• 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

SARS-CoV-2 感染和疾病结局的非人类灵长类动物模型:进展和意义。

SARS-CoV-2 infection and disease outcomes in non-human primate models: advances and implications.

机构信息

State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, National Institute of Diagnostics and Vaccine Development in Infectious Diseases, School of Life Sciences, School of Public Health, Xiamen University, Xiamen, People's Republic of China.

Department of Microbiology, Howard University College of Medicine, Washington, DC, USA.

出版信息

Emerg Microbes Infect. 2021 Dec;10(1):1881-1889. doi: 10.1080/22221751.2021.1976598.

DOI:10.1080/22221751.2021.1976598
PMID:34490832
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8451603/
Abstract

SARS-CoV-2 has been the causative pathogen of the pandemic of COVID-19, resulting in catastrophic health issues globally. It is important to develop human-like animal models for investigating the mechanisms that SARS-CoV-2 uses to infect humans and cause COVID-19. Several studies demonstrated that the non-human primate (NHP) is permissive for SARS-CoV-2 infection to cause typical clinical symptoms including fever, cough, breathing difficulty, and other diagnostic abnormalities such as immunopathogenesis and hyperplastic lesions in the lung. These NHP models have been used for investigating the potential infection route and host immune response to SARS-CoV-2, as well as testing vaccines and drugs. This review aims to summarize the benefits and caveats of NHP models currently available for SARS-CoV-2, and to discuss key topics including model optimization, extended application, and clinical translation.

摘要

SARS-CoV-2 是 COVID-19 大流行的病原体,在全球范围内造成了灾难性的健康问题。开发类人动物模型对于研究 SARS-CoV-2 感染人类和导致 COVID-19 的机制非常重要。多项研究表明,非人类灵长类动物(NHP)允许 SARS-CoV-2 感染,导致典型的临床症状,包括发热、咳嗽、呼吸困难和其他诊断异常,如肺部的免疫发病机制和增生性病变。这些 NHP 模型已被用于研究 SARS-CoV-2 的潜在感染途径和宿主免疫反应,以及测试疫苗和药物。本综述旨在总结目前用于 SARS-CoV-2 的 NHP 模型的优点和注意事项,并讨论关键主题,包括模型优化、扩展应用和临床转化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a3d/8451603/704ef7025667/TEMI_A_1976598_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a3d/8451603/704ef7025667/TEMI_A_1976598_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a3d/8451603/704ef7025667/TEMI_A_1976598_F0001_OC.jpg

