INTRODUCTION

A sexually transmitted infection (STI) is defined as an infection that results from transmission of a pathogenic organism by sexual contact (i.e., any genital or anal contact with another person’s genitals, anus, or mouth) and that accounts for a noticeable amount of illness in the general population or in a defined subpopulation [1][2]. Although there is no consensus on when the terms STI and sexually transmitted disease (STD) should be used, the American Sexual Health Association (ASHA) makes a distinction between the two terms [3]. The concept of “a disease,” as in STD, suggests a clear medical problem, usually some obvious signs or symptoms. However, most people infected with one or the other of several of the most common STIs do not manifest signs or symptoms, or have mild signs and symptoms that can be easily overlooked. A sexually transmitted virus or bacterium can infect its host, which may or may not result in “a disease.” In this article, we use the term STI.

–

Organisms such as hepatitis B virus (HBV) that cause infections via sexual transmission can also cause infections via other routes, such as percutaneous transmission by contaminated needles and vertical transmission in utero or during delivery. As a typical STI, HBV infection is present in all types of populations. Sexual contact and vertical transmission from mother to infant are responsible for the large majority of HBV infections worldwide [4].

–

HBV infection as an STI is well documented. It is mainly common among men who have sex with men (MSM), because multiple partners are common in this population; and anal sex is usually more traumatic than vaginal intercourse, resulting in increased risk of exposure to blood [4][5]. HBV infection is also extremely common among heterosexual individuals who have multiple sex partners or contact with sex workers [6].

–

Routine immunization with hepatitis B (HB) vaccine is strongly recommended for the prevention of HBV infection in MSM and other individuals at risk for STIs. HB vaccination of adults has been found to be effective at conferring immunity to individuals who are exposed to HBV via sexual transmission. However, the first priority is directly preventing the spread of HBV by the most reliable and appropriate method, which is use of a condom for safe sexual contact.

–

Chronic HBV infection is the cause of chronic hepatitis, cirrhosis, and hepatocellular carcinoma (HCC) [7]. The goals of antiviral therapy for patients with chronic HBV are to slow the progression of chronic liver disease and decrease the development of complications, including cirrhosis and HCC. At present, pegylated interferon alfa (PEG-IFN-α), entecavir, and tenofovir disoproxil fumarate (tenofovir) are available for the treatment of HBV infection [8]. Sodium taurocholate cotransporting polypeptide (NTCP) was recently identified as the receptor for HBV entry into hepatocytes [9]. Because NTCP is essential for HBV infection, it may have potential as a new therapeutic target.

–

The purpose of this article is to provide up-to-date information on HBV and HBV infection as a major STI.

ETIOLOGY AND MECHANISMS OF HBV INFECTION

Etiology

Hepatitis B virus (HBV)

HBV is classified in the family Hepadnaviridae. It is a very small, partially double-stranded DNA virus. Humans are known to be the only natural host. HBV reaches the liver through the systemic circulation and can only replicate in hepatocytes [10]. Since HBV is a hepatotropic virus, injury to the liver results from the immune-mediated destruction of infected hepatocytes [6].

–

The infectious HB virion has a diameter of 42-47 nm and is a double-shelled particle in serum. Its concentration can be as high as 108 virions per mL [6][10]. The infectious HB virion consists of an outer lipoprotein coat (also called envelope) containing hepatitis B surface antigen (HBsAg). HBsAg surrounds an inner nucleocapsid composed of hepatitis B core antigen (HBcAg) that encapsidates the HBV genome and DNA polymerase [11][12].

–

Genome structure and proteins

The HBV genome consists of a partially double-stranded, circular DNA molecule. Its total genome is 1700-2800 nucleotides long or 3020-3320 nucleotides long (for the short and full-length strand, respectively). Every nucleotide in the genome is active in 4 highly overlapping coding regions, or open reading frames (ORFs), as shown in Fig. 1 [13][14][15][16]. The polymerase gene (P gene) encodes the key enzyme for replication of the genome [13]. The enzyme has DNA polymerase (DNA Pol), reverse transcriptase (RT) and RNase H activities, and also acts as the terminal protein (TP) [13][17]. The core gene (C gene) has at least two in-frame start codons, and encodes HBcAg and HBeAg [13]. HBcAg is the protein that encapsidates the viral DNA. It can also be expressed on the surface of hepatocytes, and evokes the cellular immune response [18]. HBeAg is a marker of active viral replication [13]. Secreted HBeAg is significantly more efficient than intracellular HBcAg at producing T-cell tolerance [19]. The surface gene (S gene) encodes three different envelope glycoproteins, known as the pre-S1, pre-S2, and S proteins. The pre-S1 protein (large HBsAg) is the largest of the HBV surface proteins, and is produced starting at the first initiation codon of the ORF. The pre-S2 protein (middle HBsAg) is produced starting at the second initiation codon. The S protein (small HBsAg), which is commonly referred to as HBsAg or the Australia antigen, is produced starting at the third initiation codon. The X gene encodes the multifunctional X protein [13]. It controls the level of HBV replication and acts as a cofactor in the development of HCC [20].

–

FIGURE 1: Structure and organization of the HBV genome [16]. The four protein-coding regions are shown by semicircular arrows. They include the precore (pre-C) and core gene (C gene); the polymerase gene (P gene); the X gene; and the envelope genes pre-S1, pre-S2, and S (S gene). The positions of the direct repeats (DR1 and DR2) are indicated. Genome positions may change, depending on the HBV genotype [16]. Abbreviations: HBV, hepatitis B virus; P gene, the polymerase gene; C gene, the core gene; S gene, the surface gene.

Natural history of HBV infection

HBV infection can cause acute hepatitis, acute liver failure, or chronic hepatitis, or can cause an asymptomatic infection. Chronic HBV infection can result in cirrhosis or HCC. The probability that a person with HBV infection will progress to chronic infection is strongly dependent on the person’s age at the time of HBV infection [21]. More than 90% of HBV-infected infants and 25%-50% of children infected between the ages of 1 and 5 years will develop chronic hepatitis. More than 25% of HBV-infected infants and children older than 6 years will develop HBV-related cirrhosis and HCC [10]. The rate of progression to cirrhosis and HCC is less than 1% per year for patients in the inactive chronic hepatitis stage, while the rate of progression to cirrhosis may be 2%-10% per year for patients in the immune active stage. By contrast, less than 10% of older children and adults with acute hepatitis progress to chronic infection. The progression from cirrhosis to HCC may occur in 2%-4% of adult patients per year [22].

–

In addition to age when first infected, the rates of progression of HBV infection are generally affected by gender, the level of HBV replication, HBV genotypes and variants, coinfecting viruses (hepatitis C virus [HCV], hepatitis delta virus [HDV], human immunodeficiency virus [HIV]), host lifestyle (drinking, smoking), exposure to carcinogenic substances, host genetic factors, and probably comorbidities (metabolic syndrome, diabetes and obesity) [22].

–

The natural history of chronic HBV infection can be separated into five stages, which are not necessarily sequential [23]. These stages are summarized in Table 1 [6].

Table 1. Stages of chronic HBV infection [6]. Abbreviations: HBV, hepatitis B virus; HBeAg, hepatitis B e antigen; ALT, alanine aminotransferase; anti-HBe, antibody to hepatitis B e antigen; HCC, hepatocellular carcinoma; HIV, human immunodeficiency virus.

–

Stage 1:”Immune tolerant”

The initial stage represents the incubation period. When HBV is actively replicating, HBV DNA, HBeAg, and HBsAg are detected in the serum [24]. The serum alanine aminotransferase (ALT) is only slightly or not elevated, and the infected person is not symptomatic. The immune response is limited to production of antibody to hepatitis B core antigen (anti-HBc) (immunoglobulin M [IgM] followed by immunoglobulin G [IgG]); however, these antibodies do not neutralize the infection [25]. This first stage occurs more frequently and has a longer duration in babies infected during delivery or during the first years of life [23]. There are only few or no findings of fibrosis. In this stage, though treatment is not generally indicated, monitoring is required.

–

Stage 2:”Immune active” (HBeAg-positive chronic hepatitis)

HBeAg can be detected in the serum. A somewhat lower level of HBV DNA is seen in some patients, who are clearing HBV, than in stage 1 [24]. Compared with the previous stage, the serum ALT level is higher, and there is moderate or severe liver necroinflammation and more rapid progression of fibrosis [23][26][27][28]. For patients with chronic HBV infection, 10 years or more may pass before cirrhosis develops, immune clearance takes place, or HCC develops. The immune response reduces the level of HBV replication, and begins to clear HBeAg and HBsAg. The rate of development of antibody to hepatitis B e antigen (anti-HBe) and HBeAg clearance (HBeAg seroconversion) is 10%-20% per year. Chronic infection will develop in 80%-90% of infected infants [29], whereas less than 5% of infected adults will fail to resolve acute hepatitis [30]. This stage ends with HBeAg seroconversion [23]. In this stage, treatment may be indicated.

–

Stage 3: Inactive chronic hepatitis “immune control” (previously called inactive carrier)

The stage of inactive chronic hepatitis may follow the seroconversion to anti-HBe and clearance of HBeAg. The stage is characterized by very low or undetectable HBV DNA in the serum and serum aminotransferase levels in the reference range [23]. Through immunological control of HBV infection, the majority of patients will have a favorable outcome with very low risk of cirrhosis or HCC [31][32]. HBsAg is still present in the serum, but HBsAg clearance and development of antibody to hepatitis B surface antigen (anti-HBs) may occur spontaneously in 1%-3% of cases per year [33]. In this stage, although treatment is not generally indicated, monitoring for reactivation and HCC is required.

–

Stage 4:”Immune escape” (HBeAg-negative chronic hepatitis)

The HBeAg-negative chronic hepatitis stage may follow clearance of HBeAg and development of anti-HBe during the inactive chronic infection stage (stage 3) or directly from the immune active/clearance stage (stage 2). It is important to distinguish inactive HBV carriers from individuals negative for HBeAg who have chronic hepatitis. The former patients will have a good outcome with a very low risk of complications, while the latter have a high risk of progressive liver disease, including decompensated cirrhosis and HCC [23]. In this stage, treatment may be indicated.

–

Stage 5:”Reactivation” or “acute-on-chronic hepatitis”

In the final stage, HBV reactivation may occur spontaneously or may be triggered by cancer chemotherapy or other immunosuppressive therapies, and may result in serious acute-on-chronic hepatitis. Occult HBV infection is defined as persistence of HBV DNA in the liver of individuals in whom HBsAg is undetectable in the blood. Individuals who have cleared HBsAg and are negative for serum HBV DNA but anti-HBc positive may develop reactivation if they are being treated with potent immunosuppressive medications [6].

–

HBsAg loss before the onset of cirrhosis is associated with improved outcome, with a reduced risk of cirrhosis, decompensation, and HCC [23]. If cirrhosis develops before natural or treatment-induced clearance of HBsAg, patients remain at risk of HCC [34]. In this stage, treatment is indicated.

–

HBV life cycle

NTCP was recently identified as a receptor for HBV entry, which enabled the establishment of a susceptible cell line that can efficiently support HBV infection. This discovery should lead to a deeper understanding of the requirements for effective HBV infection and clarification of the molecular mechanism of HBV entry.

–

The replication cycle of HBV begins with entry of the virus into hepatocytes, which is mediated by the binding of the pre-S1 region on the virion envelope to the hepatocellular NTCP [13]. The virion is then uncoated and transported into the nucleus. The viral relaxed circular DNA (rcDNA) or linear DNA genome, with a protein attached to the 5’ end of the minus strand and a short RNA attached to the 5’ end of the plus strand [35], is converted into covalently closed circular DNA (cccDNA) through covalent ligation [14].

–

This cccDNA is responsible for viral persistence and is highly resistant to antiviral therapy. It serves as the template for the transcription of viral mRNAs. The pregenome mRNA serves for the synthesis of core protein (nucleocapsid subunit) and viral reverse transcriptase. The viral genome is replicated by reverse transcription of pregenomic RNA. During this process, both the protein and the RNA are removed [35]. The reverse transcriptase binds to the 5’ end of its own mRNA template, and the complex is then packaged into nucleocapsids, where viral DNA synthesis occurs. These nucleocapsids can also move into the nucleus to increase the copy numbers of cccDNA. Since cccDNA does not undergo semiconservative replication, all cccDNA copies result from viral DNA made in the cytoplasm via the reverse transcription pathway [36].

–

An increase in the level of viral envelope proteins inhibits synthesis of high levels of cccDNA, which can be toxic to hepatocytes. Once partially double-stranded DNA has been produced, nucleocapsids can undergo a maturation event that enables them to obtain an outer envelope via budding into the ER. The mature nucleocapsids may be recycled into the nucleus to mediate viral persistence, or secreted as Dane particles through exocytosis to infect other hepatocytes [35] (Fig. 2) [37][38][39].

