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肿瘤免疫和免疫治疗反应的微环境调控。

Microenvironmental regulation of tumour immunity and response to immunotherapy.

机构信息

CellCarta, Antwerp, Belgium.

Genentech, South San Francisco, CA, USA.

出版信息

J Pathol. 2021 Jul;254(4):374-383. doi: 10.1002/path.5681. Epub 2021 May 19.

Abstract

The confluence of immunology and oncology has led to a lot of uncertainty and questions about relevant biomarkers. Despite the complexity of the tumour microenvironment, most clinical studies have relied on a single-parameter immunohistochemical assay to prospectively select patients for checkpoint inhibitor therapy; the results of this strategy have been highly variable and often less than optimal. While great efforts have been made to identify additional or alternative biomarkers, pathologists, drug developers, and clinicians alike have faced technical, logistical, and regulatory challenges on how to implement them successfully. In this review, we will discuss these challenges; we will also highlight recent advances in dissecting the functional diversity of immune cell populations within the tumour microenvironment and their potential for improved, biomarker-driven therapeutic strategies. The dynamic nature and cellular diversity of the tumour microenvironment may challenge past models of a single biomarker predicting patient response and clinical outcome. © 2021 The Authors. The Journal of Pathology published by John Wiley & Sons, Ltd. on behalf of The Pathological Society of Great Britain and Ireland.

摘要

免疫与肿瘤学的结合带来了许多不确定性和相关生物标志物的问题。尽管肿瘤微环境非常复杂,但大多数临床研究都依赖于单一参数免疫组织化学检测,以前瞻性地选择接受检查点抑制剂治疗的患者;该策略的结果差异很大,通常并不理想。尽管人们已经做出了巨大努力来确定其他的或替代的生物标志物,但病理学家、药物开发商和临床医生都面临着如何成功实施这些生物标志物的技术、后勤和监管方面的挑战。在这篇综述中,我们将讨论这些挑战;我们还将强调最近在剖析肿瘤微环境中免疫细胞群体的功能多样性及其在改进生物标志物驱动的治疗策略方面的潜力。肿瘤微环境的动态性质和细胞多样性可能挑战了过去的单一生物标志物预测患者反应和临床结局的模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2eb6/8252752/e0833de24799/PATH-254-374-g002.jpg

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