Chikuma Shunsuke, Kanamori Mitsuhiro, Mise-Omata Setsuko, Yoshimura Akihiko
Department of Microbiology and Immunology, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.
Cancer Sci. 2017 Apr;108(4):574-580. doi: 10.1111/cas.13194. Epub 2017 Apr 19.
Inhibition of immune checkpoint molecules, PD-1 and CTLA4, has been shown to be a promising cancer treatment. PD-1 and CTLA4 inhibit TCR and co-stimulatory signals. The third T cell activation signal represents the signals from the cytokine receptors. The cytokine interferon-γ (IFNγ) plays an important role in anti-tumor immunity by activating cytotoxic T cells (CTLs). Most cytokines use the Janus kinase (JAK)/signal transducer and activator of transcription (STAT) pathway, and the suppressors of cytokine signaling (SOCS) family of proteins are major negative regulators of the JAK/STAT pathway. Among SOCS proteins, CIS, SOCS1, and SOCS3 proteins can be considered the third immunocheckpoint molecules since they regulate cytokine signals that control the polarization of CD4 T cells and the maturation of CD8 T cells. This review summarizes recent progress on CIS, SOCS1, and SOCS3 in terms of their anti-tumor immunity and potential applications.
免疫检查点分子PD-1和CTLA4的抑制作用已被证明是一种很有前景的癌症治疗方法。PD-1和CTLA4抑制TCR和共刺激信号。第三个T细胞激活信号代表来自细胞因子受体的信号。细胞因子干扰素-γ(IFNγ)通过激活细胞毒性T细胞(CTL)在抗肿瘤免疫中发挥重要作用。大多数细胞因子使用Janus激酶(JAK)/信号转导和转录激活因子(STAT)途径,细胞因子信号抑制因子(SOCS)蛋白家族是JAK/STAT途径的主要负调节因子。在SOCS蛋白中,CIS、SOCS1和SOCS3蛋白可被视为第三个免疫检查点分子,因为它们调节控制CD4 T细胞极化和CD8 T细胞成熟的细胞因子信号。本文综述了CIS、SOCS1和SOCS3在抗肿瘤免疫及其潜在应用方面的最新进展。