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自身免疫性甲状腺疾病患者的血清中存在胰岛素自身抗体。

Autoantibodies to insulin are present in sera of patients with autoimmune thyroid disease.

作者信息

Nuovo J A, Baker J R, Wartofsky L, Lukes Y G, Burman K D

机构信息

Department of Medicine, Walter Reed Army Medical Center, Washington, DC 20307-5001.

出版信息

Diabetes. 1988 Mar;37(3):317-20. doi: 10.2337/diab.37.3.317.

Abstract

It has been clinically suspected that patients with autoimmune thyroid disease are at an increased risk of developing other autoimmune diseases later in life. To determine the presence and potential importance of a more generalized deregulation of immune response in patients with Grave's disease and Hashimoto's disease, sera from 33 patients with Graves' disease and 16 patients with Hashimoto's disease were screened for the presence of anti-insulin antibodies and anti-insulin-receptor antibodies. An enzyme-linked immunosorbent assay was used to identify the presence of IgG against human insulin. The optical density indicating the presence of IgG against insulin in sera from patients with Graves' disease averaged .172 +/- .024 (mean +/- SE; range .010-.802), compared to the mean normal value of .098 +/- .0009 (range .012-.238) in 33 control subjects. Ten of 33 patients with Graves' disease had values greater than .200, whereas control sera values were less than .200 in all but one case (P less than .005, Graves' sera vs. controls). The sera from patients with Hashimoto's disease had a mean optical density of .110 +/- .016, with 15 of 16 values between .010 and .200. These values were not significantly different from controls with an insulin-binding inhibition assay. Anti-insulin-receptor antibodies were not detected in any of 33 patients with Graves' disease, and cytoplasmic islet cell antibodies were not detected in sera from seven patients with Graves' disease who had insulin-binding antibodies. These data support the hypothesis that the immunologic response in autoimmune thyroid disease may be more heterogeneous and polyclonal than previously believed.

摘要

临床上一直怀疑自身免疫性甲状腺疾病患者在日后患其他自身免疫性疾病的风险会增加。为了确定格雷夫斯病和桥本氏病患者免疫反应更普遍失调的存在及其潜在重要性,对33例格雷夫斯病患者和16例桥本氏病患者的血清进行了抗胰岛素抗体和抗胰岛素受体抗体检测。采用酶联免疫吸附测定法鉴定抗人胰岛素IgG的存在。格雷夫斯病患者血清中抗胰岛素IgG存在的光密度平均值为0.172±0.024(均值±标准误;范围0.010 - 0.802),而33名对照受试者血清的平均正常值为0.098±0.0009(范围0.012 - 0.238)。33例格雷夫斯病患者中有10例的值大于0.200,而对照血清的值除1例以外均小于0.200(P < 0.005,格雷夫斯病血清与对照血清)。桥本氏病患者血清的平均光密度为0.110±0.016,16个值中有15个在0.010至0.200之间。通过胰岛素结合抑制试验,这些值与对照无显著差异。33例格雷夫斯病患者中均未检测到抗胰岛素受体抗体,7例有胰岛素结合抗体的格雷夫斯病患者血清中未检测到胰岛细胞胞浆抗体。这些数据支持了这样的假说,即自身免疫性甲状腺疾病中的免疫反应可能比以前认为的更加异质性和多克隆性。

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