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单纯疱疹病毒 1 型感染的控制:基于 CRISPR/Cas 的治疗和诊断方法的发展方向。

Control of HSV-1 Infection: Directions for the Development of CRISPR/Cas-Based Therapeutics and Diagnostics.

机构信息

Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Vavilov Str., 32, 119991 Moscow, Russia.

Center for Precision Genome Editing and Genetic Technologies for Biomedicine, Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Vavilov Str., 32, 119991 Moscow, Russia.

出版信息

Int J Mol Sci. 2024 Nov 17;25(22):12346. doi: 10.3390/ijms252212346.


DOI:10.3390/ijms252212346
PMID:39596412
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11595115/
Abstract

It is estimated that nearly all individuals have been infected with herpesviruses, with herpes simplex virus type 1 (HSV-1) representing the most prevalent virus. In most cases, HSV-1 causes non-life-threatening skin damage in adults. However, in patients with compromised immune systems, it can cause serious diseases, including death. The situation is further complicated by the emergence of strains that are resistant to both traditional and novel antiviral drugs. It is, therefore, imperative that new methods of combating HSV-1 and other herpesviruses be developed without delay. CRISPR/Cas systems may prove an effective means of controlling herpesvirus infections. This review presents the current understanding of the underlying molecular mechanisms of HSV-1 infection and discusses four potential applications of CRISPR/Cas systems in the fight against HSV-1 infections. These include the search for viral and cellular genes that may serve as effective targets, the optimization of anti-HSV-1 activity of CRISPR/Cas systems in vivo, the development of CRISPR/Cas-based HSV-1 diagnostics, and the validation of HSV-1 drug resistance mutations.

摘要

据估计,几乎所有个体都曾感染过疱疹病毒,其中单纯疱疹病毒 1 型(HSV-1)最为常见。在大多数情况下,HSV-1 会导致成年人非致命性的皮肤损伤。然而,在免疫系统受损的患者中,它可能导致严重疾病,甚至死亡。更为复杂的是,一些病毒株对传统和新型抗病毒药物都具有耐药性。因此,急需开发新的方法来对抗 HSV-1 和其他疱疹病毒。CRISPR/Cas 系统可能是控制疱疹病毒感染的有效手段。本文综述了 HSV-1 感染的潜在分子机制,并讨论了 CRISPR/Cas 系统在对抗 HSV-1 感染中的四种潜在应用,包括寻找可能作为有效靶点的病毒和细胞基因、优化 CRISPR/Cas 系统在体内的抗 HSV-1 活性、开发基于 CRISPR/Cas 的 HSV-1 诊断方法以及验证 HSV-1 耐药性突变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55a5/11595115/9ce596c0a5c3/ijms-25-12346-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55a5/11595115/12fd203e9cfc/ijms-25-12346-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55a5/11595115/9ce596c0a5c3/ijms-25-12346-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55a5/11595115/12fd203e9cfc/ijms-25-12346-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55a5/11595115/9ce596c0a5c3/ijms-25-12346-g002.jpg

相似文献

[1]
Control of HSV-1 Infection: Directions for the Development of CRISPR/Cas-Based Therapeutics and Diagnostics.

Int J Mol Sci. 2024-11-17

[2]
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[3]
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[4]
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[6]
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[7]
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[10]
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引用本文的文献

[1]
Advancing gene editing therapeutics: Clinical trials and innovative delivery systems across diverse diseases.

Mol Ther Nucleic Acids. 2025-8-5

本文引用的文献

[1]
Suppression of HSV-1 infection and viral reactivation by CRISPR-Cas9 gene editing in 2D and 3D culture models.

Mol Ther Nucleic Acids. 2024-7-19

[2]
Rapid diagnosis of herpes simplex virus 1 and 2 bloodstream infections utilizing a sample-to-answer platform.

J Clin Microbiol. 2024-9-11

[3]
Practical updates in clinical antiviral resistance testing.

J Clin Microbiol. 2024-8-14

[4]
CRISPR/Cas9-mediated genome editing of the thymidine kinase gene in a clinical HSV-1 isolate identifies F289S as novel acyclovir-resistant mutation.

Antiviral Res. 2024-8

[5]
Models of Herpes Simplex Virus Latency.

Viruses. 2024-5-8

[6]
CRISPR-Cas Systems and Genome Editing: Beginning the Era of CRISPR/Cas Therapies for Humans.

Int J Mol Sci. 2024-5-13

[7]
Performance characteristics of highly automated HSV-1 and HSV-2 IgG testing.

J Clin Microbiol. 2024-6-12

[8]
A Revision of Herpes Simplex Virus Type 1 Transcription: First, Repress; Then, Express.

Microorganisms. 2024-1-26

[9]
Engineering Cas9: next generation of genomic editors.

Appl Microbiol Biotechnol. 2024-2-14

[10]
A rapid isothermal CRISPR-Cas13a diagnostic test for genital infection.

iScience. 2023-11-27

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