• 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

用于艾滋病病毒和艾滋病研究的人源化小鼠。

Humanized mice for HIV and AIDS research.

作者信息

Victor Garcia J

机构信息

Division of Infectious Diseases, UNC Center for AIDS Research, University of North Carolina School of Medicine, Genetic Medicine Building, Rm. 2043, Chapel Hill, NC 27599-7042, United States.

出版信息

Curr Opin Virol. 2016 Aug;19:56-64. doi: 10.1016/j.coviro.2016.06.010. Epub 2016 Jul 19.

DOI:10.1016/j.coviro.2016.06.010
PMID:27447446
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5021593/
Abstract

HIV has a very limited species tropism that prevents the use of most conventional small animal models for AIDS research. The in vivo analysis of HIV/AIDS has benefited extensively from novel chimeric animal models that accurately recapitulate key aspects of the human condition. Specifically, immunodeficient mice that are systemically repopulated with human hematolymphoid cells offer a viable alternative for the study of a multitude of highly relevant aspects of HIV replication, pathogenesis, therapy, transmission, prevention, and eradication. This article summarizes some of the multiple contributions that humanized mouse models of HIV infection have made to the field of AIDS research. These models have proven to be highly informative and hold great potential for accelerating multiple aspects of HIV research in the future.

摘要

人类免疫缺陷病毒(HIV)具有非常有限的物种嗜性,这使得大多数传统的小动物模型无法用于艾滋病研究。HIV/AIDS的体内分析在很大程度上受益于新型嵌合动物模型,这些模型能够准确地重现人类病情的关键方面。具体而言,用人造血淋巴细胞进行全身再填充的免疫缺陷小鼠为研究HIV复制、发病机制、治疗、传播、预防和根除等众多高度相关方面提供了可行的替代方案。本文总结了HIV感染人源化小鼠模型对艾滋病研究领域所做出的多项贡献。这些模型已被证明具有很高的信息量,并且在未来加速HIV研究的多个方面具有巨大潜力。

相似文献

1
Humanized mice for HIV and AIDS research.用于艾滋病病毒和艾滋病研究的人源化小鼠。
Curr Opin Virol. 2016 Aug;19:56-64. doi: 10.1016/j.coviro.2016.06.010. Epub 2016 Jul 19.
2
Humanized Mouse Models for Human Immunodeficiency Virus Infection.人源化小鼠模型用于人类免疫缺陷病毒感染。
Annu Rev Virol. 2017 Sep 29;4(1):393-412. doi: 10.1146/annurev-virology-101416-041703. Epub 2017 Jul 26.
3
Humanized mouse models of HIV infection.HIV 感染的人源化小鼠模型。
AIDS Rev. 2011 Jul-Sep;13(3):135-48.
4
The SCID-hu mouse: an in-vivo model for HIV-1 pathogenesis and stem cell gene therapy for AIDS.重症联合免疫缺陷-人源化小鼠:一种用于HIV-1发病机制研究及艾滋病干细胞基因治疗的体内模型。
Semin Immunol. 1996 Aug;8(4):215-21. doi: 10.1006/smim.1996.0027.
5
In vivo platforms for analysis of HIV persistence and eradication.用于分析HIV持续性和根除的体内平台。
J Clin Invest. 2016 Feb;126(2):424-31. doi: 10.1172/JCI80562. Epub 2016 Feb 1.
6
BLT humanized mice as a small animal model of HIV infection.BLT人源化小鼠作为HIV感染的小动物模型。
Curr Opin Virol. 2015 Aug;13:75-80. doi: 10.1016/j.coviro.2015.05.002. Epub 2015 Jun 12.
7
HIV-1 infection and CD4 T cell depletion in the humanized Rag2-/-gamma c-/- (RAG-hu) mouse model.人源化Rag2-/-γc-/-(RAG-hu)小鼠模型中的HIV-1感染与CD4 T细胞耗竭
Retrovirology. 2006 Nov 1;3:76. doi: 10.1186/1742-4690-3-76.
8
[Investigation of HIV-1 pathogenesis using humanized mouse model].[利用人源化小鼠模型对HIV-1发病机制的研究]
Uirusu. 2016;66(1):91-100. doi: 10.2222/jsv.66.91.
9
Improvements and Limitations of Humanized Mouse Models for HIV Research: NIH/NIAID "Meet the Experts" 2015 Workshop Summary.用于HIV研究的人源化小鼠模型的改进与局限:美国国立卫生研究院/美国国立过敏和传染病研究所2015年“与专家见面”研讨会总结
AIDS Res Hum Retroviruses. 2016 Feb;32(2):109-19. doi: 10.1089/AID.2015.0258.
10
Novel humanized murine models for HIV research.用于艾滋病病毒研究的新型人源化小鼠模型。
Curr HIV/AIDS Rep. 2009 Feb;6(1):13-9. doi: 10.1007/s11904-009-0003-2.

