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血管微环境、肿瘤免疫与免疫治疗。

Vascular Microenvironment, Tumor Immunity and Immunotherapy.

机构信息

Department of Radiation Oncology, University of Pennsylvania, Philadelphia, PA, United States.

出版信息

Front Immunol. 2021 Dec 20;12:811485. doi: 10.3389/fimmu.2021.811485. eCollection 2021.

Abstract

Immunotherapy holds great promise for treating cancer. Nonetheless, T cell-based immunotherapy of solid tumors has remained challenging, largely due to the lack of universal tumor-specific antigens and an immunosuppressive tumor microenvironment (TME) that inhibits lymphocyte infiltration and activation. Aberrant vascularity characterizes malignant solid tumors, which fuels the formation of an immune-hostile microenvironment and induces tumor resistance to immunotherapy, emerging as a crucial target for adjuvant treatment in cancer immunotherapy. In this review, we discuss the molecular and cellular basis of vascular microenvironment-mediated tumor evasion of immune responses and resistance to immunotherapy, with a focus on vessel abnormality, dysfunctional adhesion, immunosuppressive niche, and microenvironmental stress in tumor vasculature. We provide an overview of opportunities and challenges related to these mechanisms. We also propose genetic programming of tumor endothelial cells as an alternative approach to recondition the vascular microenvironment and to overcome tumor resistance to immunotherapy.

摘要

免疫疗法在治疗癌症方面有很大的前景。然而,基于 T 细胞的实体瘤免疫疗法仍然具有挑战性,主要是因为缺乏普遍的肿瘤特异性抗原和抑制淋巴细胞浸润和激活的免疫抑制肿瘤微环境(TME)。恶性实体瘤的特征是血管异常,这会促进免疫抑制微环境的形成,并导致肿瘤对免疫疗法产生耐药性,成为癌症免疫治疗中辅助治疗的一个重要靶点。在这篇综述中,我们讨论了血管微环境介导的肿瘤逃避免疫反应和对免疫治疗的耐药性的分子和细胞基础,重点讨论了血管异常、功能失调的黏附、免疫抑制龛位和肿瘤血管中的微环境应激。我们概述了与这些机制相关的机会和挑战。我们还提出了对肿瘤内皮细胞进行基因编程作为一种替代方法,以重新调节血管微环境并克服肿瘤对免疫治疗的耐药性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/faf1/8720970/ae05ba4cbc3d/fimmu-12-811485-g001.jpg

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