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抗原呈递细胞在非小细胞肺癌(NSCLC)中的作用。

Function of antigen-presenting cells in non-small-cell lung cancer (NSCLC).

作者信息

Kumar R Ilaya, Jain Kavya, Rai Karan Raj, Arora Prashasti, Gururajan Harshnna, Sarkar Koustav

机构信息

Department of Biotechnology, School of Bioengineering, College of Engineering and Technology, SRM Institute of Science and Technology, Kattankulathur, Chennai, Tamil Nadu, 603203, India.

出版信息

Med Oncol. 2025 Apr 12;42(5):162. doi: 10.1007/s12032-025-02703-7.

Abstract

The most common type of lung cancer called NSCLC avoids immune monitoring by blocking antigen display and T cell response activation. Anti-tumor immunity requires the essential function of antigen-presenting cells (APCs) which include dendritic cells and macrophages and B cells. NSCLC causes APCs to stop their normal function because they fail to properly display tumor antigens and activate adaptive immune responses. APC dysfunction in NSCLC is mainly caused by the tumor microenvironment (TME) which actively reprograms these cells through inhibitory cytokines and metabolic constraints and immune checkpoints. As a result, NSCLC exhibits poor responses to immunotherapies, such as checkpoint inhibitors. The analysis of APC-TME interactions enables researchers to develop strategies that will enhance APC function along with antigen presentation while improving immunotherapy effectiveness. The research examines APC dysfunction in NSCLC together with its TME mechanisms and develops therapeutic strategies to combat immune suppression for better clinical results.

摘要

最常见的肺癌类型即非小细胞肺癌(NSCLC),它通过阻断抗原呈递和T细胞反应激活来逃避免疫监测。抗肿瘤免疫需要抗原呈递细胞(APC)发挥重要作用,这些细胞包括树突状细胞、巨噬细胞和B细胞。NSCLC会导致APC停止其正常功能,因为它们无法正确呈递肿瘤抗原并激活适应性免疫反应。NSCLC中的APC功能障碍主要由肿瘤微环境(TME)引起,肿瘤微环境通过抑制性细胞因子、代谢限制和免疫检查点来积极重塑这些细胞。因此,NSCLC对免疫疗法(如检查点抑制剂)反应不佳。对APC与TME相互作用的分析使研究人员能够制定策略,在提高免疫治疗效果的同时增强APC功能以及抗原呈递。该研究考察了NSCLC中的APC功能障碍及其TME机制,并制定治疗策略来对抗免疫抑制,以获得更好的临床效果。

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