Barnes Tristan A, Amir Eitan
Department of Medical Oncology and Hematology, Princess Margaret Cancer, Toronto, ON M5G 2M9, Canada.
Br J Cancer. 2017 Aug 8;117(4):451-460. doi: 10.1038/bjc.2017.220. Epub 2017 Jul 13.
Interactions between immune and malignant cells have been known to have clinical relevance for decades. The potential for immune control is now being therapeutically enhanced with checkpoint inhibitors and other novel agents to improve outcomes in cancer. The importance of the immune infiltrate as a prognostic marker is increasingly relevant. In this minireview, we present an overview of the immune infiltrate and its spatial organisation, and summarise the prognostic value of immune cells in different cancer types. International collaborative efforts are standardising histopathologic reporting of the immune infiltrate, to allow application of these parameters in the clinical and research settings. In general terms, a 'pro-inflammatory' tumour microenvironment and infiltrating CD8-expressing T lymphocytes are associated with improved clinical outcomes in a broad range of tumour types. The inhibitory function of other immune cells, for example, myeloid-derived suppressor cells and regulatory T cells, appear to have a major role in disrupting the capacity for the immune control of cancers.
几十年来,人们已经知道免疫细胞与恶性细胞之间的相互作用具有临床相关性。目前,通过检查点抑制剂和其他新型药物,免疫控制的潜力正在治疗上得到增强,以改善癌症治疗效果。免疫浸润作为一种预后标志物的重要性日益凸显。在这篇综述中,我们概述了免疫浸润及其空间组织,并总结了不同癌症类型中免疫细胞的预后价值。国际合作正在使免疫浸润的组织病理学报告标准化,以便在临床和研究环境中应用这些参数。一般来说,“促炎”肿瘤微环境和浸润的表达CD8的T淋巴细胞与多种肿瘤类型的临床预后改善相关。其他免疫细胞的抑制功能,例如髓源性抑制细胞和调节性T细胞,似乎在破坏癌症免疫控制能力方面起主要作用。