• 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

鸡对柔嫩艾美耳球虫的免疫:外周血T细胞亚群的表型和功能变化

Immunity to eimeria tenella in chickens: phenotypical and functional changes in peripheral blood T-cell subsets.

作者信息

Breed D G, Dorrestein J, Vermeulen A N

机构信息

Department of Parasitology, Intervet International BV, Boxmeer, The Netherlands.

出版信息

Avian Dis. 1996 Jan-Mar;40(1):37-48.

PMID:8713046
Abstract

The changes in peripheral blood leukocyte (PBL) T-cell subsets following Eimeria tenella infection in outbred white leghorn chickens were studied, using a panel of murine monoclonal antibodies specific for the chicken homologues of the mammalian CD3, CD8, and CD4 markers on day-to-day samples of PBLs. Both flow cytometric analysis (FCA) and immunofluorescence microscopy with fixed cells on slides were used as read-out systems. The changes in the composition of the T-cell subsets measured with both techniques were similar. At 8 days post primary infection, a sharp transitory increase in the proportion of CD8-expressing cells was found. With FCA, CD8-expressing cells could be discriminated in CD8(Dim+) and CD8(Bright+) populations, which have not been described before. The proportion of CD4-expressing cells was decreased at days 9-10 after primary infection, which coincided with a less marked decrease in CD3-expressing cells. Such effects were not seen after secondary infection. When PBLs collected at day 8 post primary infection were stimulated in vitro with E. tenella sporozoite antigen, the response was higher than that in uninfected control chickens. The effects we observed coincide with the onset of recovery from primary infection. We speculate that the increase in CD8-expressing PBLs is the result of stimulation and expansion of a specific subset involved in the induction of protective immunity against Eimeria tenella.

摘要

利用一组针对哺乳动物CD3、CD8和CD4标记物的鸡同源物的鼠单克隆抗体,对非近亲繁殖的白来航鸡感染柔嫩艾美耳球虫后外周血白细胞(PBL)T细胞亚群的变化进行了研究,样本为每日采集的PBL。流式细胞术分析(FCA)和对载玻片上固定细胞进行免疫荧光显微镜检查均用作读出系统。两种技术测量的T细胞亚群组成变化相似。初次感染后8天,发现表达CD8的细胞比例急剧短暂增加。通过FCA,可以在CD8(Dim+)和CD8(Bright+)群体中区分表达CD8的细胞,这是以前未曾描述过的。初次感染后第9 - 10天,表达CD4的细胞比例下降,同时表达CD3的细胞也有较不明显的下降。二次感染后未观察到此类效应。当用柔嫩艾美耳球虫子孢子抗原体外刺激初次感染后第8天采集的PBL时,其反应高于未感染的对照鸡。我们观察到的效应与初次感染恢复的开始相吻合。我们推测,表达CD8的PBL增加是参与诱导针对柔嫩艾美耳球虫保护性免疫的特定亚群受到刺激和扩增的结果。

