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三级淋巴结构异质性决定肿瘤免疫和临床应用前景。

Tertiary lymphoid structural heterogeneity determines tumour immunity and prospects for clinical application.

机构信息

Department of Interventional Radiology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, 450052, China.

Medical School of Zhengzhou University, Zhengzhou, Henan, China.

出版信息

Mol Cancer. 2024 Apr 6;23(1):75. doi: 10.1186/s12943-024-01980-6.

Abstract

Tertiary lymphoid structures (TLS) are clusters of immune cells that resemble and function similarly to secondary lymphoid organs (SLOs). While TLS is generally associated with an anti-tumour immune response in most cancer types, it has also been observed to act as a pro-tumour immune response. The heterogeneity of TLS function is largely determined by the composition of tumour-infiltrating lymphocytes (TILs) and the balance of cell subsets within the tumour-associated TLS (TA-TLS). TA-TLS of varying maturity, density, and location may have opposing effects on tumour immunity. Higher maturity and/or higher density TLS are often associated with favorable clinical outcomes and immunotherapeutic response, mainly due to crosstalk between different proportions of immune cell subpopulations in TA-TLS. Therefore, TLS can be used as a marker to predict the efficacy of immunotherapy in immune checkpoint blockade (ICB). Developing efficient imaging and induction methods to study TA-TLS is crucial for enhancing anti-tumour immunity. The integration of imaging techniques with biological materials, including nanoprobes and hydrogels, alongside artificial intelligence (AI), enables non-invasive in vivo visualization of TLS. In this review, we explore the dynamic interactions among T and B cell subpopulations of varying phenotypes that contribute to the structural and functional diversity of TLS, examining both existing and emerging techniques for TLS imaging and induction, focusing on cancer immunotherapies and biomaterials. We also highlight novel therapeutic approaches of TLS that are being explored with the aim of increasing ICB treatment efficacy and predicting prognosis.

摘要

三级淋巴结构 (TLS) 是免疫细胞的簇集,其形态和功能类似于次级淋巴器官 (SLO)。虽然 TLS 通常与大多数癌症类型中的抗肿瘤免疫反应相关,但也观察到它可以作为促肿瘤免疫反应。TLS 功能的异质性在很大程度上取决于肿瘤浸润淋巴细胞 (TIL) 的组成以及肿瘤相关 TLS (TA-TLS) 中细胞亚群的平衡。不同成熟度、密度和位置的 TA-TLS 可能对肿瘤免疫有相反的影响。更高的成熟度和/或更高的 TLS 密度通常与有利的临床结果和免疫治疗反应相关,主要是由于 TA-TLS 中不同比例的免疫细胞亚群之间的串扰。因此,TLS 可用作预测免疫检查点阻断 (ICB) 免疫治疗疗效的标志物。开发有效的成像和诱导方法来研究 TA-TLS 对于增强抗肿瘤免疫至关重要。将成像技术与生物材料(包括纳米探针和水凝胶)以及人工智能 (AI) 相结合,可以实现 TLS 的非侵入性体内可视化。在这篇综述中,我们探讨了不同表型的 T 和 B 细胞亚群之间的动态相互作用,这些相互作用促成了 TLS 的结构和功能多样性,同时还研究了现有的和新兴的 TLS 成像和诱导技术,重点关注癌症免疫疗法和生物材料。我们还强调了正在探索的 TLS 的新治疗方法,旨在提高 ICB 治疗效果和预测预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5338/10998345/86e82f642b66/12943_2024_1980_Fig1_HTML.jpg

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