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
相关论文
共 34 条
[1]   The dynamic co-evolution of memory and regulatory CD4+ T cells in the periphery [J].
Akbar, Arne N. ;
Vukmanovic-Stejic, Milica ;
Taams, Leonie S. ;
Macallan, Derek C. .
NATURE REVIEWS IMMUNOLOGY, 2007, 7 (03) :231-237
[2]   T-cell receptor activation of human CD4+ T cells shifts the innate TLR response from CXCL8hiIFN-γnull to CXCL8loIFN-γhi [J].
Akhade, Ajay S. ;
Qadri, Ayub .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2015, 45 (09) :2628-2637
[3]   HTSeq-a Python']Python framework to work with high-throughput sequencing data [J].
Anders, Simon ;
Pyl, Paul Theodor ;
Huber, Wolfgang .
BIOINFORMATICS, 2015, 31 (02) :166-169
[4]  
[Anonymous], 2010, GENOME BIOL
[5]   Quantifying Thymic Export: Combining Models of Naive T Cell Proliferation and TCR Excision Circle Dynamics Gives an Explicit Measure of Thymic Output [J].
Bains, Iren ;
Thiebaut, Rodolphe ;
Yates, Andrew J. ;
Callard, Robin .
JOURNAL OF IMMUNOLOGY, 2009, 183 (07) :4329-4336
[6]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[7]  
Berthold MR., 2009, ACM SIGKDD Explor. Newsl., V11, P26, DOI [DOI 10.1145/1656274.1656280, DOI 10.1145/1656274]
[8]  
Brennecke P, 2013, NAT METHODS, V10, P1093, DOI [10.1038/nmeth.2645, 10.1038/NMETH.2645]
[9]   Gene expression profile of adult T-cell acute lymphocytic leukemia identifies distinct subsets of patients with different response to therapy and survival [J].
Chiaretti, S ;
Li, XC ;
Gentleman, R ;
Vitale, A ;
Vignetti, M ;
Mandelli, F ;
Ritz, J ;
Foa, R .
BLOOD, 2004, 103 (07) :2771-2778
[10]   Critical Role of IL-17RA in Immunopathology of Influenza Infection [J].
Crowe, Christopher R. ;
Chen, Kong ;
Pociask, Derek A. ;
Alcorn, John F. ;
Krivich, Cameron ;
Enelow, Richard I. ;
Ross, Ted M. ;
Witztum, Joseph L. ;
Kolls, Jay K. .
JOURNAL OF IMMUNOLOGY, 2009, 183 (08) :5301-5310