• 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

相似文献

1
Animal models and SARS-CoV-2-induced pulmonary and neurological injuries.动物模型与 SARS-CoV-2 诱导的肺部和神经系统损伤。
Mem Inst Oswaldo Cruz. 2023 Jan 20;117:e220239. doi: 10.1590/0074-02760220239. eCollection 2023.
2
Natural and genetically-modified animal models to investigate pulmonary and extrapulmonary manifestations of COVID-19.用于研究 COVID-19 肺部和肺外表现的天然和基因修饰动物模型。
Int Rev Immunol. 2024;43(1):13-32. doi: 10.1080/08830185.2022.2089666. Epub 2022 Jun 25.
3
Ferrets: A powerful model of SARS-CoV-2.雪貂:SARS-CoV-2 的强大模型。
Zool Res. 2023 Mar 18;44(2):323-330. doi: 10.24272/j.issn.2095-8137.2022.351.
4
Characterization of Three Variants of SARS-CoV-2 In Vivo Shows Host-Dependent Pathogenicity in Hamsters, While Not in K18-hACE2 Mice.三种体内 SARS-CoV-2 变体的特征表明其在仓鼠中有宿主依赖性致病性,而在 K18-hACE2 小鼠中则没有。
Viruses. 2022 Nov 21;14(11):2584. doi: 10.3390/v14112584.
5
Susceptibility of ferrets, cats, dogs, and other domesticated animals to SARS-coronavirus 2.雪貂、猫、狗和其他驯养动物对 SARS-CoV-2 的易感性。
Science. 2020 May 29;368(6494):1016-1020. doi: 10.1126/science.abb7015. Epub 2020 Apr 8.
6
The K18-Human ACE2 Transgenic Mouse Model Recapitulates Non-severe and Severe COVID-19 in Response to an Infectious Dose of the SARS-CoV-2 Virus.K18-Human ACE2 转基因小鼠模型对 SARS-CoV-2 病毒感染剂量的反应可重现非重症和重症 COVID-19。
J Virol. 2022 Jan 12;96(1):e0096421. doi: 10.1128/JVI.00964-21. Epub 2021 Oct 20.
7
SARS CoV-2 (Delta Variant) Infection Kinetics and Immunopathogenesis in Domestic Cats.SARS CoV-2(Delta 变异株)感染家猫的动力学和免疫发病机制。
Viruses. 2022 Jun 1;14(6):1207. doi: 10.3390/v14061207.
8
Infectious Clones Produce SARS-CoV-2 That Causes Severe Pulmonary Disease in Infected K18-Human ACE2 Mice.传染性克隆产生的 SARS-CoV-2 可导致感染 K18-Human ACE2 小鼠发生严重肺部疾病。
mBio. 2021 Apr 20;12(2):e00819-21. doi: 10.1128/mBio.00819-21.
9
SARS CoV-2 infections in animals, two years into the pandemic.新冠病毒(SARS-CoV-2)在动物中的感染,大流行两年后的情况。
Arch Virol. 2022 Dec;167(12):2503-2517. doi: 10.1007/s00705-022-05609-1. Epub 2022 Oct 7.
10
A longitudinal molecular and cellular lung atlas of lethal SARS-CoV-2 infection in K18-hACE2 transgenic mice.K18-hACE2 转基因小鼠致死性 SARS-CoV-2 感染的纵向分子和细胞肺部图谱。
EBioMedicine. 2024 Jan;99:104932. doi: 10.1016/j.ebiom.2023.104932. Epub 2023 Dec 19.

引用本文的文献

1
Establishment and characterization of an hhTMPRSS2 knock-in mouse model to study SARS-CoV-2.建立并鉴定 hhTMPRSS2 基因敲入小鼠模型以研究 SARS-CoV-2。
Front Immunol. 2024 Jul 10;15:1428711. doi: 10.3389/fimmu.2024.1428711. eCollection 2024.

