Immunobiology Department, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02129, USA.
Immunobiology Department, Massachusetts General Hospital and Harvard Medical School, Boston, MA 02129, USA.
Trends Mol Med. 2017 Nov;23(11):1037-1046. doi: 10.1016/j.molmed.2017.09.007. Epub 2017 Oct 12.
Immune checkpoint inhibitors (ICIs) have revolutionized cancer therapy but exhibit variable efficacy and relapse and can induce autoimmunity. Tumor necrosis factor (TNF) receptor 2 (TNFR2) is a signaling molecule found on the surface of a subset of potent regulatory T cells (Ts) that can activate the proliferation of these cells through nuclear factor kappa B (NF-κB). TNFR2 is also abundantly expressed on the surface of many human tumors. We propose that blocking TNFR2 might target abundant TNFR2 tumor-infiltrating Ts and directly kill TNFR2-expressing tumors. We also posit that TNFR2 inhibitors might potentially constitute safer and more targeted alternatives to ICI cancer treatment because the expression of TNFR2 on immune cells, concentrated in the tumor microenvironment of various cancers, appears to be more selective than that of checkpoint molecules.
免疫检查点抑制剂 (ICIs) 彻底改变了癌症治疗方法,但疗效和复发率存在差异,并且可能引发自身免疫。肿瘤坏死因子 (TNF) 受体 2 (TNFR2) 是一种信号分子,存在于一部分具有强大调节作用的 T 细胞 (Ts) 的表面,可通过核因子 κB (NF-κB) 激活这些细胞的增殖。TNFR2 也大量表达在许多人类肿瘤的表面。我们提出,阻断 TNFR2 可能靶向丰富的 TNFR2 肿瘤浸润性 Ts,并直接杀死 TNFR2 表达的肿瘤。我们还假设,TNFR2 抑制剂可能潜在地构成更安全、更具针对性的 ICI 癌症治疗替代方案,因为 TNFR2 在免疫细胞上的表达,集中在各种癌症的肿瘤微环境中,似乎比检查点分子更具选择性。