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• W2079381553 abstract "Self-peptide/major histocompatibility complex (MHC) complexes profoundly influence the biology of T lymphocytes. They promote the selection of the T cell receptor (TCR) repertoire in the thymus, maintain the homeostasis of peripheral T cells prior to encounter with antigen, and modify the responsiveness of T cells to foreign antigens. In addition, they can serve as antigens for autoaggressive T cells that induce autoimmune diseases. The complete sequencing of the genomes of human, mouse, and many pathogenic organisms now provides us with a comprehensive list of all possible proteins that may be the source of foreign antigenic and self-peptides. A computational approach using profile-based similarity searches on potential self-MHC-binding peptides can be used to efficiently predict self-peptides with biological activities. The common feature of the identified peptides is similarity to antigen. Thus, self-peptides may form 'hazy' images of the universe of antigens that are used as templates to create and maintain the TCR repertoire." @default.
• W2079381553 created "2016-06-24" @default.
• W2079381553 creator A5059688755 @default.
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• W2079381553 creator A5087430495 @default.
• W2079381553 date "2002-12-01" @default.
• W2079381553 modified "2023-10-18" @default.
• W2079381553 title "Genomics-based identification of self-ligands with T cell receptor-specific biological activity" @default.
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• W2079381553 doi "https://doi.org/10.1034/j.1600-065x.2002.19011.x" @default.
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