• 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
Mouse models to study dengue virus immunology and pathogenesis.用于研究登革病毒免疫学和发病机制的小鼠模型。
Front Immunol. 2014 Apr 10;5:151. doi: 10.3389/fimmu.2014.00151. eCollection 2014.
2
Type I interferon signals in macrophages and dendritic cells control dengue virus infection: implications for a new mouse model to test dengue vaccines.巨噬细胞和树突状细胞中的I型干扰素信号控制登革病毒感染:对用于测试登革疫苗的新型小鼠模型的启示。
J Virol. 2014 Jul;88(13):7276-85. doi: 10.1128/JVI.03827-13. Epub 2014 Apr 16.
3
Defining New Therapeutics Using a More Immunocompetent Mouse Model of Antibody-Enhanced Dengue Virus Infection.利用更具免疫活性的抗体增强型登革病毒感染小鼠模型来定义新的治疗方法。
mBio. 2015 Sep 15;6(5):e01316-15. doi: 10.1128/mBio.01316-15.
4
A lethal murine infection model for dengue virus 3 in AG129 mice deficient in type I and II interferon receptors leads to systemic disease.在缺乏I型和II型干扰素受体的AG129小鼠中建立的登革病毒3致死性小鼠感染模型可导致全身性疾病。
J Virol. 2015 Jan 15;89(2):1254-66. doi: 10.1128/JVI.01320-14. Epub 2014 Nov 12.
5
A mouse model for studying dengue virus pathogenesis and immune response.一种用于研究登革病毒发病机制和免疫反应的小鼠模型。
Ann N Y Acad Sci. 2009 Sep;1171 Suppl 1:E12-23. doi: 10.1111/j.1749-6632.2009.05057.x.
6
Utility of humanized BLT mice for analysis of dengue virus infection and antiviral drug testing.人源化BLT小鼠在登革病毒感染分析和抗病毒药物测试中的应用
J Virol. 2014 Feb;88(4):2205-18. doi: 10.1128/JVI.03085-13. Epub 2013 Dec 11.
7
Mouse models of dengue virus infection and disease.登革病毒感染与疾病的小鼠模型。
Antiviral Res. 2008 Nov;80(2):87-93. doi: 10.1016/j.antiviral.2008.06.010. Epub 2008 Jul 9.
8
Differential replicative ability of clinical dengue virus isolates in an immunocompetent C57BL/6 mouse model.临床登革病毒分离株在免疫健全的C57BL/6小鼠模型中的差异复制能力。
BMC Microbiol. 2015 Sep 29;15:189. doi: 10.1186/s12866-015-0520-7.
9
Virus-like particle secretion and genotype-dependent immunogenicity of dengue virus serotype 2 DNA vaccine.登革病毒2型DNA疫苗的病毒样颗粒分泌及基因型依赖性免疫原性
J Virol. 2014 Sep;88(18):10813-30. doi: 10.1128/JVI.00810-14. Epub 2014 Jul 9.
10
Dengue and Zika virus infections are enhanced by live attenuated dengue vaccine but not by recombinant DSV4 vaccine candidate in mouse models.登革热和 Zika 病毒感染可被减毒活疫苗增强,但在小鼠模型中,重组 DSV4 候选疫苗不会增强登革热感染。
EBioMedicine. 2020 Oct;60:102991. doi: 10.1016/j.ebiom.2020.102991. Epub 2020 Sep 16.

