Generation of T cell help through a MHC class I-Restricted TCR

被引:38
作者
Kessels, Helmut W. H. G.
Schepers, Koen
van den Boom, Marly D.
Topham, David J.
Schumacher, Ton N. M.
机构
[1] Netherlands Canc Inst, Div Immunol, NL-1066 CX Amsterdam, Netherlands
[2] Univ Rochester, Aab Inst Biomed Sci, David H Smith Ctr Vaccine Biol & Immunol, Dept Microbiol & Immunol, Rochester, NY 14642 USA
关键词
D O I
10.4049/jimmunol.177.2.976
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
CD4(+) T cells that are activated by a MHC class II/peptide encounter can induce maturation of APCs and promote cytotoxic CD8(+) T cell responses. Unfortunately, the number of well-defined tumor-specific CD4(+) T cell epitopes that can be exploited for adoptive immunotherapy is limited. To determine whether Th cell responses can be generated by redirecting CD4(+) T cells to MHC class I ligands, we have introduced MHC class I-restricted TCRs into postthymic murine CD4(+) T cells and examined CD4(+) T cell activation and helper function in vitro and in vivo. These experiments indicate that Ag-specific CD4(+) T cell help can be induced by the engagement of MHC class I-restricted TCRs in peripheral CD4(+) T cells but that it is highly dependent on the coreceptor function of the CD8 beta-chain. The ability to generate Th cell immunity by infusion of MHC class I-restricted Th cells may prove useful for the induction of tumor-specific T cell immunity in cases where MHC class II-associated epitopes are lacking.
引用
收藏
页码:976 / 982
页数:7
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