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基孔肯雅病毒感染中的Toll样受体(TLR)反应:激活机制、免疫逃逸以及TLR激动剂在疫苗开发中的应用

Toll-like Receptor (TLR) Response in Chikungunya Virus Infection: Mechanism of Activation, Immune Evasion, and Use of TLR Agonists in Vaccine Development.

作者信息

Kayesh Mohammad Enamul Hoque, Kohara Michinori, Tsukiyama-Kohara Kyoko

机构信息

Department of Microbiology and Public Health, Faculty of Animal Science and Veterinary Medicine, Patuakhali Science and Technology University, Barishal 8210, Bangladesh.

Transboundary Animal Diseases Center, Joint Faculty of Veterinary Medicine, Kagoshima University, Kagoshima 890-0065, Japan.

出版信息

Vaccines (Basel). 2025 Aug 13;13(8):856. doi: 10.3390/vaccines13080856.

DOI:10.3390/vaccines13080856
PMID:40872941
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12390013/
Abstract

CHIKV is a re-emerging mosquito-borne arthritogenic alphavirus associated with large outbreaks and severe joint pain, and it poses a growing global health threat. Toll-like receptors (TLRs), as key pattern recognition receptors, detect viral components and initiate antiviral immune responses. Increasing evidence highlights the role of TLR signaling in shaping CHIKV infection outcomes, though its precise contribution remains unclear. CHIKV has developed mechanisms to evade host innate immune surveillance, promoting viral replication. TLR agonists show promise as vaccine adjuvants by enhancing immune responses. In this review, we summarize current insights into TLR-mediated immunity during CHIKV infection, the virus's innate immune evasion strategies, and the potential of TLR agonists in improving vaccine efficacy.

摘要

基孔肯雅病毒(CHIKV)是一种再度出现的、由蚊子传播的致关节炎甲病毒,与大规模疫情爆发及严重关节疼痛相关,对全球健康构成日益严重的威胁。Toll样受体(TLRs)作为关键的模式识别受体,可检测病毒成分并启动抗病毒免疫反应。越来越多的证据凸显了TLR信号传导在塑造CHIKV感染结果中的作用,但其确切贡献仍不清楚。CHIKV已形成逃避宿主天然免疫监视的机制,从而促进病毒复制。TLR激动剂通过增强免疫反应,有望成为疫苗佐剂。在本综述中,我们总结了目前对CHIKV感染期间TLR介导的免疫、病毒的天然免疫逃避策略以及TLR激动剂在提高疫苗效力方面潜力的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a16/12390013/f74c975ad017/vaccines-13-00856-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a16/12390013/9745312a1914/vaccines-13-00856-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a16/12390013/f74c975ad017/vaccines-13-00856-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a16/12390013/9745312a1914/vaccines-13-00856-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a16/12390013/f74c975ad017/vaccines-13-00856-g002.jpg

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本文引用的文献

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TLR2 and TLR4 bridge physiological and pathological inflammation in the reproductive system.Toll样受体2(TLR2)和Toll样受体4(TLR4)在生殖系统中连接生理炎症和病理炎症。
Commun Biol. 2025 Jul 5;8(1):1008. doi: 10.1038/s42003-025-08424-x.
2
X-linked polymorphisms in TLR7 and TLR8 genes are associated with protection against Chikungunya fever.Toll样受体7(TLR7)和Toll样受体8(TLR8)基因中的X连锁多态性与抵御基孔肯雅热有关。
Mem Inst Oswaldo Cruz. 2025 Jun 13;120:e230224. doi: 10.1590/0074-02760230224. eCollection 2025.
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Pro inflammatory IL-1β: A potential biomarker for chronic chikungunya arthritis condition.
促炎白细胞介素-1β:慢性基孔肯雅热关节炎病情的一种潜在生物标志物。
Hum Immunol. 2025 Jul;86(4):111336. doi: 10.1016/j.humimm.2025.111336. Epub 2025 Jun 16.
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Global burden of chikungunya virus infections and the potential benefit of vaccination campaigns.基孔肯雅病毒感染的全球负担以及疫苗接种运动的潜在益处。
Nat Med. 2025 Jun 10. doi: 10.1038/s41591-025-03703-w.
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IFITMs exhibit antiviral activity against Chikungunya and Zika virus infection via the alteration of TLRs and RLRs signaling pathways.干扰素诱导跨膜蛋白(IFITMs)通过改变Toll样受体(TLRs)和视黄酸诱导基因-I样受体(RLRs)信号通路,对基孔肯雅病毒和寨卡病毒感染表现出抗病毒活性。
Sci Rep. 2025 May 6;15(1):15769. doi: 10.1038/s41598-025-00663-6.
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Lancet. 2025 Apr 19;405(10487):1343-1352. doi: 10.1016/S0140-6736(25)00345-9. Epub 2025 Mar 27.
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Lancet. 2025 Apr 19;405(10487):1353-1361. doi: 10.1016/S0140-6736(25)00372-1. Epub 2025 Mar 27.
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Viruses. 2025 Jan 29;17(2):191. doi: 10.3390/v17020191.
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