Mycoplasma superantigen is a CDR3-dependent ligand for the T cell antigen receptor

被引:45
作者
Hodtsev, AS
Choi, YW
Spanopoulou, E
Posnett, DN
机构
[1] CUNY Mt Sinai Sch Med, Ruttenberg Canc Ctr, Howard Hughes Med Inst, New York, NY 10029 USA
[2] Rockefeller Univ, Howard Hughes Med Inst, New York, NY 10021 USA
[3] Cornell Univ Med Coll, Grad Sch Med Sci, Program Immunol, New York, NY 10021 USA
[4] Cornell Univ Med Coll, Dept Med, New York, NY 10021 USA
关键词
D O I
10.1084/jem.187.3.319
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Superantigens are defined as proteins that activate a large number of T cells through interaction with the V beta region of the T cell antigen receptor (TCR). Here we demonstrate that the superantigen produced by Mycoplasma ai arthritidis (MAM), unlike six bacterial superantigens tested, interacts not only with the V beta region but also with the CDR3 (third complementarity-determining region) of TCR-beta. Although MAN shares typical features with other superantigens, direct interaction with CDR3-beta is a feature of nominal peptide antigens situated in the antigen groove of major histocompatibility complex (MHC) molecules rather than superantigens. During peptide recognition, V beta and V alpha. domains of the TCR form contacts with MHC and the V beta-dependent and is apparently stabilized by direct contacts with the CDR3-beta region. Thus, MAM represents a new type of ligand for TCR, distinct from both conventional peptide antigens and other known superantigens.
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页码:319 / 327
页数:9
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