T cell receptor crossreactivity as a general property of T cell recognition

被引:57
作者
Wucherpfennig, KW [1 ]
机构
[1] Dana Farber Canc Inst, Dept Canc Immunol & AIDS, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Neurol, Boston, MA 02115 USA
关键词
T cell receptor; crossreactivity; molecular mimicry; autoimmunity;
D O I
10.1016/j.molimm.2003.11.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
TCR recognition of MHC/peptide complexes directs many aspects of T cell biology, including thymic selection, survival of naive T cells and differentiation into effector and memory T cells. It was widely thought that TCR recognition is highly specific, with an individual T cell being capable of only recognizing a particular peptide and closely related sequence variants. By considering the structural requirements for peptide binding to MHC molecules and TCR recognition of MHC/peptide complexes, we demonstrated that T cell clones could recognize a number of peptides from different organisms that are remarkably distinct in their primary sequence. These peptides are particularly diverse at those sequence positions buried in pockets of the MHC binding site, while a higher degree of similarity is present at a limited number of peptide residues that create the interface with the TCR. Many examples have now been documented for human and murine T cells, indicating that TCR crossreactivity represents a general feature of TCR recognition. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1009 / 1017
页数:9
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