• 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

用于 SARS-CoV-2 研究的细胞和动物模型。

Cell and Animal Models for SARS-CoV-2 Research.

机构信息

Microbe Evolution Phylogeny Infection, Institut pour la Recherche et le Developpement, Assistance Publique Hopitaux de Marseille, Aix-Marseille University, 13005 Marseille, France.

Institue Hospitalo, Universitaire Mediterranée Infection, 13005 Marseille, France.

出版信息

Viruses. 2022 Jul 9;14(7):1507. doi: 10.3390/v14071507.

DOI:10.3390/v14071507
PMID:35891487
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9319816/
Abstract

During the last two years following the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic, development of potent antiviral drugs and vaccines has been a global health priority. In this context, the understanding of virus pathophysiology, the identification of associated therapeutic targets, and the screening of potential effective compounds have been indispensable advancements. It was therefore of primary importance to develop experimental models that recapitulate the aspects of the human disease in the best way possible. This article reviews the information concerning available SARS-CoV-2 preclinical models during that time, including cell-based approaches and animal models. We discuss their evolution, their advantages, and drawbacks, as well as their relevance to drug effectiveness evaluation.

摘要

在严重急性呼吸综合征冠状病毒 2 (SARS-CoV-2) 大流行后的近两年,开发有效的抗病毒药物和疫苗一直是全球卫生的重点。在这方面,对病毒病理生理学的理解、相关治疗靶点的确定以及潜在有效化合物的筛选是必不可少的进展。因此,开发尽可能再现人类疾病特征的实验模型至关重要。本文综述了在此期间有关 SARS-CoV-2 临床前模型的信息,包括基于细胞的方法和动物模型。我们讨论了它们的演变、优缺点,以及它们在评估药物疗效方面的相关性。

相似文献

1
Cell and Animal Models for SARS-CoV-2 Research.用于 SARS-CoV-2 研究的细胞和动物模型。
Viruses. 2022 Jul 9;14(7):1507. doi: 10.3390/v14071507.
2
Experimental Models of SARS-CoV-2 Infection: Possible Platforms to Study COVID-19 Pathogenesis and Potential Treatments.SARS-CoV-2 感染的实验模型:研究 COVID-19 发病机制和潜在治疗方法的可能平台。
Annu Rev Pharmacol Toxicol. 2022 Jan 6;62:25-53. doi: 10.1146/annurev-pharmtox-121120-012309. Epub 2021 Feb 19.
3
Antiviral Efficacies of FDA-Approved Drugs against SARS-CoV-2 Infection in Ferrets.抗 SARS-CoV-2 感染的 FDA 批准药物在雪貂中的抗病毒疗效。
mBio. 2020 May 22;11(3):e01114-20. doi: 10.1128/mBio.01114-20.
4
Molecular Virology of SARS-CoV-2 and Related Coronaviruses.SARS-CoV-2 及相关冠状病毒的分子病毒学。
Microbiol Mol Biol Rev. 2022 Jun 15;86(2):e0002621. doi: 10.1128/mmbr.00026-21. Epub 2022 Mar 28.
5
Animal models for studying coronavirus infections and developing antiviral agents and vaccines.用于研究冠状病毒感染和开发抗病毒药物和疫苗的动物模型。
Antiviral Res. 2022 Jul;203:105345. doi: 10.1016/j.antiviral.2022.105345. Epub 2022 May 21.
6
Emergence, Transmission, and Potential Therapeutic Targets for the COVID-19 Pandemic Associated with the SARS-CoV-2.与严重急性呼吸综合征冠状病毒2(SARS-CoV-2)相关的2019冠状病毒病大流行的出现、传播及潜在治疗靶点
Cell Physiol Biochem. 2020 Aug 25;54(4):767-790. doi: 10.33594/000000254.
7
Approaches and advances in the development of potential therapeutic targets and antiviral agents for the management of SARS-CoV-2 infection.SARS-CoV-2 感染管理中潜在治疗靶点和抗病毒药物开发的方法和进展。
Eur J Pharmacol. 2020 Oct 15;885:173450. doi: 10.1016/j.ejphar.2020.173450. Epub 2020 Jul 31.
8
SARS-CoV-2: Structure, Biology, and Structure-Based Therapeutics Development.SARS-CoV-2:结构、生物学和基于结构的治疗药物研发。
Front Cell Infect Microbiol. 2020 Nov 25;10:587269. doi: 10.3389/fcimb.2020.587269. eCollection 2020.
9
Comprehensive Analysis of SARS-COV-2 Drug Targets and Pharmacological Aspects in Treating the COVID-19.全面分析 SARS-CoV-2 药物靶点及治疗 COVID-19 的药理学作用
Curr Mol Pharmacol. 2022;15(2):393-417. doi: 10.2174/1874467214666210811120635.
10
Molecular mechanisms of the novel coronavirus SARS-CoV-2 and potential anti-COVID19 pharmacological targets since the outbreak of the pandemic.新型冠状病毒 SARS-CoV-2 的分子机制以及大流行爆发以来潜在的抗 COVID19 药理学靶点。
Food Chem Toxicol. 2020 Dec;146:111805. doi: 10.1016/j.fct.2020.111805. Epub 2020 Oct 8.

