• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

CRISPR-Cas 基因组编辑技术在人类病毒感染中的治疗潜力。

Therapeutic potentials of CRISPR-Cas genome editing technology in human viral infections.

机构信息

Student Research Committee, Department of Medical Biotechnology, School of Advanced Technologies in Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

UKM Medical Molecular Biology Institute, Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia.

出版信息

Biomed Pharmacother. 2022 Apr;148:112743. doi: 10.1016/j.biopha.2022.112743. Epub 2022 Feb 25.

DOI:10.1016/j.biopha.2022.112743
PMID:35228065
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8872819/
Abstract

Viral infections are a common cause of morbidity worldwide. The emergence of Coronavirus Disease 2019 (COVID-19) has led to more attention to viral infections and finding novel therapeutics. The CRISPR-Cas9 system has been recently proposed as a potential therapeutic tool for the treatment of viral diseases. Here, we review the research progress in the use of CRISPR-Cas technology for treating viral infections, as well as the strategies for improving the delivery of this gene-editing tool in vivo. Key challenges that hinder the widespread clinical application of CRISPR-Cas9 technology are also discussed, and several possible directions for future research are proposed.

摘要

病毒感染是全球发病率的常见原因。2019 年冠状病毒病(COVID-19)的出现导致人们更加关注病毒感染和寻找新的治疗方法。CRISPR-Cas9 系统最近被提议作为治疗病毒疾病的潜在治疗工具。在这里,我们回顾了使用 CRISPR-Cas 技术治疗病毒感染的研究进展,以及改善该基因编辑工具体内递送的策略。还讨论了阻碍 CRISPR-Cas9 技术广泛临床应用的关键挑战,并提出了未来研究的几个可能方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d20c/8872819/973ff449a10d/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d20c/8872819/b07532a19607/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d20c/8872819/db0d19b2cce5/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d20c/8872819/597cd575810b/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d20c/8872819/973ff449a10d/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d20c/8872819/b07532a19607/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d20c/8872819/db0d19b2cce5/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d20c/8872819/597cd575810b/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d20c/8872819/973ff449a10d/gr4_lrg.jpg

相似文献

1
Therapeutic potentials of CRISPR-Cas genome editing technology in human viral infections.CRISPR-Cas 基因组编辑技术在人类病毒感染中的治疗潜力。
Biomed Pharmacother. 2022 Apr;148:112743. doi: 10.1016/j.biopha.2022.112743. Epub 2022 Feb 25.
2
Gene Therapy with CRISPR/Cas9 Coming to Age for HIV Cure.基因治疗与 CRISPR/Cas9 渐趋成熟,有望攻克 HIV。
AIDS Rev. 2017 Oct-Dec;19(3):167-172.
3
CRISPR/Cas Technology: The Unique Synthetic Biology Genome-Editing Tool Shifting the Paradigm in Viral Diagnostics, Defense, and Therapeutics.CRISPR/Cas 技术:改变病毒诊断、防御和治疗范式的独特合成生物学基因组编辑工具。
Annu Rev Biomed Eng. 2024 Jul;26(1):247-272. doi: 10.1146/annurev-bioeng-081723-013033. Epub 2024 Jun 20.
4
Recent Progress and Future Prospective in HBV Cure by CRISPR/Cas.CRISPR/Cas 治愈乙型肝炎病毒的最新进展和未来展望
Viruses. 2021 Dec 21;14(1):4. doi: 10.3390/v14010004.
5
CRISPR/Cas9 and Genome Editing for Viral Disease-Is Resistance Futile?CRISPR/Cas9与用于病毒疾病的基因组编辑——抗性是否徒劳?
ACS Infect Dis. 2018 Jun 8;4(6):871-880. doi: 10.1021/acsinfecdis.7b00273. Epub 2018 Mar 21.
6
CRISPR-Cas based genome editing for eradication of human viruses.基于 CRISPR-Cas 的基因组编辑技术用于清除人类病毒。
Prog Mol Biol Transl Sci. 2024;208:43-58. doi: 10.1016/bs.pmbts.2024.07.012. Epub 2024 Aug 17.
7
CRISPR-Cas based targeting of host and viral genes as an antiviral strategy.基于 CRISPR-Cas 的宿主和病毒基因靶向作为抗病毒策略。
Semin Cell Dev Biol. 2019 Dec;96:53-64. doi: 10.1016/j.semcdb.2019.04.004. Epub 2019 Apr 8.
8
Gene Editing: A New Tool for Viral Disease.基因编辑:病毒病的新工具。
Annu Rev Med. 2017 Jan 14;68:401-411. doi: 10.1146/annurev-med-051215-031129. Epub 2016 Aug 26.
9
COVID-19 one year later: a retrospect of CRISPR-Cas system in combating COVID-19.COVID-19 一年后:CRISPR-Cas 系统抗击 COVID-19 的回顾。
Int J Biol Sci. 2021 May 13;17(8):2080-2088. doi: 10.7150/ijbs.60655. eCollection 2021.
10
CRISPR/Cas9-based tools for targeted genome editing and replication control of HBV.用于乙肝病毒靶向基因组编辑和复制控制的基于CRISPR/Cas9的工具。
Virol Sin. 2015 Oct;30(5):317-25. doi: 10.1007/s12250-015-3660-x. Epub 2015 Oct 22.

