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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 ( approximately 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.

Original publication

DOI

10.4049/jimmunol.0901607

Type

Journal article

Journal

J Immunol

Publication Date

01/10/2009

Volume

183

Pages

4337 - 4345

Keywords

Animals, CD8-Positive T-Lymphocytes, Cell Line, Tumor, Clone Cells, Cross Reactions, Cross-Priming, Epitopes, T-Lymphocyte, Humans, Male, Mice, Mice, Inbred BALB C, Mice, Inbred C57BL, Mice, Knockout, Mice, Transgenic, Peptide Fragments, Peptide Library, Predictive Value of Tests, Protein Binding