Alloantibodies can Discriminate Class I Major Histocompatibility Complex Molecules Associated with Various Endogenous Peptides
Molecules encoded by a single major histocompatibility complex class I gene can associate with any one of a large number of peptide ligands. T-cell receptors have the capacity to discriminate among these peptide-class I complexes and in many cases bind only a single peptide-class I complex with suff...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 1993-08, Vol.90 (15), p.6949-6951 |
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Sprache: | eng |
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Zusammenfassung: | Molecules encoded by a single major histocompatibility complex class I gene can associate with any one of a large number of peptide ligands. T-cell receptors have the capacity to discriminate among these peptide-class I complexes and in many cases bind only a single peptide-class I complex with sufficient affinity to trigger effector function. In contrast, it is generally assumed that class I-specific alloantibodies are indifferent to peptide heterogeneity, being directed toward allele-specific determinants on the molecule. In this report, three monoclonal antibodies were used to precipitate Kbmolecules from cell lysates. Surprisingly, in each case a different set of peptides was found to be associated with Kbas detected by peptide-dependent Kb-specific alloreactive cytolytic T lymphocytes or by biochemical resolution. These results demonstrate that the affinity of binding by alloantibodies can be affected by the endogenous peptide ligand. |
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ISSN: | 0027-8424 1091-6490 |
DOI: | 10.1073/pnas.90.15.6949 |