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树突状细胞对人畜共患DNA和RNA病毒的免疫反应

Immune Responses of Dendritic Cells to Zoonotic DNA and RNA Viruses.

作者信息

Miao Xinyu, Han Yixuan, Yin Yinyan, Yang Yang, Chen Sujuan, Jiao Xinan, Qin Tao, Peng Daxin

机构信息

College of Veterinary Medicine, Yangzhou University, Yangzhou 225009, China.

Jiangsu Co-Innovation Center for the Prevention and Control of Important Animal Infectious Disease and Zoonoses, Yangzhou 225009, China.

出版信息

Vet Sci. 2025 Jul 24;12(8):692. doi: 10.3390/vetsci12080692.

DOI:10.3390/vetsci12080692
PMID:40872644
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12389827/
Abstract

Viral infections persistently challenge global health through immune evasion and zoonotic transmission. Dendritic cells (DCs) play a central role in antiviral immunity by detecting viral nucleic acids via conserved pattern recognition receptors, triggering interferon-driven innate responses and cross-presentation-mediated activation of cytotoxic CD8 T cells. This study synthesizes DC-centric defense mechanisms against viral subversion, encompassing divergent nucleic acid sensing pathways for zoonotic DNA and RNA viruses, viral counterstrategies targeting DC maturation and interferon signaling, and functional specialization of DC subsets in immune coordination. Despite advances in DC-based vaccine platforms, clinical translation is hindered by cellular heterogeneity, immunosuppressive microenvironments, and limitations in antigen delivery. Future research should aim to enhance the efficiency of DC-mediated immunity, thereby establishing a robust scientific foundation for the development of next-generation vaccines and antiviral therapies. A more in-depth exploration of DC functions and regulatory mechanisms may unlock novel strategies for antiviral intervention, ultimately paving the way for improved prevention and treatment of viral infections.

摘要

病毒感染通过免疫逃逸和人畜共患病传播持续挑战全球健康。树突状细胞(DCs)在抗病毒免疫中发挥核心作用,通过保守的模式识别受体检测病毒核酸,触发干扰素驱动的固有反应以及交叉呈递介导的细胞毒性CD8 T细胞活化。本研究综合了以DC为中心的抗病毒颠覆防御机制,包括针对人畜共患DNA和RNA病毒的不同核酸传感途径、针对DC成熟和干扰素信号传导的病毒应对策略,以及DC亚群在免疫协调中的功能特化。尽管基于DC的疫苗平台取得了进展,但细胞异质性、免疫抑制微环境和抗原递送限制阻碍了其临床转化。未来的研究应旨在提高DC介导的免疫效率,从而为下一代疫苗和抗病毒疗法的开发奠定坚实的科学基础。对DC功能和调节机制进行更深入的探索可能会解锁抗病毒干预的新策略,最终为改善病毒感染的预防和治疗铺平道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffb3/12389827/bfbdf3b58e3f/vetsci-12-00692-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffb3/12389827/bfbdf3b58e3f/vetsci-12-00692-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffb3/12389827/bfbdf3b58e3f/vetsci-12-00692-g001.jpg

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本文引用的文献

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Antigen recognition and immune response to monkeypox virus infection: implications for Mpox vaccine design - a narrative review.猴痘病毒感染的抗原识别与免疫反应:对猴痘疫苗设计的启示——一篇叙述性综述
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Challenges in the Therapeutic Exploitation of Chemokine Receptor-Mediated Internalization of Nanocarriers.化学趋化因子受体介导的纳米载体内化的治疗开发中的挑战。
Front Biosci (Landmark Ed). 2024 Oct 10;29(10):350. doi: 10.31083/j.fbl2910350.
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The unique immune evasion mechanisms of the mpox virus and their implication for developing new vaccines and immunotherapies.猴痘病毒独特的免疫逃逸机制及其对开发新型疫苗和免疫疗法的意义。
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Vaccinia Virus: Mechanisms Supporting Immune Evasion and Successful Long-Term Protective Immunity.牛痘病毒:支持免疫逃逸和成功的长期保护免疫的机制。
Viruses. 2024 May 29;16(6):870. doi: 10.3390/v16060870.
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The nuclear localization signal of monkeypox virus protein P2 orthologue is critical for inhibition of IRF3-mediated innate immunity.猴痘病毒蛋白 P2 同源物的核定位信号对于抑制 IRF3 介导的固有免疫至关重要。
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