免疫检查点阻断通过扩增效应 CD8⁺ T 细胞克隆增强淋巴细胞清除性化疗诱导的抗肿瘤免疫
Immune Checkpoint Blockade Augments Lymphodepleting Chemotherapy-Induced Antitumor Immunity by Expanding Effector CD8+ T-cell Clones.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Stromal Factors as a Target for Immunotherapy in Melanoma and Non-Melanoma Skin Cancers.
Stromal Factors as a Target for Immunotherapy in Melanoma and Non-Melanoma Skin Cancers.
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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,已广泛用于不仅晚期黑色素瘤,还有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的免疫治疗中发挥重要作用,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的疗效非常重要。这篇综述文章特别关注TAMs及相关因素。在TILs中,TAMs及其相关因素可能是免疫治疗如抗PD1抗体治疗的最佳生物标志物。根据所呈现的研究,针对晚期黑色素瘤和非黑色素瘤皮肤癌的TAM靶向治疗将在未来得到发展。
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.
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