Suppr超能文献

从慢性恰加斯病小鼠获得的心脏特异性CD4 + T细胞系,可在心脏免疫小鼠中诱发心肌炎,并在无克氏锥虫的情况下导致正常心脏移植排斥反应。

A heart-specific CD4+ T-cell line obtained from a chronic chagasic mouse induces carditis in heart-immunized mice and rejection of normal heart transplants in the absence of Trypanosoma cruzi.

作者信息

Ribeiro-Dos-Santos R, Mengel J O, Postol E, Soares R A, Ferreira-Fernandez E, Soares M B, Pontes-De-Carvalho L C

机构信息

Centro de Pesquisas Gonçalo Moniz, FIOCRUZ, Bahia, Brazil.

出版信息

Parasite Immunol. 2001 Feb;23(2):93-101. doi: 10.1046/j.1365-3024.2001.00368.x.

Abstract

To study the role of autoreactive T cells in the pathogenesis of cardiomyopathy in Chagas' disease, we generated a cell line by repeated in vitro antigenic stimulation of purified splenic CD4+ T lymphocytes from a chronically Trypanosoma cruzi-infected mouse. Cells from this line were confirmed to be CD4+ CD8- and proliferated upon stimulation with soluble heart antigens from different animal species, as well as with T. cruzi antigen, in the presence of syngeneic feeder cells. In vitro antigen stimulation of the cell line produced a Th1 cytokine profile, with high levels of IFNgamma and IL-2 and absence of IL-4, IL-5 and IL-10. The cell line also terminated the beating of fetal heart clusters in vitro when cocultured with irradiated syngeneic normal spleen cells. In situ injection of the cell line into well established heart transplants also induced the cessation of heart beating. Finally, adoptive transfer of the cell line to heart-immunized or T. cruzi-infected BALB/c nude mice caused intense heart inflammation.

摘要

为研究自身反应性T细胞在恰加斯病心肌病发病机制中的作用,我们通过对来自慢性克氏锥虫感染小鼠的纯化脾CD4⁺ T淋巴细胞进行反复体外抗原刺激,建立了一个细胞系。该细胞系的细胞经证实为CD4⁺ CD8⁻,在同基因饲养细胞存在的情况下,用来自不同动物物种的可溶性心脏抗原以及克氏锥虫抗原刺激后会增殖。对该细胞系进行体外抗原刺激产生了Th1细胞因子谱,IFNγ和IL-2水平高,而IL-4、IL-5和IL-10缺失。当与经照射的同基因正常脾细胞共培养时,该细胞系在体外也会使胎儿心脏细胞团停止跳动。将该细胞系原位注射到已建立的心脏移植模型中也会导致心跳停止。最后,将该细胞系过继转移到心脏免疫或克氏锥虫感染的BALB/c裸鼠中会引起严重的心脏炎症。

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