TCR repertoire of suppressor CD8+CD28- T cell populations

被引:21
|
作者
Pennesi, G
Liu, ZR
Ciubotariu, R
Jiang, SP
Colovai, A
Cortesini, R
Suciu-Foca, N
Harris, P
机构
[1] Columbia Univ Coll Phys & Surg, Dept Pathol, New York, NY 10032 USA
[2] Univ Roma La Sapienza, Dept Surg, Ist Clin Chirurg 2, Serv Trapianti Organo, Rome, Italy
关键词
T suppressor cells; T cell receptor; TCR V beta spectratyping;
D O I
10.1016/S0198-8859(98)00134-7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The cellular basis of graft rejection and the development of strategies for specific suppression of T cell responses against allogeneic and xenogeneic transplants represents an area of active investigation. Recently, a population of MHC-class I restricted CD8(+)CD28(-) T suppressor cells (Ts) which are able to inhibit specifically the proliferative response of allospecific, xenospecific and nominal-antigen specific CD4(+) T helper cells (Th) has been identified. We have studied the TCR V beta gene repertoire expressed by CD8(+)CD28(-) Ts isolated from allospecific, xenospecific, and nominal antigen-specific T cell lines (TCL). A limited V beta repertoire has been found in all TCLs studied. The most restricted TCR V beta usage was observed within the population of Ts from xenospecific TCLs. The TCR V beta usage within the Ts subset of TCL differs from the TCR repertoire expressed by the CD4(+) Th subset of the same TCL. This is consistent with the fact that Ts and Th cells recognize distinct MHC/antigen complexes. The finding that the TCR repertoire used by Ts is limited opens new avenues for studying the mechanisms of transplant rejection. Human Immunology 60, 291-304 (1999). (C) American Society for Histocompatibility and Immunogenetics, 1999 Published by Elsevier Science Inc.
引用
收藏
页码:291 / 304
页数:14
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