慢性乙型肝炎病毒感染中CD8+T细胞功能障碍的研究进展

细胞与分子免疫学杂志 Pub Date : 2025-05-01
Nan Zhang, Chuanhai Li, Rongjie Zhao, Liwen Zhang, Qing Ouyang, Liyun Zou, Ji Zhang
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引用次数: 0

摘要

乙型肝炎病毒(HBV)特异性CD8+ T细胞在控制HBV感染中发挥核心作用;然而,在慢性HBV感染期间,它们的功能受损,表现为功能障碍状态。最近的研究表明,慢性HBV感染中的CD8+ T细胞功能障碍不同于其他病毒感染或肿瘤中观察到的经典衰竭。2024年,几项关键性研究进一步阐明了慢性HBV感染中CD8+ T细胞功能障碍的新机制,并确定了新的治疗靶点,包括4-1BB和转化生长因子-β (TGF-β)。本文在阐述CD8+ T细胞在慢性HBV感染中的功能障碍及其机制的基础上,重点总结了这些最新研究的主要发现,并探讨了它们的转化价值和临床意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Research progress on CD8+T cell dysfunction in chronic hepatitis B virus infection].

Hepatitis B virus (HBV)-specific CD8+ T cells play a central role in controlling HBV infection; however, their function is impaired during chronic HBV infection, manifesting as a state of dysfunction. Recent studies have revealed that CD8+ T cell dysfunction in chronic HBV infection differs from the classical exhaustion observed in other viral infections or tumors. In 2024, several pivotal studies further elucidated novel mechanisms underlying CD8+ T cell dysfunction in chronic HBV infection and identified new therapeutic targets, including 4-1BB and transforming growth factor-beta (TGF-β). This review, while elucidating the dysfunction of CD8+ T cells in chronic HBV infection and its underlying mechanisms, focuses on summarizing the key findings from these latest studies and explores their translational value and clinical significance.

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