IL-17+ γδ T cells as kick-starters of inflammation

被引:238
作者
Papotto, Pedro H. [1 ]
Ribot, Julie C. [1 ]
Silva-Santos, Bruno [1 ]
机构
[1] Univ Lisbon, Fac Med, Inst Med Mol, Lisbon, Portugal
基金
欧洲研究理事会;
关键词
EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; LISTERIA-MONOCYTOGENES INFECTION; PSORIASIFORM SKIN INFLAMMATION; CENTRAL-NERVOUS-SYSTEM; MULTIPLE-SCLEROSIS; TH17; CELLS; PROINFLAMMATORY IL-17(+); RECEPTOR REPERTOIRE; INTERFERON-GAMMA; INNATE IMMUNITY;
D O I
10.1038/ni.3726
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Shortly after the discovery of interleukin 17 (IL-17)-producing CD4(+) helper T cells (T(H)17 cells), it was found that gamma delta T cells can also secrete large amounts of this pro-inflammatory cytokine. A decade later, it is now known that IL-17(+) gamma delta T cells (gamma delta 17 T cells) are often the main providers of IL-17A in various models of inflammatory diseases, while they also contribute to protective immune responses to infectious organisms. Due to an intricate thymic program of differentiation, gamma delta 17 T cells are able to respond faster than T(H)17 cells do and thus predominate in the early stages of inflammatory responses. Here we review the current knowledge of the development, activation and pathophysiological functions of gamma delta 17 T cells, aiming to increase the awareness in the community of the therapeutic potential of this 'other side' of IL-17-mediated immune responses.
引用
收藏
页码:604 / 611
页数:8
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