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白细胞介素7和T细胞受体信号调节CD4记忆细胞的稳态。

Interleukin 7 and T cell receptor signals regulate homeostasis of CD4 memory cells.

作者信息

Seddon Benedict, Tomlinson Peter, Zamoyska Rose

机构信息

Division of Molecular Immunology, National Institute for Medical Research, The Ridgeway, Mill Hill, London NW7 1AA, UK.

出版信息

Nat Immunol. 2003 Jul;4(7):680-6. doi: 10.1038/ni946. Epub 2003 Jun 15.

DOI:10.1038/ni946
PMID:12808452
Abstract

Immunological memory depends on the long-term maintenance of memory T cells. Although the factors that maintain CD8 T cell memory are well understood, those responsible for CD4 memory are not well defined. We have shown here that interleukin 7 (IL-7) was an important survival factor for CD4 memory T cells that together with T cell receptor (TCR) signals regulated homeostasis of the CD4 memory population in lymphopenic conditions and in the intact immune system. Thus, IL-7 contributes to the maintenance of all naive and memory T cell subsets, and therefore controls the overall size of the T cell pool.

摘要

免疫记忆依赖于记忆性T细胞的长期维持。尽管维持CD8 T细胞记忆的因素已为人熟知,但负责CD4记忆的因素尚不明确。我们在此表明,白细胞介素7(IL-7)是CD4记忆性T细胞的重要存活因子,它与T细胞受体(TCR)信号共同调节淋巴细胞减少条件下以及完整免疫系统中CD4记忆群体的稳态。因此,IL-7有助于维持所有幼稚和记忆性T细胞亚群,从而控制T细胞库的整体规模。

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Interleukin 7 and T cell receptor signals regulate homeostasis of CD4 memory cells.白细胞介素7和T细胞受体信号调节CD4记忆细胞的稳态。
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TCR and IL-7 receptor signals can operate independently or synergize to promote lymphopenia-induced expansion of naive T cells.T细胞受体(TCR)信号和白细胞介素-7受体(IL-7受体)信号可以独立发挥作用,也可以协同作用,以促进淋巴细胞减少诱导的初始T细胞扩增。
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