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难治性格雷夫斯病患者血清白细胞介素-10水平升高。

Increase of serum interleukin-10 in intractable Graves' disease.

作者信息

Takeoka Keiko, Watanabe Mikio, Matsuzuka Fumio, Miyauchi Akira, Iwatani Yoshinori

机构信息

Division of Biomedical Informatics, Course of Health Science, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.

出版信息

Thyroid. 2004 Mar;14(3):201-5. doi: 10.1089/105072504773297876.

DOI:10.1089/105072504773297876
PMID:15072702
Abstract

The intractability of Graves' disease (GD) and the severity of Hashimoto's disease (HD) vary among patients. We previously reported that peripheral immunoglobulin (Ig) G3-secreting cells were increased in patients with intractable GD (i.e., requiring continuous antithyroid drug therapy). Isotype switching to IgG3 is induced by interleukin (IL)-4 and IL-10. To clarify which of these cytokines is related to the intractability or severity of autoimmune thyroid disease (AITD), we examined the serum concentrations of IL-10 and IL-4 by enzyme immunoassay in 166 patients with AITD and in 53 healthy controls. The serum IL-10 concentration was significantly higher in patients with GD and continuously positive for thyrotropin (TSH) receptor antibody (TRAb) despite more than 5 years of antithyroid drugs treatment than in patients with GD in remission. The serum IL-4 concentration did not differ between these two groups of patients. However, the serum IL-10 concentration was not related to the severity of HD. These results indicate that IL-10, but not IL-4, is related to the intractability of GD, but not to the severity of HD.

摘要

格雷夫斯病(GD)的难治性和桥本甲状腺炎(HD)的严重程度在患者之间存在差异。我们之前报道过,难治性GD患者(即需要持续抗甲状腺药物治疗的患者)外周分泌免疫球蛋白(Ig)G3的细胞增多。向IgG3的同种型转换是由白细胞介素(IL)-4和IL-10诱导的。为了阐明这些细胞因子中的哪一种与自身免疫性甲状腺疾病(AITD)的难治性或严重程度相关,我们通过酶免疫测定法检测了166例AITD患者和53例健康对照者血清中IL-10和IL-4的浓度。在接受抗甲状腺药物治疗超过5年但促甲状腺激素(TSH)受体抗体(TRAb)仍持续呈阳性的GD患者中,血清IL-10浓度显著高于处于缓解期的GD患者。这两组患者的血清IL-4浓度没有差异。然而,血清IL-10浓度与HD的严重程度无关。这些结果表明,与GD的难治性相关的是IL-10而非IL-4,且IL-10与HD的严重程度无关。

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