Sapoznik Sivan, Hammer Ohad, Ortenberg Rona, Besser Michal J, Ben-Moshe Tehila, Schachter Jacob, Markel Gal
Ella Institute for Melanoma, Sheba Medical Center, Ramat Gan 52621, Israel.
Clin Dev Immunol. 2012;2012:818214. doi: 10.1155/2012/818214. Epub 2012 Apr 23.
The immune system fights cancer and sometimes temporarily eliminates it or reaches an equilibrium stage of tumor growth. However, continuous immunological pressure also selects poorly immunogenic tumor variants that eventually escape the immune control system. Here, we focus on metastatic melanoma, a highly immunogenic tumor, and on anti-melanoma immunotherapies, which recently, especially following the FDA approval of Ipilimumab, gained interest from drug development companies. We describe new immunomodulatory approaches currently in the development pipeline, focus on the novel CEACAM1 immune checkpoint, and compare its potential to the extensively described targets, CTLA4 and PD1. This paper combines multi-disciplinary approaches and describes anti-melanoma immunotherapies from molecular, medical, and business angles.
免疫系统对抗癌症,有时能暂时消除癌症或使肿瘤生长达到平衡阶段。然而,持续的免疫压力也会选择免疫原性差的肿瘤变体,这些变体最终会逃脱免疫控制系统。在此,我们聚焦于转移性黑色素瘤,一种高度免疫原性的肿瘤,以及抗黑色素瘤免疫疗法,最近,尤其是在FDA批准伊匹单抗之后,抗黑色素瘤免疫疗法引起了制药公司的兴趣。我们描述了目前正在研发中的新免疫调节方法,重点关注新型癌胚抗原相关细胞黏附分子1(CEACAM1)免疫检查点,并将其潜力与已被广泛描述的靶点细胞毒性T淋巴细胞相关蛋白4(CTLA4)和程序性死亡受体1(PD1)进行比较。本文结合了多学科方法,从分子、医学和商业角度描述了抗黑色素瘤免疫疗法。