共 43 条
Coordinated expression of ig-like inhibitory MHC class I receptors and acquisition of cytotoxic function in human CD8+ T cells
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作者:

Anfossi, N
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机构: INSERM, Unite 463, Inst Biol, F-44035 Nantes 01, France

Doisne, JM
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机构: INSERM, Unite 463, Inst Biol, F-44035 Nantes 01, France

Peyrat, MA
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机构: INSERM, Unite 463, Inst Biol, F-44035 Nantes 01, France

Ugolini, S
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机构: INSERM, Unite 463, Inst Biol, F-44035 Nantes 01, France

Bonnaud, O
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机构: INSERM, Unite 463, Inst Biol, F-44035 Nantes 01, France

Bossy, D
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机构: INSERM, Unite 463, Inst Biol, F-44035 Nantes 01, France

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Moreau, JF
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机构: INSERM, Unite 463, Inst Biol, F-44035 Nantes 01, France

Delfraissy, JF
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机构: INSERM, Unite 463, Inst Biol, F-44035 Nantes 01, France

Dechanet-Merville, J
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机构: INSERM, Unite 463, Inst Biol, F-44035 Nantes 01, France

Bonneville, M
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机构:
INSERM, Unite 463, Inst Biol, F-44035 Nantes 01, France INSERM, Unite 463, Inst Biol, F-44035 Nantes 01, France

Venet, A
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机构: INSERM, Unite 463, Inst Biol, F-44035 Nantes 01, France

Vivier, E
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机构: INSERM, Unite 463, Inst Biol, F-44035 Nantes 01, France
机构:
[1] INSERM, Unite 463, Inst Biol, F-44035 Nantes 01, France
[2] Univ Bordeaux 3, CIRID, CNRS, UMR 5164, Bordeaux, France
[3] Fac Med Paris Sud, INSERM, Equipe 0109, F-94276 Le Kremlin Bicetre, France
[4] Beckman Coulter Immunotech, Marseille, France
[5] Univ Mediterranee, CNRS, INSERM, Ctr Immunol Marseille Luminy, Marseille, France
关键词:
D O I:
10.4049/jimmunol.173.12.7223
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
MHC class I-specific inhibitory receptors are expressed by a subset of memory-phenotype CD8(+) T cells. Similar to NK cells, MHC class I-specific inhibitory receptors might subserve on T cells an important negative control that participates to the prevention of autologous damage. We analyzed here human CD8(+) T cells that express the Ig-like MHC class I-specific inhibitory receptors: killer cell Ig-like receptor (KIR) and CD85j. The cell surface expression of Ig-like inhibitory MHC class I receptors was found to correlate with an advanced stage of CD8(+) T cell maturation as evidenced by the reduced proliferative potential of KIR+ and CD85j(+). T cells associated with their high intracytoplasmic perforin content. This concomitant regulation might represent a safety mechanism to control potentially harmful cytolytic CD8(+) T cells, by raising their activation threshold. Yet, KIR+ and CD85j(+) T cells present distinct features. KIR(+)CD8(+) T cells are poor IFN-gamma producers upon TCR engagement. In addition, KIR are barely detectable at the surface of virus-specific T cells during the course of CMV or HIV-1 infection. By contrast, CD85j(+)CD8(+) T cells produce IFN-gamma upon TCR triggering, and represent a large fraction of virus-specific T cells. Thus, the cell surface expression of Ig-like inhibitory MHC class I receptors is associated with T cell engagement into various stages of the cytolytic differentiation pathway, and the cell surface expression of CD85j or KIR witnesses to the history of qualitatively and/or quantitatively distinct T cell activation events.
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页码:7223 / 7229
页数:7
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