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甲状腺相关眼病中针对胰岛素样生长因子-1结合位点的自身抗体。

Autoantibodies to IGF-1 binding sites in thyroid associated ophthalmopathy.

作者信息

Weightman D R, Perros P, Sherif I H, Kendall-Taylor P

机构信息

Endocrine Unit, University of Newcastle Department of Medicine, Medical School, Newcastle-Upon-Tyne.

出版信息

Autoimmunity. 1993;16(4):251-7. doi: 10.3109/08916939309014643.

Abstract

Graves' disease is an autoimmune disorder but the nature of the association between hyperthyroidism and ophthalmopathy is not yet understood. Serum autoantibodies to orbital tissues have previously been identified and the cross-reactivity with orbital and thyroid antigens has been implicated in the development of thyroid-associated ophthalmopathy (TAO). The ophthalmopathy of Graves' disease is remarkable for the hypertrophy of extraocular muscles and proliferation of fibroblasts within the orbit; features which suggest a possible involvement of growth factors. The present study was therefore undertaken to investigate the interaction of IgGs extracted from the sera of patients with Graves' disease, with or without overt ophthalmopathy, with respect to IGF-1 receptor binding sites on fibroblasts from human orbital tissue. IGF-1 binding sites were demonstrated on human orbital fibroblast monolayers grown from eye muscle explants. These cells exhibited a population of high affinity IGF-1 binding sites (Kd, 0.5nM SEM +/- 0.05). IgG prepared from sera taken from patients with Graves' disease (n = 23) significantly inhibited [125I]IGF-1 binding to orbital fibroblasts when compared to IgGs prepared from normal volunteers (n = 13, p < 0.002). It was found that 12 of 23 (52%) patients' IgG samples gave rise to significant levels of inhibition of [125I]IGF-1 binding to orbital fibroblasts. The IgG preparations did not bind directly to IGF-1. This study demonstrates that IgG prepared from patients with Graves' disease with or without overt ophthalmopathy interact with IGF-1 binding sites on orbital fibroblasts whereas IgG from normal subjects had no significant effect.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

格雷夫斯病是一种自身免疫性疾病,但甲状腺功能亢进与眼病之间关联的本质尚未明确。此前已鉴定出针对眼眶组织的血清自身抗体,且与眼眶和甲状腺抗原的交叉反应被认为与甲状腺相关眼病(TAO)的发生有关。格雷夫斯病的眼病以眼外肌肥大和眼眶内成纤维细胞增殖为显著特征;这些特征提示生长因子可能参与其中。因此,本研究旨在调查从格雷夫斯病患者血清中提取的免疫球蛋白(IgG),无论有无明显眼病,与人眼眶组织成纤维细胞上胰岛素样生长因子-1(IGF-1)受体结合位点的相互作用。在从眼肌外植体生长的人眼眶成纤维细胞单层上证实了IGF-1结合位点。这些细胞表现出一群高亲和力的IGF-1结合位点(解离常数Kd为0.5nM,标准误±0.05)。与从正常志愿者(n = 13)制备的IgG相比,从格雷夫斯病患者(n = 23)血清中制备的IgG显著抑制[125I]IGF-1与眼眶成纤维细胞的结合(p < 0.002)。发现23例患者中有12例(52%)的IgG样本对[125I]IGF-1与眼眶成纤维细胞的结合产生显著抑制水平。IgG制剂不直接与IGF-1结合。本研究表明,无论有无明显眼病,格雷夫斯病患者制备的IgG与眼眶成纤维细胞上的IGF-1结合位点相互作用,而正常受试者的IgG则无显著影响。(摘要截短至250字)

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