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健康受试者中对促甲状腺素受体免疫显性表位有反应的T细胞系频率较高。

High frequency of T-cell lines responsive to immunodominant epitopes of thyrotropin receptor in healthy subjects.

作者信息

Molteni M, Zulian C, Scrofani S, Della Bella S, Bonara P, Kohn L D, Scorza R

机构信息

Istituto di Medicina Interna, Malattie Infettive e Immunopatologia, Università degli Studi di Milano, IRCCS Ospedale Maggiore di Milano, Italy.

出版信息

Thyroid. 1998 Mar;8(3):241-7. doi: 10.1089/thy.1998.8.241.

Abstract

In this study we analyzed the proliferative response to the extracellular domain of thyrotropin receptor (TSHR-ECD) of T-cell lines raised from healthy subjects. We found high frequencies of cell lines reactive to TSHR-ECD, ranging from 12% to 37%. The response of the cell lines to a set of overlapping peptides of TSHR-ECD showed that the most recognized epitopes by T lymphocytes are on the C-terminal portion. In particular, the regions of residues 360-396 and 258-277 are immunodominant in T-lymphocyte reactivity. A group of cell lines specific for the peptides of TSHR-ECD lost the response to the peptides during time in culture. However, these lines were still responsive to TSHR extracellular domain. The cloning of one of these lines showed three types of T-cell clones: (1) CD4+ clones (n = 4) highly responsive to the TSHR-ECD; (2) CD4+ clones (n = 4) low responsive to TSHR-ECD; (3) CD8+ clones (n = 9) not responsive to TSHR-ECD. The first group of clones was stable during time in culture, while the second group was characterized by the loss of the specific response to TSHR-ECD after some weeks from the first analysis. The observation of a spontaneous anergy in the second group of CD4+ clones suggests that mechanisms of control of the lymphocyte response to TSHR-ECD could be activated in vitro.

摘要

在本研究中,我们分析了从健康受试者中培养的T细胞系对促甲状腺激素受体细胞外结构域(TSHR-ECD)的增殖反应。我们发现对TSHR-ECD有反应的细胞系频率很高,范围从12%到37%。细胞系对一组TSHR-ECD重叠肽的反应表明,T淋巴细胞最识别的表位位于C末端部分。特别是,360-396位残基和258-277位残基区域在T淋巴细胞反应性中具有免疫优势。一组对TSHR-ECD肽具有特异性的细胞系在培养过程中对这些肽失去了反应。然而,这些细胞系仍然对TSHR细胞外结构域有反应。对其中一个细胞系的克隆显示出三种类型的T细胞克隆:(1)对TSHR-ECD高度反应的CD4+克隆(n = 4);(2)对TSHR-ECD低反应的CD4+克隆(n = 4);(3)对TSHR-ECD无反应的CD8+克隆(n = 9)。第一组克隆在培养过程中是稳定的,而第二组的特征是在首次分析几周后对TSHR-ECD的特异性反应丧失。第二组CD4+克隆中出现自发无反应性的观察结果表明,淋巴细胞对TSHR-ECD反应的控制机制可能在体外被激活。

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