引用本文的文献

1
Optimization of A549 Cell Transfection Efficiency with a Plasmid Encoding the N-Protein of the SARS-CoV-2 Virus.使用编码严重急性呼吸综合征冠状病毒2(SARS-CoV-2)病毒N蛋白的质粒优化A549细胞转染效率
Dokl Biochem Biophys. 2025 Apr;521(1):157-159. doi: 10.1134/S1607672924601136. Epub 2025 Apr 11.
2
Effects of immunoproteasome inhibition on acute respiratory infection with murine hepatitis virus strain 1.免疫蛋白酶体抑制对小鼠肝炎病毒1型急性呼吸道感染的影响。
J Virol. 2024 Dec 17;98(12):e0123824. doi: 10.1128/jvi.01238-24. Epub 2024 Nov 7.
3
Induced pluripotent stem cells (iPSCs): molecular mechanisms of induction and applications.诱导多能干细胞(iPSCs):诱导的分子机制与应用。
Signal Transduct Target Ther. 2024 Apr 26;9(1):112. doi: 10.1038/s41392-024-01809-0.
4
Features of SARS-CoV-2 Replication in Various Types of Reptilian and Fish Cell Cultures.各种类型的爬行动物和鱼类细胞培养物中 SARS-CoV-2 的复制特征。
Viruses. 2023 Nov 29;15(12):2350. doi: 10.3390/v15122350.
5
Current state-of-the-art and potential future therapeutic drugs against COVID-19.针对新型冠状病毒肺炎的当前最先进技术及潜在的未来治疗药物。
Front Cell Dev Biol. 2023 Aug 25;11:1238027. doi: 10.3389/fcell.2023.1238027. eCollection 2023.
6
The Isolation and In Vitro Differentiation of Primary Fetal Baboon Tracheal Epithelial Cells for the Study of SARS-CoV-2 Host-Virus Interactions.用于研究 SARS-CoV-2 宿主-病毒相互作用的原代狒狒胎气管上皮细胞的分离和体外分化。
Viruses. 2023 Mar 28;15(4):862. doi: 10.3390/v15040862.
7
Therapeutic strategies for COVID-19: progress and lessons learned.COVID-19 的治疗策略:进展与经验教训。
Nat Rev Drug Discov. 2023 Jun;22(6):449-475. doi: 10.1038/s41573-023-00672-y. Epub 2023 Apr 19.
8
The Role of Viral Infections in the Onset of Autoimmune Diseases.病毒感染在自身免疫性疾病发病中的作用。
Viruses. 2023 Mar 18;15(3):782. doi: 10.3390/v15030782.
9
Ocular Symptoms Associated with COVID-19 Are Correlated with the Expression Profile of Mouse SARS-CoV-2 Binding Sites.与 COVID-19 相关的眼部症状与小鼠 SARS-CoV-2 结合位点的表达谱相关。
Viruses. 2023 Jan 26;15(2):354. doi: 10.3390/v15020354.
10
Animal Models to Test SARS-CoV-2 Vaccines: Which Ones Are in Use and Future Expectations.用于测试新型冠状病毒疫苗的动物模型:哪些正在使用及未来展望
Pathogens. 2022 Dec 23;12(1):20. doi: 10.3390/pathogens12010020.

