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全身性I型干扰素与局部TLR7/8激动剂协同作用以抑制转移性肿瘤。

Systemic IFN-I Synergizes with Topical TLR7/8 Agonists to Suppress Metastatic Tumors.

作者信息

Xu Haiting, Wang Chenghui, Xiao Bo

机构信息

State Key Laboratory of Resource Insects, College of Sericulture, Textile, and Biomass Sciences, Southwest University, Chongqing 400715, China.

Department of Laboratory Medicine, Key Laboratory for Human Disease Gene Study of Sichuan Province and the Department of Laboratory Medicine, Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu, Sichuan 611731, China.

出版信息

Research (Wash D C). 2025 Jun 21;8:0739. doi: 10.34133/research.0739. eCollection 2025.

Abstract

Advancing targeted cancer immunotherapy is pivotal for overcoming distant metastasis and tumor relapse. The recent study in by Sanlorenzo et al. demonstrates a breakthrough strategy combining systemic type I interferon with topical Toll-like receptor 7/8 agonists, where oral imiquimod primes plasmacytoid dendritic cells (DCs) to produce type I interferon, thereby sensitizing conventional DCs in tumors to local Toll-like receptor 7 activation. This approach triggers c-Jun-dependent IL-12 production and CCL2-mediated plasmacytoid DC recruitment, enabling localized and systemic tumor suppression. Importantly, the therapy synergizes with PD-1 blockade to prevent recurrence, representing a significant advance in DC-targeted cancer immunotherapy.

摘要

推进靶向癌症免疫疗法对于克服远处转移和肿瘤复发至关重要。Sanlorenzo等人最近的研究展示了一种将全身性I型干扰素与局部Toll样受体7/8激动剂相结合的突破性策略,其中口服咪喹莫特可促使浆细胞样树突状细胞(DCs)产生I型干扰素,从而使肿瘤中的常规DCs对局部Toll样受体7激活敏感。这种方法触发c-Jun依赖性白细胞介素-12的产生以及CCL2介导的浆细胞样DC募集,实现局部和全身性肿瘤抑制。重要的是,该疗法与PD-1阻断协同作用以预防复发,代表了DC靶向癌症免疫疗法的重大进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b352/12180689/c7de7923e9c7/research.0739.fig.001.jpg

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