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用甲状腺球蛋白特异性细胞毒性T细胞杂交瘤进行免疫可诱导抗甲状腺球蛋白抗体:单克隆抗甲状腺球蛋白自身抗体的特性。

Immunization with thyroglobulin-specific cytotoxic T cell hybridoma induces anti-thyroglobulin antibodies: characteristics of monoclonal anti-thyroglobulin auto-antibody.

作者信息

Bedin C, Mignon-Godefroy K, Brazillet M P, Tang H, Charreire J

机构信息

INSERM U. 283, Hôpital Cochin, Paris, France.

出版信息

Cell Immunol. 1993 Feb;146(2):227-37. doi: 10.1006/cimm.1993.1022.

Abstract

We have produced five monoclonal autoantibodies (mA-Abs) to thyroglobulin (Tg) and more precisely to one epitope located within the < 10-kDa pTg tryptic fragment suspension capable of inducing experimental autoimmune thyroiditis (EAT). They were selected from spleen cells from CBA/J mouse immunized with the syngeneic cytotoxic T cell hybridoma HTC2. HTC2 cells are specific for one Tg epitope located within the EAT inducer pTg tryptic fragments and are able to prevent EAT induction by pTg. The restricted specificity of the humoral response previously observed in vivo was further demonstrated and defined in vitro at the single cell level. Competitive studies for binding to pTg or to the < 10-kDa pTg tryptic fragments demonstrated that HTC2-induced anti-Tg mA-Abs recognized an epitope(s) located in the < 10-kDa pTg tryptic fragment (as did 3B8G9, one conventional anti-Tg mA-Ab we selected). We ruled out the possibility that HTC2-induced anti-Tg A-Abs belong to the group of the natural A-Abs due to the lack of recognition of actin, dsDNA, TNP-ovalbumin, tubulin, their isotypes (IgG1 or Ig2a), and their affinities (in the 10(-7) M order of magnitude). The results strengthen the hypothesis that T and B cells sharing the same specificity can express similar idiotopes on their respective receptors for antigen. They also demonstrate the existence of a regulatory idiotypic network that could explain the protection from EAT after injection of inactivated HTC2 cells or its anti-clonotypic mAb.

摘要

我们制备了五种针对甲状腺球蛋白(Tg)的单克隆自身抗体(mA-Abs),更确切地说是针对位于<10-kDa pTg胰蛋白酶片段悬浮液中一个表位的抗体,该悬浮液能够诱导实验性自身免疫性甲状腺炎(EAT)。它们是从用同基因细胞毒性T细胞杂交瘤HTC2免疫的CBA/J小鼠的脾细胞中筛选出来的。HTC2细胞对位于EAT诱导剂pTg胰蛋白酶片段内的一个Tg表位具有特异性,并且能够阻止pTg诱导EAT。先前在体内观察到的体液反应的受限特异性在单细胞水平上在体外得到了进一步证实和界定。与pTg或<10-kDa pTg胰蛋白酶片段结合的竞争性研究表明,HTC2诱导的抗Tg mA-Abs识别位于<10-kDa pTg胰蛋白酶片段中的一个表位(我们选择的一种传统抗Tg mA-Ab 3B8G9也是如此)。由于缺乏对肌动蛋白、双链DNA、TNP-卵清蛋白、微管蛋白、它们的同种型(IgG1或Ig2a)以及它们的亲和力(在10^(-7) M数量级)的识别,我们排除了HTC2诱导的抗Tg A-Abs属于天然A-Abs组的可能性。这些结果强化了这样的假设,即具有相同特异性的T细胞和B细胞可以在它们各自的抗原受体上表达相似的独特型。它们还证明了存在一个调节性独特型网络,这可以解释注射灭活的HTC2细胞或其抗克隆型单克隆抗体后对EAT的保护作用。

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