Innate lymphoid cell regulation of adaptive immunity

被引:42
|
作者
Withers, David R. [1 ]
机构
[1] Univ Birmingham, Inst Immunol & Immunotherapy, Coll Med & Dent Sci, Birmingham B15 2TT, W Midlands, England
基金
英国惠康基金;
关键词
innate lymphoid cells; memory; spleen and lymph nodes; T cells; CD4(+) T-CELLS; ROR-GAMMA-T; TRANSCRIPTION FACTOR GATA-3; TISSUE-INDUCER CELLS; NK CELLS; GENE-EXPRESSION; OX40; LIGAND; ADULT; FETAL; CD30;
D O I
10.1111/imm.12639
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Innate lymphoid cells (ILCs) were identified principally as non-T-cell sources of key cytokines, able to provide rapid and early production of these molecules in the support of tissue homeostasis, repair and response to infection. As our understanding of these cells has developed, it has become evident that ILCs can impact on lymphocytes through a range of mechanisms. Hence, an exciting area of research has evolved in determining the extent to which ILCs may regulate adaptive immune responses. This review will focus initially on our current understanding of where ILC populations are located and what this means for potential cellular interactions. Mechanisms underpinning such interactions and how they may contribute to controlling adaptive immunity will then be considered.
引用
收藏
页码:123 / 130
页数:8
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