Adaptive from Innate: Human IFN-γ+CD4+ T Cells Can Arise Directly from CXCL8-Producing Recent Thymic Emigrants in Babies and Adults

被引:23
作者
Das, Abhishek [1 ]
Rouault-Pierre, Kevin [2 ]
Kamdar, Shraddha [1 ]
Gomez-Tourino, Iria [1 ]
Wood, Kristie [3 ]
Donaldson, Ian [4 ]
Mein, Charles A. [4 ]
Bonnet, Dominique [2 ]
Hayday, Adrian C. [1 ,2 ]
Gibbons, Deena L. [1 ]
机构
[1] Kings Coll London, Peter Gorer Dept Immunobiol, London SE1 9RT, England
[2] Francis Crick Inst, London NW1 1AT, England
[3] Guys Hosp, Natl Inst Hlth Res, Biomed Res Ctr, Genom Res Platform, London SE1 9RT, England
[4] Barts & London Queen Marys Sch Med & Dent, John Vane Sci Ctr, Genome Ctr, London EC1M 6BQ, England
基金
英国惠康基金;
关键词
EXPRESSION; RECEPTOR; DIFFERENTIATION; INFLAMMATION; CHEMOKINES; MECHANISM; CYTOKINES; LEUKEMIA; MEMORY;
D O I
10.4049/jimmunol.1700551
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We recently demonstrated that the major effector function of neonatal CD4(+) T cells is to produce CXCL8, a prototypic cytokine of innate immune cells. In this article, we show that CXCL8 expression, prior to proliferation, is common in newly arising T cells (so-called "recent thymic emigrants") in adults, as well as in babies. This effector potential is acquired in the human thymus, prior to TCR signaling, but rather than describing end-stage differentiation, such cells, whether isolated from neonates or adults, can further differentiate into IFN-gamma-producing CD4(+) T cells. Thus, the temporal transition of host defense from innate to adaptive immunity is unexpectedly mirrored at the cellular level by the capacity of human innate-like CXCL8-producing CD4(+) T cells to transition directly into Th1 cells.
引用
收藏
页码:1696 / 1705
页数:10
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