Clinical implication of immune checkpoint inhibitor on the chronic hepatitis B virus infection

乙型肝炎表面抗原 医学 乙型肝炎病毒 免疫学 免疫系统 病毒学 病毒 乙型肝炎 慢性肝炎 抗原 免疫耐受 内科学
作者
Satoru Hagiwara,Naoshi Nishida,Hiroshi Ida,Kazuomi Ueshima,Yasunori Minami,Masahiro Takita,Tomoko Aoki,Masahiro Morita,Hirokazu Cishina,Yoriaki Komeda,Akihiro Yoshida,Hidetoshi Hayashi,Kazuhiko Nakagawa,Masatoshi Kudo
出处
期刊:Hepatology Research [Wiley]
卷期号:52 (9): 754-761 被引量:4
标识
DOI:10.1111/hepr.13798
摘要

Aim The risk of hepatitis B virus (HBV) reactivation with immune checkpoint inhibitors (ICIs) is an important issue that has not yet been fully investigated. ICI is also expected to have an antiviral effect on HBV due to its immune tolerance inhibitory effect. We herein investigated the risk of HBV reactivation and the antiviral effect of ICI administration. Methods This study included 892 patients on ICIs between September 2014 and May 2021 at our hospital. The frequency of HBV reactivation and antiviral effects were investigated. Results Among the 892 patients who underwent ICI, 27 were hepatitis B surface antigen (HBsAg) positive. HBV reactivation was evaluated in 24 cases, among which 4.1% (1/24) had HBV reactivation. Nucleic acid analog prophylaxis was not administered to patients with reactivation. In a study of 15 cases, the amount of HBsAg decreased from baseline; 2.18 ± 0.77 log to 48 weeks later; 1.61 ± 1.38 log (p = 0.17). Forty-eight weeks after the start of ICI, disappearance of HBsAg was observed in two out of 15 cases (13.3%), and one case each with and without nucleic acid analog. Conclusion In rare cases, HBsAg-positive patients may be reactivated by ICI administration. On the other hand, when ICI is administered, it is expected to have an antiviral effect on HBV due to its immune tolerance inhibitory effect, and future drug development is expected. This article is protected by copyright. All rights reserved.
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