• 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
Intragranulomatous necrosis in pulmonary granulomas is not related to resistance against Mycobacterium tuberculosis infection in experimental murine models induced by aerosol.在气溶胶诱导的实验性小鼠模型中,肺肉芽肿内的肉芽肿内坏死与抗结核分枝杆菌感染的抵抗力无关。
Int J Exp Pathol. 2006 Apr;87(2):139-49. doi: 10.1111/j.0959-9673.2006.00472.x.
2
Intragranulomatous necrosis in lungs of mice infected by aerosol with Mycobacterium tuberculosis is related to bacterial load rather than to any one cytokine or T cell type.经气溶胶感染结核分枝杆菌的小鼠肺部的肉芽肿内坏死与细菌载量有关,而非与任何一种细胞因子或T细胞类型有关。
Microbes Infect. 2006 Mar;8(3):628-36. doi: 10.1016/j.micinf.2005.08.014. Epub 2006 Jan 13.
3
Towards a 'human-like' model of tuberculosis: intranasal inoculation of LPS induces intragranulomatous lung necrosis in mice infected aerogenically with Mycobacterium tuberculosis.迈向“类人”肺结核模型:经鼻接种脂多糖可在经空气感染结核分枝杆菌的小鼠中诱导肺肉芽肿内坏死。
Scand J Immunol. 2001 Jan;53(1):65-71. doi: 10.1046/j.1365-3083.2001.00842.x.
4
Widespread bronchogenic dissemination makes DBA/2 mice more susceptible than C57BL/6 mice to experimental aerosol infection with Mycobacterium tuberculosis.广泛的支气管源性播散使DBA/2小鼠比C57BL/6小鼠更易受到结核分枝杆菌实验性气溶胶感染。
Infect Immun. 2003 Oct;71(10):5845-54. doi: 10.1128/IAI.71.10.5845-5854.2003.
5
Interferon-gamma-dependent mechanisms of mycobacteria-induced pulmonary immunopathology: the role of angiostasis and CXCR3-targeted chemokines for granuloma necrosis.干扰素-γ依赖性分枝杆菌诱导的肺部免疫病理学机制:血管生成抑制和靶向CXCR3趋化因子在肉芽肿坏死中的作用
J Pathol. 2007 Jul;212(3):295-305. doi: 10.1002/path.2185.
6
Mycobacterium bovis with different genotypes and from different hosts induce dissimilar immunopathological lesions in a mouse model of tuberculosis.不同基因型和不同宿主来源的牛分枝杆菌在结核病小鼠模型中会引发不同的免疫病理损伤。
Clin Exp Immunol. 2009 Jul;157(1):139-47. doi: 10.1111/j.1365-2249.2009.03923.x.
7
Different types of pulmonary granuloma necrosis in immunocompetent vs. TNFRp55-gene-deficient mice aerogenically infected with highly virulent Mycobacterium avium.在经空气感染高毒力鸟分枝杆菌的免疫健全小鼠与肿瘤坏死因子受体p55基因缺陷小鼠中不同类型的肺肉芽肿坏死情况
J Pathol. 1999 Sep;189(1):127-37. doi: 10.1002/(SICI)1096-9896(199909)189:1<127::AID-PATH398>3.0.CO;2-S.
8
The lymphotoxin beta receptor is critically involved in controlling infections with the intracellular pathogens Mycobacterium tuberculosis and Listeria monocytogenes.淋巴毒素β受体在控制细胞内病原体结核分枝杆菌和单核细胞增生李斯特菌的感染中起着关键作用。
J Immunol. 2003 May 15;170(10):5210-8. doi: 10.4049/jimmunol.170.10.5210.
9
The integrated stress response mediates necrosis in murine Mycobacterium tuberculosis granulomas.整合应激反应介导了鼠分枝杆菌肉芽肿中的细胞坏死。
J Clin Invest. 2021 Feb 1;131(3). doi: 10.1172/JCI130319.
10
Structural deficiencies in granuloma formation in TNF gene-targeted mice underlie the heightened susceptibility to aerosol Mycobacterium tuberculosis infection, which is not compensated for by lymphotoxin.肿瘤坏死因子基因靶向小鼠肉芽肿形成的结构缺陷是其对气溶胶结核分枝杆菌感染易感性增加的基础,而淋巴毒素无法弥补这一缺陷。
J Immunol. 1999 Mar 15;162(6):3504-11.

