Comparative analysis of the CD8+ T cell repertoires of H‐2 class I wild‐type/HLA‐A2.1 and H‐2 class I knockout/HLA‐A2.1 transgenic mice

HHD transgenic mice which express HLA‐A2.1 monochain molecules in a H‐2 class I– context have an improved capacity to develop HLA‐A2.1‐restricted cytotoxic T lymphocyte (CTL) responses as compared with classical A2.1/Kb transgenic mice, which express heterodimeric HLA‐A2.1 molecules in a H‐2 class I...

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Veröffentlicht in:International immunology 2002-08, Vol.14 (8), p.925-934
Hauptverfasser: Firat, Hüseyin, Cochet, Madeleine, Rohrlich, Pierre‐Simon, Garcia‐Pons, Francisco, Darche, Sylvie, Danos, Olivier, Lemonnier, François A., Langlade‐Demoyen, Pierre
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Sprache:eng
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Zusammenfassung:HHD transgenic mice which express HLA‐A2.1 monochain molecules in a H‐2 class I– context have an improved capacity to develop HLA‐A2.1‐restricted cytotoxic T lymphocyte (CTL) responses as compared with classical A2.1/Kb transgenic mice, which express heterodimeric HLA‐A2.1 molecules in a H‐2 class I wild‐type context. A detailed TCR analysis of HLA‐A2.1‐restricted CD8+ T cells educated and mobilized in both strains of mice was undertaken. Focusing on TCR β chains, comparative PCR analysis of naive and immune CD8+ T cell repertoires were performed. In spite of lower cell surface expression of HLA class I molecules and lower overall number of CD8+ T cells, HHD mice educate a qualitatively normally diversified CD8+ T cell repertoire and mobilize a larger variety of CD8+ T cells in response to HLA‐A2.1‐restricted antigens compared with A2.1/Kb mice. These observations provide the molecular bases accounting for the fact that HHD mice represent the most versatile animal model currently available for preclinical studies of HLA‐A2.1‐restricted CTL responses.
ISSN:0953-8178
1460-2377
1460-2377
DOI:10.1093/intimm/dxf056