• 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

用等量致死剂量的刚地弓形虫攻击后不同小鼠品系的免疫反应。

Immune responses of different mouse strains after challenge with equivalent lethal doses of Toxoplasma gondii.

作者信息

Lee Y H, Kasper L H

机构信息

Department of Parasitology, College of Medicine, Chungnam National University, 6 Munhwa-dong, Chung-gu, Daejeon 301-131, Korea.

出版信息

Parasite. 2004 Mar;11(1):89-97. doi: 10.1051/parasite/200411189.

DOI:10.1051/parasite/200411189
PMID:15071833
Abstract

Most immunological studies that utilize different strains of inbred mice following T. gondii infection fail to compensate for differences in host susceptibility to the size of the parasite innoculum. To address this concern, susceptible C57BL/6 and resistant CBA/J mice were orally infected with either an equivalent 50% lethal dose (LD50) of brain cysts of the 76K strain of T. gondii (15 cysts in C57BL/6, 400 cysts in CBA/J) or the same dose of parasites in each mouse strain. C57BL/6 mice receiving 400 cysts (LD50 of CBA/J mice) died post infection, whereas CBA/J mice that received 15 cysts (LD50 of C57BL/6 mice) survived. Parasite loads in the brains and serum Toxoplasma-specific IgG1 titers of LD50-infected C57BL/6 mice were significantly higher than those in LD50- or 15 cysts-infected CBA/J mice, whereas splenocyte proliferation to Toxoplasma antigen and the percentage of CD8 alpha+ T cells were reduced in LD50-infected C57BL/6 mice. In contrast, serum IgG2a and IgM titers, the percentage of gamma delta T cells and IFN-gamma expression of spleen of LD50-infected CBA/J mice were higher than those of either 15 cysts-infected CBA/J mice or LD50-infected C57BL/6 mice. These observations demonstrate that the immune response between LD50-infected C57BL/6 and CBA/J mice was more prominent when compared to C57BL/6 or CBA/J mice receiving the same parasite inoculum. These observations would suggest that caution must be excersized in the planning and interpretation of data when the size of the parasite inoculum has not been adjusted for mouse strain.

摘要

大多数利用不同近交系小鼠感染弓形虫后的免疫研究,未能弥补宿主对寄生虫接种量大小易感性的差异。为解决这一问题,将易感的C57BL/6小鼠和抗性的CBA/J小鼠经口感染等量的76K株弓形虫脑包囊的50%致死剂量(LD50)(C57BL/6小鼠为15个包囊,CBA/J小鼠为400个包囊),或在每个小鼠品系中接种相同剂量的寄生虫。接受400个包囊(CBA/J小鼠的LD50)的C57BL/6小鼠在感染后死亡,而接受15个包囊(C57BL/6小鼠的LD50)的CBA/J小鼠存活。LD50感染的C57BL/6小鼠脑内的寄生虫载量和血清弓形虫特异性IgG1滴度显著高于LD50或15个包囊感染的CBA/J小鼠,而LD50感染的C57BL/6小鼠对弓形虫抗原的脾细胞增殖和CD8α+T细胞百分比降低。相反,LD50感染的CBA/J小鼠的血清IgG2a和IgM滴度、γδT细胞百分比以及脾脏的IFN-γ表达高于15个包囊感染的CBA/J小鼠或LD50感染的C5 BL/6小鼠。这些观察结果表明,与接受相同寄生虫接种量的C57BL/6或CBA/J小鼠相比,LD50感染的C57BL/6和CBA/J小鼠之间的免疫反应更为显著。这些观察结果表明,在未根据小鼠品系调整寄生虫接种量的情况下,在规划和解释数据时必须谨慎。