–

FIGURE 2: Schematic representation of the HBV lifecycle, from entry into hepatocytes to release from hepatocytes. Entry: HBV (Dane particle) obtains entry into hepatocytes by binding to the receptor NTCP [37][38][39] and possible additional hepatocyte-specific factors on the cell surface. The HBV membrane fuses with the membrane of the host hepatocyte, and the virion is endocytosed. Uncoating: The HBV membrane releases the viral DNA (partially double-stranded circular DNA) with the core particle into the cytoplasm [39]. The viral membrane is lost (uncoating). The viral nucleocapsid containing the viral genomic DNA is transported into the nucleus in the relaxed circular form. Repair and cccDNA formation: In the nucleus, the viral DNA polymerase synthesizes fully double-stranded DNA, and fully double-stranded DNA is converted to a cccDNA by the viral DNA polymerase [38][39]. The formation of cccDNA remains poorly understood. It is most likely formed via the DNA repair mechanism [38]. Transcription: cccDNA is transcribed into the pregenomic and subgenomic mRNAs by host RNA polymerase [38][39]. Translation and re-verse transcription: Pregenomic RNA is the template for the translation of both DNA polymerase and the core proteins, and for reverse transcription. The DNA polymerase binds to the packaging signal of the pregenomic RNA, and both are then combined into the viral capsid, which is the core particle [38][39]. The HBV genome matures in the core particle via reverse transcription of pregenomic mRNA to DNA [39]. DNA synthesis: After synthesis of the (-) strand DNA and (+) strand DNA, the nucleocapsid, containing partially-double stranded circular DNA, is generated. Assembly: HBsAg and the nucleocapsid containing partially double-stranded circular DNA are assembled together to become a new complete virion [39]. Release: The mature HBV virion (Dane particle) is released from the infected hepatocyte or is recycled back into the nucleus for amplification of cccDNA [38]. Other events: The C gene directs the synthesis of two major gene products: HBcAg (p21c), which comprises the nucleocapsid; and HBeAg (p17e), which is a secreted antigen. Noninfectious particles (empty particles), which are composed of HBsAg, a 22-kDa precore protein (p22cr), and HBeAg, are also produced as a trap for the host immune system, in order to protect the infectious Dane particles. Serologic testing can assess HBeAg, p22cr, and HBcAg as hepatitis B core-related antigen (HBcrAg). Abbreviations: HBV, hepatitis B virus; NTCP, sodium taurocholate cotransporting polypeptide; cccDNA, covalently closed circular DNA; RC-DNA, relaxed circular DNA; HBsAg, hepatitis B virus surface antigen; HBcAg, HBV core antigen; HBV e antigen, HBeAg; p22cr, precore protein; HBcrAg, hepatitis B core-related antigen.

EPIDEMIOLOGY: INCIDENCE AND PREVALENCE

Incidence: worldwide view and HIV/HBV coinfection

More than one third of the world’s population are estimated to be infected with HBV. About 5% of the world’s population are chronic carriers of HBV, and HBV infection causes more than one million deaths every year [40]. The HBsAg carrier rate varies from 0.1% to 20% of different populations worldwide. In low-risk regions, the highest incidence of infection is seen in teenagers and young adults.

–

Based on the data from Western cohorts, HIV/HBV coinfection has a profound impact on almost every aspect of the natural history of HBV infection [6]. The consequences include higher rates of chronicity after acute HBV infection, higher levels of HBV replication and rates of reactivation, less spontaneous clearance, higher rates of occult HBV infection (i.e., detectable HBV DNA positivity in the absence of HBsAg seropositivity), more rapid progression to cirrhosis and HCC, higher rates of liver-related mortality, and decreased treatment response compared with individuals without HIV coinfection [41][42]. Recent longitudinal cohort studies have found that coinfection with HBV also can lead to increased rates of progression to acquired immune deficiency syndrome (AIDS)-related outcomes and all-cause mortality [43][44]. An estimated 5% to 15% of the 34 million HIV-infected individuals worldwide are coinfected with HBV, as a chronic infection [45][46]. The burden of coinfection is greatest in Southeast Asia and sub-Saharan Africa [6].

–

Prevalence: international statistics

An estimated 240 million people are chronically infected with hepatitis B [47]. The prevalence of chronic HBV infection varies geographically, ranging from 1% to 20%. Populations with high rates include Alaskan Eskimos, Asian-Pacific islanders, Australian aborigines, and populations of the Indian subcontinent, sub-Saharan Africa, and Central Asia. In some locations, such as Vietnam, the rate is as high as 30% [48]. The prevalence of the HBV carrier state is related to differences in the mode of transmission, including iatrogenic transmission, and the age of primary infection.

–

In low-prevalence (<2%) regions, the lifetime risk of HBV infection is less than 20%. Sexual transmission and percutaneous transmission during early adulthood are the main routes of spreading the infection. About 12% of HBV-infected individuals live in the low-prevalence regions, which include North America, northern and western Europe, Australia, and New Zealand [48]. In these areas, most HBV infections occur in adolescents and young adults belonging to relatively well defined high-risk groups, which include injection drug users, MSM, healthcare workers, and patients who undergo regular blood transfusions or hemodialysis [48][49].

–

In intermediate-prevalence (3%-5%) regions, sexual and percutaneous transmission and vertical transmission during delivery are the major routes of infection. These regions include eastern and southern Europe, Japan, the Mediterranean basin, the Middle East, Latin and South America, and Central Asia. One study reported that approximately 43% of HBV-infected individuals live in southern, central, and western Asia; eastern Europe; Russia; and Central and South America. The lifetime risk of HBV infection is 20%-60% [48]. The persistently high rates of chronic infection are mostly due to infections occurring in infants and children.

–

In high-prevalence (10%-20%) regions, transmission occurs predominantly in infants and children. During early childhood, HBV is transmitted vertically from the mother to infant or occurs via close contact. In some regions, percutaneous exposure to contaminated needles or an unsafe injection is also a possible route of HBV infection. Since most infections in children are asymptomatic, there is little evidence of acute HBV-related disease, but the rates of chronic liver disease and HCC in adults are high. Approximately 45% of individuals infected with HBV live in high-prevalence regions. The lifetime risk of infection is higher than 60%, as demonstrated by the presence of anti-HBc in sera [48]. The high-prevalence regions are mostly regions with developing economies and large populations. They include China, Southeast Asia, Indonesia, sub-Saharan Africa, the Pacific Islands, parts of the Middle East, and the Amazon Basin [48].

–

HBV serotypes and genotypes

Based on some of the antigenic determinants of HBsAg, nine serological types – referred to as subtypes adw2, adw4, adrq+, adrq-, ayw1, ayw2, ayw3, ayw4 and ayr – have been identified [50]. Ten genotypes of HBV (A-J) have been identified, and these correspond to specific geographic distributions [51]. Genotype A is more frequently found in North America, northwestern Europe, India, and Africa. Genotypes B and C are endemic to Asia, and genotype D predominates in eastern Europe and the Mediterranean [52]. Type E is found in western Africa; type F, in South America; and type G, in France, Germany, Central America, Mexico, and the United States. Type H is prevalent in Central America [48]; type I, in Vietnam; and type J (possible recombination with type C), in Japan [53].

–

HIV-seropositive MSM populations predominantly coinfected with HBV genotype A have been reported in European countries and Japan [54][55][56]. The prevalence of HBV genotype A is significantly higher in the MSM population than in the rest of the population [56]. In addition, Araujo et al. speculated in their review that HBV subgenotypes A2 and C are likely to predominate in populations at high risk of infection via sexual transmission [57]. Additionally, HBV genotype A develops into a persistent infection more often than genotype C [58][59].

–

Individuals infected with genotypes C and F have higher rates of HCC than individuals infected with genotypes B and D [6]. Evidence increasingly suggests that genotype C and F affect disease severity and response to treatment [60][61][62]. Results of studies in Asia suggest that patients infected by HBV genotype C show a more rapid progression to cirrhosis and HCC than patients infected by genotype B [63][64][65], and subgenotypes of HBV genotype C are probably responsible for the increased rate of HCC in patients who were positive for HBeAg [66]. Studies in Europe and North America have found that higher proportions of patients with chronic hepatitis associated with genotype D infection progressed to cirrhosis and HCC than those with chronic hepatitis associated with genotype A infection [26][67][68][69].

PATHOPHYSIOLOGY / SEROLOGY / SIGNS AND SYMPTOMS

Pathophysiology

Pathological findings

Currently, most liver biopsies are performed to confirm the existence of chronic hepatitis and to determine its level of activity. This section mainly describes chronic hepatitis, which plays an important role in HBV infection.

–

1) Acute hepatitis B

Because acute hepatitis B is always diagnosed by clinical symptoms and serologic markers related to HBV infection, liver biopsies are not often performed. In general, acute hepatitis shows more areas of spotty parenchymal inflammation and more severe damage than typical chronic hepatitis. The lesions mainly contain diffuse sinusoidal and portal mononuclear infiltrates (lymphocytes, plasma cells, Kupffer cells), swollen hepatocytes and/or necrotic hepatocytes (also called apoptotic or acidophilic hepatocytes, or Councilman bodies) [70][71]. Cell plates and sinusoids may be indistinct in more severe cases as a result of hepatocyte swelling, filling of sinusoids by mononuclear inflammatory cells, and regenerating hepatocytes. Significant lobular necrosis leads to acute liver failure [70].

–

2) Chronic hepatitis B and cirrhosis

In chronic HBV infection, there is a varying degree of predominantly lymphocytic portal inflammation with interface hepatitis and spotty lobular inflammation. The inflammation is minimal in the immune-tolerant or inactive chronic infection stages, but is prominent in the immune-active stage. Bridging necrosis is identified as inflammation “connecting” portal tracts to one another or to central veins [71]. Confluent necrosis affects multiple contiguous hepatocytes. Inflammation is typically associated with scarring, which can vary from a mild portal extension to periportal fibrous strands, bridging fibrosis, and cirrhosis. Livers that develop central to portal bridging necrosis or confluent necrosis are likely to have a higher fibrosis stage. The Scheuer classification for grading and staging of chronic hepatitis is often used, as shown in Table 2 [72].

–

The hepatocytes that express a high level of HBsAg may have a “ground-glass” cytoplasm, which can be highlighted by special immunohistochemical stains (Shikata’s orcein and Victoria blue). Ground-glass hepatocytes may also be seen in other conditions [73].

–

TABLE 2. Scheuer classification for grading and staging of chronic hepatitis [72].

Cirrhosis is diagnosed when the loss of normal central-portal relationships is observed. The atypical enlargement of nuclei with an increase in the nuclear-cytoplasmic ratio, known as “large cell change”, is very common in cirrhosis. This cytologic abnormality should only be used to support the evidence of regeneration and architectural abnormalities, which is used for diagnosing cirrhosis [70].

–

Diagnosis

Serologic markers related to HBV infection

The serologic markers of HBV infection are as follows: HBsAg and the corresponding antibody anti-HBs, HBeAg and the corresponding antibody anti-HBe, immunoglobulin M antibody to hepatitis B core antigen (IgM anti-HBc), immunoglobulin G antibody to hepatitis B core antigen (IgG anti-HBc), and serum HBV DNA. The diagnosis of acute or chronic HBV infection requires serologic testing (Table 3) [2]. The first detectable markers in acute HBV infection are HBsAg and IgM anti-HBc.

–

Total anti-HBc is present over the entire lifetime of the infected individual. It is found in individuals with chronic HBV infection and in those who recover from HBV infection [10]. The presence of anti-HBc alone might indicate acute, resolved, or chronic infection, or a false-positive result [2]. HBsAg and HBeAg can be used as surrogate markers of HBV replication [74]. HBsAg is eliminated from the sera of individuals who recover from HBV infection, and anti-HBs is detectable during recovery [10]. Detection of HBsAg indicates early acute infection. To ensure that an HBsAg-positive test result is not false positive, samples with repeatedly reactive HBsAg results should be tested with a US Food and Drug Administration (FDA)-cleared neutralizing confirmatory test [2]. HBeAg is a marker of high levels of viral replication. Detection of HBeAg indicates that the blood and body fluids of an infected person are highly infectious. Detection of anti-HBeAg indicates inactive chronic hepatitis. The persistence of HBeAg for longer than 10 weeks and/or HBsAg and serum HBV DNA for longer than 6 months, indicates transition to chronic HBV infection [74]. Detection of anti-HBs indicates immunity against HBV. Anti-HBs can also be detected in individuals who were immunized by the HB vaccine. Most individuals who recover from HBV infection are expected to be positive for both anti-HBs and anti-HBc [10]. Individuals positive for anti-HBc only are unlikely to be infectious, except under unusual circumstances, including direct percutaneous exposure to large quantities of blood (e.g., blood transfusion and organ transplantation) from individuals positive for anti-HBc only [2].

