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Serum IL-1 beta predicts de novo hepatitis B virus reactivation during direct-acting antiviral therapy for hepatitis C, not during anti-cancer/immunosuppressive therapy

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Title: Serum IL-1 beta predicts de novo hepatitis B virus reactivation during direct-acting antiviral therapy for hepatitis C, not during anti-cancer/immunosuppressive therapy
Authors: Kawagishi, Naoki Browse this author
Suda, Goki Browse this author →KAKEN DB
Sakamori, Ryotaro Browse this author
Matsui, Takeshi Browse this author
Onozawa, Masahiro Browse this author →KAKEN DB
Yang, Zijian Browse this author
Yoshida, Sonoe Browse this author
Ohara, Masatsugu Browse this author
Kimura, Megumi Browse this author
Kubo, Akinori Browse this author
Maehara, Osamu Browse this author
Fu, Qingjie Browse this author
Hosoda, Shunichi Browse this author
Tokuchi, Yoshimasa Browse this author
Suzuki, Kazuharu Browse this author
Nakai, Masato Browse this author
Sho, Takuya Browse this author
Morikawa, Kenichi Browse this author
Natsuizaka, Mitsuteru Browse this author
Ogawa, Koji Browse this author →KAKEN DB
Sakai, Hajime Browse this author
Ohnishi, Shunsuke Browse this author
Baba, Masaru Browse this author
Takehara, Tetsuo Browse this author
Sakamoto, Naoya Browse this author →KAKEN DB
Issue Date: 7-Oct-2022
Publisher: Nature Portfolio
Journal Title: Scientific reports
Volume: 12
Issue: 1
Start Page: 16800
Publisher DOI: 10.1038/s41598-022-21315-z
Abstract: De novo hepatitis B virus (HBV) reactivation occurs during direct-acting antiviral (DAA) treatment in hepatitis C virus (HCV)-infected patients with resolved HBV infection. We evaluated the predictive factors, mechanical insight, and differences of cytokine levels during anti-cancer/immunosuppressive and DAA. Eleven, 35, and 19 HCV-infected patients with previous HBV infection with HBV reactivation during DAA treatment, previous HBV infection without HBV reactivation during DAA treatment, and without HBV infection resolution receiving DAA treatment, respectively, were enrolled. Clinical data and baseline cytokine levels were analyzed. Low baseline serum interleukin (IL)-1 beta levels predicted de novo HBV reactivation during DAA treatment (odds ratio: 47.6, 95% confidence interval: 6.94-333.3). HCV-infected patients with the IL-1 beta gene single nucleotide polymorphism rs16944 AA allele had significantly higher IL-1 beta levels; no HCV-infected patient with the IL-1 beta AA allele experienced HBV reactivation during DAA treatment. Compared to HCV-infected patients with HBV infection resolution, non-HCV infected patients with or without HBV reactivation during anti-cancer/immunosuppressive therapy or bone marrow transplantation had remarkably lower baseline IL-1 beta levels. Low IL-1 beta levels were not associated with HBV reactivation. IL-1 beta levels before DAA for HCV-infected patients with resolved HBV infection could predict HBV reactivation during DAA treatment.
Type: article
URI: http://hdl.handle.net/2115/87372
Appears in Collections:医学院・医学研究院 (Graduate School of Medicine / Faculty of Medicine) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

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