引用本文的文献

1
Mouse Models for Pathogenesis: Show and Do Not Tell.发病机制的小鼠模型:展示而非讲述。
Pathogens. 2022 Dec 28;12(1):49. doi: 10.3390/pathogens12010049.
2
Cording Bacilli Have a Key Role in the Progression towards Active Tuberculosis, Which is Stopped by Previous Immune Response.条索状杆菌在活动性肺结核的进展中起关键作用,而先前的免疫反应可阻止这一进展。
Microorganisms. 2020 Feb 8;8(2):228. doi: 10.3390/microorganisms8020228.
3
Extracellular Sphingomyelinase Rv0888 of Contributes to Pathological Lung Injury of in Mice Inducing Formation of Neutrophil Extracellular Traps.细胞外神经酰胺酶 Rv0888 有助于诱导中性粒细胞胞外陷阱形成的 诱导的小鼠肺部病理性损伤。
Front Immunol. 2018 Apr 4;9:677. doi: 10.3389/fimmu.2018.00677. eCollection 2018.
4
A spotlight on liquefaction: evidence from clinical settings and experimental models in tuberculosis.聚焦液化:来自结核病临床病例和实验模型的证据
Clin Dev Immunol. 2011;2011:868246. doi: 10.1155/2011/868246. Epub 2011 Mar 13.
5
Man and mouse TB: contradictions and solutions.人类与小鼠结核病:矛盾与解决方案
Tuberculosis (Edinb). 2009 May;89(3):195-8. doi: 10.1016/j.tube.2009.02.002. Epub 2009 Apr 2.
6
Induction of a specific strong polyantigenic cellular immune response after short-term chemotherapy controls bacillary reactivation in murine and guinea pig experimental models of tuberculosis.在小鼠和豚鼠结核病实验模型中,短期化疗后诱导出特定的强烈多抗原细胞免疫反应可控制细菌再激活。
Clin Vaccine Immunol. 2008 Aug;15(8):1229-37. doi: 10.1128/CVI.00094-08. Epub 2008 Jun 4.
7
Intranasal inoculation of mice with Yersinia pseudotuberculosis causes a lethal lung infection that is dependent on Yersinia outer proteins and PhoP.用假结核耶尔森菌对小鼠进行鼻内接种会导致致命的肺部感染,这种感染依赖于耶尔森菌外膜蛋白和PhoP。
Infect Immun. 2007 Jan;75(1):429-42. doi: 10.1128/IAI.01287-06. Epub 2006 Oct 30.

本文引用的文献

1
Pillars Article: M-1/M-2 Macrophages and the Th1/Th2 Paradigm. . 2000. 164: 6166-6173.支柱文章:M-1/M-2巨噬细胞与Th1/Th2范式。. 2000年。164: 6166 - 6173。
J Immunol. 2017 Oct 1;199(7):2194-2201. doi: 10.4049/jimmunol.1701141.
2
THE CORRELATION BETWEEN THE HISTOLOGICAL CHANGES AND THE FATE OF LIVING TUBERCLE BACILLI IN THE ORGANS OF TUBERCULOUS RABBITS.结核兔器官内组织学变化与活菌命运的相关性。
J Exp Med. 1932 Jan 1;55(1):31-54. doi: 10.1084/jem.55.1.31.
3
IL-4 in tuberculosis: implications for vaccine design.白细胞介素-4在结核病中的作用:对疫苗设计的启示
Trends Immunol. 2004 Sep;25(9):483-8. doi: 10.1016/j.it.2004.06.005.
4
Immunity to tuberculosis.对结核病的免疫力。
Annu Rev Immunol. 2004;22:599-623. doi: 10.1146/annurev.immunol.22.012703.104635.
5
M. tuberculosis persistence, latency, and drug tolerance.结核分枝杆菌的持续存在、潜伏和耐药性。
Tuberculosis (Edinb). 2004;84(1-2):29-44. doi: 10.1016/j.tube.2003.08.003.
6
Catalase-peroxidase activity has no influence on virulence in a murine model of tuberculosis.过氧化氢酶-过氧化物酶活性对结核小鼠模型的毒力没有影响。
Tuberculosis (Edinb). 2003;83(6):351-9. doi: 10.1016/s1472-9792(03)00056-8.
7
Widespread bronchogenic dissemination makes DBA/2 mice more susceptible than C57BL/6 mice to experimental aerosol infection with Mycobacterium tuberculosis.广泛的支气管源性播散使DBA/2小鼠比C57BL/6小鼠更易受到结核分枝杆菌实验性气溶胶感染。
Infect Immun. 2003 Oct;71(10):5845-54. doi: 10.1128/IAI.71.10.5845-5854.2003.
8
Towards a 'human-like' model of tuberculosis: intranasal inoculation of LPS induces intragranulomatous lung necrosis in mice infected aerogenically with Mycobacterium tuberculosis.迈向“类人”肺结核模型:经鼻接种脂多糖可在经空气感染结核分枝杆菌的小鼠中诱导肺肉芽肿内坏死。
Scand J Immunol. 2001 Jan;53(1):65-71. doi: 10.1046/j.1365-3083.2001.00842.x.
9
Evolution of granulomas in lungs of mice infected aerogenically with Mycobacterium tuberculosis.经空气感染结核分枝杆菌的小鼠肺部肉芽肿的演变
Scand J Immunol. 2000 Aug;52(2):156-63. doi: 10.1046/j.1365-3083.2000.00763.x.
10
Resistance ranking of some common inbred mouse strains to Mycobacterium tuberculosis and relationship to major histocompatibility complex haplotype and Nramp1 genotype.一些常见近交系小鼠品系对结核分枝杆菌的抗性排名及其与主要组织相容性复合体单倍型和Nramp1基因型的关系
Immunology. 1998 Feb;93(2):270-4. doi: 10.1046/j.1365-2567.1998.00419.x.

