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甲巯咪唑可阻断格雷夫斯病患者的甲状腺细胞产生的IgG,但不阻断甲状腺细胞产生的γ干扰素HLA - DR表达。

Methimazole blocks Graves' IgG but not interferon-gamma HLA-DR expression by thyroid cells.

作者信息

Bodolay E, Suranyi P, Juhasz F, Stenszky V, Balazs C, Farid N R

机构信息

2nd Department of Medicine, Medical College, Debrecen, Hungary.

出版信息

Immunol Lett. 1988 Jul;18(3):167-71. doi: 10.1016/0165-2478(88)90015-6.

Abstract

We have expanded our early observation that a potent Graves' IgG preparation induces HLA-DR expression on thyroid cells, by showing that four randomly-selected Graves' IgG's were also capable of inducing DR antigens on thyroid cells. The effect of Graves' IgG was specific to thyroid cells, as it did not induce MHC Class II molecule expression on endothelial cells whereas interferon-gamma and immune complexes did so. The anti-thyroid drug methimazole was capable of rapidly reducing Graves' IgG-induced DR expression but to a much lesser extent than brought about by interferon-gamma. We conclude that Graves' IgG propagates thyroid-specific autoaggression by continued induction of DR antigens and than an important means whereby methimazole brings about remission is by reducing this induction.

摘要

我们扩展了早期的观察结果,即一种强效的格雷夫斯病IgG制剂可诱导甲状腺细胞表达HLA-DR,通过表明随机选择的四种格雷夫斯病IgG也能够诱导甲状腺细胞上的DR抗原。格雷夫斯病IgG的作用对甲状腺细胞具有特异性,因为它不会在内皮细胞上诱导MHC II类分子表达,而干扰素-γ和免疫复合物则会。抗甲状腺药物甲巯咪唑能够迅速降低格雷夫斯病IgG诱导的DR表达,但程度远低于干扰素-γ。我们得出结论,格雷夫斯病IgG通过持续诱导DR抗原促进甲状腺特异性自身攻击,而甲巯咪唑实现缓解的一个重要方式是减少这种诱导。

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