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单核细胞和巨噬细胞对[35S]甲巯咪唑的摄取。

The accumulation of [35S]methimazole by monocytes and macrophages.

作者信息

Weetman A P, Gunn C, Hall R, McGregor A M

出版信息

Acta Endocrinol (Copenh). 1984 Nov;107(3):366-70. doi: 10.1530/acta.0.1070366.

Abstract

We have used an automatic cell harvester and micro culture techniques to examine the accumulation of [35S]methimazole by monocytes, macrophages and lymphocytes. Significant temperature-dependent accumulation of the drug was found in resting monocytes and macrophages; this was increased up to 4-fold by phagocytosis. Lymphocytes accumulated little or no drug and myeloma and leukaemic cell lines accumulated none. These results show that two interrelated cells with endogenous peroxidatic activity take up the antithyroid drug methimazole providing further support for the concept that immunosuppression by this drug in Graves' disease is mediated via an action on antigen-presenting cells.

摘要

我们使用自动细胞收集器和微量培养技术,检测单核细胞、巨噬细胞和淋巴细胞对[35S]甲巯咪唑的摄取情况。发现静息单核细胞和巨噬细胞对该药物的摄取存在显著的温度依赖性;吞噬作用可使其增加至4倍。淋巴细胞摄取的药物很少或几乎不摄取,骨髓瘤和白血病细胞系则不摄取。这些结果表明,两种具有内源性过氧化物酶活性的相关细胞摄取抗甲状腺药物甲巯咪唑,这为该药物在格雷夫斯病中通过作用于抗原呈递细胞介导免疫抑制这一概念提供了进一步支持。

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