引用本文的文献

1
Targeting Metastasis: Exploring the Impact of Microbial Infections on Cancer Progression Through Innovative Biological Models.靶向转移:通过创新生物学模型探索微生物感染对癌症进展的影响
Curr Microbiol. 2025 Jun 7;82(7):328. doi: 10.1007/s00284-025-04306-x.
2
Nucleoside Reverse Transcriptase Inhibitor (NRTI)-Induced Neuropathy and Mitochondrial Toxicity: Limitations of the Poly-γ Hypothesis and the Potential Roles of Autophagy and Drug Transport.核苷类逆转录酶抑制剂(NRTI)所致神经病变和线粒体毒性:多聚-γ假说的局限性以及自噬和药物转运的潜在作用
Pharmaceutics. 2024 Dec 13;16(12):1592. doi: 10.3390/pharmaceutics16121592.
3

本文引用的文献

1
In vivo analysis of the effect of panobinostat on cell-associated HIV RNA and DNA levels and latent HIV infection.帕比司他对细胞相关HIV RNA和DNA水平及潜伏性HIV感染影响的体内分析。
Retrovirology. 2016 May 21;13(1):36. doi: 10.1186/s12977-016-0268-7.
2
CD19xCD3 DART protein mediates human B-cell depletion in vivo in humanized BLT mice.CD19xCD3 DART 蛋白介导人源化 BLT 小鼠体内人 B 细胞耗竭。
Mol Ther Oncolytics. 2016 Mar 2;3:15024. doi: 10.1038/mto.2015.24. eCollection 2016.
3
Quantitation of Productively Infected Monocytes and Macrophages of Simian Immunodeficiency Virus-Infected Macaques.
Nonhuman primate models of pediatric viral diseases.
儿科病毒性疾病的非人灵长类动物模型。
Front Cell Infect Microbiol. 2024 Dec 3;14:1493885. doi: 10.3389/fcimb.2024.1493885. eCollection 2024.
4
Making a Monkey out of Human Immunodeficiency Virus/Simian Immunodeficiency Virus Pathogenesis: Immune Cell Depletion Experiments as a Tool to Understand the Immune Correlates of Protection and Pathogenicity in HIV Infection.将人类免疫缺陷病毒/猴免疫缺陷病毒发病机制搞得一团糟:免疫细胞耗竭实验作为一种工具,用于理解 HIV 感染中的免疫保护相关性和致病性的免疫相关性。
Viruses. 2024 Jun 17;16(6):972. doi: 10.3390/v16060972.
5
A novel humanized mouse model for HIV and tuberculosis co-infection studies.一种用于 HIV 和结核病合并感染研究的新型人源化小鼠模型。
Front Immunol. 2024 May 10;15:1395018. doi: 10.3389/fimmu.2024.1395018. eCollection 2024.
6
A Novel Humanized Mouse Model for HIV and Tuberculosis Co-infection Studies.一种用于HIV和结核病合并感染研究的新型人源化小鼠模型。
bioRxiv. 2024 Mar 7:2024.03.05.583545. doi: 10.1101/2024.03.05.583545.
7
Examining Chronic Inflammation, Immune Metabolism, and T Cell Dysfunction in HIV Infection.探讨 HIV 感染中的慢性炎症、免疫代谢和 T 细胞功能障碍。
Viruses. 2024 Jan 31;16(2):219. doi: 10.3390/v16020219.
8
Experimental models for HIV latency and molecular tools for reservoir quantification-an update.HIV 潜伏期的实验模型和储存库定量的分子工具——更新。
Clin Microbiol Rev. 2023 Dec 20;36(4):e0001323. doi: 10.1128/cmr.00013-23. Epub 2023 Nov 15.
9
Single-Cell Transcriptomics of /HIV Co-Infection.单细胞转录组学分析 /HIV 共感染。
Cells. 2023 Sep 17;12(18):2295. doi: 10.3390/cells12182295.
10
Humanized Mice for Studies of HIV-1 Persistence and Elimination.用于研究HIV-1持续性和清除的人源化小鼠
Pathogens. 2023 Jun 27;12(7):879. doi: 10.3390/pathogens12070879.
猴免疫缺陷病毒感染猕猴中产生性感染的单核细胞和巨噬细胞的定量分析。
J Virol. 2016 May 27;90(12):5643-5656. doi: 10.1128/JVI.00290-16. Print 2016 Jun 15.
4
A long-acting formulation of the integrase inhibitor raltegravir protects humanized BLT mice from repeated high-dose vaginal HIV challenges.整合酶抑制剂拉替拉韦的长效制剂可保护人源化BLT小鼠免受反复高剂量阴道HIV攻击。
J Antimicrob Chemother. 2016 Jun;71(6):1586-96. doi: 10.1093/jac/dkw042. Epub 2016 Mar 21.
5
Macrophages and HIV-1: An Unhealthy Constellation.巨噬细胞与HIV-1:一个不健康的组合。
Cell Host Microbe. 2016 Mar 9;19(3):304-10. doi: 10.1016/j.chom.2016.02.013.
6
Macrophages sustain HIV replication in vivo independently of T cells.巨噬细胞在体内可独立于T细胞维持HIV复制。
J Clin Invest. 2016 Apr 1;126(4):1353-66. doi: 10.1172/JCI84456. Epub 2016 Mar 7.
7
ART influences HIV persistence in the female reproductive tract and cervicovaginal secretions.抗逆转录病毒疗法会影响艾滋病毒在女性生殖道和宫颈阴道分泌物中的持续存在。
J Clin Invest. 2016 Mar 1;126(3):892-904. doi: 10.1172/JCI64212. Epub 2016 Feb 8.
8
In vivo platforms for analysis of HIV persistence and eradication.用于分析HIV持续性和根除的体内平台。
J Clin Invest. 2016 Feb;126(2):424-31. doi: 10.1172/JCI80562. Epub 2016 Feb 1.
9
Nanoformulations of Rilpivirine for Topical Pericoital and Systemic Coitus-Independent Administration Efficiently Prevent HIV Transmission.用于局部性交前和全身非性交依赖给药的利匹韦林纳米制剂可有效预防艾滋病毒传播。
PLoS Pathog. 2015 Aug 13;11(8):e1005075. doi: 10.1371/journal.ppat.1005075. eCollection 2015 Aug.
10
BLT humanized mice as a small animal model of HIV infection.BLT人源化小鼠作为HIV感染的小动物模型。
Curr Opin Virol. 2015 Aug;13:75-80. doi: 10.1016/j.coviro.2015.05.002. Epub 2015 Jun 12.