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单纯疱疹病毒 1 型感染相关疾病的治疗及疫苗研发、载体治疗应用的最新综述

An updated review of HSV-1 infection-associated diseases and treatment, vaccine development, and vector therapy application.

机构信息

Department of Endocrine, The Third Affiliated Hospital of Xinxiang Medical University, Xinxiang Medical University, Xinxiang, Henan, China.

School of Basic Medical Sciences, Xinxiang Medical University, Xinxiang, Henan, China.

出版信息

Virulence. 2024 Dec;15(1):2425744. doi: 10.1080/21505594.2024.2425744. Epub 2024 Nov 13.


DOI:10.1080/21505594.2024.2425744
PMID:39508503
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11562918/
Abstract

Herpes simplex virus type 1 (HSV-1) is a globally widespread virus that causes and associates with a wide range of diseases, including herpes simplex encephalitis, herpes simplex keratitis, and herpes labialis. The interaction between HSV-1 and the host involves complex immune response mechanisms, including recognition of viral invasion, maintenance of latent infection, and triggering of reactivation. Antiviral therapy is the core treatment for HSV-1 infections. Meanwhile, vaccine development employs different strategies and methods, and several promising vaccine types have emerged, such as live attenuated, protein subunit, and nucleic acid vaccines, offering new possibilities for the prevention of HSV-1 infection. Moreover, HSV-1 can be modified into a therapeutic vector for gene therapy and tumour immunotherapy. This review provides an in-depth summary of HSV-1 infection-associated innate and adaptive immune responses, disease pathogenesis, current therapeutic approaches, recent advances in vaccine development, and vector therapy applications for cancer treatment. Through a systematic review of multiple aspects of HSV-1, this study aims to provide a comprehensive and detailed reference for the public on the prevention, control, and treatment of HSV-1.

摘要

单纯疱疹病毒 1 型(HSV-1)是一种在全球广泛传播的病毒,可引起多种疾病,并与之相关联,包括单纯疱疹性脑炎、单纯疱疹性角膜炎和唇疱疹。HSV-1 与宿主的相互作用涉及复杂的免疫反应机制,包括识别病毒入侵、维持潜伏感染和触发再激活。抗病毒治疗是 HSV-1 感染的核心治疗方法。同时,疫苗的开发采用了不同的策略和方法,已经出现了几种有前途的疫苗类型,如减毒活疫苗、蛋白亚单位疫苗和核酸疫苗,为预防 HSV-1 感染提供了新的可能性。此外,HSV-1 可以被改造成治疗性载体,用于基因治疗和肿瘤免疫治疗。本综述深入总结了 HSV-1 感染相关的先天和适应性免疫反应、疾病发病机制、当前的治疗方法、疫苗开发的最新进展以及用于癌症治疗的载体治疗应用。通过对 HSV-1 的多个方面进行系统综述,本研究旨在为公众提供关于 HSV-1 的预防、控制和治疗的全面、详细的参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/215c/11562918/3e3611d842c4/KVIR_A_2425744_F0006_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/215c/11562918/01d8ce3dd706/KVIR_A_2425744_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/215c/11562918/39993e18d4b5/KVIR_A_2425744_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/215c/11562918/6663e667755e/KVIR_A_2425744_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/215c/11562918/09d3c64fe95c/KVIR_A_2425744_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/215c/11562918/839914f56b7b/KVIR_A_2425744_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/215c/11562918/3e3611d842c4/KVIR_A_2425744_F0006_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/215c/11562918/01d8ce3dd706/KVIR_A_2425744_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/215c/11562918/39993e18d4b5/KVIR_A_2425744_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/215c/11562918/6663e667755e/KVIR_A_2425744_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/215c/11562918/09d3c64fe95c/KVIR_A_2425744_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/215c/11562918/839914f56b7b/KVIR_A_2425744_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/215c/11562918/3e3611d842c4/KVIR_A_2425744_F0006_OC.jpg

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[7]
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Magnesium Oxide Nanoparticles: A New Frontier in Antiviral Therapy Against Herpes Simplex Virus Type 1.

Adv Virol. 2025-8-17

[2]
The Procaine-Based ProcCluster Impedes the Second Envelopment Process of Herpes Simplex Virus Type 1.

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[3]
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Int J Mol Sci. 2025-7-13

[4]
Neutralizing Antibodies: Role in Immune Response and Viral Vector Based Gene Therapy.

Int J Mol Sci. 2025-5-29

[5]
Immunological Control of Herpes Simplex Virus Type 1 Infection: A Non-Thermal Plasma-Based Approach.

Viruses. 2025-4-23

[6]
Development of viral infectious clones and their applications based on yeast and bacterial artificial chromosome platforms.

Mol Biomed. 2025-4-29

[7]
Co-expression of HSV-1 ICP34.5 enhances the expression of gene delivered by self-amplifying RNA and mitigates its immunogenicity.

FEBS Open Bio. 2025-7

[8]
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Front Immunol. 2025-3-18

[9]
Post-translational modifications as a key mechanism for herpes simplex virus type I evasion of host innate immunity.

Front Microbiol. 2025-2-11

本文引用的文献

[1]
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Rev Med Virol. 2024-5

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Front Immunol. 2024

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Sci Adv. 2024-3

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