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由A组链球菌M蛋白诱发的人细胞毒性T淋巴细胞。

Human cytotoxic T lymphocytes evoked by group A streptococcal M proteins.

作者信息

Dale J B, Beachey E H

机构信息

Veterans Administration Medical Center, Memphis Tennessee.

出版信息

J Exp Med. 1987 Dec 1;166(6):1825-35. doi: 10.1084/jem.166.6.1825.

Abstract

Purified group A streptococcal M proteins were used to stimulate peripheral blood lymphocytes from normal adult volunteers. The activated lymphocytes were cytotoxic against cultured human heart cells, as well as liver cells, fibroblasts, and K562 cells, but showed only minimal cytotoxicity against several animal cell types. The cytotoxic activity evoked by type 5 M protein was dose and time dependent. Rabbit antisera against pep M5 that contained heart-crossreactive antibodies partially inhibited cytotoxicity against heart cells, but had no effect on other target cells, suggesting that a fraction of the effector lymphocytes may be recognizing M protein-crossreactive cell surface antigens. All of the cytotoxic activity was recovered from a CD3+ population of lymphocytes obtained from a fluorescence-activated cell sorter, and CD4+ and CD8+ cells were also cytotoxic. M protein-responsive T cell clones were generated that showed specificity for heart and K562 cells, in addition to clones that were cytotoxic against both cell lines. Our data show that streptococcal M protein evokes cytotoxic T lymphocytes against multiple human but not animal target cells. Some of the effector cells may be specific for cultured myocardial cells, but their role in the pathogenesis of rheumatic carditis will require further studies of lymphocytes from patients with acute rheumatic fever and carditis.

摘要

纯化的A组链球菌M蛋白用于刺激正常成年志愿者的外周血淋巴细胞。活化的淋巴细胞对培养的人心脏细胞、肝细胞、成纤维细胞和K562细胞具有细胞毒性,但对几种动物细胞类型仅表现出最小的细胞毒性。5型M蛋白诱发的细胞毒性活性呈剂量和时间依赖性。含有心脏交叉反应抗体的抗M5肽兔抗血清部分抑制了对心脏细胞的细胞毒性,但对其他靶细胞没有影响,这表明一部分效应淋巴细胞可能识别M蛋白交叉反应性细胞表面抗原。所有细胞毒性活性均从通过荧光激活细胞分选仪获得的CD3+淋巴细胞群体中恢复,并且CD4+和CD8+细胞也具有细胞毒性。产生了对心脏和K562细胞具有特异性的M蛋白反应性T细胞克隆,以及对两种细胞系均具有细胞毒性的克隆。我们的数据表明,链球菌M蛋白可诱发针对多种人类而非动物靶细胞的细胞毒性T淋巴细胞。一些效应细胞可能对培养的心肌细胞具有特异性,但其在风湿性心肌炎发病机制中的作用需要对急性风湿热和心肌炎患者的淋巴细胞进行进一步研究。

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