引用本文的文献

1
Ferroptosis and non-coding RNAs in breast cancer: insights into CAF and TAM interactions.乳腺癌中的铁死亡与非编码RNA:对癌症相关成纤维细胞和肿瘤相关巨噬细胞相互作用的见解
Discov Oncol. 2025 Aug 31;16(1):1658. doi: 10.1007/s12672-025-03507-x.
2
The role of pioneering transcription factors, chromatin accessibility and epigenetic reprogramming in oncogenic viruses.先驱转录因子、染色质可及性和表观遗传重编程在致癌病毒中的作用。
Front Microbiol. 2025 Jun 16;16:1602497. doi: 10.3389/fmicb.2025.1602497. eCollection 2025.
3
The CRISPR-Cas revolution in head and neck cancer: a new era of targeted therapy.

本文引用的文献

1
Epigenetic Dysregulations in Merkel Cell Polyomavirus-Driven Merkel Cell Carcinoma.Merkel 细胞多瘤病毒驱动的 Merkel 细胞癌中的表观遗传失调。
Int J Mol Sci. 2021 Oct 24;22(21):11464. doi: 10.3390/ijms222111464.
2
Targeting the Regulatory Subunit R2Alpha of Protein Kinase A in Human Glioblastoma through shRNA-Expressing Lentiviral Vectors.通过表达 shRNA 的慢病毒载体靶向人神经胶质瘤中的蛋白激酶 A 的调节亚基 R2Alpha。
Viruses. 2021 Jul 13;13(7):1361. doi: 10.3390/v13071361.
3
The application of CRISPR/Cas9 system in cervical carcinogenesis.
CRISPR-Cas技术在头颈癌领域的变革:靶向治疗的新时代。
Funct Integr Genomics. 2025 May 30;25(1):113. doi: 10.1007/s10142-025-01612-2.
4
Application of CRISPR/Cas gene editing for infectious disease control in poultry.CRISPR/Cas基因编辑在禽类传染病防控中的应用。
Open Life Sci. 2025 May 20;20(1):20251095. doi: 10.1515/biol-2025-1095. eCollection 2025.
5
Recent Advances in Antiviral Drug Delivery Strategies.抗病毒药物递送策略的最新进展
AAPS PharmSciTech. 2025 Mar 4;26(3):73. doi: 10.1208/s12249-025-03053-3.
6
NOX4 modulates breast cancer progression through cancer cell metabolic reprogramming and CD8 T cell antitumor activity.NOX4通过癌细胞代谢重编程和CD8 T细胞抗肿瘤活性调节乳腺癌进展。
Front Immunol. 2025 Feb 7;16:1534936. doi: 10.3389/fimmu.2025.1534936. eCollection 2025.
7
Construction and Stability of All-in-One Adenovirus Vectors Simultaneously Expressing Four and Eight Multiplex Guide RNAs and Cas9 Nickase.同时表达四个和八个多重向导 RNA 和 Cas9 尼克酶的一体式腺病毒载体的构建和稳定性。
Int J Mol Sci. 2024 Aug 12;25(16):8783. doi: 10.3390/ijms25168783.
8
Let's make it personal: CRISPR tools in manipulating cell death pathways for cancer treatment.让我们个体化治疗:CRISPR 工具在操控细胞死亡通路以治疗癌症中的应用。