在气溶胶诱导的实验性小鼠模型中,肺肉芽肿内的肉芽肿内坏死与抗结核分枝杆菌感染的抵抗力无关。

Intragranulomatous necrosis in pulmonary granulomas is not related to resistance against Mycobacterium tuberculosis infection in experimental murine models induced by aerosol.

作者信息

Guirado Evelyn, Gordillo Sergi, Gil Olga, Díaz Jorge, Tapia Gustavo, Vilaplana Cristina, Ausina Vicenç, Cardona Pere-Joan

机构信息

Unitat de Tuberculosi Experimental, Department of Microbiology, Fundació Institut per a la Investigació en Ciències de la Salut Germans Trias i Pujol and Universitat Autònoma de Barcelona, Catalonia, Spain.

出版信息

Int J Exp Pathol. 2006 Apr;87(2):139-49. doi: 10.1111/j.0959-9673.2006.00472.x.

DOI:10.1111/j.0959-9673.2006.00472.x
PMID:16623758
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2517358/
Abstract

Intragranulomatous necrosis is a primary feature in the natural history of human tuberculosis (TB). Unfortunately, this phenomenon is not usually seen in the experimental TB murine model. Artificial induction of this necrosis in pulmonary granulomas (INPG) may be achieved through aerosol inoculation of lipopolysaccharide (LPS) 3 weeks after Mycobacterium tuberculosis infection. At week 9 post-infection, the centre of primary granulomas became larger, showing eosinophilic necrosis. Interestingly, INPG induction was related to mice strains C57BL/6 and 129/Sv, but not to BALB/c and DBA/2. Furthermore, the same pattern was obtained with the induction of infection using a clinical M. tuberculosis strain (UTE 0335R) that naturally induces INPG. In all the mice strains tested, the study of pulmonary mRNA expression revealed a tendency to increase or to maintain the expression of RANTES, interferon-gamma, tumour necrosis factor and iNOS, in both LPS- and UTE 0335R-induced INPG, thus suggesting that this response must be necessary but not sufficient for inducing INPG. Our work supports that INPG induction is a local phenomenon unrelated to the resistant (C57BL/6 and BALB/c) or susceptible (129/Sv and DBA/2) background of mice strains against M. tuberculosis infection.

摘要

肉芽肿内坏死是人类结核病自然病程中的一个主要特征。不幸的是,这种现象在实验性结核小鼠模型中通常看不到。在结核分枝杆菌感染3周后,通过气溶胶接种脂多糖(LPS)可人工诱导肺部肉芽肿发生这种坏死(INPG)。感染后第9周,原发性肉芽肿的中心变大,呈现嗜酸性坏死。有趣的是,INPG的诱导与小鼠品系C57BL/6和129/Sv有关,但与BALB/c和DBA/2无关。此外,使用自然诱导INPG的临床结核分枝杆菌菌株(UTE 0335R)诱导感染也得到了相同的模式。在所有测试的小鼠品系中,对肺部mRNA表达的研究表明,在LPS和UTE 0335R诱导的INPG中,RANTES、干扰素-γ、肿瘤坏死因子和诱导型一氧化氮合酶的表达均有增加或维持的趋势,因此表明这种反应对于诱导INPG是必要的,但不是充分的。我们的研究支持INPG的诱导是一种局部现象,与小鼠品系对结核分枝杆菌感染的抗性(C57BL/6和BALB/c)或易感性(129/Sv和DBA/2)背景无关。