Type 1 innate Lymphoid Cell Biology: Lessons Learnt from Natural Killer Cells

被引:65
作者
Jiao, Yuhao [1 ,2 ,3 ]
Huntington, Nicholas D. [1 ,2 ]
Belz, Gabrielle T. [1 ,2 ]
Seillet, Cyril [1 ,2 ]
机构
[1] Walter & Eliza Hall Inst Med Res, Mol Immunol Div, Melbourne, Vic, Australia
[2] Univ Melbourne, Dept Med Biol, Melbourne, Vic, Australia
[3] Tsinghua Univ, Sch Med, Beijing, Peoples R China
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
innate lymphoid cells; immunity; immune protection; lymphocyte subsets; GVHD; tumor rejection; LISTERIA-MONOCYTOGENES INFECTION; APOPTOSIS-INDUCING LIGAND; VERSUS-HOST-DISEASE; NK-CELLS; MEDIATED CYTOTOXICITY; TISSUE RESIDENCY; TUMOR-METASTASIS; T-CELLS; MOUSE; TRAIL;
D O I
10.3389/fimmu.2016.00426
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Group 1 innate lymphoid cells (ILCs) comprise the natural killer (NK) cells and ILC1s that reside within peripheral tissues. Several different ILC1 subsets have recently been characterized; however, no unique markers have been identified that uniquely define these subsets. Whether ILC1s and NK cells are in fact distinct lineages, or alternately exhibit transitional molecular programs that allow them to adapt to different tissue niches remains an open question. NK cells are the prototypic member of the Group 1 ILCs and have been historically assigned the functions of what now appears to be a multi-subset family that are distributed throughout the body. This raises the question of whether each of these populations mediate distinct functions during infection and tumor immuno-surveillance. Here, we review the diversity of the Group 1 ILC subsets in their transcriptional regulation, localization, mobility, and receptor expression, and highlight the challenges in unraveling the individual functions of these different populations of cells.
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页数:8
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