Das Abhishek, Rouault-Pierre Kevin, Kamdar Shraddha, Gomez-Tourino Iria, Wood Kristie, Donaldson Ian, Mein Charles A, Bonnet Dominique, Hayday Adrian C, Gibbons Deena L
Peter Gorer Department of Immunobiology, King's College London, London SE1 9RT, United Kingdom.
The Francis Crick Institute, London NW1 1AT, United Kingdom.
J Immunol. 2017 Sep 1;199(5):1696-1705. doi: 10.4049/jimmunol.1700551. Epub 2017 Jul 28.
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-γ-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.
我们最近证明,新生儿CD4 T细胞的主要效应功能是产生CXCL8,这是一种先天性免疫细胞的典型细胞因子。在本文中,我们表明,在增殖之前,CXCL8的表达在成年人以及婴儿新出现的T细胞(所谓的“近期胸腺迁出者”)中很常见。这种效应潜能在人类胸腺中,在TCR信号传导之前就已获得,但这些细胞,无论从新生儿还是成年人中分离出来,并非处于终末分化阶段,而是可以进一步分化为产生IFN-γ的CD4 T细胞。因此,宿主防御从先天性免疫到适应性免疫的时间转变,在细胞水平上意外地反映为人类产生先天性样CXCL8的CD4 T细胞直接转变为Th1细胞的能力。