相似文献

1
SARS-CoV-2 infection and disease outcomes in non-human primate models: advances and implications.SARS-CoV-2 感染和疾病结局的非人类灵长类动物模型:进展和意义。
Emerg Microbes Infect. 2021 Dec;10(1):1881-1889. doi: 10.1080/22221751.2021.1976598.
2
Waning antibodies from inactivated SARS-CoV-2 vaccination offer protection against infection without antibody-enhanced immunopathology in rhesus macaque pneumonia models.灭活 SARS-CoV-2 疫苗产生的抗体衰减提供了针对感染的保护,而不会在恒河猴肺炎模型中引起抗体增强的免疫病理学。
Emerg Microbes Infect. 2021 Dec;10(1):2194-2198. doi: 10.1080/22221751.2021.2002670.
3
SARS-CoV-2: Immune Response Elicited by Infection and Development of Vaccines and Treatments.SARS-CoV-2:感染引起的免疫反应和疫苗及治疗的发展。
Front Immunol. 2020 Dec 11;11:569760. doi: 10.3389/fimmu.2020.569760. eCollection 2020.
4
Designing therapeutic strategies to combat severe acute respiratory syndrome coronavirus-2 disease: COVID-19.设计治疗策略以对抗严重急性呼吸综合征冠状病毒 2 型疾病:COVID-19。
Drug Dev Res. 2021 Feb;82(1):12-26. doi: 10.1002/ddr.21720. Epub 2020 Jul 30.
5
Age-associated SARS-CoV-2 breakthrough infection and changes in immune response in a mouse model.年龄相关的 SARS-CoV-2 突破感染及在小鼠模型中的免疫反应变化。
Emerg Microbes Infect. 2022 Dec;11(1):368-383. doi: 10.1080/22221751.2022.2026741.
6
Similarities and Dissimilarities of COVID-19 and Other Coronavirus Diseases.新型冠状病毒病与其他冠状病毒病的异同。
Annu Rev Microbiol. 2021 Oct 8;75:19-47. doi: 10.1146/annurev-micro-110520-023212. Epub 2021 Jan 25.
7
Potential Therapeutic Targets and Vaccine Development for SARS-CoV-2/COVID-19 Pandemic Management: A Review on the Recent Update.SARS-CoV-2/COVID-19 大流行管理的潜在治疗靶点和疫苗开发:近期进展综述。
Front Immunol. 2021 Jun 30;12:658519. doi: 10.3389/fimmu.2021.658519. eCollection 2021.
8
Host metabolism dysregulation and cell tropism identification in human airway and alveolar organoids upon SARS-CoV-2 infection.SARS-CoV-2 感染后人类气道和肺泡类器官中的宿主代谢失调和细胞嗜性鉴定。
Protein Cell. 2021 Sep;12(9):717-733. doi: 10.1007/s13238-020-00811-w. Epub 2020 Dec 12.
9
Insights into COVID-19 Vaccine Development Based on Immunogenic Structural Proteins of SARS-CoV-2, Host Immune Responses, and Herd Immunity.基于 SARS-CoV-2 的免疫原性结构蛋白、宿主免疫反应和群体免疫的 COVID-19 疫苗开发的新见解。
Cells. 2021 Oct 29;10(11):2949. doi: 10.3390/cells10112949.
10
Animal models for SARS-CoV-2.用于 SARS-CoV-2 的动物模型。
Curr Opin Virol. 2021 Jun;48:73-81. doi: 10.1016/j.coviro.2021.03.009. Epub 2021 Apr 6.

引用本文的文献

1
Decisive reversal of lethal coronavirus disease 2019 in senescent hamster by synchronic antiviral and immunoregulatory intervention.通过同步抗病毒和免疫调节干预决定性逆转衰老仓鼠的致死性2019冠状病毒病
MedComm (2020). 2024 Jul 19;5(8):e642. doi: 10.1002/mco2.642. eCollection 2024 Aug.
2
Immunobiology of COVID-19: Mechanistic and therapeutic insights from animal models.新型冠状病毒病的免疫生物学:来自动物模型的机制和治疗见解。
Zool Res. 2024 Jul 18;45(4):747-766. doi: 10.24272/j.issn.2095-8137.2024.062.
3
SARS-CoV-2 in Captive Nonhuman Primates, Spain, 2020-2023.

