SELECTION OF LYMPHOCYTES-T BEARING LIMITED T-CELL RECEPTOR-BETA CHAINS IN THE RESPONSE TO A HUMAN PATHOGEN

被引:50
作者
WANG, XH
OHMEN, JD
UYEMURA, K
REA, TH
KRONENBERG, M
MODLIN, RL
机构
[1] UNIV CALIF LOS ANGELES,SCH MED,DIV DERMATOL,52-121 CHS,10833 LE CONTE AVE,LOS ANGELES,CA 90024
[2] UNIV CALIF LOS ANGELES,SCH MED,DEPT MICROBIOL & IMMUNOL,LOS ANGELES,CA 90024
[3] UNIV SO CALIF,SCH MED,DERMATOL SECT,LOS ANGELES,CA 90033
关键词
CELL-MEDIATED IMMUNITY; DELAYED-TYPE HYPERSENSITIVITY; MAJOR HISTOCOMPATIBILITY COMPLEX; LEPROSY;
D O I
10.1073/pnas.90.1.188
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Delayed-type hypersensitivity (DTH) is a classic measure of T-cell responsiveness to foreign antigen. To estimate the extent of the T-cell repertoire in the DTH response to a human pathogen, we measured T-cell receptor (TCR) beta-chain variable-region (V(beta)) gene usage in reversal reactions in leprosy. Reversal reactions represent naturally occurring DTH responses in leprosy, in which augmentation of T-cell responses to Mycobacterium leprae is concomitant with clearance of bacilli from lesions. T cells using the V(beta)6-, V(beta)12-, V(beta)14-, and V(beta)19-encoded TCRs were strikingly overrepresented in the lesions of patients as compared to blood and pre-DTH lesions from the same individuals. Furthermore, these data indicate a possible association between the predominant expression of a V(beta) gene segment in lesions and the major histocompatibility complex class II haplotype of the individual. V(beta)6 was prominent in the lesions of four patients who were DR15, a marker of resistance in leprosy infection. Sequence analysis of V(beta)6 TCRs showed frequent use of V(beta)6.1 and J(beta)2.7 gene segments and a conserved amino acid motif in the V-J junction in a reversal-reaction lesion, but not in blood from the same patient. The limited TCR repertoire expressed by the infiltrating T cells suggests that a limited set of antigens is recognized in the DTH response to a human pathogen. We suggest that the mechanism by which major histocompatibility complex haplotype influences DTH in this disease involves the presentation of specific peptides, with subsequent selection of specific TCRs followed by local oligoclonal expansion.
引用
收藏
页码:188 / 192
页数:5
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