Format: Abstract
Send to
J Gastroenterol. 2016 Nov;51(11):1073-1080. Epub 2016 Mar 4.
Antiviral effects of anti-HBs immunoglobulin and vaccine on HBs antigen seroclearance for chronic hepatitis B infection.
Tsuge M1,2,3, Hiraga N1,3, Uchida T1,3, Kan H1,3, Miyaki E1,3, Masaki K1,3, Ono A1,3, Nakahara T1,3, Abe-Chayama H1,3, Zhang Y1,3, Naswa MG1,3, Kawaoka T1,3, Miki D1,3,4, Imamura M1,3, Kawakami Y1,3, Aikata H1,3, Ochi H1,3, Hayes CN1,3, Chayama K5,6,7.
Author information
Abstract
BACKGROUND AND AIMS:
Interferon and nucleotide/nucleoside analogues are the main treatments for chronic hepatitis B. These drugs effectively reduce serum hepatitis B virus (HBV) DNA titers but fail to sufficiently reduce hepatitis B surface antigen (HBsAg) levels. Following the recent identification of sodium taurocholate cotransporting polypeptide as a receptor for HBV entry, inhibition of HBV entry has become an attractive therapeutic target for chronic hepatitis B treatment. We therefore evaluated the antiviral effects of antibody to HBsAg (anti-HBs) immunoglobulin (HBIG), which can inhibit HBV entry, by in an vivo study and a clinical trial.
METHODS:
In the in vivo study, HBV-infected mice were generated from human hepatocyte chimeric mice and treated with HBIG. A clinical trial evaluating HBIG therapy in patients was also performed.
RESULTS:
In the mouse study, HBV DNA titers were reduced and serum HBsAg titers decreased to undetectable levels following high-dose HBIG injection. On the basis of this result, eight chronic hepatitis B patients, who had received long-term nucleotide analogue treatment, were treated with monthly HBIG injections as an additional treatment. After 1 year of treatment, an HBsAg level reduction of more than 1 log IU/mL was observed in four patients, and three patients became anti-HBs positive. No adverse events occurred during HBIG therapy.
CONCLUSION:
These results suggest that monthly HBIG injection might benefit patients with chronic hepatitis B whose HBsAg titer becomes lower following long-term nucleotide/nucleoside analogue treatment.
KEYWORDS:
Anti-HBs immunoglobulin; Chronic hepatitis B; Hepatitis B surface antigen loss; Human hepatocyte chimeric mouse