Role of silent hepatitis B virus in chronic hepatitis B surface antigen(-)liver disease

Citation
I. Chemin et al., Role of silent hepatitis B virus in chronic hepatitis B surface antigen(-)liver disease, ANTIVIR RES, 52(2), 2001, pp. 117-123
Citations number
30
Categorie Soggetti
Microbiology
Journal title
ANTIVIRAL RESEARCH
ISSN journal
01663542 → ACNP
Volume
52
Issue
2
Year of publication
2001
Pages
117 - 123
Database
ISI
SICI code
0166-3542(200111)52:2<117:ROSHBV>2.0.ZU;2-M
Abstract
Despite a number of studies documenting hepatitis B virus (HBV) infection i n the absence of hepatitis B surface antigen (HBsAg) a causal relationship between silent HBV infection and liver disease remain difficult to establis h. In particular, both the prevalence and clinical significance of this obs ervation are poorly understood. Why is HBV replication apparently so low in these patients? A number of studies have tried to elucidate the mechanism of HBsAg negative: infections, and considerable data documenting HBV infect ivity or reinfection in the absence of detectable HBsAg support the hypothe sis that in some of these cases, HBV is undergoing low-level replication in the liver and this, in several situations including: (1) chronic liver dis ease, alcoholic liver disease, hepatocellular carcinoma; (2) viral reactiva tion following cancer chemotherapy or immunosuppression and (3) transmissio n via transfusion or from human serum to chimpanzees. In a recent study inc luding 50 patients with chronic liver disease of unknown etiology we could detect serum HBV DNA by nested polymerase chain reaction (PCR) in 15/50 pat ients (50% at the cirrhosis stage) in the absence of HBsAg; in the liver of the 15 patients both HBcAg and/or HBsAg can be detected at very low-level. Viral host factors allowing HBV persistence in the absence of HBsAg can de pend on several mechanisms. Coinfections with HCV can explain only a propor tion of HBsAg(-) HBV infections. Secondly, HBV mutations in the core promot or region leading to a minimal viral replication, or mutations in the HBsAg -encoding region might explain the absence of serological recognition. Fina lly, it is possible that in some cases host immune mechanisms can maintain HBV infection in a latent state until transmission to another individual wh o subsequently develops a more active infection especially when immunosuppr essive therapy is employed. Existence of HBsAg(-) HBV infections should be taken into account by the use of sensitive PCR tests for prevention of vira l transmission in the settings of blood donations and organ transplants. (C ) 2001 Elsevier Science B.V. All rights reserved.