–

TABLE 3. Interpretation of results of serologic tests for HBV infection [2]. Symbol for negative test result, “–“; symbol for positive test result, “+.” Abbreviations: HBV, hepatitis B virus; HBsAg, hepatitis B surface antigen; anti-HBc, antibody to hepatitis B core antigen, IgM anti-HBc, immunoglobulin M antibody to hepatitis B core antigen; HBIG, hepatitis B immune globulin.

Acute hepatitis B

The incubation period (duration from exposure to HBV to onset of symptoms) of HBV-infected individuals with acute hepatitis ranges from 60 to 150 days, with an average of 90 days [75][76]. The signs and symptoms of acute hepatitis B are described in detail in the “Signs and symptoms” section. As mentioned previously, the clinical manifestations of acute HBV infection are age dependent [10]. Over 90% of infants with HBV infection are asymptomatic, while the typical manifestations of acute hepatitis are prominent in 5% to 15% of newly infected young children (aged 1–5 years) and in 33% to 50% of children older than 6 years of age [10][21]. Serologic markers related to acute hepatitis B are described in the subsection “Serologic markers related to HBV infection”. As described in that subsection, the persistence of HBeAg indicates the transition to chronic HBV infection [74].

–

Chronic HBV infection

The natural history of HBV infection, including the transition to chronic infection, is described in the “Etiology” section. Chronic HBV infection is defined as either the presence of HBsAg in the serum for at least 6 months or the presence of HBsAg in a person who tests negative for IgM anti-HBc [10]. Unlike individuals who recover from acute HBV infection, patients with chronic HBV infection do not produce anti-HBs, and serum HBsAg positivity typically persists for a long period of time [10]. In patients with chronic HBV infection, the disappearance of HBeAg and detection of anti-HBe usually indicate a reduction in viral load [77]. Each year, approximately 0.5% of adults with chronic HBV infection will clear HBsAg and produce anti-HBs [78][79][80]. Although patients with chronic HBV infection die of causes unrelated to HBV, chronic HBV infection is responsible for most of the morbidity associated with HBV [10]. Follow-up studies of individuals first infected with HBV when they were infants or young children, show that approximately 15% to 25% of patients with chronic infection die prematurely from cirrhosis or HCC [81][82].

–

Signs and symptoms

Symptoms and physical findings

The manifestations of HBV infection during the acute phase vary from subclinical hepatitis to acute hepatitis and acute hepatic failure. During the chronic phase, disease progression varies from asymptomatic chronic infection to chronic hepatitis, cirrhosis, and HCC [83]. The findings on physical examination vary from minimal to remarkable, according to disease severity. The signs, symptoms, and findings on physical examination are listed in Table 4.

–

TABLE 4. Manifestations of hepatitis B virus infection.

Acute hepatitis B is an illness that begins with general fatigue, loss of appetite, nausea, vomiting, body aches, low-grade fever, dark urine, and jaundice. The illness lasts for several weeks and then gradually improves in most affected individuals. A few individuals may develop more severe liver disease (acute hepatic failure) and may die. In addition, acute hepatitis B infection may be entirely asymptomatic and may go unrecognized [84].

–

Some acute hepatitis B patients (about 1%) may develop acute liver failure, which is characterized by evidence of decompensated liver disease and is fatal in up to 50% of cases [83]. Patients with acute liver failure can present with the following signs and symptoms: hepatic encephalopathy, somnolence, disturbed sleep patterns, mental confusion, coma, ascites, variceal bleeding, and coagulopathy.

–

Individuals with chronic HBV infection may be asymptomatic or may manifest the signs and symptoms associated with chronic hepatic inflammation. Patients with chronic active hepatitis, especially during the replicative stage, can manifest symptoms similar to acute hepatitis (fatigue, anorexia, nausea, and mild upper quadrant pain or discomfort). Physical examination of patients with chronic HBV infection can reveal the typical characteristics of chronic liver disease, including hepatomegaly, splenomegaly, muscle wasting, palmar erythema, spider angioma, and vasculitis.

–

In cases with progressive liver disease, the following manifestations may be present: hepatic decompensation, hepatic encephalopathy, somnolence, disturbed sleep patterns, mental confusion, coma, ascites, variceal bleeding, coagulopathy, ascites, jaundice, peripheral edema, gynecomastia, testicular atrophy, and collateral abdominal veins (caput medusa). Pleural effusion and hepatopulmonary and portopulmonary syndrome may occur in patients with cirrhosis. Patients with cirrhosis may have the following findings: ascites, jaundice, history of variceal bleeding, peripheral edema, gynecomastia, testicular atrophy, and collateral abdominal veins.

–

Extrahepatic manifestations

Extrahepatic manifestations of HBV infection occur in 1% to 10% of patients, and include serum-sickness-like syndrome, acute necrotizing vasculitis (polyarteritis nodosa), membranous glomerulonephritis (MGN) [85], and papular acrodermatitis of childhood (Gianotti-Crosti syndrome) [86][87]. Serum-sickness-like syndrome occurs in the setting of acute hepatitis B, often preceding the onset of jaundice [88]. The manifestations often subside shortly after the onset of jaundice, but can persist throughout the duration of acute hepatitis B [11]. About 30% to 50% of people with acute necrotizing vasculitis (polyarteritis nodosa) are HBV carriers [89]. HBV-associated nephropathy has been described in adults but is more common in children [90][91]. MGN is the most common form. Other immune-mediated hematological disorders, such as essential mixed cryoglobulinemia and aplastic anemia, can also occur [11].

–

A variety of cutaneous lesions can appear during the early course of viral hepatitis, including transient maculopapular rash.

TRANSMISSION AND PROTECTION

Transmission

As described previously, HBV is transmitted mainly via percutaneous or permucosal exposure to HBV-containing body fluids. The most critical source of infection is blood (serum) [92]. HBV transmission has been found to occur through various forms of human contact, including vertical transmission from mother to newborn, sexual contact, close household contact, needle sharing, and occupational (healthcare) exposure (horizontal transmission) [10]. HBV transmission can result from the accidental inoculation of small amounts of blood or other body fluids during medical procedures [6]. Nowadays, blood transfusion and organ transplantation are extremely rare routes for HBV transmission. This section will primarily focus on sexual transmission, which is a common route of HBV infection.

–

HBV is efficiently transmitted by sexual contact [10]. The primary risk factors are unprotected sex with an HBV-infected partner, mainly unvaccinated MSM and heterosexual individuals with multiple sex partners or contact with sex workers [6]. MSM have long been known to have high rates of STIs [93]. They continue to show higher seroprevalence rates of HBV-related markers than the general population [94]. Progression through the infection stages is very rapid, and the immune tolerant stage is sometimes absent [24][95].

–

Heterosexual transmission is still important, as shown by the 40% transmission rate to nonimmune partners of patients with acute HBV hepatitis or chronic HBV infection [96][97]. The seroprevalence rates of HBV-related markers are positively correlated with increasing numbers of current and lifetime heterosexual partners [98][99].

–

Protection

Behavioral approaches

The 2015 Centers for Disease Control and Prevention (CDC) guidelines describe five major strategies for the prevention and control of STIs (Table 5) [100]. For primary prevention, the first approach is to change the sexual behavior that can increase the risk of STIs. Information on sexual behavior that can increase the risk of STIs should be provided tactfully. In addition, adolescents and young adults should be made aware that some of the information on protection against STIs may be inaccurate [100]. Correcting misinformation on protection against STIs may also reduce the incidence of high-risk sexual behavior [101]. One of the most reliable methods for preventing an STI is refraining from sexual contact, which includes oral, vaginal, and anal sex [100].

–

TABLE 5. Major strategies for prevention and control of STIs [100]. Abbreviation: STIs, sexually transmitted infections.

Over the past 10 years, condom use by unprotected heterosexuals has increased in the United States, suggesting that information on the prevention of STIs is being widely disseminated and understood [102]. Additionally, possible sexual partners should be tested for STIs before sexual contact is initiated [100]. If one partner has an STI or his/her infection status is unknown, a new condom should be used for each sexual contact.

–

In summary, safe sex practices, including minimizing the number of sex partners and using barrier protection, can reduce the risk of HBV infection.

–

Hepatitis B immune globulin (HBIG) and hepatitis B (HB) vaccine

Both HBIG and HB vaccines have been approved for preventing HBV infection [103][104].

–

HBIG is prepared from human plasma containing a high concentration of anti-HBs and provides short-term (3 to 6 months) protection from HBV infection. It is typically used as post-exposure prophylaxis along with HB vaccination for individuals who have never been vaccinated or who have not responded to HB vaccination. The recommended dose of HBIG is 0.06 mL/kg [100].

–

HB vaccines contain HBsAg that is produced by a recombinant yeast strain [105]. Epidemiologic studies have not found any evidence of an underlying association between HB vaccination and sudden infant death syndrome or other causes of death during the first year of life [106][107]. Thus, HB vaccination can be considered safe.

–

HB vaccination is the most effective method of preventing HBV infection [108]. The introduction of universal HB vaccination for newborns has been reported to be a very reasonable and cost-effective strategy [109][110]. The World Health Organization (WHO) has now included HB vaccination in the Expanded Program on Immunization [22]. WHO recommends that all infants receive HB vaccine as soon as possible after birth, preferably within 24 hours. In 2013, 183 WHO member states immunized infants against HBV as a part of their routine vaccination schedule, and 81% of children received HB vaccines [47].

–

HB vaccine is available for younger children, adolescents, and healthy adults [2]. In adolescents and healthy adults (aged younger than 40 years), approximately 30% to 55% of recipients achieve protective antibody responses (i.e., anti-HBs ≥10 mIU/mL) after the first vaccination, 75% after the second, and over 90% after the third. Therefore, HB vaccination can be thought to induce protective antibody response (anti-HBs ≥ 10 mIU/mL) in the majority of recipients. Regardless of the specific patient considerations needed when an HB vaccination schedule is selected, a complete vaccine series should be administered [100]. Recommendations on the HB vaccine dosage and schedule vary, depending on the product used and the recipient’s age [2]. Details on HB vaccination are described in guidelines [6][104].

–

HB vaccine-induced immune memory has been established to last for more than 20 years [111][112][113]. According to the 2015 CDC guidelines, periodic monitoring of anti-HBs levels after routine HB vaccination is not needed, and booster doses of HB vaccine are not currently recommended [2]. However, the American Red Cross report suggests that HB-vaccine-induced immune memory might be limited; although HB vaccination can prevent clinical liver injury (hepatitis), 100% of subclinical infections cannot be prevented [114]. Indeed, although HB vaccine is sufficiently effective at preventing the development of clinical disease (hepatitis), it cannot prevent 100% of HBV infections, resulting in detectable anti-HBc [114]. Additionally, there is a report of acute hepatitis B infection in a patient who received five HB vaccinations [115]. An MSM patient, who received several HB vaccinations and showed an anti-HBs serological response of >10 mIU/mL (accepted threshold for protection), was reported to have developed a chronic HBV genotype F infection [116]. These cases suggest that monitoring anti-HBs levels after routine vaccination might be necessary for certain patients. When the anti-HBs level is too low to provide protection from HBV infection (anti-HBs <10 mIU/mL), a booster vaccination should be administered. Although HB vaccines are highly immunogenic, postvaccination serologic testing might be indicated for infants whose mothers were infected at delivery, individuals with occupational exposure to blood, sexually active individuals such as MSM, or immunosuppressed individuals [10].

–

Pre-exposure vaccination

In 1992, WHO recommended that all countries should introduce universal HB vaccination into their routine immunization programs [117]. HB vaccination is recommended for all unvaccinated children and adolescents, all unvaccinated adults with risk of HBV infection (especially MSM, adults with multiple sex partners, and drug users), and all adults desiring protection from HBV infection [104]. HB vaccine should be routinely offered to all unvaccinated persons who attend STI clinics or seek evaluation or treatment for STIs in other settings, especially correctional facilities, facilities providing treatment and prevention services for substance use disorder, and settings serving MSM (e.g., HIV care and prevention settings) [2].