本文引用的文献

1
In vitro and in vivo differences in neurovirulence between D614G, Delta And Omicron BA.1 SARS-CoV-2 variants.D614G、Delta 和奥密克戎 BA.1 SARS-CoV-2 变体之间神经毒力的体外和体内差异。
Acta Neuropathol Commun. 2022 Sep 5;10(1):124. doi: 10.1186/s40478-022-01426-4.
2
Microgliosis and neuronal proteinopathy in brain persist beyond viral clearance in SARS-CoV-2 hamster model.在 SARS-CoV-2 仓鼠模型中,病毒清除后,脑内小胶质细胞增生和神经元蛋白病变仍然存在。
EBioMedicine. 2022 May;79:103999. doi: 10.1016/j.ebiom.2022.103999. Epub 2022 Apr 16.
3
Fatal Neurodissemination and SARS-CoV-2 Tropism in K18-hACE2 Mice Is Only Partially Dependent on hACE2 Expression.K18-hACE2小鼠中的致命性神经播散和SARS-CoV-2嗜性仅部分依赖于hACE2表达。
Viruses. 2022 Mar 5;14(3):535. doi: 10.3390/v14030535.
4
Distinct spatial arrangements of ACE2 and TMPRSS2 expression in Syrian hamster lung lobes dictates SARS-CoV-2 infection patterns.叙利亚仓鼠肺叶中 ACE2 和 TMPRSS2 表达的不同空间排列决定了 SARS-CoV-2 的感染模式。
PLoS Pathog. 2022 Mar 7;18(3):e1010340. doi: 10.1371/journal.ppat.1010340. eCollection 2022 Mar.
5
Characterization of Two Heterogeneous Lethal Mouse-Adapted SARS-CoV-2 Variants Recapitulating Representative Aspects of Human COVID-19.两种异质性致死性适应小鼠的 SARS-CoV-2 变异株的特征,再现了人类 COVID-19 的代表性方面。
Front Immunol. 2022 Feb 7;13:821664. doi: 10.3389/fimmu.2022.821664. eCollection 2022.
6
SARS-CoV-2 Omicron virus causes attenuated disease in mice and hamsters.新冠病毒奥密克戎变异株在小鼠和仓鼠中引起轻症疾病。
Nature. 2022 Mar;603(7902):687-692. doi: 10.1038/s41586-022-04441-6. Epub 2022 Jan 21.
7
Recovery of anosmia in hamsters infected with SARS-CoV-2 is correlated with repair of the olfactory epithelium.感染 SARS-CoV-2 的仓鼠的嗅觉丧失恢复与嗅上皮修复有关。
Sci Rep. 2022 Jan 12;12(1):628. doi: 10.1038/s41598-021-04622-9.
8
Pulmonary lesions induced by SARS-CoV-2 infection in domestic cats.猫感染 SARS-CoV-2 引起的肺部病变。
Vet Pathol. 2022 Jul;59(4):696-706. doi: 10.1177/03009858211066840. Epub 2021 Dec 29.
9
Histologic pulmonary lesions of SARS-CoV-2 in 4 nonhuman primate species: An institutional comparative review.四种非人类灵长类动物的 SARS-CoV-2 组织肺部病变:机构间比较回顾。
Vet Pathol. 2022 Jul;59(4):673-680. doi: 10.1177/03009858211067468. Epub 2021 Dec 29.
10
Microglia Do Not Restrict SARS-CoV-2 Replication following Infection of the Central Nervous System of K18-Human ACE2 Transgenic Mice.小胶质细胞在 K18-Human ACE2 转基因小鼠中枢神经系统感染后并不限制 SARS-CoV-2 的复制。
J Virol. 2022 Feb 23;96(4):e0196921. doi: 10.1128/jvi.01969-21. Epub 2021 Dec 22.

动物模型与 SARS-CoV-2 诱导的肺部和神经系统损伤。

Animal models and SARS-CoV-2-induced pulmonary and neurological injuries.

机构信息

Fundação Oswaldo Cruz-Fiocruz, Instituto Oswaldo Cruz, Laboratório de Desenvolvimento Tecnológico em Virologia, Rio de Janeiro, RJ, Brasil.

Fundação Oswaldo Cruz-Fiocruz, Instituto de Tecnologia em Imunobiológicos, Laboratório de Experimentação Animal, Rio de Janeiro, RJ, Brasil.

出版信息

Mem Inst Oswaldo Cruz. 2023 Jan 20;117:e220239. doi: 10.1590/0074-02760220239. eCollection 2023.

DOI:10.1590/0074-02760220239
PMID:36700583
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9870265/
Abstract

Laboratory animals are essential mainly for experiments aiming to study pathogenesis and evaluate antivirals and vaccines against emerging human infectious diseases. Preclinical studies of coronavirus disease 19 (COVID-19) pathogenesis have used several animal species as models: transgenic human ACE2 mice (K18 mice), inbred BALB/c or C57BL/6N mice, ferrets, minks, domestic cats and dogs, hamsters, and macaques. However, the choice of an animal model relies on several limitations. Besides the host susceptibility, the researcher's experience with animal model management and the correct interpretation of clinical and laboratory records are crucial to succeed in preclinical translational research. Here, we summarise pathological and clinical findings correlated with virological data and immunological changes observed from severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) experimental infections using different well-established SARS-CoV-2 animal model species. This essay aims to critically evaluate the current state of animal model translation to clinical data, as described in the human SARS-CoV-2 infection.

摘要

实验动物主要用于旨在研究发病机制和评估针对新发人类传染病的抗病毒药物和疫苗的实验。针对新型冠状病毒病 19(COVID-19)发病机制的临床前研究已经使用了几种动物物种作为模型:转人 ACE2 基因的小鼠(K18 小鼠)、近交 BALB/c 或 C57BL/6N 小鼠、雪貂、水貂、家猫和狗、仓鼠和猕猴。然而,动物模型的选择取决于几个限制因素。除了宿主易感性外,研究人员对动物模型管理的经验以及对临床和实验室记录的正确解释对于成功进行临床前转化研究至关重要。在这里,我们总结了与病毒学数据相关的病理和临床发现以及使用不同成熟的 SARS-CoV-2 动物模型观察到的免疫变化,这些动物模型被感染了严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)。本文旨在批判性地评估目前根据人类 SARS-CoV-2 感染情况将动物模型转化为临床数据的情况。