Strength of TCR-Peptide/MHC Interactions and In Vivo T Cell Responses

被引:157
作者
Corse, Emily [1 ]
Gottschalk, Rachel A. [1 ,2 ]
Allison, James P. [1 ,3 ]
机构
[1] Howard Hughes Med Inst, Dept Immunol, Chevy Chase, MD 20815 USA
[2] Mem Sloan Kettering Canc Ctr, Ludwig Ctr Canc Immunotherapy, New York, NY 10021 USA
[3] Weill Cornell Grad Sch Med Sci, Immunol & Microbial Pathogenesis Program, New York, NY 10065 USA
关键词
MAJOR HISTOCOMPATIBILITY COMPLEX; DENDRITIC CELLS; LYMPH-NODES; IMMUNOLOGICAL SYNAPSE; ANTIGEN PERSISTENCE; AVIDITY MATURATION; RECEPTOR LIGATION; IMMUNE-RESPONSE; AFFINITY; ACTIVATION;
D O I
10.4049/jimmunol.1003650
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 TCR can detect subtle differences in the strength of interaction with peptide/MHC ligand and transmit this information to influence downstream events in T cell responses. Manipulation of the factor commonly referred to as TCR signal strength can be achieved by changing the amount or quality of peptide/MHC ligand. Recent work has enhanced our understanding of the many variables that contribute to the apparent cumulative strength of TCR stimulation during immunogenic and tolerogenic T cell responses. In this review, we consider data from in vitro studies in the context of in vivo immune responses and discuss in vivo consequences of manipulation of strength of TCR stimulation, including influences on T cell-APC interactions, the magnitude and quality of the T cell response, and the types of fate decisions made by peripheral T cells. The Journal of Immunology, 2011, 186: 5039-5045.
引用
收藏
页码:5039 / 5045
页数:7
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