• 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

放射性标记骨髓细胞归巢和接触敏感性证明迟发型超敏反应在慢性伯氏疟原虫感染期间的保护作用。

Role of delayed type hypersensitivity responses in protection during chronic Plasmodium berghei infection as evidenced by homing of radiolabelled bone marrow cells and contact sensitivity.

作者信息

Wangoo A, Ganguly N K, Mahajan R C

机构信息

Department of Parasitology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.

出版信息

Jpn J Exp Med. 1990 Apr;60(2):45-50.

PMID:2200902
Abstract

A comparative study of specific and non-specific immunosuppression has been carried out in acute and chronic Plasmodium berghei infected mice in an in vivo system. In our previous studies, immunosuppression during acute P. berghei infection was attributed to T lymphocytes when we studied modulation of blastogenic response of lymphocytes in an in vitro system. In the present study, delayed type hypersensitivity (DTH) was evident from the homing of radiolabelled bone marrow cells into the delayed lesions of antigen challenged foot pads during chronic infection. This response was suppressed during acute infection especially in early stages. A greater concentration of bone marrow cells in the liver and spleen occurred during chronic infection in comparison with acute infection. When radiolabelled bone marrow cells from infected mice were injected into the normal mice previously given malaria antigen in foot pads, no significant change in homing pattern in liver, spleen or foot pads was observed. Contact sensitivity to picryl chloride was suppressed during acute infection, but was intact during chronic infection. Since these responses are mediated by T lymphocytes, significance of these responses is discussed.

摘要

在体内系统中,对感染伯氏疟原虫的急性和慢性小鼠进行了特异性和非特异性免疫抑制的比较研究。在我们之前的研究中,当我们在体外系统中研究淋巴细胞的增殖反应调节时,急性伯氏疟原虫感染期间的免疫抑制归因于T淋巴细胞。在本研究中,慢性感染期间放射性标记的骨髓细胞归巢到抗原攻击的脚垫延迟病变中,延迟型超敏反应(DTH)很明显。这种反应在急性感染期间尤其是早期受到抑制。与急性感染相比,慢性感染期间肝脏和脾脏中的骨髓细胞浓度更高。当将来自感染小鼠的放射性标记骨髓细胞注射到先前在脚垫中给予疟疾抗原的正常小鼠中时,在肝脏、脾脏或脚垫中的归巢模式没有观察到显著变化。急性感染期间对苦味酸氯的接触敏感性受到抑制,但慢性感染期间保持完整。由于这些反应是由T淋巴细胞介导的,因此讨论了这些反应的意义。

相似文献

1
Role of delayed type hypersensitivity responses in protection during chronic Plasmodium berghei infection as evidenced by homing of radiolabelled bone marrow cells and contact sensitivity.放射性标记骨髓细胞归巢和接触敏感性证明迟发型超敏反应在慢性伯氏疟原虫感染期间的保护作用。
Jpn J Exp Med. 1990 Apr;60(2):45-50.
2
Cell-mediated immunity in mice vaccinated against malaria.接种疟疾疫苗的小鼠的细胞介导免疫
Clin Exp Immunol. 1978 Nov;34(2):147-58.
3
Delayed-type hypersensitivity initiation by early-acting cells that are antigen mismatched or MHC incompatible with late-acting, delayed-type hypersensitivity effector T cells.由与迟发型超敏反应效应T细胞抗原不匹配或MHC不相容的早期作用细胞引发的迟发型超敏反应。
J Immunol. 1991 Jan 15;146(2):469-75.
4
Two distinct types of non-specific immunosuppression in murine malaria.小鼠疟疾中两种不同类型的非特异性免疫抑制。
Clin Exp Immunol. 1980 Dec;42(3):428-35.
5
Supplementation of CXCL12 (CXCL12) induces homing of CD11c+ dendritic cells to the spleen and enhances control of Plasmodium berghei malaria in BALB/c mice.补充趋化因子CXCL12可诱导CD11c+树突状细胞归巢至脾脏,并增强对BALB/c小鼠伯氏疟原虫疟疾的控制。
Immunology. 2005 Jul;115(3):399-406. doi: 10.1111/j.1365-2567.2005.02178.x.
6
An in vitro assay for T cell immunity to malaria in mice.一种针对小鼠疟疾T细胞免疫的体外检测方法。
J Immunol. 1976 May;116(5):1280-3.
7
Plasmodium berghei XAT: contribution of gammadelta T cells to host defense against infection with blood-stage nonlethal malaria parasite.伯氏疟原虫XAT:γδT细胞在宿主抵御血液期非致死性疟原虫感染中的作用
Exp Parasitol. 2007 Dec;117(4):368-75. doi: 10.1016/j.exppara.2007.05.002. Epub 2007 May 13.
8
MHC class I-dependent presentation of exoerythrocytic antigens to CD8+ T lymphocytes is required for protective immunity against Plasmodium berghei.针对伯氏疟原虫的保护性免疫需要将红细胞外抗原呈递给CD8 + T淋巴细胞的MHC I类依赖性呈递。
J Immunol. 1996 May 1;156(9):3374-81.
9
Immunosuppression in murine malaria: suppressor role of macrophages and their products during acute and chronic Plasmodium berghei infection.小鼠疟疾中的免疫抑制:伯氏疟原虫急性和慢性感染期间巨噬细胞及其产物的抑制作用
APMIS. 1990 May;98(5):407-14.
10
Early lymphocyte trapping in malaria infections: a particulate antigen mediated phenomenon.疟疾感染中的早期淋巴细胞捕获:一种颗粒抗原介导的现象。
J Parasitol. 1984 Jun;70(3):391-7.