• 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

在抵抗性 BALB/c 小鼠急性弓形虫感染期间,CD4(+)CD25(+)Foxp3(+)T 调节细胞的部分耗竭显著增加发病率。

Partial depletion of CD4(+)CD25(+)Foxp3(+) T regulatory cells significantly increases morbidity during acute phase Toxoplasma gondii infection in resistant BALB/c mice.

机构信息

Toxoplasmosis Laboratory, Operational Direction Communicable and Infectious Diseases, Scientific Institute of Public Health, Site Uccle, 642 rue Engeland, 1180 Brussels, Belgium.

出版信息

Microbes Infect. 2011 Apr;13(4):394-404. doi: 10.1016/j.micinf.2011.01.006. Epub 2011 Jan 22.

DOI:10.1016/j.micinf.2011.01.006
PMID:21262371
Abstract

CD4(+)CD25(+)Foxp3(+) T regulatory (Treg) cells, are known to regulate responses to infectious agents. Here we compared disease progression in BALB/c and C57BL/6(B6) mice infected perorally with Toxoplasma gondii for 7 days and examined the affect of partial depletion of Treg cells in these mice. BALB/c mice were seen to be resistant to peroral infection whereas B6 mice were susceptible in terms of mortality. Although the depletion of Treg cells before infection had no effect on the survival of B6 or BALB/c mice, it resulted in increased parasite burdens in BALB/c mice, especially in the lamina propria, but not in B6 mice. Pro-inflammatory cytokines were also increased in Treg cells depleted BALB/c mice as compared to B6 mice. In addition Treg cell depleted BALB/c mice displayed increased ileal histopathology compared to their non-treated counterparts. These findings provide evidence for the contribution of Treg cells, in the resistance of BALB/c mice against peroral T. gondii infection.

摘要

CD4(+)CD25(+)Foxp3(+)T 调节性 (Treg) 细胞,已知可调节对感染因子的反应。在这里,我们比较了 BALB/c 和 C57BL/6(B6) 小鼠经口感染弓形虫 7 天后的疾病进展,并研究了在这些小鼠中部分耗尽 Treg 细胞的影响。BALB/c 小鼠对经口感染具有抗性,而 B6 小鼠则在死亡率方面易感。尽管在感染前耗尽 Treg 细胞对 B6 或 BALB/c 小鼠的存活没有影响,但它导致 BALB/c 小鼠中的寄生虫负担增加,特别是在固有层,但在 B6 小鼠中没有。与 B6 小鼠相比,Treg 细胞耗尽的 BALB/c 小鼠中的促炎细胞因子也增加了。此外,与未治疗的对照相比,Treg 细胞耗尽的 BALB/c 小鼠显示出回肠组织病理学增加。这些发现为 Treg 细胞在 BALB/c 小鼠抵抗经口 T. gondii 感染中的作用提供了证据。

相似文献

1
Partial depletion of CD4(+)CD25(+)Foxp3(+) T regulatory cells significantly increases morbidity during acute phase Toxoplasma gondii infection in resistant BALB/c mice.在抵抗性 BALB/c 小鼠急性弓形虫感染期间,CD4(+)CD25(+)Foxp3(+)T 调节细胞的部分耗竭显著增加发病率。
Microbes Infect. 2011 Apr;13(4):394-404. doi: 10.1016/j.micinf.2011.01.006. Epub 2011 Jan 22.
2
Increased CD4+CD25+Foxp3+ regulatory T cells in tolerance induced by portal venous injection.门静脉注射诱导的耐受中CD4+CD25+Foxp3+调节性T细胞增加。
Surgery. 2009 Jun;145(6):663-74. doi: 10.1016/j.surg.2009.01.016. Epub 2009 Apr 19.
3
Depletion of CD25⁺ cells during acute toxoplasmosis does not significantly increase mortality in Swiss OF1 mice.在急性弓形虫病期间耗尽 CD25⁺细胞不会显著增加瑞士 OF1 小鼠的死亡率。
Mem Inst Oswaldo Cruz. 2012 Mar;107(2):155-62. doi: 10.1590/s0074-02762012000200002.
4
Reduction of Foxp3+ cells by depletion with the PC61 mAb induces mortality in resistant BALB/c mice infected with Toxoplasma gondii.用PC61单克隆抗体清除Foxp3+细胞会导致感染刚地弓形虫的抗性BALB/c小鼠死亡。
J Biomed Biotechnol. 2010;2010:786078. doi: 10.1155/2010/786078. Epub 2009 Dec 13.
5
Depletion with PC61 mAb before Toxoplasma gondii infection eliminates mainly Tregs in BALB/c mice, but activated cells in C57BL/6J mice.在弓形虫感染前用PC61单克隆抗体清除细胞,主要清除BALB/c小鼠中的调节性T细胞,但清除C57BL/6J小鼠中的活化细胞。
FEMS Immunol Med Microbiol. 2011 Aug;62(3):362-7. doi: 10.1111/j.1574-695X.2011.00805.x. Epub 2011 May 6.
6
Anti-CD25 antibody-mediated depletion of effector T cell populations enhances susceptibility of mice to acute but not chronic Toxoplasma gondii infection.抗CD25抗体介导的效应T细胞群体耗竭增强了小鼠对急性而非慢性弓形虫感染的易感性。
J Immunol. 2009 Apr 1;182(7):3985-94. doi: 10.4049/jimmunol.0803053.
7
Adoptive transfer of CD4(+)Foxp3(+) regulatory T cells to C57BL/6J mice during acute infection with Toxoplasma gondii down modulates the exacerbated Th1 immune response.在急性感染刚地弓形虫期间,将CD4(+)Foxp3(+)调节性T细胞过继转移至C57BL/6J小鼠可下调加剧的Th1免疫反应。
Microbes Infect. 2015 Aug;17(8):586-95. doi: 10.1016/j.micinf.2015.04.002. Epub 2015 Apr 18.
8
BALB/c mice have more CD4+CD25+ T regulatory cells and show greater susceptibility to suppression of their CD4+CD25- responder T cells than C57BL/6 mice.与C57BL/6小鼠相比,BALB/c小鼠拥有更多的CD4+CD25+调节性T细胞,并且其CD4+CD25-反应性T细胞受到抑制的易感性更高。
J Leukoc Biol. 2005 Jul;78(1):114-21. doi: 10.1189/jlb.0604341. Epub 2005 Apr 21.
9
CD4+ Foxp3+ regulatory T cells mediate Toxoplasma gondii-induced T-cell suppression through an IL-2-related mechanism but independently of IL-10.CD4+Foxp3+调节性 T 细胞通过与 IL-2 相关的机制介导弓形虫诱导的 T 细胞抑制,但不依赖于 IL-10。
Eur J Immunol. 2011 Dec;41(12):3529-41. doi: 10.1002/eji.201141507. Epub 2011 Oct 20.
10
Regulatory T cells are necessary for implantation and maintenance of early pregnancy but not late pregnancy in allogeneic mice.调节性 T 细胞对于同种异体小鼠的早期妊娠着床和维持是必要的,但对于晚期妊娠则不是必需的。
J Reprod Immunol. 2010 Jun;85(2):121-9. doi: 10.1016/j.jri.2010.02.006. Epub 2010 May 2.