相似文献

1
Immune responses of different mouse strains after challenge with equivalent lethal doses of Toxoplasma gondii.用等量致死剂量的刚地弓形虫攻击后不同小鼠品系的免疫反应。
Parasite. 2004 Mar;11(1):89-97. doi: 10.1051/parasite/200411189.
2
Mucosal and systemic cellular immune responses induced by Toxoplasma gondii antigens in cyst orally infected mice.经口感染包囊型弓形虫抗原诱导的小鼠黏膜及全身细胞免疫反应
Immunology. 1993 Mar;78(3):421-9.
3
Immune responses associated with early survival after peroral infection with Toxoplasma gondii.经口感染刚地弓形虫后与早期存活相关的免疫反应。
J Immunol. 1989 May 1;142(9):3247-55.
4
Infection of mice by a Toxoplasma gondii isolate from an AIDS patient: virulence and activation of hosts' immune responses are independent of parasite genotype.
Parasite Immunol. 1999 Dec;21(12):649-57. doi: 10.1046/j.1365-3024.1999.00273.x.
5
Strain- and Dose-Dependent Reduction of Burden in Pigs Is Associated with Interferon-Gamma Production by CD8 Lymphocytes in a Heterologous Challenge Model.在异源攻击模型中,猪体内负担的应变和剂量依赖性降低与CD8淋巴细胞产生的γ干扰素相关。
Front Cell Infect Microbiol. 2017 Jun 8;7:232. doi: 10.3389/fcimb.2017.00232. eCollection 2017.
6
Humoral responses and immune protection in mice immunized with irradiated T. gondii tachyzoites and challenged with three genetically distinct strains of T. gondii.经照射的弓形虫速殖子免疫小鼠的体液反应和免疫保护,并用三种遗传上不同的弓形虫分离株进行攻毒。
Immunol Lett. 2011 Aug 30;138(2):187-96. doi: 10.1016/j.imlet.2011.04.007. Epub 2011 Apr 25.
7
Evaluation of three recombinant multi-antigenic vaccines composed of surface and secretory antigens of Toxoplasma gondii in murine models of experimental toxoplasmosis.评价三种由弓形虫表面和分泌抗原组成的重组多抗原疫苗在实验性弓形虫病小鼠模型中的效果。
Vaccine. 2011 Jan 17;29(4):821-30. doi: 10.1016/j.vaccine.2010.11.002. Epub 2010 Nov 16.
8
Evaluation of immunization with tachyzoite excreted-secreted proteins in a novel susceptible mouse model (A/Sn) for Toxoplasma gondii.在一种新型的对刚地弓形虫易感的小鼠模型(A/Sn)中对速殖子排泄-分泌蛋白免疫接种的评估。
Exp Parasitol. 2008 Nov;120(3):227-34. doi: 10.1016/j.exppara.2008.07.015. Epub 2008 Jul 31.
9
Decreased resistance of B cell-deficient mice to infection with Toxoplasma gondii despite unimpaired expression of IFN-gamma, TNF-alpha, and inducible nitric oxide synthase.B细胞缺陷小鼠对刚地弓形虫感染的抵抗力降低,尽管其γ干扰素、肿瘤坏死因子-α和诱导型一氧化氮合酶的表达未受影响。
J Immunol. 2000 Mar 1;164(5):2629-34. doi: 10.4049/jimmunol.164.5.2629.
10
Protection against lethal toxoplasmosis in mice by an avirulent strain of Toxoplasma gondii: stimulation of IFN-gamma and TNF-alpha response.无毒力株刚地弓形虫对小鼠致死性弓形虫病的保护作用:IFN-γ和TNF-α反应的刺激
Exp Parasitol. 1999 Dec;93(4):231-40. doi: 10.1006/expr.1999.4457.

引用本文的文献

1
Effective factors in the pathogenesis of .……发病机制中的有效因素。 你提供的原文不完整,“of”后面缺少具体内容。
Heliyon. 2024 May 19;10(10):e31558. doi: 10.1016/j.heliyon.2024.e31558. eCollection 2024 May 30.
2
The effector GRA83 modulates the host's innate immune response to regulate parasite infection.效应子 GRA83 调节宿主的固有免疫反应以调节寄生虫感染。
mSphere. 2023 Oct 24;8(5):e0026323. doi: 10.1128/msphere.00263-23. Epub 2023 Sep 28.
3
Expression of cytokines and co-stimulatory molecules in the Toxoplasma gondii-infected dendritic cells of C57BL/6 and BALB/c mice.
弓形虫感染的 C57BL/6 和 BALB/c 小鼠树突状细胞中细胞因子和共刺激分子的表达。
Parasites Hosts Dis. 2023 May;61(2):138-146. doi: 10.3347/PHD.22150. Epub 2023 May 23.
4
Current and Future Strategies for the Diagnosis and Treatment of the Alpha-Gal Syndrome (AGS).α-半乳糖综合征(AGS)诊断与治疗的当前及未来策略
J Asthma Allergy. 2022 Jul 18;15:957-970. doi: 10.2147/JAA.S265660. eCollection 2022.
5
Targeted Transcriptomic Analysis of C57BL/6 and BALB/c Mice During Progressive Chronic Infection Reveals Changes in Host and Parasite Gene Expression Relating to Neuropathology and Resolution.靶向转录组分析慢性感染过程中的 C57BL/6 和 BALB/c 小鼠,揭示与神经病理学和恢复相关的宿主和寄生虫基因表达变化。
Front Cell Infect Microbiol. 2021 Mar 18;11:645778. doi: 10.3389/fcimb.2021.645778. eCollection 2021.
6
Influence of the Host and Parasite Strain on the Immune Response During Infection.宿主和寄生虫株对感染期间免疫反应的影响。
Front Cell Infect Microbiol. 2020 Oct 15;10:580425. doi: 10.3389/fcimb.2020.580425. eCollection 2020.
7
Overview of inactivating mutations in the protein-coding genome of the mouse reference strain C57BL/6J.小鼠参考品系 C57BL/6J 蛋白编码基因组中失活突变概述。
JCI Insight. 2018 Jul 12;3(13):121758. doi: 10.1172/jci.insight.121758.
8
The Pathogenic Potential of a Microbe.微生物的致病潜力
mSphere. 2017 Feb 22;2(1). doi: 10.1128/mSphere.00015-17. eCollection 2017 Jan-Feb.
9
Novel Approaches Reveal that Toxoplasma gondii Bradyzoites within Tissue Cysts Are Dynamic and Replicating Entities In Vivo.新方法揭示组织囊肿内的刚地弓形虫缓殖子在体内是动态且可复制的实体。
mBio. 2015 Sep 8;6(5):e01155-15. doi: 10.1128/mBio.01155-15.
10
Molecular Mechanisms of Differentiation of Murine Pro-Inflammatory γδ T Cell Subsets.小鼠促炎性γδ T细胞亚群分化的分子机制
Front Immunol. 2013 Dec 5;4:431. doi: 10.3389/fimmu.2013.00431.