The Yin and Yang of Targeting KLRG1+ Tregs and Effector Cells

被引:18
作者
Borys, Samantha M. [1 ]
Bag, Arup K. [2 ]
Brossay, Laurent [1 ]
Adeegbe, Dennis O. [2 ]
机构
[1] Brown Univ Alpert Med Sch, Dept Mol Microbiol & Immunol, Div Biol & Med, Providence, RI USA
[2] H Lee Moffitt Canc Ctr & Res Inst, Dept Immunol, Tampa, FL USA
来源
FRONTIERS IN IMMUNOLOGY | 2022年 / 13卷
关键词
regulatory T cells (T reg); cancer; KLRG1; immune modulation; Treg targeting; REGULATORY T-CELLS; FUNCTION-ASSOCIATED ANTIGEN; E-CADHERIN; RECEPTOR KLRG1; CUTTING EDGE; EPITHELIAL-CELLS; IL-2; RECEPTOR; EXPRESSION; NK; DIFFERENTIATION;
D O I
10.3389/fimmu.2022.894508
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The literature surrounding KLRG1 has primarily focused on NK and CD8(+) T cells. However, there is evidence that the most suppressive Tregs express KLRG1. Until now, the role of KLRG1 on Tregs has been mostly overlooked and remains to be elucidated. Here we review the current literature on KLRG1 with an emphasis on the KLRG1(+) Treg subset role during cancer development and autoimmunity. KLRG1 has been recently proposed as a new checkpoint inhibitor target, but these studies focused on the effects of KLRG1 blockade on effector cells. We propose that when designing anti-tumor therapies targeting KLRG1, the effects on both effector cells and Tregs will have to be considered.
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页数:8
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