Abstract A176: Overcoming CD8 T-cell suppression in the tumor microenvironment

Adam N. Cartwright, Peng Jiang, A. Saadatpour, Guocheng Yuan, Shirley X. Liu, K. Wucherpfennig
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Abstract

CD8 T-cell-mediated antitumor immunity is required for the control and elimination of tumors. However, tumors are able to overcome immune response resulting in immunosuppression, tumor growth, and metastatic spread. CD8 T-cells are controlled through a homeostatic network of positive and negative feedback loops. These negative signals are exploited by the tumor and associated suppressive cell populations in the tumor microenvironment. Immunotherapies targeted to receptors that control these negative signals, termed immune checkpoint inhibitors, have provided robust and durable responses to a number of cancers. Unfortunately, only a subset of patients will respond to current immunotherapies. This is due to the accruement of suppressive and inhibitory mechanisms employed by the tumor and its microenvironment. These include expression of inhibitory ligands, release of immune-suppressive factors, and the recruitment of suppressive cell populations. Furthermore, the administration of immune checkpoint inhibitors can enhance tumor acquisition of a more suppressive phenotype, diminishing immune responses through additional inhibitory pathways. We therefore propose that further CD8 T-cell-intrinsic negative regulators most likely exist, which can be targeted to improve antitumor responses. Here, we have used functional genomic approaches to identify pathways that can be targeted to advance anti-tumor responses, either in combination with anti-PD-1 or to overcome suppressive mechanisms employed by the tumor microenvironment. Using both in vivo and in vitro assays, we have identified both a novel target that provides an enhancement to CD8 T-cell effector function when in combination with PD-1 checkpoint blockade, and CD8 T-cell-intrinsic pathways that are modulated by the presence of suppressive cells associated with the tumor microenvironment. Citation Format: Adam N.R Cartwright, Peng Jiang, Assieh Saadatpour, Guo-Cheng Yuan, Shirley X. Liu, Kai W. Wucherpfennig. Overcoming CD8 T-cell suppression in the tumor microenvironment [abstract]. In: Proceedings of the Fourth CRI-CIMT-EATI-AACR International Cancer Immunotherapy Conference: Translating Science into Survival; Sept 30-Oct 3, 2018; New York, NY. Philadelphia (PA): AACR; Cancer Immunol Res 2019;7(2 Suppl):Abstract nr A176.
A176:克服肿瘤微环境中CD8 t细胞抑制
CD8 t细胞介导的抗肿瘤免疫是控制和消除肿瘤所必需的。然而,肿瘤能够克服免疫反应,导致免疫抑制、肿瘤生长和转移扩散。CD8 t细胞是通过一个由正负反馈回路组成的稳态网络来控制的。这些负信号被肿瘤和肿瘤微环境中相关的抑制细胞群利用。针对控制这些负信号的受体的免疫疗法,称为免疫检查点抑制剂,已经为许多癌症提供了强大而持久的反应。不幸的是,只有一小部分患者对目前的免疫疗法有反应。这是由于肿瘤及其微环境所采用的抑制和抑制机制的积累。这些包括抑制性配体的表达、免疫抑制因子的释放和抑制性细胞群的募集。此外,免疫检查点抑制剂的施用可以增强肿瘤获得更具抑制性的表型,通过额外的抑制途径减少免疫反应。因此,我们提出CD8 t细胞内在负调节因子很可能存在,可以靶向改善抗肿瘤反应。在这里,我们使用功能基因组方法来确定可以靶向推进抗肿瘤反应的途径,无论是与抗pd -1结合,还是克服肿瘤微环境所采用的抑制机制。通过体内和体外实验,我们已经确定了一个新的靶点,当与PD-1检查点阻断结合时,可以增强CD8 t细胞效应功能,以及CD8 t细胞的内在途径,这些途径由与肿瘤微环境相关的抑制性细胞的存在所调节。引用格式:Adam N.R Cartwright, Jiang Peng, Assieh Saadatpour,袁国成,Shirley X. Liu, Kai W. Wucherpfennig。克服肿瘤微环境中CD8 t细胞的抑制[摘要]。第四届CRI-CIMT-EATI-AACR国际癌症免疫治疗会议:将科学转化为生存;2018年9月30日至10月3日;纽约,纽约。费城(PA): AACR;癌症免疫学杂志2019;7(2增刊):摘要nr A176。
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