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依赖受体酪氨酸激酶 c-MET 的反应性中性粒细胞反应限制了癌症免疫治疗。

Reactive Neutrophil Responses Dependent on the Receptor Tyrosine Kinase c-MET Limit Cancer Immunotherapy.

机构信息

Laboratory of Experimental Dermatology, Department of Dermatology, University of Magdeburg, 39120 Magdeburg, Germany; Laboratory of Experimental Dermatology, Department of Dermatology and Allergy, University of Bonn, 53105 Bonn, Germany; Unit for RNA Biology, Department of Clinical Chemistry and Clinical Pharmacology, University of Bonn, 53105 Bonn, Germany.

Laboratory of Experimental Dermatology, Department of Dermatology, University of Magdeburg, 39120 Magdeburg, Germany; Laboratory of Experimental Dermatology, Department of Dermatology and Allergy, University of Bonn, 53105 Bonn, Germany; Immunology in Cancer and Infection Laboratory, QIMR Berghofer Medical Research Institute, Herston, QLD 4006, Australia.

出版信息

Immunity. 2017 Oct 17;47(4):789-802.e9. doi: 10.1016/j.immuni.2017.09.012.

Abstract

Inhibitors of the receptor tyrosine kinase c-MET are currently used in the clinic to target oncogenic signaling in tumor cells. We found that concomitant c-MET inhibition promoted adoptive T cell transfer and checkpoint immunotherapies in murine cancer models by increasing effector T cell infiltration in tumors. This therapeutic effect was independent of tumor cell-intrinsic c-MET dependence. Mechanistically, c-MET inhibition impaired the reactive mobilization and recruitment of neutrophils into tumors and draining lymph nodes in response to cytotoxic immunotherapies. In the absence of c-MET inhibition, neutrophils recruited to T cell-inflamed microenvironments rapidly acquired immunosuppressive properties, restraining T cell expansion and effector functions. In cancer patients, high serum levels of the c-MET ligand HGF correlated with increasing neutrophil counts and poor responses to checkpoint blockade therapies. Our findings reveal a role for the HGF/c-MET pathway in neutrophil recruitment and function and suggest that c-MET inhibitor co-treatment may improve responses to cancer immunotherapy in settings beyond c-MET-dependent tumors.

摘要

受体酪氨酸激酶 c-MET 的抑制剂目前被用于临床靶向肿瘤细胞中的致癌信号。我们发现,在小鼠癌症模型中,同时抑制 c-MET 可通过增加效应 T 细胞在肿瘤中的浸润来促进过继性 T 细胞转移和检查点免疫疗法。这种治疗效果不依赖于肿瘤细胞内在的 c-MET 依赖性。从机制上讲,c-MET 抑制会损害中性粒细胞对细胞毒性免疫疗法的反应性动员和募集到肿瘤和引流淋巴结中。在没有 c-MET 抑制的情况下,募集到 T 细胞炎症微环境中的中性粒细胞会迅速获得免疫抑制特性,限制 T 细胞的扩增和效应功能。在癌症患者中,c-MET 配体 HGF 的血清水平升高与中性粒细胞计数增加和对检查点阻断疗法的反应不佳相关。我们的研究结果揭示了 HGF/c-MET 途径在中性粒细胞募集和功能中的作用,并表明在超出 c-MET 依赖性肿瘤的情况下,c-MET 抑制剂联合治疗可能会改善对癌症免疫疗法的反应。

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