Usuku K, Joshi N, Hatem C J, Alper C A, Schoenfeld D A, Hauser S L
Department of Neurology, Massachusetts General Hospital, Boston 02114.
Immunogenetics. 1993;38(3):193-8. doi: 10.1007/BF00211519.
The influence of the environment and of the major histocompatibility complex (MHC) in shaping the human T-cell receptor beta-chain variable region (TCRBV) repertoire has not been systematically studied. Here, expression of TCRBV gene families was estimated by a sensitive polymerase chain reaction (PCR)-based method. Serial studies of peripheral blood, performed at 2-week intervals over a 3-month period, revealed that fluctuation in the expression of many TCRBV genes occurred in healthy individuals and in the absence of clinically evident infections. Fluctuation of TCRBV4, TCRBV5.2, TCRBV9, and TCRBV13.1 genes were present in all subjects. Additional TCRBV genes fluctuated in some but not in other individuals. Comparison of the TCRBV repertoire between these unrelated individuals indicated differences in the mean expression of TCRBV5.1, TCRBV9, TCRBV11, TCRBV15, TCRBV17, and TCRBV20 genes. For any TCRBV gene, intersubject differences were generally of a magnitude of twofold or less. Larger differences characterized the TCRBV repertoire of CD4 compared to CD8 cells. Some differences, for example over-representation of TCRBV2 and TCRBV5.1 on CD4, and TCRBV10, TCRBV14, and TCRBV16 on CD8 cells, were present in most subjects. Individuals homozygous for DR2- or DR3-bearing extended MHC haplotypes displayed similar individual variability of TCRBV expression. These data indicate that the circulating TCRBV repertoire in humans is both dynamic and diverse. Both environment and MHC effects contribute to the diversity of TCRBV expression.
环境和主要组织相容性复合体(MHC)对人类T细胞受体β链可变区(TCRBV)库形成的影响尚未得到系统研究。在此,通过一种基于聚合酶链反应(PCR)的灵敏方法来估计TCRBV基因家族的表达。在3个月的时间里,每隔2周对外周血进行系列研究,结果显示,在健康个体且无临床明显感染的情况下,许多TCRBV基因的表达会发生波动。所有受试者均出现TCRBV4、TCRBV5.2、TCRBV9和TCRBV13.1基因的波动。其他TCRBV基因在部分个体中出现波动,但在其他个体中未出现。对这些不相关个体的TCRBV库进行比较,结果表明TCRBV5.1、TCRBV9、TCRBV11、TCRBV15、TCRBV17和TCRBV20基因的平均表达存在差异。对于任何TCRBV基因,个体间差异通常在两倍或更小范围内。与CD8细胞相比,CD4细胞的TCRBV库差异更大。在大多数受试者中存在一些差异,例如CD4细胞上TCRBV2和TCRBV5.1的过度表达,以及CD8细胞上TCRBV10、TCRBV14和TCRBV16的过度表达。携带DR2或DR3的扩展MHC单倍型纯合个体表现出相似的TCRBV表达个体变异性。这些数据表明,人类循环中的TCRBV库既具有动态性又具有多样性。环境和MHC效应均有助于TCRBV表达的多样性。