The low frequency of self-peptide–specific T cells in the human preimmune repertoire has so far precluded their direct evaluation. Here, we report an unexpected high frequency of T cells specific for the self-antigen Melan-A/MART-1 in CD8 single–positive thymocytes from human histocompatibility leukocyte antigen-A2 healthy individuals, which is maintained in the peripheral blood of newborns and adults. Postthymic replicative history of Melan-A/MART-1–specific CD8 T cells was independently assessed by quantifying T cell receptor excision circles and telomere length ex vivo. We provide direct evidence that the large T cell pool specific for the self-antigen Melan-A/MART-1 is mostly generated by thymic output of a high number of precursors. This represents the only known naive self-peptide–specific T cell repertoire directly accessible in humans.
Thymic Selection Generates a Large T Cell Pool Recognizing a Self-Peptide in Humans
A. Zippelius and M.J. Pittet contributed equally to this work.
Abbreviations used in this paper: CB, cord blood; DP, double positive; flow FISH, fluorescence in situ hybridization and flow cytometry; HD, healthy donor; Melan-A, Melan-A/MART-1; SP, single positive; TILN, tumor infiltrated lymph node; TREC, T cell receptor excision circles.
Alfred Zippelius, Mikaël J. Pittet, Pascal Batard, Nathalie Rufer, Magda de Smedt, Philippe Guillaume, Kim Ellefsen, Danila Valmori, Danielle Liénard, Jean Plum, H. Robson MacDonald, Daniel E. Speiser, Jean-Charles Cerottini, Pedro Romero; Thymic Selection Generates a Large T Cell Pool Recognizing a Self-Peptide in Humans . J Exp Med 18 February 2002; 195 (4): 485–494. doi: https://doi.org/10.1084/jem.20011658
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