Division of Gastroenterology and Hepatology, Erasmus MC, University Medical Center, Rotterdam, Netherlands.
Front Immunol. 2020 Mar 4;11:401. doi: 10.3389/fimmu.2020.00401. eCollection 2020.
Treatment of chronic hepatitis B virus (HBV) infection is highly effective in suppressing viral replication, but complete cure is rarely achieved. In recent years, substantial progress has been made in the development of immunotherapy to treat cancer. Applying these therapies to improve the management of chronic HBV infection is now being attempted, and has become an area of active research. Immunotherapy with vaccines and checkpoint inhibitors can boost T cell functions , and therefore may be used to reinvigorate the impaired HBV-specific T cell response. However, whether these approaches will suffice and restore antiviral T cell immunity to induce long-term HBV control remains an open question. Recent efforts have begun to describe the phenotype and function of HBV-specific T cells on the single epitope level. An improved understanding of differing T cell specificities and their contribution to HBV control will be instrumental for advancement of the field. In this review, we outline correlates of successful versus inadequate T cell responses to HBV, and discuss the rationale behind therapeutic vaccines and checkpoint inhibitors for the treatment of chronic HBV infection.
治疗慢性乙型肝炎病毒(HBV)感染在抑制病毒复制方面非常有效,但很少能实现完全治愈。近年来,癌症免疫疗法的发展取得了重大进展。现在正在尝试将这些疗法应用于改善慢性 HBV 感染的管理,这已成为一个活跃的研究领域。疫苗和检查点抑制剂的免疫疗法可以增强 T 细胞的功能,因此可能用于重振受损的 HBV 特异性 T 细胞反应。然而,这些方法是否足以恢复抗病毒 T 细胞免疫以诱导长期 HBV 控制仍然是一个悬而未决的问题。最近的研究工作已经开始描述 HBV 特异性 T 细胞在单个表位水平上的表型和功能。更好地了解不同的 T 细胞特异性及其对 HBV 控制的贡献,将有助于该领域的发展。在这篇综述中,我们概述了成功和不充分的 T 细胞对 HBV 反应的相关性,并讨论了治疗性疫苗和检查点抑制剂治疗慢性 HBV 感染的基本原理。