Hepatitis B surface antigen seroclearance: Immune mechanisms, clinical impact, importance for drug development

HBsAg seroclearance occurs rarely in the natural history of chronic hepatitis B (CHB) infection and is associated with improved clinical outcomes. Many factors are associated with HBsAg seroconversion, including immune and viral factors. However, the immune mechanisms associated with HBsAg seroclear...

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Published inJournal of hepatology Vol. 73; no. 2; pp. 409 - 422
Main Authors Tout, Issam, Loureiro, Dimitri, Mansouri, Abdellah, Soumelis, Vassili, Boyer, Nathalie, Asselah, Tarik
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.08.2020
Elsevier Science Ltd
Elsevier
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ISSN0168-8278
1600-0641
1600-0641
DOI10.1016/j.jhep.2020.04.013

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Summary:HBsAg seroclearance occurs rarely in the natural history of chronic hepatitis B (CHB) infection and is associated with improved clinical outcomes. Many factors are associated with HBsAg seroconversion, including immune and viral factors. However, the immune mechanisms associated with HBsAg seroclearance are still difficult to elucidate. HBsAg seroclearance is the ideal aim of HBV treatment. Unfortunately, this goal is rarely achieved with current treatments. Understanding the mechanisms of HBsAg loss appears to be important for the development of curative HBV treatments. While studies from animal models give insights into the potential immune mechanisms and interactions occurring between the immune system and HBsAg, they do not recapitulate all features of CHB in humans and are subject to variability due to their complexity. In this article, we review recent studies on these immune factors, focusing on their influence on CHB progression and HBsAg seroconversion. These data provide new insights for the development of therapeutic approaches to partially restore the anti-HBV immune response. Targeting HBsAg will ideally relieve the immunosuppressive effects on the immune system and help to restore anti-HBV immune responses.
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ISSN:0168-8278
1600-0641
1600-0641
DOI:10.1016/j.jhep.2020.04.013