Suppr超能文献

用弓形虫的保护性F3G3抗原对小鼠进行疫苗接种可激活CD4 + 但不激活CD8 + T细胞,并诱导产生弓形虫特异性IgG抗体。

Vaccination of mice with the protective F3G3 antigen of Toxoplasma gondii activates CD4+ but not CD8+ T cells and induces Toxoplasma specific IgG antibody.

作者信息

Brinkmann V, Remington J S, Sharma S D

机构信息

Department of Medicine, Stanford University School of Medicine, CA 94305.

出版信息

Mol Immunol. 1993 Mar;30(4):353-8. doi: 10.1016/0161-5890(93)90064-i.

Abstract

A major cytoplasmic Toxoplasma gondii (T. gondii) antigen recognized by monoclonal antibody F3G3 (F3G3-Ag), as well as two surface antigens recognized by monoclonal antibodies 2G11 and 1E11 respectively (2G11-Ag; 1E11-Ag), were isolated from crude Toxoplasma sonicates using affinity chromatography. Purified F3G3-Ag induced long term protection against Toxoplasma infection in mice and induced Toxoplasma specific IgG antibody. CD4+ but not CD8+ T cells from immune animals proliferated and produced IL-2 upon restimulation with either Toxoplasma sonicate or F3G3-Ag in vitro. Furthermore, CD4+ T cells from mice immunized with F3G3-Ag responded to purified 2G11- and 1E11-Ag. In contrast, CD4+ T cells from mice immunized with 2G11-Ag responded to Toxoplasma sonicate and 2G11-Ag, but not to F3G3- or 1E11-Ag. The results may indicate that the protective F3G3-Ag shares immunogenic epitopes present also on 2G11- and 1E11-Ag, since the F3G3-Ag used for the vaccination did not contain detectable amounts of 2G11- or 1E11-Ag, and none of the antigens displayed any mitogenicity. Taken together the results show that the cytoplasmic F3G3-Ag of T. gondii induces CD4+ T helper cells, Toxoplasma specific IgG antibodies and long term protection against Toxoplasma infection, but does not induce detectable sensitization of the CD8+ T cell compartment.

摘要

利用亲和层析从粗制的弓形虫超声裂解物中分离出一种被单克隆抗体F3G3识别的主要细胞质弓形虫(T. gondii)抗原(F3G3-Ag),以及分别被单克隆抗体2G11和1E11识别的两种表面抗原(2G11-Ag;1E11-Ag)。纯化的F3G3-Ag可诱导小鼠对弓形虫感染产生长期保护,并诱导产生弓形虫特异性IgG抗体。来自免疫动物的CD4+而非CD8+ T细胞在体外被弓形虫超声裂解物或F3G3-Ag再次刺激后会增殖并产生IL-2。此外,用F3G3-Ag免疫的小鼠的CD4+ T细胞对纯化的2G11-Ag和1E11-Ag有反应。相比之下,用2G11-Ag免疫的小鼠的CD4+ T细胞对弓形虫超声裂解物和2G11-Ag有反应,但对F3G3-Ag或1E11-Ag无反应。这些结果可能表明,具有保护作用的F3G3-Ag与2G11-Ag和1E11-Ag上也存在的免疫原性表位相同,因为用于疫苗接种的F3G3-Ag不含可检测量的2G11-Ag或1E11-Ag,且这些抗原均未表现出任何促有丝分裂活性。综合这些结果表明,弓形虫的细胞质F3G3-Ag可诱导CD4+辅助性T细胞、弓形虫特异性IgG抗体以及对弓形虫感染的长期保护,但不会诱导CD8+ T细胞区室产生可检测到的致敏反应。

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