CXCR6 is required for antitumor efficacy of intratumoral CD8+T cell

细胞毒性T细胞 CD8型 癌症研究 T细胞 肿瘤微环境 嵌合抗原受体 免疫学 免疫疗法 免疫系统 生物 抗原 体外 生物化学
作者
Binglin Wang,Yi Wang,Xiaofan Sun,Guoliang Deng,Wei Huang,Xingxin Wu,Yanghong Gu,Zhigang Tian,Zhimin Fan,Qiang Xu,Hongqi Chen,Yang Sun
出处
期刊:Journal for ImmunoTherapy of Cancer [BMJ]
卷期号:9 (8): e003100-e003100 被引量:81
标识
DOI:10.1136/jitc-2021-003100
摘要

Background Increasing infiltration of CD8 + T cells within tumor tissue predicts a better prognosis and is essential for response to checkpoint blocking therapy. Furthermore, current clinical protocols use unfractioned T cell populations as the starting point for transduction of chimeric antigen receptors (CARs)-modified T cells, but the optimal T cell subtype of CAR-modified T cells remains unclear. Thus, accurately identifying a group of cytotoxic T lymphocytes with high antitumor efficacy is imperative. Inspired by the theory of yin and yang, we explored a subset of CD8 + T cell in cancer with the same phenotypic characteristics as highly activated inflammatory T cells in autoimmune diseases. Methods Combination of single-cell RNA sequencing, general transcriptome sequencing data and multiparametric cytometric techniques allowed us to map CXCR6 expression on specific cell type and tissue. We applied Cxcr6 −/− mice, immune checkpoint therapies and bone marrow chimeras to identify the function of CXCR6 + CD8 + T cells. Transgenic Cxcr6 −/− OT-I mice were employed to explore the functional role of CXCR6 in antigen-specific antitumor response. Results We identified that CXCR6 was exclusively expressed on intratumoral CD8 + T cell. CXCR6 + CD8 + T cells were more immunocompetent, and chimeras with specific deficiency on CD8 + T cells showed weaker antitumor activity. In addition, Cxcr6 −/− mice could not respond to anti-PD-1 treatment effectively. High tumor expression of CXCR6 was not mainly caused by ligand-receptor chemotaxis of CXCL16/CXCR6 but induced by tumor tissue self. Induced CXCR6 + CD8 + T cells possessed tumor antigen specificity and could enhance the effect of anti-PD-1 blockade to retard tumor progression. Conclusions This study may contribute to the rational design of combined immunotherapy. Alternatively, CXCR6 may be used as a biomarker for effective CD8 + T cell state before adoptive cell therapy, providing a basis for tumor immunotherapy.
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