Center of Integrated Protein Science Munich (CIPS-M) & Division of Clinical Pharmacology, Klinikum der Universität München, Lindwurmstrasse 2a, 80337 Munich, Germany, Member of the German Center of Lung Research.
Immunotherapy. 2019 Feb;11(3):201-213. doi: 10.2217/imt-2018-0111.
Cancer immunotherapy has changed the treatment landscape for cancer patients, especially for those with metastatic spread. While the immunotherapeutic armamentarium is constantly growing, as exemplified by approved compounds, clinical outcome remains variable both within and across entities. A sufficient infiltration into the tumor microenvironment and successful activation of effector T lymphocytes against tumor cells have been identified as predictors for responses to T cell-based immunotherapies. However, tumor cells have developed a variety of mechanisms to reduce T cell homing and access to the tumor tissue to prevent activity of anticancer immunity. As a consequence, investigations have interrogated strategies to improve the efficacy of cancer immunotherapies by enhancing T cell infiltration into tumor tissues. In this review, we summarize mechanisms of how tumor tissue shapes immune suppressive microenvironment to prevent T cell access to the tumor site. We focus on current strategies to improve cancer immunotherapies through enhancing T cell infiltration.
癌症免疫疗法改变了癌症患者的治疗格局,特别是对于转移性癌症患者。尽管免疫治疗手段不断增加,例如已批准的化合物,但在实体瘤内和实体瘤之间,临床疗效仍然存在差异。充分浸润肿瘤微环境并成功激活效应 T 淋巴细胞对抗肿瘤细胞已被确定为 T 细胞为基础的免疫治疗反应的预测因子。然而,肿瘤细胞已经发展出多种机制来减少 T 细胞归巢和进入肿瘤组织,以防止抗癌免疫的活性。因此,研究已经探讨了通过增强 T 细胞浸润到肿瘤组织中来提高癌症免疫疗法疗效的策略。在这篇综述中,我们总结了肿瘤组织如何塑造免疫抑制微环境以防止 T 细胞进入肿瘤部位的机制。我们重点介绍了通过增强 T 细胞浸润来改善癌症免疫疗法的当前策略。