相似文献

1
Immunity to eimeria tenella in chickens: phenotypical and functional changes in peripheral blood T-cell subsets.鸡对柔嫩艾美耳球虫的免疫:外周血T细胞亚群的表型和功能变化
Avian Dis. 1996 Jan-Mar;40(1):37-48.
2
Changes in intestinal intra-epithelial and systemic T-cell subpopulations after an Eimeria infection in chickens: comparative study between E acervulina and E tenella.鸡艾美耳球虫感染后肠道上皮内和全身T细胞亚群的变化:堆型艾美耳球虫和柔嫩艾美耳球虫的比较研究
Vet Res. 1996;27(4-5):503-14.
3
Peripheral blood lymphocytes from Eimeria tenella infected chickens produce gamma-interferon after stimulation in vitro.来自感染柔嫩艾美耳球虫鸡的外周血淋巴细胞在体外刺激后产生γ-干扰素。
Parasite Immunol. 1997 Mar;19(3):127-35. doi: 10.1046/j.1365-3024.1997.d01-191.x.
4
Studies on construction of a recombinant Eimeria tenella SO7 gene expressing Escherichia coli and its protective efficacy against homologous infection.重组柔嫩艾美耳球虫SO7基因表达大肠杆菌的构建及其对同源感染的保护效果研究
Parasitol Int. 2010 Dec;59(4):517-23. doi: 10.1016/j.parint.2010.06.010. Epub 2010 Jul 1.
5
Analysis of chicken cytokine and chemokine gene expression following Eimeria acervulina and Eimeria tenella infections.堆型艾美耳球虫和柔嫩艾美耳球虫感染后鸡细胞因子和趋化因子基因表达分析
Vet Immunol Immunopathol. 2006 Dec 15;114(3-4):209-23. doi: 10.1016/j.vetimm.2006.07.007. Epub 2006 Sep 20.
6
Characterization of phenotype related responsiveness of peripheral blood lymphocytes from Eimeria tenella infected chickens.柔嫩艾美耳球虫感染鸡外周血淋巴细胞表型相关反应性的特征分析
Parasite Immunol. 1997 Dec;19(12):563-9. doi: 10.1046/j.1365-3024.1997.d01-174.x.
7
Changes in immune-related gene expression and intestinal lymphocyte subpopulations following Eimeria maxima infection of chickens.巨型艾美耳球虫感染鸡后免疫相关基因表达及肠道淋巴细胞亚群的变化
Vet Immunol Immunopathol. 2006 Dec 15;114(3-4):259-72. doi: 10.1016/j.vetimm.2006.08.006. Epub 2006 Oct 12.
8
Protective immunity of recombinant Mycobacterium bovis BCG expressing rhomboid gene against Eimeria tenella challenge.表达菱形基因的重组牛分枝杆菌卡介苗对柔嫩艾美耳球虫攻击的保护性免疫
Vet Parasitol. 2009 Mar 23;160(3-4):198-203. doi: 10.1016/j.vetpar.2008.11.006. Epub 2008 Nov 13.
9
Transgenic Eimeria tenella expressing enhanced yellow fluorescent protein targeted to different cellular compartments stimulated dichotomic immune responses in chickens.表达靶向不同细胞区室的增强型黄色荧光蛋白的转基因柔嫩艾美耳球虫刺激鸡的二分免疫应答。
J Immunol. 2011 Oct 1;187(7):3595-602. doi: 10.4049/jimmunol.1100043. Epub 2011 Aug 29.
10
[The T and B immunity systems in eimeriosis (Eimeria tenella) in domestic chickens].
Parazitologiia. 1996 Jul-Aug;30(4):336-42.

引用本文的文献

1
Coccidiosis: Recent Progress in Host Immunity and Alternatives to Antibiotic Strategies.球虫病:宿主免疫及抗生素替代策略的最新进展
Vaccines (Basel). 2022 Jan 29;10(2):215. doi: 10.3390/vaccines10020215.
2
Involvement of T Cell Immunity in Avian Coccidiosis.T 细胞免疫在禽类球虫病中的作用。
Front Immunol. 2019 Nov 22;10:2732. doi: 10.3389/fimmu.2019.02732. eCollection 2019.
3
Responses to dietary levels of methionine in broilers medicated or vaccinated against coccidia under Eimeria tenella-challenged condition.在柔嫩艾美耳球虫攻击条件下,给肉鸡投喂抗球虫药或进行球虫疫苗接种后,其对不同蛋氨酸日粮水平的反应。
BMC Vet Res. 2018 Apr 25;14(1):140. doi: 10.1186/s12917-018-1470-8.
4
T cell reactions of Eimeria bovis primary and challenge-infected calves.牛艾美耳球虫初次感染和攻虫感染犊牛的 T 细胞反应。
Parasitol Res. 2010 Feb;106(3):595-605. doi: 10.1007/s00436-009-1705-5.
5
Recent advances in biology and immunobiology of Eimeria species and in diagnosis and control of infection with these coccidian parasites of poultry.艾美耳球虫属的生物学和免疫生物学研究进展以及家禽这些球虫寄生虫感染的诊断与防控
Clin Microbiol Rev. 2002 Jan;15(1):58-65. doi: 10.1128/CMR.15.1.58-65.2002.