Cell Biol Toxicol. 2024 Jul 29;40(1):61. doi: 10.1007/s10565-024-09907-z.
9
Gene editing in allergic diseases: Identification of novel pathways and impact of deleting allergen genes.基因编辑在过敏性疾病中的应用:新型通路的鉴定和过敏原基因缺失的影响。
J Allergy Clin Immunol. 2024 Jul;154(1):51-58. doi: 10.1016/j.jaci.2024.03.016. Epub 2024 Mar 29.
10
Recent Advances in CRISPR/Cas9-Mediated Genome Editing in Leishmania Strains.CRISPR/Cas9 介导的利什曼原虫株基因组编辑的最新进展。
Acta Parasitol. 2024 Mar;69(1):121-134. doi: 10.1007/s11686-023-00756-0. Epub 2023 Dec 21.
CRISPR/Cas9 系统在宫颈癌发生中的应用。
Cancer Gene Ther. 2022 May;29(5):466-474. doi: 10.1038/s41417-021-00366-w. Epub 2021 Aug 4.
4
CRISPR/Cas9-based inactivation of human papillomavirus oncogenes E6 or E7 induces senescence in cervical cancer cells.基于 CRISPR/Cas9 的人乳头瘤病毒致癌基因 E6 或 E7 的失活诱导宫颈癌细胞衰老。
Virology. 2021 Oct;562:92-102. doi: 10.1016/j.virol.2021.07.005. Epub 2021 Jul 14.
5
Inhibition of Hepatitis B Virus by AAV8-Derived CRISPR/SaCas9 Expressed From Liver-Specific Promoters.由肝脏特异性启动子表达的AAV8衍生的CRISPR/SaCas9对乙型肝炎病毒的抑制作用
Front Microbiol. 2021 Jun 26;12:665184. doi: 10.3389/fmicb.2021.665184. eCollection 2021.
6
Knowledge From London and Berlin: Finding Threads to a Functional HIV Cure.伦敦与柏林的经验:探寻功能性 HIV 治愈方法。
Front Immunol. 2021 May 27;12:688747. doi: 10.3389/fimmu.2021.688747. eCollection 2021.
7
Adenovirus Structure: What Is New?腺病毒结构:有哪些新进展?
Int J Mol Sci. 2021 May 15;22(10):5240. doi: 10.3390/ijms22105240.
8
CRISPR is a useful biological tool for detecting nucleic acid of SARS-CoV-2 in human clinical samples.CRISPR是一种用于检测人类临床样本中SARS-CoV-2核酸的有用生物工具。
Biomed Pharmacother. 2021 Aug;140:111772. doi: 10.1016/j.biopha.2021.111772. Epub 2021 May 27.
9
HIV-based lentiviral vectors: origin and sequence differences.基于HIV的慢病毒载体:起源与序列差异。
Mol Ther Methods Clin Dev. 2021 Mar 27;21:451-465. doi: 10.1016/j.omtm.2021.03.018. eCollection 2021 Jun 11.
10
Latest Advances of Virology Research Using CRISPR/Cas9-Based Gene-Editing Technology and Its Application to Vaccine Development.基于 CRISPR/Cas9 的基因编辑技术在病毒学研究中的最新进展及其在疫苗开发中的应用。
Viruses. 2021 Apr 28;13(5):779. doi: 10.3390/v13050779.