Research progress on immune tolerance mechanisms in liver metastatic tumors and the "Liver-metastasis-oriented shared-mechanism therapeutic strategy" approach.

Medical review (Berlin, Germany) Pub Date : 2026-02-26 eCollection Date: 2026-02-01 DOI:10.1515/mr-2025-0077
Qing Zhang, Wenjing Wang, Hongli Yu, Fuchuan Wang, Xiong Chen, Zhipeng Liang, Yinying Lu
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Abstract

Liver metastases pose a serious challenge in the field of systemic cancer treatment, as this organ has a particular microenvironment that favours malignant cells disseminating to settle there. We outline major steps of liver immune tolerance in metastasis including pre-metastatic niche formation, immune evasion during circulation, establishment of an intrahepatic immune desert and metabolism, myeloid cell networks and gut microbiome-mediated coordinated tolerance. We then combine new combination and integrative therapies that are intended to break this tolerance; these include immunochemotherapy regimens, synergistic antiangiogenics and immunotherapies, dual immune checkpoint blockade and myeloid-cell reprogramming, combined locoregional and systemic therapies and new microenvironmental targeting. Each strategy is assessed with regard to its potential disruption of hepatic immune quiescence, improved clinical translation and durable antitumour activity. We suggest a proposed solution termed Liver-metastasis-oriented shared-mechanism therapeutic strategy, which may target multiple metastatic bottlenecks due to similarities. This framework provides a basis for personalizing combination therapies and designing future clinical trials for treating liver metastases, with organ-specific considerations and will be the subject of a commentary.

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肝转移瘤免疫耐受机制研究进展及“以肝转移为导向的共享机制治疗策略”
肝转移是系统性癌症治疗领域的一个严峻挑战,因为该器官具有特殊的微环境,有利于恶性细胞在那里扩散定居。我们概述了肝脏免疫耐受在转移中的主要步骤,包括转移前生态位的形成、循环中的免疫逃避、肝内免疫沙漠和代谢的建立、骨髓细胞网络和肠道微生物群介导的协调耐受。然后我们结合新的联合疗法和综合疗法来打破这种耐受性;这些包括免疫化疗方案、协同抗血管生成和免疫疗法、双重免疫检查点封锁和髓细胞重编程、局部和全身联合治疗以及新的微环境靶向治疗。评估每一种策略对肝免疫静止的潜在破坏,改善临床转化和持久的抗肿瘤活性。我们提出了一种解决方案,称为肝转移导向的共享机制治疗策略,它可能针对多个转移瓶颈,由于相似性。该框架为个性化联合治疗和设计未来治疗肝转移的临床试验提供了基础,并考虑到器官特异性,将成为评论的主题。
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