Hibberd M L, Wong F S, Nicholson L B, Demaine A G
Department of Medicine, King's College School of Medicine and Dentistry, London.
Immunology. 1993 Jul;79(3):398-402.
The human T-cell antigen receptor (TcR) V beta repertoire was investigated following in vivo reimmunization with tetanus toxoid (TT). Four healthy subjects were immunized subcutaneously with TT, and 24 samples of peripheral blood T cells were taken at intervals over several weeks and used to generate TcR-C beta chain-specific first-strand cDNA. A semi-quantitative assay utilizing the polymerase chain reaction (PCR) was used to measure the amount of 22 different TcR-V beta gene transcripts in the cDNA. A peak increase in the amount of V beta 2, 4, 6, 13.1 and 14 occurred 14 days post-immunization, with each V beta increased in at least two of the four subjects. No obvious changes in the other 17 V beta genes were found. A secondary antibody response to TT occurred in all subjects by day 14. These results show that it is now possible to characterize the in vivo kinetics of the human TcR repertoire following stimulation with a conventional antigen.
在用破伤风类毒素(TT)进行体内再次免疫后,对人T细胞抗原受体(TcR)Vβ谱系进行了研究。4名健康受试者皮下注射TT,在数周内定期采集24份外周血T细胞样本,并用于生成TcR-Cβ链特异性第一链cDNA。利用聚合酶链反应(PCR)的半定量分析方法来测定cDNA中22种不同TcR-Vβ基因转录本的量。免疫后14天,Vβ2、4、6、13.1和14的量出现峰值增加,且在4名受试者中的至少两名中,每种Vβ均增加。未发现其他17种Vβ基因有明显变化。到第14天时,所有受试者均出现了对TT的二次抗体应答。这些结果表明,现在有可能对用传统抗原刺激后人TcR谱系的体内动力学特征进行描述。