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肝转移中的调节性 T 细胞:在肿瘤进展中新出现且各异的作用

英文原题:Regulatory T cells in liver metastases: emerging and divergent roles in tumour progression.

查看英文原题

Regulatory T cells in liver metastases: emerging and divergent roles in tumour progression.

PubMed 2025/11/05(内容时间) eGastroenterology Q1 · IF 10.5(JCR 2025)

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中文摘要

肝转移(LMs)带来了显著的发病率和死亡率负担,导致许多原发性恶性肿瘤预后更差。尽管癌症治疗取得了进展,如免疫治疗、分子治疗、额外的化疗方案以及手术切除的优化,但针对肝转移的有效治疗仍然难以实现。近期免疫肿瘤学研究揭示了肝转移微环境中不同的肿瘤微环境(TME)特征,这些特征与每种原发肿瘤或起源器官特有的内在微环境特征相互作用。调节性T细胞(Tregs)被认为与肝脏TME的免疫抑制性质有关,但其确切相互作用机制尚未完全阐明。已有文献记录了Tregs在数量、功能及与其他TIL(肿瘤浸润淋巴细胞)比例方面的差异,且不同原发肿瘤的LMs中研究结果相互矛盾。这些结果可能归因于每种器官特异性肿瘤的潜在生物学特性,以及在转移级联逐步进展过程中形成的独特肝脏TME。在本综述中,我们探讨了不同起源肿瘤LMs中肝内Tregs常相互矛盾的研究发现,并就这些观察到的差异提供潜在机制的见解,以及对未来治疗策略的启示。

展开英文摘要原文

Liver metastases (LMs) pose a significant burden of morbidity and mortality, resulting in a worse prognosis for many primary malignancies. Despite advancements in cancer treatment, such as immunotherapy, molecular therapies, additional lines of chemotherapy and optimisation of surgical resection, effective therapy against hepatic metastases remains elusive. Recent studies in immuno-oncology have implicated distinct tumour microenvironment (TME) signatures in the hepatic metastatic niche, which interplay with the intrinsic microenvironmental features specific to each primary tumour or organ of origin. Regulatory T cells (Tregs) have been implicated in the immunosuppressive nature of the hepatic TME, yet the exact mechanisms of interaction have not been fully elucidated.

Discrepancies in number, function and proportion of Tregs to other tumour-infiltrating lymphocytes have been documented, with conflicting findings in the LMs from different primary tumours. These results may be attributable to the underlying biology of each organ-specific tumour and the unique hepatic TME that forms during the stepwise progression of the metastatic cascade.

In this review, we explore the often-contradicting findings of intrahepatic Tregs in LMs from different originating tumours and offer insight into potential mechanisms for these observed differences with implications for future therapeutic strategies.

论文信息

作者
Wu G、Yang T、Gholami S、DePeralta D、Weiss M、Deng M、Wang P、Huang H
单位
Division of Hepatology, Center for Immunology and Inflammation, Departments of Medicine and Surgery at Northwell Health, Institute of Translational Research, Feinstein Institutes for Medical Research, Manhasset, New York, USA.United States
文献类型
综述
期刊
eGastroenterology2025
原文标识
PubMed 41209659 · DOI 10.1136/egastro-2025-100257