本文引用的文献

1
Accelerated passage of gene-modified monkeys by hormone-induced precocious puberty.通过激素诱导的性早熟加速基因编辑猴的传代
Natl Sci Rev. 2021 May 4;8(7):nwab083. doi: 10.1093/nsr/nwab083. eCollection 2021 Jul.
2
Prevention and Attenuation of Covid-19 with the BNT162b2 and mRNA-1273 Vaccines.BNT162b2 和 mRNA-1273 疫苗对新冠病毒的预防和衰减作用。
N Engl J Med. 2021 Jul 22;385(4):320-329. doi: 10.1056/NEJMoa2107058. Epub 2021 Jun 30.
3
An infectivity-enhancing site on the SARS-CoV-2 spike protein targeted by antibodies.
2020-2023 年西班牙圈养非人灵长类动物中的 SARS-CoV-2。
Emerg Infect Dis. 2024 Jun;30(6):1253-1257. doi: 10.3201/eid3006.231247.
4
Predicting the presence of infectious virus from PCR data: A meta-analysis of SARS-CoV-2 in non-human primates.从 PCR 数据预测传染性病毒的存在:非人类灵长类动物中 SARS-CoV-2 的荟萃分析。
PLoS Pathog. 2024 Apr 29;20(4):e1012171. doi: 10.1371/journal.ppat.1012171. eCollection 2024 Apr.
5
Monitoring and immunogenicity of SARS-CoV-2 vaccination of laboratory rhesus monkeys (Macaca mulatta).实验室恒河猴(Macaca mulatta)接种 SARS-CoV-2 疫苗的监测和免疫原性。
Sci Rep. 2023 Feb 25;13(1):3274. doi: 10.1038/s41598-023-30473-7.
6
Protective roles and protective mechanisms of neutralizing antibodies against SARS-CoV-2 infection and their potential clinical implications.中和抗体对 SARS-CoV-2 感染的保护作用和保护机制及其潜在的临床意义。
Front Immunol. 2023 Jan 19;14:1055457. doi: 10.3389/fimmu.2023.1055457. eCollection 2023.
7
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.
8
A Heterologous Challenge Rescues the Attenuated Immunogenicity of SARS-CoV-2 Omicron BA.1 Variant in Syrian Hamster Model.一种异源挑战可挽救 SARS-CoV-2 奥密克戎 BA.1 变异株在叙利亚仓鼠模型中的减毒免疫原性。
J Virol. 2023 Feb 28;97(2):e0168422. doi: 10.1128/jvi.01684-22. Epub 2023 Jan 18.
9
Prospects of animal models and their application in studies on adaptive immunity to SARS-CoV-2.SARS-CoV-2 适应性免疫的动物模型及其应用前景。
Front Immunol. 2022 Sep 16;13:993754. doi: 10.3389/fimmu.2022.993754. eCollection 2022.
10
Application of animal models to compare and contrast the virulence of current and future potential SARS-CoV-2 variants.应用动物模型来比较和对比当前及未来潜在的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)变体的毒力。
Biosaf Health. 2022 Jun;4(3):154-160. doi: 10.1016/j.bsheal.2022.05.001. Epub 2022 May 5.
新冠病毒刺突蛋白上一个被抗体靶向的增强感染性位点。
Cell. 2021 Jun 24;184(13):3452-3466.e18. doi: 10.1016/j.cell.2021.05.032. Epub 2021 May 24.
4
A core-shell structured COVID-19 mRNA vaccine with favorable biodistribution pattern and promising immunity.一种具有有利生物分布模式和有前景免疫效果的核壳结构 COVID-19 mRNA 疫苗。
Signal Transduct Target Ther. 2021 May 31;6(1):213. doi: 10.1038/s41392-021-00634-z.
5
BNT162b2 vaccine induces neutralizing antibodies and poly-specific T cells in humans.BNT162b2 疫苗可在人体内诱导中和抗体和多特异性 T 细胞。
Nature. 2021 Jul;595(7868):572-577. doi: 10.1038/s41586-021-03653-6. Epub 2021 May 27.
6
COVID-19 reinfection: a rapid systematic review of case reports and case series.COVID-19 再感染:病例报告和病例系列的快速系统评价。
J Investig Med. 2021 Aug;69(6):1253-1255. doi: 10.1136/jim-2021-001853. Epub 2021 May 18.
7
The olfactory route is a potential way for SARS-CoV-2 to invade the central nervous system of rhesus monkeys.嗅觉途径可能是 SARS-CoV-2 入侵恒河猴中枢神经系统的一种方式。
Signal Transduct Target Ther. 2021 Apr 24;6(1):169. doi: 10.1038/s41392-021-00591-7.
8
Multiple SARS-CoV-2 variants escape neutralization by vaccine-induced humoral immunity.多种 SARS-CoV-2 变异株逃避疫苗诱导的体液免疫中和作用。
Cell. 2021 Apr 29;184(9):2372-2383.e9. doi: 10.1016/j.cell.2021.03.013. Epub 2021 Mar 12.
9
Evidence of escape of SARS-CoV-2 variant B.1.351 from natural and vaccine-induced sera.SARS-CoV-2 变体 B.1.351 从自然和疫苗诱导的血清中逃逸的证据。
Cell. 2021 Apr 29;184(9):2348-2361.e6. doi: 10.1016/j.cell.2021.02.037. Epub 2021 Feb 23.
10
Antibody resistance of SARS-CoV-2 variants B.1.351 and B.1.1.7.SARS-CoV-2 变体 B.1.351 和 B.1.1.7 的抗体抗性。
Nature. 2021 May;593(7857):130-135. doi: 10.1038/s41586-021-03398-2. Epub 2021 Mar 8.