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• W1994379419 endingPage "359" @default.
• W1994379419 startingPage "351" @default.
• W1994379419 abstract "Alloreactive T cells are often specific for individual peptides that are bound to allogeneic major histocompatibility complex (MHC) molecules. Other alloreactive T cells are reported to be peptide-independent or to recognize MHC conformational changes that are induced by multiple peptides. We tested 12 anti-HLA-B7 alloreactive cytotoxic T lymphocyte (CTL) clones that bind a restricted region of HLA-B7, including three CTL clones that were generated in a protocol designed to stimulate peptide-independent T cells. All 12 CTLs recognized multiple point mutations in the HLA-B7 peptide-binding groove. Eleven of the 12 CTLs recognized specific peptides that eluted in one or two fractions on high-performance liquid chromatography (HPLC). None of the CTLs promiscuously recognized 16 HLA-B7-binding synthetic peptides, although one CTL recognized minor by-products in one synthetic peptide preparation. CTL clone KID-9 cross-reacted with allogeneic HLA-B7 and HLA-B27 molecules and recognized a distinct peptide bound to each MHC molecule. CTL clone KD-11 recognized peptides that eluted in two HPLC fractions and recognized HLA-B7-transfected peptide antigen processing defective T2 cells. These results indicate that CTL allorecognition is peptide-specific whether the allogeneic MHC molecules are expressed on normal cells or antigen processing-deficient cells." @default.
• W1994379419 created "2016-06-24" @default.
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• W1994379419 date "1997-07-01" @default.
• W1994379419 modified "2023-10-17" @default.
• W1994379419 title "ALLOREACTIVE CYTOTOXIC T LYMPHOCYTES FOCUS ON SPECIFIC MAJOR HISTOCOMPATIBILITY COMPLEX-BOUND PEPTIDES1" @default.
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• W1994379419 doi "https://doi.org/10.1097/00007890-199707270-00030" @default.
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