剧目
T细胞受体
乙型肝炎病毒
免疫系统
免疫学
乙型肝炎
表位
病毒学
免疫
肝细胞癌
慢性肝炎
获得性免疫系统
抗原
T细胞
医学
癌症研究
病毒
物理
声学
作者
Xueying Li,Anqi Zheng,Jiabang Liu,Mengfen Shi,Baolin Liao,Shi Xie,Rong Yan,Yifan Gan,Xuan Zuo,Mingxing Gong,Hongkai Wu,Zhanhui Wang
标识
DOI:10.1016/j.antiviral.2023.105608
摘要
Challenges in assessing hepatitis B virus (HBV)-specific T cell immunity as an immunological biomarker still remain in chronic hepatitis B (CHB), such as the requirement of large quantities of cells. This study aims to conveniently assess HBV-specific T cells immunity in chronic HBV infected patients. We obtained T cell receptor β chains (TCRβs) from public databases and six acute hepatitis B patients to establish an HBV-specific TCRβs dataset. For some TCRs from one acute patient, their specificities and epitopes were verified. The potential HBV-specific TCRβs from CHB patients were analyzed using GLIPH2 and established dataset. By analyzing two antiviral therapy cohorts including 42 CHB patients, we showed that individuals with better therapy response may depend more on newly emerging potential HBV-specific TCRβs. In a cross-sectional study containing 207 chronic HBV infected patients, the results exhibited that the characteristics of potential HBV-specific clusters were divergent between CHB and hepatocellular carcinoma patients. Our strategy could profile potential HBV-specific TCRβ repertoire using a small blood sample, which will complement traditional methods for assessing the HBV-specific T cell immunity.
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