Suppr超能文献

针对人类胰岛素受体而非大鼠胰岛素受体的人类自身抗体。

Human autoantibodies directed against the human, but not the rat, insulin receptor.

作者信息

De Pirro R, Rossetti L, Montemurro A, Lauro R, Gammeltoft S, Maddux B A, Goldfine I D

出版信息

J Clin Endocrinol Metab. 1985 Nov;61(5):986-9. doi: 10.1210/jcem-61-5-986.

Abstract

Prior studies with monoclonal antibodies produced against the human insulin receptor in mice revealed that these antibodies may be species specific. Whether species-specific antibodies to the insulin receptor occur spontaneously in patients, however, has not been previously investigated. Recently, we found that the serum immunoglobulin G from a patient with lupus nephritis, insulin resistance, and hypoglycemia contained multiple subpopulations of antibodies directed at the human insulin receptor. We report herein that one such subpopulation has a high affinity for the human insulin receptor. This antibody subpopulation at 10 nM half-maximally inhibited [125I]insulin binding to human IM-9 lymphocytes, circulating erythrocytes and monocytes, isolated adipocytes, and placenta membranes. In contrast, this antibody subpopulation did not inhibit [125I]insulin binding to isolated rat adipocytes and hepatocytes, even at concentrations as high as 100 nM. These studies indicate that species-specific antibodies can occur spontaneously in patients with antiinsulin receptor antibodies.

摘要

先前在小鼠中针对人胰岛素受体产生单克隆抗体的研究表明,这些抗体可能具有物种特异性。然而,患者体内是否会自发产生针对胰岛素受体的物种特异性抗体,此前尚未得到研究。最近,我们发现一名患有狼疮性肾炎、胰岛素抵抗和低血糖症患者的血清免疫球蛋白G中含有多种针对人胰岛素受体的抗体亚群。我们在此报告,其中一个这样的亚群对人胰岛素受体具有高亲和力。该抗体亚群在10 nM时可半数最大抑制[125I]胰岛素与人IM-9淋巴细胞、循环红细胞和单核细胞、分离的脂肪细胞及胎盘膜的结合。相比之下,即使在浓度高达100 nM时,该抗体亚群也不会抑制[125I]胰岛素与分离的大鼠脂肪细胞和肝细胞的结合。这些研究表明,抗胰岛素受体抗体患者体内可自发产生物种特异性抗体。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验