–

Postexposure prophylaxis

Both passive-active postexposure prophylaxis (simultaneous administration of HBIG and HB vaccine at separate sites) and active postexposure prophylaxis (administration of HB vaccination alone) have been demonstrated to be highly effective for preventing HBV infection [103]. Unvaccinated individuals or those known not to have received a complete HB vaccine series should receive both HBIG and HB vaccine as soon as possible (preferably ≤24 hours) after exposure to blood or body fluids containing HBsAg. HB vaccine should be administered at the same time as HBIG, but at a separate injection site; and the HB vaccine series should be completed, using the age-appropriate vaccine dose and schedule [2]. Individuals with certification that they received a complete HB vaccine series and who have never undergone post-vaccination serologic testing should receive a single vaccine booster dose. These individuals should be treated according to guidelines for the management of individuals with occupational exposure to blood or body fluids that contain HBV [118].

TREATMENT AND CURABILITY

Treatment

The primary treatment goals for patients with HBV infection are preventing the progression to severe liver disease. The prevention of cirrhosis, hepatic failure, and HCC are most important. The risk factors for progression of chronic HBV include male gender, older age, family history of HCC, elevated alpha-fetoprotein (AFP) level, and coinfection with other viruses (HCV, HDV, or HIV) [119].

–

For the best outcome, a synergistic approach that decreases the viral load and uses immunotherapeutic interventions to boost the immune response is needed [120]. The prevention of HCC often includes antiviral treatment using pegylated interferon (PEG-IFN) or nucleos(t)ide analogues (NAs), which are described later [121].

–

Overall management for types of HBV infection

Patients with acute hepatitis B are treated by supportive care, with no specific treatment. Patient care is focused on maintaining comfort and adequate nutritional balance, including replacement of fluids lost from vomiting and diarrhea. Patients with chronic HBV infection should be referred for evaluation to a provider experienced in the management of chronic HBV infection [122]. A variety of treatment algorithms have been proposed, including ones from the American Association for the Study of Liver Diseases (AASLD) [28], the European Association for the Study of the Liver (EASL) [23], the Asian Pacific Association for the Study of the Liver (APASL) [123], the Canadian Association for the Study of the Liver (CASL) [124], and the National Institute for Health and Clinical Excellence (NICE) [125].

–

In general, for patients with chronic HBV infection who are positive for serum HBeAg, treatment is advised when the serum level of HBV DNA is at or greater than 20,000 IU/mL (10⁵ copies/mL) (or >2,000 IU/mL [EASL recommendation]) and the serum ALT level is elevated (>20 U/L for females and 30 U/L for males) for 3-6 months. For patients with chronic HBV infection who are negative for HBeAg, treatment is advised when the serum level of HBV DNA is at or greater than 2,000 IU/mL (10⁴ copies/mL) and the serum ALT is elevated (>20 U/L for females and 30 U/L for males) for 3-6 months [126].

–

Treatment of HIV infection with nucleos(t)ide analogs active against HBV greatly improves the outcomes of hepatic disease, including cirrhosis and HCC, in HIV-HBV coinfected patients, especially when tenofovir is part of the antiviral regimen [127]. HBV/HDV coinfection should be treated with PEG-IFN therapy [128].

–

The National Institutes of Health (NIH) also advises that immediate therapy is not usually indicated for the following patients: 1) patients who are in the immune-tolerant stage, with chronic hepatitis B and high serum levels of HBV DNA but normal serum ALT levels or little activity on liver biopsy; 2) patients who are in an inactive chronically infected/low replicative stage and have low serum levels of or undetectable HBV DNA and normal serum ALT levels; and 3) patients who are not immunosuppressed and have latent HBV infection, defined as detection of HBV DNA in the absence of HBsAg [126].

–

Pharmacologic management

The therapeutic agents cleared by FDA for the treatment of chronic hepatitis B can achieve sustained suppression of HBV replication and remission of liver disease [122]. Currently, PEG-IFN-α 2a, entecavir, and tenofovir are available for the treatment of HBV infection. These are the main treatments that have been approved worldwide. Lamivudine, telbivudine, and adefovir are now “nonpreferred” agents, and considered to be of historical interest [129].

–

Pegylated interferon alpha 2a (PEG-IFN-α 2a)

IFNs are naturally produced cytokines. They induce direct antiviral activity by stimulating the host’s antiviral immune response and mediating conflicting effects on viral replication. PEG-IFN-α 2a has a longer half-life and enhanced efficacy relative to standard IFN-α. Pegylation lowers the rate of absorption following subcutaneous injection, reduces renal clearance, and decreases the immunogenicity of IFN [130].

–

The advantages of IFN therapy are the absence of viral resistance, the finite course of treatment (normally 48 weeks), an increased chance of sustained virological response (SVR), and HBeAg and HBsAg clearance; compared with patients treated by NAs [131]. A 48-week regimen of PEG-IFN-α 2a has been found to induce HBeAg seroconversion in 27% of patients and disappearance of serum HBV DNA in 25% of patients [130]. Long-term studies have demonstrated that IFN treatment is associated with a significant reduction in the risk of cirrhosis and HCC, even in patients who fail to clear HBeAg [24]. However, IFN has a poor side-effect profile (including persistent flu-like symptoms and psychiatric complications) compared with NAs, requires subcutaneous injection, and is not recommended for patients with decompensated cirrhosis [25]. HBV genotypes A and D are important and independent predictors of IFN responsiveness in patients with chronic hepatitis B [132]. IFN treatment is more effective for patients who are most likely to benefit, especially younger patients, who have more potential years in which to develop complications from their chronic hepatitis B infection and thus have more to gain from achieving an SVR [25][95].

–

Nucleos(t)ide analogues (NAs)

The NIH recommends nucleos(t)ide therapy for the treatment of HBV-infected patients with acute liver failure as well as for cirrhotic patients who are positive for serum HBV DNA; and for patients with clinical complications, cirrhosis, advanced fibrosis with serum positive for HBV DNA, or reactivation of chronic HBV during or after chemotherapy or immunosuppression [126].

–

Entecavir, a guanosine nucleoside analogue, is a first-line agent for the treatment of HBV infection [51]. It is a powerful inhibitor of HBV polymerase. It competes with the natural substrate, deoxyguanosine triphosphate (dGTP), to inhibit HBV polymerase (reverse transcriptase) activity. The advantages of therapy with this agent include potent antiviral activity and a low rate of resistance to the drug [51], although entecavir is used less frequently than other agents for the treatment of lamivudine-resistant HBV.

–

Results of a retrospective study indicated that assessment of serum HBV DNA levels 12 months after initiation of entecavir therapy may be useful for evaluating entecavir therapy for NA-naïve, HBV-infected patients [7]. Investigators found 3 independent predictors for viral suppression lasting 3 years after the start of entecavir therapy: the lowest level of HBV DNA that can be detected, undetectable serum HBV DNA at month 12, and seronegative for HBeAg at the start of therapy. Serum HBV DNA undetectable at month 12 also increased the probability of HBeAg seroconversion and lowered the risk of drug resistance [133].

–

In another study, after 240 weeks of continuous entecavir therapy for HBeAg-positive patients, 94% of patients had less than 300 copies/mL of serum HBV DNA, and 80% had normal ALT levels. An additional 23% of patients achieved HBeAg seroconversion, and HBsAg disappeared in 1.4% of the patients. Only 1 patient developed resistance to treatment with entecavir within 5 years of treatment [134].

–

Another study found that long-term treatment with entecavir (about 6 years of cumulative therapy [range, 267-297 weeks]) for NA-naïve patients with chronic HBV infection and advanced fibrosis or cirrhosis, resulted in durable virologic suppression, continued histologic improvement, and reversal of fibrosis or cirrhosis [135].

–

Tenofovir is the newest antiviral agent. It is a nucleotide-analogue (adenosine monophosphate) inhibitor of viral reverse transcriptase. It may be used as first-line therapy for treatment-naïve patients [51]. Patients who received tenofovir continuously for 240 weeks had sustained suppression of serum HBV DNA levels (less than 400 copies/mL). The rate of viral suppression in patients negative for HBeAg was 83%, and in patients positive for HBeAg was 65%. Of the patients positive for HBeAg who received tenofovir through 240 weeks, the rate of disappearance of HBsAg was 9%, and the HBsAg seroconversion rate was 7%. The rate of disappearance of HBeAg was 46%, and the HBeAg seroconversion rate was 40%. There was no evidence of resistance to tenofovir over the treatment period [125]. Of note, follow up of the same cohort revealed that after 4.5 years of tenofovir, 87% had histological improvement, 51% had regression of fibrosis, and 74% of the patients with cirrhosis at baseline were no longer cirrhotic [136].

–

Monitoring considerations

The tests that should be used and the frequency of testing will depend on the patient’s serological profile (HBeAg-positive or -negative) and HBV DNA viral levels [126]. Patients with chronic active hepatitis should undergo blood testing (aminotransferase levels, HBV status, viral load, and AFP levels), as well as treatment.

–

For individuals with inactive chronic HBV infection, the current guidelines recommend monitoring for serum HBV DNA and ALT levels at least annually [23][28][137]. Patients with cirrhosis must be monitored for HCC by determination of AFP levels every 6 to 12 months and undergoing surveillance by abdominal ultrasonography [28][137]. Note, however, that determination of AFP levels was excluded from the AASLD guidelines [28].

–

Curability

Despite notable progress regarding many aspects of HBV infection, particularly with respect to prevention and treatment, chronic HBV infection remains strictly noncurable, because residual HBV cccDNA can always be detected in the liver, even after clearance of HBsAg and development of anti-HBs in the serum [138]. Moreover, HBV DNA sequences can integrate into the hepatocyte genome, as demonstrated in individuals seronegative for HBsAg [139]. Therefore, the term “cure” cannot be used to indicate that HBV is completely eradicated.

–

There is ongoing discussion on the meaning of “’cured’ of chronic HBV infection”. The primary treatment goal for HBV infection is to improve patient quality of life and reduce the risk of death from liver disease [140]. Large cohort studies of patients with chronic hepatitis B have found a 15% to 40% cumulative risk of developing cirrhosis. Two to five percent of patients with established cirrhosis will develop HCC [141]. Three possible types of cure are identified, which are described below [140].

–

“Absolute cure” means that the patient is free of HBV. That is, there are no HB virions and cccDNA anywhere in the body, including hepatocytes. The patient recovers to the degree of health and medical condition prior to HBV infection, and the probability of developing cirrhosis or HCC depends on age and gender. Although this type of cure is uncommon, it is the most desirable [140].

–

“Functional cure” means that HBV progression can be controlled. The patient recovers to his or her state of health equal to that of a person who has recovered spontaneously from HBV infection. Both have a similar likelihood of developing cirrhosis or HCC. Current therapy can only achieve “functional cure” through suppression of HBV replication [140].

–

“Apparent virologic cure” is defined as a sustained off-drug suppression of virologic markers and the normalization of liver function. This last definition includes an SVR, which is the ongoing suppression of viral load following the cessation of therapy, and adds the disappearance of all circulating viral markers (seroclearance), and the possible suppression of cccDNA. A complicating factor with HBV infection is that patients who have achieved a serologic resolution of infection (loss of HBsAg, undetectable serum HBV DNA, appearance of anti-HBs) can develop reactivation of their disease because of immunosuppression or the use of anti-inflammatory medications [142][143]. In addition, it is important to note that in occult HBV infection, despite the complete loss of HBsAg and undetectable or very low levels of HBV DNA in serum, there may still be an increased risk for progression to cirrhosis and the development of HCC [144].

–

An “apparent virologic cure” or “functional cure” as a desirable endpoint for therapy is supported by a recent study looking at the risk of HCC in patients with or without spontaneous seroclearance of HBV seromarkers [145]. However, none of these endpoints turned out to be a reliable indicator of favorable long-term outcome of chronic HBV infection. Thus, for the time being, HBsAg loss is viewed as the best possible predictor of a favorable long-term outcome of HBV infection and is used as an endpoint [146][147].

CONCLUSIONS

HBV infection is one of the common STIs having a major worldwide impact on a patient’s clinical health status and on public health, and is also associated with liver-related morbidity and mortality. New HBV infections in industrialized countries are becoming increasingly concentrated among individuals at risk for STIs, infants, and injection drug users. HB vaccines have been an effective prevention strategy for individuals at risk through sexual exposure, especially MSM and heterosexuals with multiple sex partners. The proper education of persons at risk for STIs may also help with their acceptance of HB vaccination.

–

Regarding the persistence of HB vaccine-induced immunity, the effectiveness of routine HB vaccination might not last long enough to prevent 100% of HBV infections. In our opinion, postvaccination serologic testing, especially for anti-HBs, should be introduced for groups at high risk for HBV infection, after careful consideration. Potential causes of vaccine failure, such as infection with HBV variants, require further study. The need for booster doses to preserve vaccine-induced immunity should be evaluated regularly, especially for infants whose mothers were infected, individuals with occupational risk, sexually active individuals such as MSM, or individuals under immunosuppression.

