Suppr超能文献

重症肌无力中的突触前膜受体反应性T淋巴细胞。

Presynaptic membrane receptor-reactive T lymphocytes in myasthenia gravis.

作者信息

Yi Q, Pirskanen R, Lefvert A K

机构信息

Immunological Research Laboratory, Karolinska Hospital, Stockholm, Sweden.

出版信息

Scand J Immunol. 1996 Jan;43(1):81-7. doi: 10.1046/j.1365-3083.1996.d01-1.x.

Abstract

The majority of patients with myasthenia gravis were shown to have T and B cells specific for a beta-bungarotoxin binding protein, presynaptic membrane receptor (PsmR). Such autoreactive T cells may be subdivided into different subsets according to the pattern of cytokine production. In this study the authors examined the subpopulation of the T cells by analysing their IFN-gamma and/or IL-4 secretion pattern. T cell response to human muscle acetylcholine receptor (AChR) was examined in parallel. PsmR-stimulated IFN-gamma secretion was found in 60%, and IL-4 secretion in 48% of the patients. Cells stimulated to secrete both IFN-gamma and IL-4 or IFN-gamma only were the most common patterns. Treatment of the cells with a mouse anti-human HLA-DR antibody abolished the secretion of cytokines. There was a positive correlation between the numbers of PsmR-reactive and AChR-reactive T cells. In conclusion, the results show that PsmR-stimulated T cells secreted IFN-gamma and/or IL-4. This T cell response is MHC class II restricted. Thus, this study indicates that both Th1/Th2 or Th0 subsets of the T cells are involved in the autoimmune response in the disease.

摘要

大多数重症肌无力患者被证明具有针对β-银环蛇毒素结合蛋白(突触前膜受体,PsmR)的T细胞和B细胞。这种自身反应性T细胞可根据细胞因子产生模式细分为不同亚群。在本研究中,作者通过分析T细胞的γ干扰素和/或白细胞介素-4分泌模式来检测T细胞亚群。同时检测了T细胞对人肌肉乙酰胆碱受体(AChR)的反应。60%的患者中发现PsmR刺激后γ干扰素分泌,48%的患者有白细胞介素-4分泌。细胞被刺激后同时分泌γ干扰素和白细胞介素-4或仅分泌γ干扰素是最常见的模式。用小鼠抗人HLA-DR抗体处理细胞可消除细胞因子的分泌。PsmR反应性T细胞数量与AChR反应性T细胞数量之间存在正相关。总之,结果表明PsmR刺激的T细胞分泌γ干扰素和/或白细胞介素-4。这种T细胞反应受MHCⅡ类分子限制。因此,本研究表明T细胞的Th1/Th2或Th0亚群均参与了该疾病的自身免疫反应。

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