本文引用的文献

1
SARS-CoV-2 VOC type and biological sex affect molnupiravir efficacy in severe COVID-19 dwarf hamster model.SARS-CoV-2 VOC 类型和生物性别影响严重 COVID-19 dwarf hamster 模型中 molnupiravir 的疗效。
Nat Commun. 2022 Jul 29;13(1):4416. doi: 10.1038/s41467-022-32045-1.
2
A broadly neutralizing antibody protects Syrian hamsters against SARS-CoV-2 Omicron challenge.一种广谱中和抗体可保护叙利亚仓鼠免受 SARS-CoV-2 奥密克戎株挑战。
Nat Commun. 2022 Jun 23;13(1):3589. doi: 10.1038/s41467-022-31259-7.
3
Breakthroughs and Applications of Organ-on-a-Chip Technology.器官芯片技术的突破与应用。
Cells. 2022 Jun 2;11(11):1828. doi: 10.3390/cells11111828.
4
Adenovirus type 5 SARS-CoV-2 vaccines delivered orally or intranasally reduced disease severity and transmission in a hamster model.口服或鼻内接种 5 型腺病毒 SARS-CoV-2 疫苗可降低仓鼠模型疾病严重程度和传播。
Sci Transl Med. 2022 Aug 17;14(658):eabn6868. doi: 10.1126/scitranslmed.abn6868.
5
Infection and transmission of ancestral SARS-CoV-2 and its alpha variant in pregnant white-tailed deer.在怀孕白尾鹿中感染和传播祖先 SARS-CoV-2 及其 alpha 变体。
Emerg Microbes Infect. 2022 Dec;11(1):95-112. doi: 10.1080/22221751.2021.2012528.
6
A potent SARS-CoV-2 neutralising nanobody shows therapeutic efficacy in the Syrian golden hamster model of COVID-19.一种强效的 SARS-CoV-2 中和纳米抗体在 COVID-19 的叙利亚金黄地鼠模型中显示出治疗效果。
Nat Commun. 2021 Sep 22;12(1):5469. doi: 10.1038/s41467-021-25480-z.
7
Low dose inocula of SARS-CoV-2 Alpha variant transmits more efficiently than earlier variants in hamsters.严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)阿尔法变体的低剂量接种物在仓鼠中比早期变体传播更有效。
Commun Biol. 2021 Sep 20;4(1):1102. doi: 10.1038/s42003-021-02640-x.
8
Safety and Immunogenicity of a Newcastle Disease Virus Vector-Based SARS-CoV-2 Vaccine Candidate, AVX/COVID-12-HEXAPRO (Patria), in Pigs.新型冠状病毒疫苗候选物 Newcastle 疾病病毒载体 AVX/COVID-19-HEXAPRO(Patria)在猪体内的安全性和免疫原性。
mBio. 2021 Oct 26;12(5):e0190821. doi: 10.1128/mBio.01908-21. Epub 2021 Sep 21.
9
A CRISPR/Cas9 genetically engineered organoid biobank reveals essential host factors for coronaviruses.CRISPR/Cas9 基因编辑类器官生物库揭示冠状病毒的关键宿主因子。
Nat Commun. 2021 Sep 17;12(1):5498. doi: 10.1038/s41467-021-25729-7.
10
Estimating clinical SARS-CoV-2 infectiousness in Vero E6 and primary airway epithelial cells.评估新型冠状病毒(SARS-CoV-2)在非洲绿猴肾细胞(Vero E6)和原代气道上皮细胞中的临床传染性。
Lancet Microbe. 2021 Nov;2(11):e571. doi: 10.1016/S2666-5247(21)00216-0. Epub 2021 Aug 27.