Fujimura Taku
Department of Dermatology, Tohoku University Graduate School of Medicine, 1-1 Seiryo-machi, Aoba-ku, Sendai 980-8574, Japan.
Int J Mol Sci. 2022 Apr 6;23(7):4044. doi: 10.3390/ijms23074044.
Immune checkpoint inhibitors (ICIs), such as anti-programmed cell death 1 (PD1) antibodies (Abs) and anti-cytotoxic T-lymphocyte associated protein 4 (CTLA4) Abs, have been widely administered for not only advanced melanoma, but also various non-melanoma skin cancers. Since profiles of tumor-infiltrating leukocytes (TILs) play important roles in immunotherapy using ICIs, it is important to evaluate cancer stromal cells such as tumor-associated macrophages (TAMs) and cancer-associated fibroblasts (CAFs), as well as stromal extracellular matrix protein, to predict the efficacy of ICIs. This review article focuses particularly on TAMs and related factors. Among TILs, TAMs and their related factors could be the optimal biomarkers for immunotherapy such as anti-PD1 Ab therapy. According to the studies presented, TAM-targeting therapies for advanced melanoma and non-melanoma skin cancer will develop in the future.
免疫检查点抑制剂(ICIs),如抗程序性细胞死亡1(PD1)抗体(Abs)和抗细胞毒性T淋巴细胞相关蛋白4(CTLA4)抗体,不仅已广泛应用于晚期黑色素瘤,还应用于各种非黑色素瘤皮肤癌。由于肿瘤浸润白细胞(TILs)的特征在使用ICIs的免疫治疗中起着重要作用,因此评估癌症基质细胞,如肿瘤相关巨噬细胞(TAMs)和癌症相关成纤维细胞(CAFs)以及基质细胞外基质蛋白,对于预测ICIs的疗效很重要。这篇综述文章特别关注TAMs及其相关因素。在TILs中,TAMs及其相关因素可能是抗PD1抗体治疗等免疫治疗的最佳生物标志物。根据所展示的研究,未来将开发针对晚期黑色素瘤和非黑色素瘤皮肤癌的TAM靶向治疗方法。