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迈向消除传染性人乳头瘤病毒:利用CRISPR/Cas技术创新

Towards the elimination of infectious HPV: exploiting CRISPR/Cas innovations.

作者信息

Liu Wei, Jiang Yingyan, Wang Cheng, Wang Min, Zhang Wei, Ren Haiying, Xu Shiyan, Qin Jinjing, Liu Pan, Jin Lianhai, Zhao Donghai

机构信息

College of Laboratory Medicine, Jilin Medical University, Jilin, China.

Department of Obstetrics and Gynecology, Affiliated hospital of Jilin medical university, Jilin, China.

出版信息

Front Cell Infect Microbiol. 2025 Aug 4;15:1627668. doi: 10.3389/fcimb.2025.1627668. eCollection 2025.

DOI:10.3389/fcimb.2025.1627668
PMID:40831701
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12358359/
Abstract

HPV has been conclusively associated with various human malignancies, making the development of prevention and treatment strategies for HPV-induced diseases a high priority. Currently, primary prevention methods include HPV immunization and routine screening, which significantly reduce the risk of HPV transmission. However, for patients diagnosed with invasive, advanced, or recurrent malignancies, non-virus-specific therapies frequently lead to drug resistance and adverse effects, resulting in minimal improvement in treatment efficacy for numerous patients. Viral genome-targeting therapy is emerging as a promising avenue for the future management of HPV infections. With the rapid advancement of genetic modification technologies, the CRISPR/Cas system has demonstrated significant potential in treating viral infections. Its ability to selectively target and edit viral genomes for elimination positions it as a highly effective approach for combating HPV. This review will explore the functions and applications of the CRISPR/Cas system as an innovative therapy for HPV. We will illustrate the prospective efficacy of CRISPR/Cas as a groundbreaking and promising cure for HPV infections, while also addressing the opportunities and challenges associated with this novel approach.

摘要

人乳头瘤病毒(HPV)已被确凿地证明与多种人类恶性肿瘤相关,这使得开发针对HPV引发疾病的预防和治疗策略成为当务之急。目前,一级预防方法包括HPV免疫接种和常规筛查,这些方法能显著降低HPV传播风险。然而,对于被诊断为侵袭性、晚期或复发性恶性肿瘤的患者,非病毒特异性疗法常常导致耐药性和不良反应,致使众多患者的治疗效果改善甚微。靶向病毒基因组的疗法正成为未来管理HPV感染的一条有前景的途径。随着基因编辑技术的迅速发展,CRISPR/Cas系统在治疗病毒感染方面已展现出巨大潜力。它能够选择性地靶向和编辑病毒基因组以实现清除,这使其成为对抗HPV的一种高效方法。本综述将探讨CRISPR/Cas系统作为一种针对HPV的创新疗法的功能及应用。我们将阐述CRISPR/Cas作为一种开创性且有前景的HPV感染治疗方法的预期疗效,同时也会探讨与这种新方法相关的机遇和挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d041/12358359/79ed9963e69c/fcimb-15-1627668-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d041/12358359/e7ec35fab820/fcimb-15-1627668-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d041/12358359/79ed9963e69c/fcimb-15-1627668-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d041/12358359/e7ec35fab820/fcimb-15-1627668-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d041/12358359/79ed9963e69c/fcimb-15-1627668-g002.jpg

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本文引用的文献

1
Generic Diagramming Platform (GDP): a comprehensive database of high-quality biomedical graphics.通用绘图平台(GDP):一个高质量生物医学图形的综合数据库。
Nucleic Acids Res. 2025 Jan 6;53(D1):D1670-D1676. doi: 10.1093/nar/gkae973.
2
iPSC-derived hypoimmunogenic tissue resident memory T cells mediate robust anti-tumor activity against cervical cancer.iPSC 衍生的低免疫原性组织驻留记忆 T 细胞介导针对宫颈癌的强大抗肿瘤活性。
Cell Rep Med. 2023 Dec 19;4(12):101327. doi: 10.1016/j.xcrm.2023.101327. Epub 2023 Dec 12.
3
Genome editing mRNA nanotherapies inhibit cervical cancer progression and regulate the immunosuppressive microenvironment for adoptive T-cell therapy.
基因编辑 mRNA 纳米疗法抑制宫颈癌进展并调节过继性 T 细胞治疗的免疫抑制微环境。
J Control Release. 2023 Aug;360:496-513. doi: 10.1016/j.jconrel.2023.07.007. Epub 2023 Jul 12.
4
Systemic delivery of specific and efficient CRISPR/Cas9 system targeting HPV16 oncogenes using LL-37 antimicrobial peptide in C57BL/6 mice.采用 LL-37 抗菌肽在 C57BL/6 小鼠中靶向 HPV16 致癌基因的系统递送特异性和高效的 CRISPR/Cas9 系统。
J Med Virol. 2023 Jul;95(7):e28934. doi: 10.1002/jmv.28934.
5
The Role of DNA Viruses in Human Cancer.DNA病毒在人类癌症中的作用。
Cancer Inform. 2023 Jun 13;22:11769351231154186. doi: 10.1177/11769351231154186. eCollection 2023.
6
Efficient engineering of human and mouse primary cells using peptide-assisted genome editing.使用肽辅助基因组编辑技术高效工程化人类和小鼠原代细胞。
Nat Biotechnol. 2024 Feb;42(2):305-315. doi: 10.1038/s41587-023-01756-1. Epub 2023 Apr 24.
7
Passive, active and endogenous organ-targeted lipid and polymer nanoparticles for delivery of genetic drugs.用于递送基因药物的被动、主动和内源性器官靶向脂质及聚合物纳米颗粒。
Nat Rev Mater. 2023;8(4):282-300. doi: 10.1038/s41578-022-00529-7. Epub 2023 Jan 19.
8
Current studies and future promises of PD-1 signal inhibitors in cervical cancer therapy.PD-1 信号抑制剂在宫颈癌治疗中的当前研究和未来前景。
Biomed Pharmacother. 2023 Jan;157:114057. doi: 10.1016/j.biopha.2022.114057. Epub 2022 Dec 1.
9
CRISPR/Cas9-HPV-liposome enhances antitumor immunity and treatment of HPV infection-associated cervical cancer.CRISPR/Cas9-人乳头瘤病毒脂质体增强抗肿瘤免疫力并治疗人乳头瘤病毒感染相关的宫颈癌。
J Med Virol. 2023 Jan;95(1):e28144. doi: 10.1002/jmv.28144. Epub 2022 Oct 11.
10
Application of CRISPR-Cas9 Gene Editing for HIV Host Factor Discovery and Validation.CRISPR-Cas9基因编辑技术在HIV宿主因子发现与验证中的应用
Pathogens. 2022 Aug 9;11(8):891. doi: 10.3390/pathogens11080891.