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遗传性血管性水肿:达那唑对C4和C1酯酶抑制剂的治疗效果

Hereditary angioedema: therapeutic effect of danazol on C4 and C1 esterase inhibitors.

作者信息

Fabiani J E, Paulin P, Simkin G, Leoni J, Palombarani S, Squiquera L

机构信息

Institute for Allergy and Immunology, Buenos Aires, Argentina.

出版信息

Ann Allergy. 1990 Apr;64(4):388-92.

PMID:2108593
Abstract

Hereditary angioedema (HAE) is an inherited deficiency of C1 esterase inhibitor (C1 inh). The two types of genetic C1 inh deficiency are type I, which is quantitative, and type II, which is functional. For the purpose of the present study, four HAE patients were selected. None of them had received any androgenic therapy. The group included three type I and one type II cases. All patients that entered the protocol received danazol, 400 mg/day for 14 days. The complement system was evaluated by monitoring C4, hemolytic complement 50% (CH50), circulating immune complexes (CIC), and antigenic and functional C1 inh during the study. The level of complement factors at the beginning and at the end of this period demonstrated a statistically significant increase in C4 and CH50 and the disappearance of CIC, while C1 inh remained unmodified. These results suggest that the therapeutic effect of danazol may have two mechanisms of action: (1) promotion of C4 synthesis by anabolic effect resulting in an improvement of the complement system with the disappearance of CIC and (2) a minor increase in C1 inh level primarily due to the lack of its consumption.

摘要

遗传性血管性水肿(HAE)是一种遗传性C1酯酶抑制剂(C1 inh)缺乏症。遗传性C1 inh缺乏症有两种类型:I型为数量缺乏型,II型为功能缺乏型。本研究选取了4例HAE患者。他们均未接受过任何雄激素治疗。该组包括3例I型和1例II型病例。所有进入该方案的患者均接受达那唑治疗,400mg/天,共14天。在研究期间,通过监测C4、50%溶血补体(CH50)、循环免疫复合物(CIC)以及抗原性和功能性C1 inh来评估补体系统。在这段时间开始和结束时的补体因子水平显示,C4和CH50有统计学意义的升高,CIC消失,而C1 inh保持不变。这些结果表明,达那唑的治疗作用可能有两种机制:(1)通过合成代谢作用促进C4合成,导致补体系统改善,CIC消失;(2)C1 inh水平略有升高,主要是由于其消耗减少。

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