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肿瘤中三级淋巴结构的异质性

英文原题:Heterogeneity of tertiary lymphoid structures in cancer.

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Heterogeneity of tertiary lymphoid structures in cancer.

PubMed 2023/12/04(内容时间) Front Immunol Q1 · IF 7(JCR 2025)

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中文摘要

免疫治疗方法,如免疫检查点阻断和基因修饰淋巴细胞的细胞免疫治疗,已成功地将免疫系统牢固地嵌入抗击癌症的路线图中。遗憾的是,大多数癌症患者尚未从这些治疗方法中获益,即使免疫反应在其肿瘤实体中的预后相关性已被证实。因此,探索诱导抗肿瘤免疫的新策略具有合理的必要性。最近,肿瘤部位异位淋巴聚集体的形成与患者预后以及有效的抗肿瘤反应之间的联系表明,操纵这些三级淋巴结构(TLS)的发生可能在激活免疫系统对抗生长中的肿瘤方面发挥关键作用。然而,调控TLS形成的机制以及对其显著异质性的清晰理解仍然缺乏。在此,我们简要总结了关于驱动TLS发展的机制的知识现状,概述了TLS异质性对癌症患者临床结局的影响,并讨论了适合模拟TLS异质性的系统,这可能有助于识别在癌症患者中诱导保护性TLS形成的新策略。

展开英文摘要原文

The success of immunotherapy approaches, such as immune checkpoint blockade and cellular immunotherapy with genetically modified lymphocytes, has firmly embedded the immune system in the roadmap for combating cancer. Unfortunately, the majority of cancer patients do not yet benefit from these therapeutic approaches, even when the prognostic relevance of the immune response in their tumor entity has been demonstrated.

Therefore, there is a justified need to explore new strategies for inducing anti-tumor immunity. The recent connection between the formation of ectopic lymphoid aggregates at tumor sites and patient prognosis, along with an effective anti-tumor response, suggests that manipulating the occurrence of these tertiary lymphoid structures (TLS) may play a critical role in activating the immune system against a growing tumor.

However, mechanisms governing TLS formation and a clear understanding of their substantial heterogeneity are still lacking.

Here, we briefly summarize the current state of knowledge regarding the mechanisms driving TLS development, outline the impact of TLS heterogeneity on clinical outcomes in cancer patients, and discuss appropriate systems for modeling TLS heterogeneity that may help identify new strategies for inducing protective TLS formation in cancer patients.

论文信息

作者
You X、Koop K、Weigert A
单位
Goethe-University Frankfurt, Faculty of Medicine, Institute of Biochemistry I, Frankfurt, Germany.Germany
文献类型
综述 · 非美国政府资助研究
期刊
Frontiers in immunology2023
原文标识
PubMed 38111571 · DOI 10.3389/fimmu.2023.1286850