Ribeiro-Dos-Santos R, Mengel J O, Postol E, Soares R A, Ferreira-Fernandez E, Soares M B, Pontes-De-Carvalho L C
Centro de Pesquisas Gonçalo Moniz, FIOCRUZ, Bahia, Brazil.
Parasite Immunol. 2001 Feb;23(2):93-101. doi: 10.1046/j.1365-3024.2001.00368.x.
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.
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。