Important note: Information in this article was accurate in 1997. The state of the art may have changed since the publication date.
Alloreactive CD8+ T cells can recognize unusual, rare, and unique processed peptide/MHC complexes.
J Immunol. 1996 Nov 15;157(10):4464-73. Unique Identifier : AIDSLINE MED/97064204 Malarkannan S; Gonzalez F; Nguyen V; Adair G; Shastri N; Department of Molecular and Cell Biology, University of; California, Berkeley 94720, USA.
Abstract:
The identity and abundance of self-peptide/MHC class I complexes that serve as ligands for alloreactive T cells remain largely unknown. Using the Kb-restricted, alloreactive T cells as a probe, the Ag precursor gene, adenosine phosphoribosyl transferase (APRT), was isolated by expression cloning. Its naturally processed product was identified as the SLVELTSL (SEL8) octapeptide. The SEL8 peptide shared five residues with the previously identified SVVEFSSL (JAL8) peptide that stimulated the same T cell, but lacked the critical phenylalanine/tyrosine residue at the primary p5 anchor position. Despite the absence of this key conserved anchor residue, SEL8 was bound tightly by Kb MHC and yet was expressed at less than 10 copies/cell. Mutations in the donor APRT gene in the APC caused a concomitant loss in the ability of APCs to stimulate T cells. The results confirm that the display of peptide/MHC complexes in cells exceeds the predictions based upon consensus motifs, and that CD8+ alloreactive and conventional Ag-specific T cells are indistinguishable in their ability to recognize unique and rare peptide/MHC class I complexes.
Keywords: Animal Cell Line CD8-Positive T-Lymphocytes/*IMMUNOLOGY Epitopes/*IMMUNOLOGY Histocompatibility Antigens Class I/*IMMUNOLOGY Isoantigens/*IMMUNOLOGY Mice NAD+ ADP-Ribosyltransferase/ANALYSIS Peptides/*IMMUNOLOGY/METABOLISM Protein Binding/IMMUNOLOGY Support, Non-U.S. Gov't Support, U.S. Gov't, P.H.S. JOURNAL ARTICLE 970228
M9721860
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