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重新编程免疫抑制性肿瘤微环境:利用血管生成和血栓形成增强免疫治疗。

Reprogramming the immunosuppressive tumor microenvironment: exploiting angiogenesis and thrombosis to enhance immunotherapy.

机构信息

College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.

School of Medicine, Cardiff University, Cardiff, United Kingdom.

出版信息

Front Immunol. 2023 Jul 3;14:1200941. doi: 10.3389/fimmu.2023.1200941. eCollection 2023.

Abstract

This review focuses on the immunosuppressive effects of tumor angiogenesis and coagulation on the tumor microenvironment (TME). We summarize previous research efforts leveraging these observations and targeting these processes to enhance immunotherapy outcomes. Clinical trials have documented improved outcomes when combining anti-angiogenic agents and immunotherapy. However, their overall survival benefit over conventional therapy remains limited and certain tumors exhibit poor response to anti-angiogenic therapy. Additionally, whilst preclinical studies have shown several components of the tumor coagulome to curb effective anti-tumor immune responses, the clinical studies reporting combinations of anticoagulants with immunotherapies have demonstrated variable treatment outcomes. By reviewing the current state of the literature on this topic, we address the key questions and future directions in the field, the answers of which are crucial for developing effective strategies to reprogram the TME in order to further the field of cancer immunotherapy.

摘要

这篇综述重点关注肿瘤血管生成和凝血对肿瘤微环境(TME)的免疫抑制作用。我们总结了以前利用这些观察结果并针对这些过程来增强免疫治疗效果的研究工作。临床试验记录了联合使用抗血管生成药物和免疫疗法可改善治疗效果。然而,与传统疗法相比,它们在总体生存获益方面仍然有限,某些肿瘤对抗血管生成治疗反应不佳。此外,虽然临床前研究表明肿瘤凝块的几个成分可抑制有效的抗肿瘤免疫反应,但报告抗凝剂与免疫疗法联合使用的临床研究显示出不同的治疗效果。通过回顾该主题的现有文献,我们探讨了该领域的关键问题和未来方向,这些问题的答案对于制定有效的策略来重新编程 TME 以进一步推进癌症免疫治疗领域至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e60/10374407/e131384179de/fimmu-14-1200941-g001.jpg

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