Neumann-Haefelin Christoph, Spangenberg Hans-Christian, Blum Hubert-E, Thimme Robert
Department of Medicine II, University Hospital Freiburg, Hugstetter Strasse 55, Freiburg D-79106, Germany.
World J Gastroenterol. 2007 Sep 28;13(36):4839-47. doi: 10.3748/wjg.v13.i36.4839.
Virus-specific CD8+ T cells are thought to be the major anti-viral effector cells in hepatitis C virus (HCV) infection. Indeed, viral clearance is associated with vigorous CD8+ T cell responses targeting multiple epitopes. In the chronic phase of infection, HCV-specific CD8+ T cell responses are usually weak, narrowly focused and display often functional defects regarding cytotoxicity, cytokine production, and proliferative capacity. In the last few years, different mechanisms which might contribute to the failure of HCV-specific CD8+ T cells in chronic infection have been identified, including insufficient CD4+ help, deficient CD8+ T cell differentiation, viral escape mutations, suppression by viral factors, inhibitory cytokines, inhibitory ligands, and regulatory T cells. In addition, host genetic factors such as the host's human leukocyte antigen (HLA) background may play an important role in the efficiency of the HCV-specific CD8+ T cell response and thus outcome of infection. The growing understanding of the mechanisms contributing to T cell failure and persistence of HCV infection will contribute to the development of successful immunotherapeutical and -prophylactical strategies.
病毒特异性CD8 + T细胞被认为是丙型肝炎病毒(HCV)感染中的主要抗病毒效应细胞。事实上,病毒清除与针对多个表位的强烈CD8 + T细胞反应相关。在感染的慢性期,HCV特异性CD8 + T细胞反应通常较弱,范围狭窄,并且在细胞毒性、细胞因子产生和增殖能力方面常常表现出功能缺陷。在过去几年中,已经确定了可能导致HCV特异性CD8 + T细胞在慢性感染中功能衰竭的不同机制,包括CD4 +辅助不足、CD8 + T细胞分化缺陷、病毒逃逸突变、病毒因子抑制、抑制性细胞因子、抑制性配体和调节性T细胞。此外,宿主遗传因素,如宿主的人类白细胞抗原(HLA)背景,可能在HCV特异性CD8 + T细胞反应的效率以及感染结果中发挥重要作用。对导致T细胞功能衰竭和HCV感染持续存在的机制的日益了解将有助于成功开发免疫治疗和预防策略。