Quantitating T Cell Cross-Reactivity for Unrelated Peptide Antigens

被引:62
|
作者
Ishizuka, Jeffrey [2 ]
Grebe, Kristie
Shenderov, Eugene [2 ]
Peters, Bjoern [3 ]
Chen, Qiongyu [2 ]
Peng, YanChun [2 ]
Wang, Lili [2 ]
Dong, Tao [2 ]
Pasquetto, Valerie [3 ]
Oseroff, Carla [3 ]
Sidney, John [3 ]
Hickman, Heather
Cerundolo, Vincenzo [2 ]
Sette, Alessandro [3 ]
Bennink, Jack R.
McMichael, Andrew [2 ]
Yewdell, Jonathan W. [1 ]
机构
[1] NIAID, Viral Dis Lab, NIH, Bethesda, MD 20892 USA
[2] Univ Oxford, John Radcliffe Hosp, Weatherall Inst Mol Med, Oxford OX3 9DU, England
[3] La Jolla Inst Allergy & Immunol, La Jolla, CA 92037 USA
来源
JOURNAL OF IMMUNOLOGY | 2009年 / 183卷 / 07期
基金
英国医学研究理事会;
关键词
TRANSGENIC MICE; INFLUENZA NUCLEOPROTEIN; REPERTOIRE DIVERSITY; HIGH-AFFINITY; RESPONSES; RECEPTOR; LYMPHOCYTES; VIRUS; CYTOMEGALOVIRUS; SPECIFICITY;
D O I
10.4049/jimmunol.0901607
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Quantitating the frequency of T cell cross-reactivity to unrelated peptides is essential to understanding T cell responses in infectious and autoimmune diseases. Here we used 15 mouse or human CD8(+) T cell clones (11 antiviral, 4 anti-self) in conjunction with a large library of defined synthetic peptides to examine nearly 30,000 TCR-peptide MHC class I interactions for cross-reactions. We identified a single cross-reaction consisting of an anti-self TCR recognizing a poxvirus peptide at relatively low sensitivity. We failed to identify any cross-reactions between the synthetic peptides in the panel and polyclonal. CD8(+) T cells raised to viral or alloantigens. These findings provide the best estimate to date of the frequency of T cell cross-reactivity to unrelated peptides (similar to 1/30,000), explaining why cross-reactions between unrelated pathogens are infrequently encountered and providing a critical parameter for understanding the scope of self-tolerance. The Journal of Immunology, 2009, 183: 4337-4345.
引用
收藏
页码:4337 / 4345
页数:9
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