References

1. . World Health Organization, "Sexually transmitted infections (STIs)", Available at: http://www.who.int/mediacentre/factsheets/fs110/en/. Accessed: 29.04.2016, 2015.
2. K.A. Workowski, G.A. Bolan, and . , "Sexually transmitted diseases treatment guidelines, 2015.", MMWR. Recommendations and reports : Morbidity and mortality weekly report. Recommendations and reports, 2015. http://www.ncbi.nlm.nih.gov/pubmed/26042815
3. . ASHA, "STDs/STIs", Available at: http://www.ashasexualhealth.org/stdsstis. Accessed 29.04.2016, 2016.
4. H.H. Handsfield, "Hepatitis A and B immunization in persons being evaluated for sexually transmitted diseases", The American Journal of Medicine, vol. 118, pp. 69-74, 2005. http://dx.doi.org/10.1016/j.amjmed.2005.07.023
5. R.S. Remis, A. Dufour, M. Alary, J. Vincelette, J. Otis, B. Mâsse, B. Turmel, R. LeClerc, R. Parent, and R. Lavoie, "Association of hepatitis B virus infection with other sexually transmitted infections in homosexual men. Omega Study Group.", American journal of public health, 2000. http://www.ncbi.nlm.nih.gov/pubmed/11029990
6. . WHO Guidelines Approved by the Guidelines Review Committee, "Guidelines for the Prevention, Care and Treatment of Persons with Chronic Hepatitis B Infection.", World Health Organization 2015., Geneva., 2015.
7. T. Chang, R.G. Gish, R. de Man, A. Gadano, J. Sollano, Y. Chao, A.S. Lok, K. Han, Z. Goodman, J. Zhu, A. Cross, D. DeHertogh, R. Wilber, R. Colonno, and D. Apelian, "A Comparison of Entecavir and Lamivudine for HBeAg-Positive Chronic Hepatitis B", New England Journal of Medicine, vol. 354, pp. 1001-1010, 2006. http://dx.doi.org/10.1056/NEJMoa051285
8. T.A. Santantonio, "Chronic hepatitis B: Advances in treatment", World Journal of Hepatology, vol. 6, pp. 284, 2014. http://dx.doi.org/10.4254/wjh.v6.i5.284
9. K. Watashi, S. Urban, W. Li, and T. Wakita, "NTCP and Beyond: Opening the Door to Unveil Hepatitis B Virus Entry", International Journal of Molecular Sciences, vol. 15, pp. 2892-2905, 2014. http://dx.doi.org/10.3390/ijms15022892
10. C.W. Shepard, "Hepatitis B Virus Infection: Epidemiology and Vaccination", Epidemiologic Reviews, vol. 28, pp. 112-125, 2006. http://dx.doi.org/10.1093/epirev/mxj009
11. T.J. Liang, "Hepatitis B: The virus and disease", Hepatology, vol. 49, pp. S13-S21, 2009. http://dx.doi.org/10.1002/hep.22881
12. N. Coppola, "Clinical significance of hepatitis B surface antigen mutants", World Journal of Hepatology, vol. 7, pp. 2729, 2015. http://dx.doi.org/10.4254/wjh.v7.i27.2729
13. S. Datta, S. Chatterjee, V. Veer, and R. Chakravarty, "Molecular Biology of the Hepatitis B Virus for Clinicians", Journal of Clinical and Experimental Hepatology, vol. 2, pp. 353-365, 2012. http://dx.doi.org/10.1016/j.jceh.2012.10.003
14. K. Kidd-Ljunggren, Y. Miyakawa, and A.H. Kidd, "Genetic variability in hepatitis B viruses", Journal of General Virology, vol. 83, pp. 1267-1280, 2002. http://dx.doi.org/10.1099/0022-1317-83-6-1267
15. A. Kay, and F. Zoulim, "Hepatitis B virus genetic variability and evolution", Virus Research, vol. 127, pp. 164-176, 2007. http://dx.doi.org/10.1016/j.virusres.2007.02.021
16. F.J. Mahoney, "Update on diagnosis, management, and prevention of hepatitis B virus infection.", Clinical microbiology reviews, 1999. http://www.ncbi.nlm.nih.gov/pubmed/10194463
17. R. Bartenschlager, and H. Schaller, "The amino-terminal domain of the hepadnaviral P-gene encodes the terminal protein (genome-linked protein) believed to prime reverse transcription.", The EMBO journal, 1988. http://www.ncbi.nlm.nih.gov/pubmed/2854056
18. H.Y. Hsu, M.H. Chang, K.H. Hsieh, C.Y. Lee, H.H. Lin, L.H. Hwang, P.J. Chen, and D.S. Chen, "Cellular immune response to HBcAg in mother-to-infant transmission of hepatitis B virus.", Hepatology (Baltimore, Md.), 1992. http://www.ncbi.nlm.nih.gov/pubmed/1568717
19. M. Chen, M. Sällberg, J. Hughes, J. Jones, L.G. Guidotti, F.V. Chisari, J. Billaud, and D.R. Milich, "Immune Tolerance Split between Hepatitis B Virus Precore and Core Proteins", Journal of Virology, vol. 79, pp. 3016-3027, 2005. http://dx.doi.org/10.1128/jvi.79.5.3016-3027.2005
20. R. Pang, E. Tse, and R.T. Poon, "Molecular pathways in hepatocellular carcinoma", Cancer Letters, vol. 240, pp. 157-169, 2006. http://dx.doi.org/10.1016/j.canlet.2005.08.031
21. B.J. McMahon, W.L. Alward, D.B. Hall, W.L. Heyward, T.R. Bender, D.P. Francis, and J.E. Maynard, "Acute hepatitis B virus infection: relation of age to the clinical expression of disease and subsequent development of the carrier state.", The Journal of infectious diseases, 1985. http://www.ncbi.nlm.nih.gov/pubmed/3973412
22. S. Locarnini, A. Hatzakis, D. Chen, and A. Lok, "Strategies to control hepatitis B: Public policy, epidemiology, vaccine and drugs", Journal of Hepatology, vol. 62, pp. S76-S86, 2015. http://dx.doi.org/10.1016/j.jhep.2015.01.018
23. . , "EASL Clinical Practice Guidelines: Management of chronic hepatitis B virus infection", Journal of Hepatology, vol. 57, pp. 167-185, 2012. http://dx.doi.org/10.1016/j.jhep.2012.02.010
24. Y. Liaw, and C. Chu, "Hepatitis B virus infection", The Lancet, vol. 373, pp. 582-592, 2009. http://dx.doi.org/10.1016/s0140-6736(09)60207-5
25. E.J. Aspinall, G. Hawkins, A. Fraser, S.J. Hutchinson, and D. Goldberg, "Hepatitis B prevention, diagnosis, treatment and care: a review", Occupational Medicine, vol. 61, pp. 531-540, 2011. http://dx.doi.org/10.1093/occmed/kqr136
26. G. Fattovich, F. Bortolotti, and F. Donato, "Natural history of chronic hepatitis B: Special emphasis on disease progression and prognostic factors", Journal of Hepatology, vol. 48, pp. 335-352, 2008. http://dx.doi.org/10.1016/j.jhep.2007.11.011
27. J.H. Hoofnagle, E. Doo, T.J. Liang, R. Fleischer, and A.S. Lok, "Management of hepatitis B: Summary of a clinical research workshop", Hepatology, vol. 45, pp. 1056-1075, 2007. http://dx.doi.org/10.1002/hep.21627
28. A.S.F. Lok, and B.J. McMahon, "Chronic hepatitis B: Update 2009", Hepatology, vol. 50, pp. 661-662, 2009. http://dx.doi.org/10.1002/hep.23190
29. M. Yuen, "Significance of hepatitis B genotype in acute exacerbation, HBeAg seroconversion, cirrhosis-related complications, and hepatocellular carcinoma", Hepatology, vol. 37, pp. 562-567, 2003. http://dx.doi.org/10.1053/jhep.2003.50098
30. R.P. Beasley, L.Y. Hwang, G.C. Lee, C.C. Lan, C.H. Roan, F.Y. Huang, and C.L. Chen, "Prevention of perinatally transmitted hepatitis B virus infections with hepatitis B immune globulin and hepatitis B vaccine.", Lancet (London, England), 1983. http://www.ncbi.nlm.nih.gov/pubmed/6138642
31. D. Tai, S. Lin, I. Sheen, C. Chu, D. Lin, and Y. Liaw, "Long-term outcome of hepatitis B e antigen-negative hepatitis B surface antigen carriers in relation to changes of alanine aminotransferase levels over time", Hepatology, vol. 49, pp. 1859-1867, 2009. http://dx.doi.org/10.1002/hep.22878
32. G.V. Papatheodoridis, N. Chrysanthos, E. Hadziyannis, E. Cholongitas, and E.K. Manesis, "Longitudinal changes in serum HBV DNA levels and predictors of progression during the natural course of HBeAg‐negative chronic hepatitis B virus infection", Journal of Viral Hepatitis, vol. 15, pp. 434-441, 2008. http://dx.doi.org/10.1111/j.1365-2893.2007.00957.x
33. M. Martinot-Peignoux, N. Boyer, M. Colombat, R. Akremi, B. Pham, S. Ollivier, C. Castelnau, D. Valla, C. Degott, and P. Marcellin, "Serum hepatitis B virus DNA levels and liver histology in inactive HBsAg carriers.", Journal of hepatology, 2002. http://www.ncbi.nlm.nih.gov/pubmed/11943427
34. J. Simonetti, L. Bulkow, B.J. McMahon, C. Homan, M. Snowball, S. Negus, J. Williams, and S.E. Livingston, "Clearance of hepatitis B surface antigen and risk of hepatocellular carcinoma in a cohort chronically infected with hepatitis B virus", Hepatology, vol. 51, pp. 1531-1537, 2009. http://dx.doi.org/10.1002/hep.23464
35. C. Seeger, and W.S. Mason, "Hepatitis B virus biology.", Microbiology and molecular biology reviews : MMBR, 2000. http://www.ncbi.nlm.nih.gov/pubmed/10704474
36. J.S. Tuttleman, C. Pourcel, and J. Summers, "Formation of the pool of covalently closed circular viral DNA in hepadnavirus-infected cells.", Cell, 1986. http://www.ncbi.nlm.nih.gov/pubmed/3768961
37. H. Yan, G. Zhong, G. Xu, W. He, Z. Jing, Z. Gao, Y. Huang, Y. Qi, B. Peng, H. Wang, L. Fu, M. Song, P. Chen, W. Gao, B. Ren, Y. Sun, T. Cai, X. Feng, J. Sui, and W. Li, "Sodium taurocholate cotransporting polypeptide is a functional receptor for human hepatitis B and D virus", eLife, vol. 1, 2012. http://dx.doi.org/10.7554/eLife.00049
38. H. Yang, and J. Kao, "Persistence of hepatitis B virus covalently closed circular DNA in hepatocytes: molecular mechanisms and clinical significance", Emerging Microbes & Infections, vol. 3, pp. 1-7, 2014. http://dx.doi.org/10.1038/emi.2014.64
39. W.H. Gerlich, "Medical Virology of Hepatitis B: how it began and where we are now", Virology Journal, vol. 10, 2013. http://dx.doi.org/10.1186/1743-422x-10-239
40. . WHO, "Hepatitis B: Surveillance and control", Available at: http://www.who.int/csr/disease/hepatitis/whocdscsrlyo20022/en/index4.html. Accessed 04.12.2015, 2016.
41. C. Hawkins, B. Christian, J. Ye, T. Nagu, E. Aris, G. Chalamilla, D. Spiegelman, F. Mugusi, S. Mehta, and W. Fawzi, "Prevalence of hepatitis B co-infection and response to antiretroviral therapy among HIV-infected patients in Tanzania", AIDS, vol. 27, pp. 919-927, 2013. http://dx.doi.org/10.1097/QAD.0b013e32835cb9c8