引用本文的文献

1
Immunobiotic and Paraprobiotic Potential Effect of in a Systemic Toxoplasmosis Murine Model.在系统性弓形虫病小鼠模型中,[具体物质]的免疫益生菌和副益生菌潜在作用。 (你原文中“in a Systemic Toxoplasmosis Murine Model”前应该有个具体物质未给出)
Microorganisms. 2020 Jan 14;8(1):113. doi: 10.3390/microorganisms8010113.
2
Microbiome Dependent Regulation of T and Th17 Cells in Mucosa.黏膜中微生物组依赖的 T 和 Th17 细胞调控。
Front Immunol. 2019 Mar 8;10:426. doi: 10.3389/fimmu.2019.00426. eCollection 2019.
3
Role of CD4+ Foxp3+ Regulatory T Cells in Protection Induced by a Live Attenuated, Replicating Type I Vaccine Strain of Toxoplasma gondii.
CD4+ Foxp3+调节性T细胞在减毒活复制型I型弓形虫疫苗株诱导的保护作用中的角色
Infect Immun. 2015 Sep;83(9):3601-11. doi: 10.1128/IAI.00217-15. Epub 2015 Jun 29.
4
Parasite distribution and associated immune response during the acute phase of Toxoplasma gondii infection in sheep.绵羊急性弓形虫感染期的寄生虫分布及相关免疫反应
BMC Vet Res. 2014 Dec 16;10:293. doi: 10.1186/s12917-014-0293-5.
5
Nematode-induced interference with vaccination efficacy targets follicular T helper cell induction and is preserved after termination of infection.线虫对疫苗接种效果的干扰靶向滤泡辅助性T细胞的诱导,并且在感染终止后依然存在。
PLoS Negl Trop Dis. 2014 Sep 25;8(9):e3170. doi: 10.1371/journal.pntd.0003170. eCollection 2014 Sep.
6
Foxp3⁺ regulatory T cells delay expulsion of intestinal nematodes by suppression of IL-9-driven mast cell activation in BALB/c but not in C57BL/6 mice.Foxp3⁺ 调节性 T 细胞通过抑制 BALB/c 而非 C57BL/6 小鼠中 IL-9 驱动的肥大细胞活化来延迟肠道线虫的排出。
PLoS Pathog. 2014 Feb 6;10(2):e1003913. doi: 10.1371/journal.ppat.1003913. eCollection 2014 Feb.
7
Heme oxygenase-1 activity is involved in the control of Toxoplasma gondii infection in the lung of BALB/c and C57BL/6 and in the small intestine of C57BL/6 mice.血红素加氧酶-1 的活性参与 BALB/c 和 C57BL/6 小鼠肺部以及 C57BL/6 小鼠小肠内弓形虫感染的调控。
Vet Res. 2013 Oct 2;44(1):89. doi: 10.1186/1297-9716-44-89.
8
Characterization of regulatory T cell (Treg) function in patients infected with Leishmania braziliensis.鉴定感染巴西利什曼原虫患者调节性 T 细胞(Treg)的功能。
Hum Immunol. 2013 Dec;74(12):1491-500. doi: 10.1016/j.humimm.2013.08.269. Epub 2013 Aug 28.
9
MAP kinase phosphatase-2 plays a key role in the control of infection with Toxoplasma gondii by modulating iNOS and arginase-1 activities in mice.丝裂原活化蛋白激酶磷酸酶-2通过调节小鼠诱导型一氧化氮合酶和精氨酸酶-1的活性在弓形虫感染的控制中发挥关键作用。
PLoS Pathog. 2013 Aug;9(8):e1003535. doi: 10.1371/journal.ppat.1003535. Epub 2013 Aug 15.
10
Toxoplasma gondii infection induces suppression in a mouse model of allergic airway inflammation.弓形虫感染诱导过敏性气道炎症小鼠模型中的抑制作用。
PLoS One. 2012;7(8):e43420. doi: 10.1371/journal.pone.0043420. Epub 2012 Aug 28.