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

被引:41
作者
Firat, H
Cochet, M
Rohrlich, PS
Garcia-Pons, F
Darche, S
Danos, O
Lemonnier, FA
Langlade-Demoyen, P
机构
[1] CNRS, URA 1923, F-91002 Evry, France
[2] Inst Pasteur, Unite Immunite Cellulaire Antivirale, Dept SIDA Retrovirus, F-75724 Paris 15, France
[3] Hop Robert Debre, F-75019 Paris, France
[4] Inst Pasteur, INSERM, U277, Unite Biol Mol Gene, F-75724 Paris 15, France
关键词
cytotoxic T lymphocyte; HLA-A2.1; MHC; transgenic; knockout;
D O I
10.1093/intimm/dxf056
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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/K-b 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 beta 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/K-b 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.
引用
收藏
页码:925 / 934
页数:10
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