Department of Molecular Biology and Biochemistry, University of California, Irvine, Irvine, CA, United States.
Front Immunol. 2021 Feb 23;12:636238. doi: 10.3389/fimmu.2021.636238. eCollection 2021.
Immune checkpoint inhibition targeting T cells has shown tremendous promise in the treatment of many cancer types and are now standard therapies for patients. While standard therapies have focused on PD-1 and CTLA-4 blockade, additional immune checkpoints have shown promise in promoting anti-tumor immunity. PSGL-1, primarily known for its role in cellular migration, has also been shown to function as a negative regulator of CD4 T cells in numerous disease settings including cancer. PSGL-1 is highly expressed on T cells and can engage numerous ligands that impact signaling pathways, which may modulate CD4 T cell differentiation and function. PSGL-1 engagement in the tumor microenvironment may promote CD4 T cell exhaustion pathways that favor tumor growth. Here we highlight that blocking the PSGL-1 pathway on CD4 T cells may represent a new cancer therapy approach to eradicate tumors.
免疫检查点抑制靶向 T 细胞在治疗多种癌症类型方面显示出巨大的潜力,现在已成为患者的标准疗法。虽然标准疗法主要集中在 PD-1 和 CTLA-4 阻断上,但其他免疫检查点在促进抗肿瘤免疫方面也显示出了希望。PSGL-1 主要因其在细胞迁移中的作用而闻名,但其在包括癌症在内的许多疾病环境中也被证明是 CD4 T 细胞的负调节剂。PSGL-1 在 T 细胞上高度表达,并能与许多影响信号通路的配体结合,从而可能调节 CD4 T 细胞的分化和功能。PSGL-1 在肿瘤微环境中的结合可能促进有利于肿瘤生长的 CD4 T 细胞衰竭途径。在这里,我们强调阻断 CD4 T 细胞上的 PSGL-1 途径可能代表一种新的癌症治疗方法来消灭肿瘤。