引用本文的文献

1
Impact of sampling technique, anticoagulant, processing delay, and temperature on murine platelet function in whole blood.采样技术、抗凝剂、处理延迟和温度对全血中鼠血小板功能的影响。
Res Pract Thromb Haemost. 2025 May 8;9(4):102883. doi: 10.1016/j.rpth.2025.102883. eCollection 2025 May.
2
The Emerging Role of Circulating T Follicular Helper Cells in Dengue Virus Immunity: Balancing Protection and Pathogenesis.循环滤泡辅助性T细胞在登革病毒免疫中的新作用:平衡保护与发病机制
Viruses. 2025 Apr 30;17(5):652. doi: 10.3390/v17050652.
3
Dengue Envelope Protein as a Cytotoxic Factor Inducing Hemorrhage and Endothelial Cell Death in Mice.登革热囊膜蛋白作为一种细胞毒性因子,诱导小鼠出血和血管内皮细胞死亡。
Int J Mol Sci. 2024 Oct 9;25(19):10858. doi: 10.3390/ijms251910858.
4
Dengue virus: pathogenesis and potential for small molecule inhibitors.登革热病毒:发病机制与小分子抑制剂的潜力。
Biosci Rep. 2024 Aug 28;44(8). doi: 10.1042/BSR20240134.
5
A Novel, Comprehensive A129 Mouse Model for Investigating Dengue Vaccines and Evaluating Pathogenesis.一种用于研究登革热疫苗和评估发病机制的新型综合A129小鼠模型。
Vaccines (Basel). 2023 Dec 15;11(12):1857. doi: 10.3390/vaccines11121857.
6
Preclinical proof of concept of a tetravalent lentiviral T-cell vaccine against dengue viruses.抗登革病毒四价慢病毒 T 细胞疫苗的临床前概念验证。
Front Immunol. 2023 Aug 15;14:1208041. doi: 10.3389/fimmu.2023.1208041. eCollection 2023.
7
Human FcγRIIIa activation on splenic macrophages drives dengue pathogenesis in mice.脾脏巨噬细胞上的人 FcγRIIIa 的激活导致小鼠登革热发病机制。
Nat Microbiol. 2023 Aug;8(8):1468-1479. doi: 10.1038/s41564-023-01421-y. Epub 2023 Jul 10.
8
The acute effects of nonstructural-1 protein dengue virus type 2 on wet liver weight, zonulin expression and serum zonulin.2型登革病毒非结构蛋白1对肝脏湿重、zonulin表达及血清zonulin的急性影响
Iran J Microbiol. 2023 Apr;15(2):311-317. doi: 10.18502/ijm.v15i2.12483.
9
Sialokinin in mosquito saliva shifts human immune responses towards intracellular pathogens.唾液神经氨酸酶使蚊虫唾液中的人类免疫反应转向细胞内病原体。
PLoS Negl Trop Dis. 2023 Feb 3;17(2):e0011095. doi: 10.1371/journal.pntd.0011095. eCollection 2023 Feb.
10
Combination of E- and NS1-Derived DNA Vaccines: The Immune Response and Protection Elicited in Mice against DENV2.E 蛋白和 NS1 衍生 DNA 疫苗的联合应用:在小鼠中诱导针对登革热病毒 2 型的免疫反应和保护作用。
Viruses. 2022 Jun 30;14(7):1452. doi: 10.3390/v14071452.

本文引用的文献

1
Hepatic dysfunction in patients infected with dengue virus.登革病毒感染患者的肝功能障碍
J Coll Physicians Surg Pak. 2014 Jan;24(1):74.
2
Live attenuated vaccine: the first clinically approved dengue vaccine?活疫苗:首个经临床批准的登革热疫苗?
Expert Rev Vaccines. 2014 Feb;13(2):185-8. doi: 10.1586/14760584.2014.870888. Epub 2013 Dec 18.
3
WHO Expert Committee on Biological Standardization.世界卫生组织生物标准化专家委员会
World Health Organ Tech Rep Ser. 2013(979):1-366, back cover.
4
Utility of humanized BLT mice for analysis of dengue virus infection and antiviral drug testing.人源化BLT小鼠在登革病毒感染分析和抗病毒药物测试中的应用
J Virol. 2014 Feb;88(4):2205-18. doi: 10.1128/JVI.03085-13. Epub 2013 Dec 11.
5
Demonstration of marmosets (Callithrix jacchus) as a non-human primate model for secondary dengue virus infection: high levels of viraemia and serotype cross-reactive antibody responses consistent with secondary infection of humans.证明卷尾猴(Callithrix jacchus)可作为登革病毒二次感染的非人灵长类动物模型:高水平的病毒血症和血清型交叉反应抗体反应与人类的二次感染一致。
J Gen Virol. 2014 Mar;95(Pt 3):591-600. doi: 10.1099/vir.0.060384-0. Epub 2013 Dec 9.
6
Role of humoral versus cellular responses induced by a protective dengue vaccine candidate.体液免疫和细胞免疫在保护性登革热候选疫苗中的作用。
PLoS Pathog. 2013 Oct;9(10):e1003723. doi: 10.1371/journal.ppat.1003723. Epub 2013 Oct 31.
7
Can non-human primates serve as models for investigating dengue disease pathogenesis?非人灵长类动物能否作为研究登革热疾病发病机制的模型?
Front Microbiol. 2013 Oct 11;4:305. doi: 10.3389/fmicb.2013.00305.
8
Transmission of dengue virus from a donor to a recipient after living donor liver transplantation.活体肝移植后登革热病毒从供体传播至受体。
Liver Transpl. 2013 Dec;19(12):1413-4. doi: 10.1002/lt.23755. Epub 2013 Oct 21.
9
Immunopathogenesis of dengue hemorrhagic fever: contribution to the study of human liver lesions.登革出血热的免疫发病机制:对人类肝脏病变研究的贡献。
J Med Virol. 2014 Jul;86(7):1193-7. doi: 10.1002/jmv.23758. Epub 2013 Sep 23.
10
Profile of hepatic involvement by dengue virus in dengue infected children.登革热感染儿童中登革病毒所致肝脏受累情况
N Am J Med Sci. 2013 Aug;5(8):480-5. doi: 10.4103/1947-2714.117313.