42. G. Wandeler, T. Gsponer, F. Bihl, E. Bernasconi, M. Cavassini, H. Kovari, P. Schmid, M. Battegay, A. Calmy, M. Egger, H. Furrer, A. Rauch, V. Aubert, J. Barth, M. Battegay, E. Bernasconi, J. Böni, H. Bucher, C. Burton-Jeangros, A. Calmy, M. Cavassini, M. Egger, L. Elzi, J. Fehr, J. Fellay, P. Francioli, H. Furrer, C. Fux, M. Gorgievski, H. Günthard, D. Haerry, B. Hasse, H. Hirsch, B. Hirschel, I. Hösli, C. Kahlert, L. Kaiser, O. Keiser, C. Kind, T. Klimkait, H. Kovari, B. Ledergerber, G. Martinetti, B. Martinez de Tejada, K. Metzner, N. Müller, D. Nadal, G. Pantaleo, A. Rauch, S. Regenass, M. Rickenbach, C. Rudin, P. Schmid, D. Schultze, F. Schöni-Affolter, J. Schüpbach, R. Speck, P. Taffé, P. Tarr, A. Telenti, A. Trkola, P. Vernazza, R. Weber, S. Yerly, and . , "Hepatitis B Virus Infection Is Associated With Impaired Immunological Recovery During Antiretroviral Therapy in the Swiss HIV Cohort Study", The Journal of Infectious Diseases, vol. 208, pp. 1454-1458, 2013. http://dx.doi.org/10.1093/infdis/jit351
43. G. Nikolopoulos, D. Paraskevis, E. Hatzitheodorou, Z. Moschidis, V. Sypsa, X. Zavitsanos, V. Kalapothaki, and A. Hatzakis, "Impact of Hepatitis B Virus Infection on the Progression of AIDS and Mortality in HIV‐Infected Individuals: A Cohort Study and Meta‐Analysis", Clinical Infectious Diseases, vol. 48, pp. 1763-1771, 2009. http://dx.doi.org/10.1086/599110
44. H.M. Chun, M.P. Roediger, K.H. Hullsiek, C.L. Thio, B.K. Agan, W.P. Bradley, S.A. Peel, L.L. Jagodzinski, A.C. Weintrob, A. Ganesan, G. Wortmann, N.F. Crum-Cianflone, J.D. Maguire, and M.L. Landrum, "Hepatitis B Virus Coinfection Negatively Impacts HIV Outcomes in HIV Seroconverters", The Journal of Infectious Diseases, vol. 205, pp. 185-193, 2011. http://dx.doi.org/10.1093/infdis/jir720
45. A.A. Modi, and J.J. Feld, "Viral hepatitis and HIV in Africa.", AIDS reviews, 2007. http://www.ncbi.nlm.nih.gov/pubmed/17474311
46. P. Easterbrook, A. Sands, and H. Harmanci, "Challenges and Priorities in the Management of HIV/HBV and HIV/HCV Coinfection in Resource-Limited Settings", Seminars in Liver Disease, vol. 32, pp. 147-157, 2012. http://dx.doi.org/10.1055/s-0032-1316476
47. . WHO, "Hepatitis B: Fact sheet", Available at: http://www.who.int/mediacentre/factsheets/fs204/en/. Accessed 29.04.2016, 2016.
48. H.S. Te, and D.M. Jensen, "Epidemiology of Hepatitis B and C Viruses: A Global Overview", Clinics in Liver Disease, vol. 14, pp. 1-21, 2010. http://dx.doi.org/10.1016/j.cld.2009.11.009
49. M. Kwak, "Occult hepatitis B virus infection", World Journal of Hepatology, vol. 6, pp. 860, 2014. http://dx.doi.org/10.4254/wjh.v6.i12.860
50. M.D. Thedja, D.H. Muljono, S.I. Ie, E. Sidarta, . Turyadi, J. Verhoef, and S. Marzuki, "Genogeography and Immune Epitope Characteristics of Hepatitis B Virus Genotype C Reveals Two Distinct Types: Asian and Papua-Pacific", PLOS ONE, vol. 10, pp. e0132533, 2015. http://dx.doi.org/10.1371/journal.pone.0132533
51. A. Kuo, and R. Gish, "Chronic Hepatitis B Infection", Clinics in Liver Disease, vol. 16, pp. 347-369, 2012. http://dx.doi.org/10.1016/j.cld.2012.03.003
52. F. Kurbanov, Y. Tanaka, and M. Mizokami, "Geographical and genetic diversity of the human hepatitis B virus", Hepatology Research, vol. 40, pp. 14-30, 2010. http://dx.doi.org/10.1111/j.1872-034X.2009.00601.x
53. K. Tatematsu, Y. Tanaka, F. Kurbanov, F. Sugauchi, S. Mano, T. Maeshiro, T. Nakayoshi, M. Wakuta, Y. Miyakawa, and M. Mizokami, "A Genetic Variant of Hepatitis B Virus Divergent from Known Human and Ape Genotypes Isolated from a Japanese Patient and Provisionally Assigned to New Genotype J", Journal of Virology, vol. 83, pp. 10538-10547, 2009. http://dx.doi.org/10.1128/jvi.00462-09
54. V. Soriano, A. Mocroft, L. Peters, J. Rockstroh, F. Antunes, N. Kirkby, S. de Wit, A.D. Monforte, R. Flisiak, J. Lundgren, and . , "Predictors of hepatitis B virus genotype and viraemia in HIV-infected patients with chronic hepatitis B in Europe", Journal of Antimicrobial Chemotherapy, vol. 65, pp. 548-555, 2010. http://dx.doi.org/10.1093/jac/dkp479
55. V. Thibault, C. Gaudy-Graffin, P. Colson, J. Gozlan, N. Schnepf, P. Trimoulet, C. Pallier, K. Saune, M. Branger, M. Coste, F.R. Thoraval, and . , "Epidemiological, virological and clinical characteristics of HBV infection in 223 HIV co-infected patients: a French multi-centre collaborative study.", Virology journal, 2013. http://www.ncbi.nlm.nih.gov/pubmed/23497042
56. S. Fujisaki, Y. Yokomaku, T. Shiino, T. Koibuchi, J. Hattori, S. Ibe, Y. Iwatani, A. Iwamoto, T. Shirasaka, M. Hamaguchi, and W. Sugiura, "Outbreak of Infections by Hepatitis B Virus Genotype A and Transmission of Genetic Drug Resistance in Patients Coinfected with HIV-1 in Japan", Journal of Clinical Microbiology, vol. 49, pp. 1017-1024, 2011. http://dx.doi.org/10.1128/jcm.02149-10
57. N.M. Araujo, R. Waizbort, and A. Kay, "Hepatitis B virus infection from an evolutionary point of view: How viral, host, and environmental factors shape genotypes and subgenotypes", Infection, Genetics and Evolution, vol. 11, pp. 1199-1207, 2011. http://dx.doi.org/10.1016/j.meegid.2011.04.017
58. K. Ito, H. Yotsuyanagi, H. Yatsuhashi, Y. Karino, Y. Takikawa, T. Saito, Y. Arase, F. Imazeki, M. Kurosaki, T. Umemura, T. Ichida, H. Toyoda, M. Yoneda, E. Mita, K. Yamamoto, K. Michitaka, T. Maeshiro, J. Tanuma, Y. Tanaka, M. Sugiyama, K. Murata, N. Masaki, M. Mizokami, and . , "Risk factors for long-term persistence of serum hepatitis B surface antigen following acute hepatitis B virus infection in Japanese adults", Hepatology, vol. 59, pp. 89-97, 2013. http://dx.doi.org/10.1002/hep.26635
59. K. Ito, H. Yotsuyanagi, M. Sugiyama, H. Yatsuhashi, Y. Karino, Y. Takikawa, T. Saito, Y. Arase, F. Imazeki, M. Kurosaki, T. Umemura, T. Ichida, H. Toyoda, M. Yoneda, Y. Tanaka, E. Mita, K. Yamamoto, K. Michitaka, T. Maeshiro, J. Tanuma, M. Korenaga, K. Murata, N. Masaki, K. Koike, M. Mizokami, and . , "Geographic distribution and characteristics of genotype A hepatitis B virus infection in acute and chronic hepatitis B patients in Japan", Journal of Gastroenterology and Hepatology, vol. 31, pp. 180-189, 2015. http://dx.doi.org/10.1111/jgh.13030
60. S.K. Fung, and A.S.F. Lok, "Hepatitis B virus genotypes: Do they play a role in the outcome of HBV infection?", Hepatology, vol. 40, pp. 790-792, 2004. http://dx.doi.org/10.1002/hep.20455
61. C.M. Croagh, "Genotypes and viral variants in chronic hepatitis B: A review of epidemiology and clinical relevance", World Journal of Hepatology, vol. 7, pp. 289, 2015. http://dx.doi.org/10.4254/wjh.v7.i3.289
62. S. Marciano, O.A. Galdame, and A.C. Gadano, "HBV Genotype F: Natural History and Treatment", Antiviral Therapy, vol. 18, pp. 485-488, 2005. http://dx.doi.org/10.3851/imp2604
63. C. Chu, and Y. Liaw, "Genotype C hepatitis B virus infection is associated with a higher risk of reactivation of hepatitis B and progression to cirrhosis than genotype B: A longitudinal study of hepatitis B e antigen-positive patients with normal aminotransferase levels at baseline", Journal of Hepatology, vol. 43, pp. 411-417, 2005. http://dx.doi.org/10.1016/j.jhep.2005.03.018
64. H.L. Chan, G.L. Wong, C. Tse, A.M. Chim, K.K. Yiu, H. Chan, J.J. Sung, and V.W. Wong, "Hepatitis B Virus Genotype C Is Associated With More Severe Liver Fibrosis Than Genotype B", Clinical Gastroenterology and Hepatology, vol. 7, pp. 1361-1366, 2009. http://dx.doi.org/10.1016/j.cgh.2009.08.004
65. M. Lee, H. Yang, J. Liu, R. Batrla-Utermann, C. Jen, U.H. Iloeje, S. Lu, S. You, L. Wang, C. Chen, and . , "Prediction models of long-term Cirrhosis and hepatocellular carcinoma risk in chronic hepatitis B patients: Risk scores integrating host and virus profiles", Hepatology, vol. 58, pp. 546-554, 2013. http://dx.doi.org/10.1002/hep.26385
66. Y. Tanaka, M. Mukaide, E. Orito, M. Yuen, K. Ito, F. Kurbanov, F. Sugauchi, Y. Asahina, N. Izumi, M. Kato, C. Lai, R. Ueda, and M. Mizokami, "Specific mutations in enhancer II/core promoter of hepatitis B virus subgenotypes C1/C2 increase the risk of hepatocellular carcinoma", Journal of Hepatology, vol. 45, pp. 646-653, 2006. http://dx.doi.org/10.1016/j.jhep.2006.06.018
67. B.J. McMahon, "Natural History of Chronic Hepatitis B", Clinics in Liver Disease, vol. 14, pp. 381-396, 2010. http://dx.doi.org/10.1016/j.cld.2010.05.007
68. A. Kramvis, M. Kew, and G. François, "Hepatitis B virus genotypes", Vaccine, vol. 23, pp. 2409-2423, 2005. http://dx.doi.org/10.1016/j.vaccine.2004.10.045
69. Y. Tanaka, I. Hasegawa, T. Kato, E. Orito, N. Hirashima, S.K. Acharya, R.G. Gish, A. Kramvis, M.C. Kew, N. Yoshihara, S.M. Shrestha, M. Khan, Y. Miyakawa, and M. Mizokami, "A case-control study for differences among hepatitis B virus infections of genotypes A (subtypes Aa and Ae) and D", Hepatology, vol. 40, pp. 747-755, 2004. http://dx.doi.org/10.1002/hep.20365
70. L. Ferrell, "Liver Pathology: Cirrhosis, Hepatitis, and Primary Liver Tumors. Update and Diagnostic Problems", Modern Pathology, vol. 13, pp. 679-704, 2000. http://dx.doi.org/10.1038/modpathol.3880119
71. H. Mani, and D.E. Kleiner, "Liver biopsy findings in chronic hepatitis B", Hepatology, vol. 49, pp. S61-S71, 2009. http://dx.doi.org/10.1002/hep.22930
72. N.D. Theise, "Liver biopsy assessment in chronic viral hepatitis: a personal, practical approach", Modern Pathology, vol. 20, pp. S3-S14, 2007. http://dx.doi.org/10.1038/modpathol.3800693
73. I. Su, H. Wang, H. Wu, and W. Huang, "Ground glass hepatocytes contain pre‐S mutants and represent preneoplastic lesions in chronic hepatitis B virus infection", Journal of Gastroenterology and Hepatology, vol. 23, pp. 1169-1174, 2008. http://dx.doi.org/10.1111/j.1440-1746.2008.05348.x
74. C. Sagnelli, M. Ciccozzi, M. Pisaturo, A. Lo Presti, E. Cella, N. Coppola, and E. Sagnelli, "The impact of viral molecular diversity on the clinical presentation and outcome of acute hepatitis B in Italy.", The new microbiologica, 2015. http://www.ncbi.nlm.nih.gov/pubmed/25915056
75. S. Krugman, L.R. Overby, I.K. Mushahwar, C. Ling, G.G. Frösner, and F. Deinhardt, "Viral Hepatitis, Type B", New England Journal of Medicine, vol. 300, pp. 101-106, 1979. http://dx.doi.org/10.1056/nejm197901183000301
76. J. Hoofnagle, and A. Di Bisceglie, "Serologic Diagnosis of Acute and Chronic Viral Hepatitis", Seminars in Liver Disease, vol. 11, pp. 73-83, 1991. http://dx.doi.org/10.1055/s-2008-1040426
