Yang Jiezuan, Lu Haifeng, Guo Renyong, Yan Dong, Ye Ping, Jin Linfeng, Chen Chunlei, Cao Hongcui, Diao Hongyan, Li Lanjuan
State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, the First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou 310003, China Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Zhejiang University, Hangzhou 310003, China.
Department of Laboratory Medicine, the First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou 310003, China.
Pathog Dis. 2015 Mar;73(2):1-9. doi: 10.1093/femspd/ftu018. Epub 2014 Dec 4.
T cell receptor beta variable (TCRBV) repertoire could imply the composition and function status of T cells in subjects with HBV infection. The gene melting spectral pattern (GMSP) can be used to determine the profile of TCRBV gene family. The molecular profile of TCRBV in peripheral lymphocytes from asymptomatic HBV carriers (AsC) remains ill-defined. Peripheral blood mononuclear cells (PBMCs) were separated and sorted, and the profiles of TCRBV complementarity-determining region 3 (CDR3) in CD4(+), CD8(+) T subsets and PBMCs were assayed using GMSP. The number of skewed TCRBV in the PBMCs was significantly lower than that in the CD4(+) or CD8(+) T subsets, and the number of monoclonal TCRBV families in the CD8(+) T subset was significantly higher than that in CD4(+) T subset. Compared to healthy donors, TCRBV11, BV13.1, BV20 and BV24 were used more frequently than other TCRBV members in PBMCs from AsC subjects. Furthermore, the relatively conserved CDR3 motifs were detected in these TCRBVs. The results indicate that the T cell response in AsC subjects involves several TCRBVs, and that the CD8(+) T subset maybe more relevant to pathogenesis of AsC. Moreover, the four relative conserved TCRBVs maybe a target for personalized treatments for persistent HBV infection.
T细胞受体β可变区(TCRBV)库可暗示乙肝病毒感染受试者体内T细胞的组成和功能状态。基因熔解光谱模式(GMSP)可用于确定TCRBV基因家族的概况。无症状乙肝病毒携带者(AsC)外周淋巴细胞中TCRBV的分子概况仍不明确。分离并分选外周血单个核细胞(PBMC),使用GMSP检测CD4(+)、CD8(+) T亚群和PBMC中TCRBV互补决定区3(CDR3)的概况。PBMC中偏斜的TCRBV数量显著低于CD4(+)或CD8(+) T亚群,且CD8(+) T亚群中单克隆TCRBV家族的数量显著高于CD4(+) T亚群。与健康供体相比,AsC受试者的PBMC中TCRBV11、BV13.1、BV20和BV24的使用频率高于其他TCRBV成员。此外,在这些TCRBV中检测到相对保守的CDR3基序。结果表明,AsC受试者的T细胞反应涉及多种TCRBV,且CD8(+) T亚群可能与AsC的发病机制更相关。此外,这四种相对保守的TCRBV可能是持续性乙肝病毒感染个性化治疗的靶点。