用于研究登革病毒免疫学和发病机制的小鼠模型。

Mouse models to study dengue virus immunology and pathogenesis.

作者信息

Zellweger Raphaël M, Shresta Sujan

机构信息

Division of Vaccine Discovery, La Jolla Institute for Allergy and Immunology , La Jolla, CA , USA.

出版信息

Front Immunol. 2014 Apr 10;5:151. doi: 10.3389/fimmu.2014.00151. eCollection 2014.

DOI:10.3389/fimmu.2014.00151
PMID:24782859
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3989707/
Abstract

The development of a compelling murine model of dengue virus (DENV) infection has been challenging, because DENV clinical isolates do not readily replicate or cause pathology in immunocompetent mice. However, research using immunocompromised mice and/or mouse-adapted viruses allows investigation of questions that may be impossible to address in human studies. In this review, we discuss the potential strengths and limitations of existing mouse models of dengue disease. Human studies are descriptive by nature; moreover, the strain, time, and sequence of infection are often unknown. In contrast, in mice, the conditions of infection are well defined and a large number of experimental parameters can be varied at will. Therefore, mouse models offer an opportunity to experimentally test hypotheses that are based on epidemiological observations. In particular, gain-of-function or loss-of-function models can be established to assess how different components of the immune system (either alone or in combination) contribute to protection or pathogenesis during secondary infections or after vaccination. In addition, mouse models have been used for pre-clinical testing of anti-viral drugs or for vaccine development studies. Conclusions based on mouse experiments must be extrapolated to DENV-infection in humans with caution due to the inherent limitations of animal models. However, research in mouse models is a useful complement to in vitro and epidemiological data, and may delineate new areas that deserve attention during future human studies.

摘要

登革病毒(DENV)感染的令人信服的小鼠模型的开发一直具有挑战性,因为DENV临床分离株在免疫健全的小鼠中不易复制或引起病变。然而,使用免疫受损小鼠和/或小鼠适应病毒的研究允许探讨一些在人体研究中可能无法解决的问题。在这篇综述中,我们讨论了现有登革热疾病小鼠模型的潜在优势和局限性。人体研究本质上是描述性的;此外,感染的毒株、时间和序列往往未知。相比之下,在小鼠中,感染条件明确,大量实验参数可以随意改变。因此,小鼠模型为基于流行病学观察的假设提供了实验检验的机会。特别是,可以建立功能获得或功能丧失模型,以评估免疫系统的不同组成部分(单独或组合)在二次感染或接种疫苗后如何促进保护或发病机制。此外,小鼠模型已用于抗病毒药物的临床前测试或疫苗开发研究。由于动物模型的固有局限性,基于小鼠实验得出的结论必须谨慎地外推至人类的DENV感染。然而,小鼠模型研究是体外和流行病学数据的有益补充,可能会勾勒出未来人体研究中值得关注的新领域。