77. B.J. McMahon, P. Holck, L. Bulkow, and M. Snowball, "Serologic and clinical outcomes of 1536 Alaska Natives chronically infected with hepatitis B virus.", Annals of internal medicine, 2001. http://www.ncbi.nlm.nih.gov/pubmed/11694101
78. W.L. Alward, B.J. McMahon, D.B. Hall, W.L. Heyward, D.P. Francis, and T.R. Bender, "The long-term serological course of asymptomatic hepatitis B virus carriers and the development of primary hepatocellular carcinoma.", The Journal of infectious diseases, 1985. http://www.ncbi.nlm.nih.gov/pubmed/2982971
79. Y.F. Liaw, I.S. Sheen, T.J. Chen, C.M. Chu, and C.C. Pao, "Incidence, determinants and significance of delayed clearance of serum HBsAg in chronic hepatitis B virus infection: a prospective study.", Hepatology (Baltimore, Md.), 1991. http://www.ncbi.nlm.nih.gov/pubmed/2010157
80. H. Adachi, S. Kaneko, E. Matsushita, Y. Inagaki, M. Unoura, and K. Kobayashi, "Clearance of HBsAg in seven patients with chronic hepatitis B.", Hepatology (Baltimore, Md.), 1992. http://www.ncbi.nlm.nih.gov/pubmed/1332920
81. R.P. Beasley, L.Y. Hwang, C.C. Lin, and C.S. Chien, "Hepatocellular carcinoma and hepatitis B virus. A prospective study of 22 707 men in Taiwan.", Lancet (London, England), 1981. http://www.ncbi.nlm.nih.gov/pubmed/6118576
82. B.J. McMahon, S.R. Alberts, R.B. Wainwright, L. Bulkow, and A.P. Lanier, "Hepatitis B-related sequelae. Prospective study in 1400 hepatitis B surface antigen-positive Alaska native carriers.", Archives of internal medicine, 1990. http://www.ncbi.nlm.nih.gov/pubmed/2158773
83. M.G. Brook, "Sexually acquired hepatitis.", Sexually transmitted infections, 2002. http://www.ncbi.nlm.nih.gov/pubmed/12181458
84. N. Terrault, B. Roche, and D. Samuel, "Management of the hepatitis B virus in the liver transplantation setting: A European and an American perspective", Liver Transplantation, vol. 11, pp. 716-732, 2005. http://dx.doi.org/10.1002/lt.20492
85. S.I. Gan, S.M. Devlin, N.W. Scott-Douglas, and K.W. Burak, "Lamivudine for the treatment of membranous glomerulopathy secondary to chronic Hepatitis B infection.", Canadian journal of gastroenterology = Journal canadien de gastroenterologie, 2005. http://www.ncbi.nlm.nih.gov/pubmed/16247526
86. J. Dienstag, "Hepatitis B as an Immune Complex Disease", Seminars in Liver Disease, vol. 1, pp. 45-57, 1981. http://dx.doi.org/10.1055/s-2008-1063929
87. C. Trepo, and L. Guillevin, "Polyarteritis Nodosa and Extrahepatic Manifestations of HBV Infection: The Case Against Autoimmune Intervention in Pathogenesis", Journal of Autoimmunity, vol. 16, pp. 269-274, 2001. http://dx.doi.org/10.1006/jaut.2000.0502
88. E. Alpert, K.J. Isselbacher, and P.H. Schur, "The Pathogenesis of Arthritis Associated with Viral Hepatitis", New England Journal of Medicine, vol. 285, pp. 185-189, 1971. http://dx.doi.org/10.1056/nejm197107222850401
89. D.J. Gocke, K. Hsu, C. Morgan, S. Bombardieri, M. Lockshin, and C.L. Christian, "Association between polyarteritis and Australia antigen.", Lancet (London, England), 1970. http://www.ncbi.nlm.nih.gov/pubmed/4098431
90. K.N. Lai, P.K. Li, S.F. Lui, T.C. Au, J.S. Tam, K.L. Tong, and F.M. Lai, "Membranous Nephropathy Related to Hepatitis B Virus in Adults", New England Journal of Medicine, vol. 324, pp. 1457-1463, 1991. http://dx.doi.org/10.1056/nejm199105233242103
91. Y. Takekoshi, M. Tanaka, N. Shida, Y. Satake, Y. Saheki, and S. Matsumoto, "Strong association between membranous nephropathy and hepatitis-B surface antigenaemia in Japanese children.", Lancet (London, England), 1978. http://www.ncbi.nlm.nih.gov/pubmed/82085
92. C. Lin, L. Liao, C. Liu, M. Yu, P. Chen, M. Lai, D. Chen, and J. Kao, "Hepatitis B viral factors in HBeAg-Negative carriers with persistently normal serum alanine aminotransferase levels", Hepatology, vol. 45, pp. 1193-1198, 2007. http://dx.doi.org/10.1002/hep.21585
93. D.E. Dietzman, J.P. Harnisch, C.G. Ray, E.R. Alexander, and K.K. Holmes, "Hepatitis B surface antigen (HBsAg) and antibody to HBsAg. Prevalence in homosexual and heterosexual men.", JAMA, 1977. http://www.ncbi.nlm.nih.gov/pubmed/579199
94. D.A. MacKellar, L.A. Valleroy, G.M. Secura, W. McFarland, D. Shehan, W. Ford, M. LaLota, D.D. Celentano, B.A. Koblin, L.V. Torian, H. Thiede, R.S. Janssen, and . , "Two decades after vaccine license: hepatitis B immunization and infection among young men who have sex with men.", American journal of public health, 2001. http://www.ncbi.nlm.nih.gov/pubmed/11392942
95. J. Kao, "Diagnosis of hepatitis B virus infection through serological and virological markers", Expert Review of Gastroenterology & Hepatology, vol. 2, pp. 553-562, 2008. http://dx.doi.org/10.1586/17474124.2.4.553
96. G.B. Yao, "Importance of perinatal versus horizontal transmission of hepatitis B virus infection in China.", Gut, 1996. http://www.ncbi.nlm.nih.gov/pubmed/8786052
97. P. Van Damme, M. Cramm, J.C. Van der Auwera, R. Vranckx, and A. Meheus, "Horizontal transmission of hepatitis B virus.", Lancet (London, England), 1995. http://www.ncbi.nlm.nih.gov/pubmed/7799703
98. M.J. Alter, J. Ahtone, I. Weisfuse, K. Starko, T.D. Vacalis, and J.E. Maynard, "Hepatitis B virus transmission between heterosexuals.", JAMA, 1986. http://www.ncbi.nlm.nih.gov/pubmed/3755769
99. M.J. Alter, P.J. Coleman, W.J. Alexander, E. Kramer, J.K. Miller, E. Mandel, S.C. Hadler, and H.S. Margolis, "Importance of heterosexual activity in the transmission of hepatitis B and non-A, non-B hepatitis.", JAMA, 1989. http://www.ncbi.nlm.nih.gov/pubmed/2503630
100. K.E. Miller, D.E. Ruiz, and J.C. Graves, "Update on the prevention and treatment of sexually transmitted diseases.", American family physician, 2003. http://www.ncbi.nlm.nih.gov/pubmed/12751653
101. R.A. Crosby, D. Newman, M.L. Kamb, J. Zenilman, . Douglas JMJr, and M. Iatesta, "Misconceptions about STD-protective behavior. Project RESPECT Study Group.", American journal of preventive medicine, 2000. http://www.ncbi.nlm.nih.gov/pubmed/11020593
102. J.A. Catania, J. Canchola, D. Binson, M.M. Dolcini, J.P. Paul, L. Fisher, K.H. Choi, L. Pollack, J. Chang, W.L. Yarber, J.R. Heiman, and T. Coates, "National trends in condom use among at-risk heterosexuals in the united states.", Journal of acquired immune deficiency syndromes (1999), 2001. http://www.ncbi.nlm.nih.gov/pubmed/11404540
103. E.E. Mast, H.S. Margolis, A.E. Fiore, E.W. Brink, S.T. Goldstein, S.A. Wang, L.A. Moyer, B.P. Bell, M.J. Alter, and . , "A comprehensive immunization strategy to eliminate transmission of hepatitis B virus infection in the United States: recommendations of the Advisory Committee on Immunization Practices (ACIP) part 1: immunization of infants, children, and adolescents.", MMWR. Recommendations and reports : Morbidity and mortality weekly report. Recommendations and reports, 2005. http://www.ncbi.nlm.nih.gov/pubmed/16371945
104. E.E. Mast, C.M. Weinbaum, A.E. Fiore, M.J. Alter, B.P. Bell, L. Finelli, L.E. Rodewald, J.M. Douglas, R.S. Janssen, J.W. Ward, and . , "A comprehensive immunization strategy to eliminate transmission of hepatitis B virus infection in the United States: recommendations of the Advisory Committee on Immunization Practices (ACIP) Part II: immunization of adults.", MMWR. Recommendations and reports : Morbidity and mortality weekly report. Recommendations and reports, 2006. http://www.ncbi.nlm.nih.gov/pubmed/17159833
105. P. Valenzuela, A. Medina, W.J. Rutter, G. Ammerer, and B.D. Hall, "Synthesis and assembly of hepatitis B virus surface antigen particles in yeast.", Nature, 1982. http://www.ncbi.nlm.nih.gov/pubmed/7045698
106. M.T. Niu, M.E. Salive, and S.S. Ellenberg, "Neonatal deaths after hepatitis B vaccine: the vaccine adverse event reporting system, 1991-1998.", Archives of pediatrics & adolescent medicine, 1999. http://www.ncbi.nlm.nih.gov/pubmed/10591306
107. E.M. Eriksen, J.A. Perlman, A. Miller, S.M. Marcy, H. Lee, C. Vadheim, K.M. Zangwill, R.T. Chen, F. DeStefano, E. Lewis, S. Black, H. Shinefield, and J.I. Ward, "Lack of association between hepatitis B birth immunization and neonatal death: a population-based study from the vaccine safety datalink project.", The Pediatric infectious disease journal, 2004. http://www.ncbi.nlm.nih.gov/pubmed/15247605
108. D. Chen, "Hepatitis B vaccination: The key towards elimination and eradication of hepatitis B", Journal of Hepatology, vol. 50, pp. 805-816, 2009. http://dx.doi.org/10.1016/j.jhep.2009.01.002
109. J.A. Arevalo, and A.E. Washington, "Cost-effectiveness of prenatal screening and immunization for hepatitis B virus.", JAMA, 1988. http://www.ncbi.nlm.nih.gov/pubmed/2961895
110. D.S. Chen, N.H. Hsu, J.L. Sung, T.C. Hsu, S.T. Hsu, Y.T. Kuo, K.J. Lo, and Y.T. Shih, "A mass vaccination program in Taiwan against hepatitis B virus infection in infants of hepatitis B surface antigen-carrier mothers.", JAMA, 1987. http://www.ncbi.nlm.nih.gov/pubmed/3573257
111. P.R. Spradling, J. Xing, R. Williams, Y. Masunu-Faleafaga, T. Dulski, A. Mahamud, J. Drobeniuc, and E.H. Teshale, "Immunity to Hepatitis B Virus (HBV) Infection Two Decades after Implementation of Universal Infant HBV Vaccination: Association of Detectable Residual Antibodies and Response to a Single HBV Challenge Dose", Clinical and Vaccine Immunology, vol. 20, pp. 559-561, 2013. http://dx.doi.org/10.1128/cvi.00694-12
112. M. Mendy, I. Peterson, S. Hossin, T. Peto, M.L. Jobarteh, A. Jeng-Barry, M. Sidibeh, A. Jatta, S.E. Moore, A.J. Hall, and H. Whittle, "Observational Study of Vaccine Efficacy 24 Years after the Start of Hepatitis B Vaccination in Two Gambian Villages: No Need for a Booster Dose", PLoS ONE, vol. 8, pp. e58029, 2013. http://dx.doi.org/10.1371/journal.pone.0058029
113. Y. Poovorawan, V. Chongsrisawat, A. Theamboonlers, G. Leroux-Roels, P.D. Crasta, and K. Hardt, "Persistence and immune memory to hepatitis B vaccine 20 years after primary vaccination of Thai infants, born to HBsAg and HBeAg positive mothers", Human Vaccines & Immunotherapeutics, vol. 8, pp. 896-904, 2012. http://dx.doi.org/10.4161/hv.19989
