Department of Molecular Microbiology and Immunology, Division of Biology and Medicine, Brown University Alpert Medical School, Providence, RI, United States.
Department of Immunology, H. Lee Moffitt Cancer Center, Tampa, FL, United States.
Front Immunol. 2022 Apr 29;13:894508. doi: 10.3389/fimmu.2022.894508. eCollection 2022.
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.
围绕 KLRG1 的文献主要集中在 NK 和 CD8 T 细胞上。然而,有证据表明,最具抑制性的 Tregs 表达 KLRG1。到目前为止,KLRG1 在 Tregs 中的作用大多被忽视,仍有待阐明。在这里,我们综述了 KLRG1 的最新文献,重点介绍了 KLRG1 在癌症发展和自身免疫中的 Treg 亚群作用。KLRG1 最近被提议作为一种新的检查点抑制剂靶点,但这些研究集中在 KLRG1 阻断对效应细胞的影响上。我们提出,在设计针对 KLRG1 的抗肿瘤治疗方法时,必须考虑到其对效应细胞和 Tregs 的影响。