Diversity, functionality, and stability of the T cell repertoire derived in vivo from a single human T cell precursor

被引:112
作者
Bousso, P
Wahn, V
Douagi, I
Horneff, G
Pannetier, C
Le Deist, F
Zepp, F
Niehues, T
Kourilsky, P
Fischer, A
de Saint Basile, G [1 ]
机构
[1] Hop Necker Enfants Malad, INSERM, U429, F-75015 Paris, France
[2] INSERM, Unite Biol Mol Gene, U277, F-75015 Paris, France
[3] Inst Pasteur, CNRS URA 1961, Unite Dev Lymphocytes, F-75015 Paris, France
[4] Univ Dusseldorf, Kinderklin, D-40225 Dusseldorf, Germany
[5] Johannes Gutenberg Univ Mainz, Kinderklin, D-55131 Mainz, Germany
关键词
D O I
10.1073/pnas.97.1.274
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In this report, we have analyzed the human T cell repertoire derived in vivo from a single T cell precursor. A unique case of X-linked severe combined immunodeficiency in which a reverse mutation occurred in an early T cell precursor was analyzed to this end. It was determined that at least 1,000 T cell clones with unique T cell receptor-β sequences were generated from this precursor. This diversity seems to be stable over time and provides protection from infections in vivo. A similar estimation was obtained in an in vitro murine model of T cell generation from a single cell precursor. Overall, our results document the large diversity potential of T cell precursors and provide a rationale for gene therapy of the block of T cell development.
引用
收藏
页码:274 / 278
页数:5
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