114. S.L. Stramer, U. Wend, D. Candotti, G.A. Foster, F.B. Hollinger, R.Y. Dodd, J. Allain, and W. Gerlich, "Nucleic Acid Testing to Detect HBV Infection in Blood Donors", New England Journal of Medicine, vol. 364, pp. 236-247, 2011. http://dx.doi.org/10.1056/NEJMoa1007644
115. H.J. Boot, L.A. van der Waaij, J. Schirm, C.G. Kallenberg, J. van Steenbergen, and B. Wolters, "Acute hepatitis B in a healthcare worker: A case report of genuine vaccination failure", Journal of Hepatology, vol. 50, pp. 426-431, 2009. http://dx.doi.org/10.1016/j.jhep.2008.07.040
116. J. O’Halloran, C. De Gascun, L. Dunford, M. Carr, J. Connell, R. Howard, W. Hall, and J. Lambert, "Hepatitis B virus vaccine failure resulting in chronic hepatitis B infection", Journal of Clinical Virology, vol. 52, pp. 151-154, 2011. http://dx.doi.org/10.1016/j.jcv.2011.06.020
117. M. Kane, "Global programme for control of hepatitis B infection.", Vaccine, 1995. http://www.ncbi.nlm.nih.gov/pubmed/7571830
118. S. Schillie, T.V. Murphy, M. Sawyer, K. Ly, E. Hughes, R. Jiles, M.A. de Perio, M. Reilly, K. Byrd, J.W. Ward, and . , "CDC guidance for evaluating health-care personnel for hepatitis B virus protection and for administering postexposure management.", MMWR. Recommendations and reports : Morbidity and mortality weekly report. Recommendations and reports, 2013. http://www.ncbi.nlm.nih.gov/pubmed/24352112
119. M.F. Sorrell, E.A. Belongia, J. Costa, I.F. Gareen, J.L. Grem, J.M. Inadomi, E.R. Kern, J.A. McHugh, G.M. Petersen, M.F. Rein, D.B. Strader, and H.T. Trotter, "National Institutes of Health consensus development conference statement: Management of hepatitis B", Hepatology, vol. 49, pp. S4-S12, 2009. http://dx.doi.org/10.1002/hep.22946
120. G. Nebbia, D. Peppa, and M.K. Maini, "Hepatitis B infection: current concepts and future challenges", QJM, vol. 105, pp. 109-113, 2012. http://dx.doi.org/10.1093/qjmed/hcr270
121. B.K. Kim, K. Han, and S.H. Ahn, "Prevention of Hepatocellular Carcinoma in Patients with Chronic Hepatitis B Virus Infection", Oncology, vol. 81, pp. 41-49, 2011. http://dx.doi.org/10.1159/000333258
122. K.C. Scott, E.M. Taylor, B. Mamo, N.D. Herr, P.J. Cronkright, K. Yun, M. Altshuler, S. Shetty, and . , "Hepatitis B screening and prevalence among resettled refugees - United States, 2006-2011.", MMWR. Morbidity and mortality weekly report, 2015. http://www.ncbi.nlm.nih.gov/pubmed/26042647
123. Y. Liaw, N. Leung, J. Kao, T. Piratvisuth, E. Gane, K. Han, R. Guan, G.K.K. Lau, S. Locarnini, and . , "Asian-Pacific consensus statement on the management of chronic hepatitis B: a 2008 update", Hepatology International, vol. 2, pp. 263-283, 2008. http://dx.doi.org/10.1007/s12072-008-9080-3
124. M. Sherman, S. Shafran, K. Burak, K. Doucette, W. Wong, N. Girgrah, E. Yoshida, E. Renner, P. Wong, and M. Deschênes, "Management of chronic hepatitis B: consensus guidelines.", Canadian journal of gastroenterology = Journal canadien de gastroenterologie, 2007. http://www.ncbi.nlm.nih.gov/pubmed/17568823
125. P.T.F. Kennedy, H.C. Lee, L. Jeyalingam, R. Malik, P. Karayiannis, D. Muir, J. Main, M. Thursz, R. Goldin, B. Smith, A. Brown, and H.C. Thomas, "NICE guidelines and a treatment algorithm for the management of chronic hepatitis B: a review of 12 years experience in west London.", Antiviral therapy, 2008. http://www.ncbi.nlm.nih.gov/pubmed/19195332
126. M.F. Sorrell, E.A. Belongia, J. Costa, I.F. Gareen, J.L. Grem, J.M. Inadomi, E.R. Kern, J.A. McHugh, G.M. Petersen, M.F. Rein, D.B. Strader, and H.T. Trotter, "National Institutes of Health Consensus Development Conference Statement: management of hepatitis B.", Annals of internal medicine, 2009. http://www.ncbi.nlm.nih.gov/pubmed/19124811
127. V. Soriano, C. de Mendoza, J.M. Peña, and P. Barreiro, "Advances in treating drug-resistant hepatitis B virus in HIV-infected patients", Expert Opinion on Pharmacotherapy, vol. 16, pp. 179-186, 2014. http://dx.doi.org/10.1517/14656566.2015.973852
128. P. Dény, and F. Zoulim, "Hepatitis B virus: From diagnosis to treatment", Pathologie Biologie, vol. 58, pp. 245-253, 2010. http://dx.doi.org/10.1016/j.patbio.2010.05.002
129. D. Mutimer, N. Naoumov, P. Honkoop, G. Marinos, M. Ahmed, R. de Man, P. McPhillips, M. Johnson, R. Williams, E. Elias, and S. Schalm, "Combination alpha-interferon and lamivudine therapy for alpha-interferon-resistant chronic hepatitis B infection: results of a pilot study.", Journal of hepatology, 1998. http://www.ncbi.nlm.nih.gov/pubmed/9672165
130. G.K. Lau, T. Piratvisuth, K.X. Luo, P. Marcellin, S. Thongsawat, G. Cooksley, E. Gane, M.W. Fried, W.C. Chow, S.W. Paik, W.Y. Chang, T. Berg, R. Flisiak, P. McCloud, and N. Pluck, "Peginterferon Alfa-2a, Lamivudine, and the Combination for HBeAg-Positive Chronic Hepatitis B", New England Journal of Medicine, vol. 352, pp. 2682-2695, 2005. http://dx.doi.org/10.1056/NEJMoa043470
131. I. Carey, and P.M. Harrison, "Monotherapy versus combination therapy for the treatment of chronic hepatitis B", Expert Opinion on Investigational Drugs, vol. 18, pp. 1655-1666, 2009. http://dx.doi.org/10.1517/13543780903241599
132. A. Erhardt, "Response to interferon alfa is hepatitis B virus genotype dependent: genotype A is more sensitive to interferon than genotype D", Gut, vol. 54, pp. 1009-1013, 2005. http://dx.doi.org/10.1136/gut.2004.060327
133. G.L. Wong, V.W. Wong, H. Chan, P.C. Tse, J. Wong, A.M. Chim, K.K. Yiu, S.H. Chu, and H.L. Chan, "Undetectable HBV DNA at month 12 of entecavir treatment predicts maintained viral suppression and HBeAg‐seroconversion in chronic hepatitis B patients at 3 years", Alimentary Pharmacology & Therapeutics, vol. 35, pp. 1326-1335, 2012. http://dx.doi.org/10.1111/j.1365-2036.2012.05098.x
134. T. Chang, C. Lai, S. Kew Yoon, S.S. Lee, H.S.M. Coelho, F.J. Carrilho, F. Poordad, W. Halota, Y. Horsmans, N. Tsai, H. Zhang, D.J. Tenney, R. Tamez, and U. Iloeje, "Entecavir treatment for up to 5 years in patients with hepatitis B e antigen-positive chronic hepatitis B", Hepatology, vol. 51, pp. 422-430, 2010. http://dx.doi.org/10.1002/hep.23327
135. E.R. Schiff, S.S. Lee, Y. Chao, S. Kew Yoon, F. Bessone, S. Wu, W. Kryczka, Y. Lurie, A. Gadano, G. Kitis, S. Beebe, D. Xu, H. Tang, and U. Iloeje, "Long-Term Treatment With Entecavir Induces Reversal of Advanced Fibrosis or Cirrhosis in Patients With Chronic Hepatitis B", Clinical Gastroenterology and Hepatology, vol. 9, pp. 274-276.e1, 2011. http://dx.doi.org/10.1016/j.cgh.2010.11.040
136. P. Marcellin, E. Gane, M. Buti, N. Afdhal, W. Sievert, I.M. Jacobson, M.K. Washington, G. Germanidis, J.F. Flaherty, R.A. Schall, J.D. Bornstein, K.M. Kitrinos, G.M. Subramanian, J.G. McHutchison, and E.J. Heathcote, "Regression of cirrhosis during treatment with tenofovir disoproxil fumarate for chronic hepatitis B: a 5-year open-label follow-up study", The Lancet, vol. 381, pp. 468-475, 2013. http://dx.doi.org/10.1016/s0140-6736(12)61425-1
137. H.B. El-Serag, and J.A. Davila, "Surveillance for hepatocellular carcinoma: in whom and how?", Therapeutic Advances in Gastroenterology, vol. 4, pp. 5-10, 2010. http://dx.doi.org/10.1177/1756283X10385964
138. B. Rehermann, and A. Bertoletti, "Immunological aspects of antiviral therapy of chronic hepatitis B virus and hepatitis C virus infections", Hepatology, vol. 61, pp. 712-721, 2015. http://dx.doi.org/10.1002/hep.27323
139. D.A. Shafritz, D. Shouval, H.I. Sherman, S.J. Hadziyannis, and M.C. Kew, "Integration of Hepatitis B Virus DNA into the Genome of Liver Cells in Chronic Liver Disease and Hepatocellular Carcinoma", New England Journal of Medicine, vol. 305, pp. 1067-1073, 1981. http://dx.doi.org/10.1056/nejm198110293051807
140. T.M. Block, R. Gish, H. Guo, A. Mehta, A. Cuconati, W. Thomas London, and J. Guo, "Chronic hepatitis B: What should be the goal for new therapies?", Antiviral Research, vol. 98, pp. 27-34, 2013. http://dx.doi.org/10.1016/j.antiviral.2013.01.006
141. G. Fattovich, T. Stroffolini, I. Zagni, and F. Donato, "Hepatocellular carcinoma in cirrhosis: incidence and risk factors.", Gastroenterology, 2004. http://www.ncbi.nlm.nih.gov/pubmed/15508101
142. K.R. Reddy, K.L. Beavers, S.P. Hammond, J.K. Lim, and Y.T. Falck-Ytter, "American Gastroenterological Association Institute Guideline on the Prevention and Treatment of Hepatitis B Virus Reactivation During Immunosuppressive Drug Therapy", Gastroenterology, vol. 148, pp. 215-219, 2015. http://dx.doi.org/10.1053/j.gastro.2014.10.039
143. R.P. Perrillo, R. Gish, and Y.T. Falck-Ytter, "American Gastroenterological Association Institute Technical Review on Prevention and Treatment of Hepatitis B Virus Reactivation During Immunosuppressive Drug Therapy", Gastroenterology, vol. 148, pp. 221-244.e3, 2015. http://dx.doi.org/10.1053/j.gastro.2014.10.038
144. T. Pollicino, and G. Raimondo, "Occult hepatitis B infection", Journal of Hepatology, vol. 61, pp. 688-689, 2014. http://dx.doi.org/10.1016/j.jhep.2014.04.036
145. J. Liu, H. Yang, M. Lee, S. Lu, C. Jen, R. Batrla-Utermann, L. Wang, S. You, C.K. Hsiao, P. Chen, and C. Chen, "Spontaneous seroclearance of hepatitis B seromarkers and subsequent risk of hepatocellular carcinoma", Gut, vol. 63, pp. 1648-1657, 2013. http://dx.doi.org/10.1136/gutjnl-2013-305785
146. S.J. Hadziyannis, V. Sevastianos, I. Rapti, D. Vassilopoulos, and E. Hadziyannis, "Sustained Responses and Loss of HBsAg in HBeAg-Negative Patients With Chronic Hepatitis B Who Stop Long-Term Treatment With Adefovir", Gastroenterology, vol. 143, pp. 629-636.e1, 2012. http://dx.doi.org/10.1053/j.gastro.2012.05.039
147. E. Hadziyannis, and S.J. Hadziyannis, "Hepatitis B surface antigen quantification in chronic hepatitis B and its clinical utility", Expert Review of Gastroenterology & Hepatology, vol. 8, pp. 185-195, 2014. http://dx.doi.org/10.1586/17474124.2014.876362