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青霉胺诱导的原发性胆汁性肝硬化中免疫复合物和免疫球蛋白的减少

Reduction of immune complexes and immunoglobulins induced by D-penicillamine in primary biliary cirrhosis.

作者信息

Epstein O, De Villiers D, Jain S, Potter B J, Thomas H C, Sherlock S

出版信息

N Engl J Med. 1979 Feb 8;300(6):274-8. doi: 10.1056/NEJM197902083000602.

Abstract

Penicillamine has an effect on immune complexes and immunoglobulins both in vivo and in vitro. We therefore studied the effect of penicillamine on immune complexes and immunoglobulins in primary biliary cirrhosis. Twenty-eight patients were randomly allocated into a treatment group receiving 600 to 900 mg of penicillamine, or a control group, and followed for a maximum of 24 months. After 12 and 24 months, serum immune complexes had fallen significantly in treated patients as compared to controls (P less than 0.05, P less than 0.01). Treatment reduced IgA, IgG and IgM concentrations, with IgM being significantly different from controls at six, 12 and 24 months (P less than 0.01). Over 24 months, serum aspartate transaminase levels fell in treated patients but rose in controls (P less than 0.01). Bilirubin concentrations increased at a slower rate in treated patients. Penicillamine may favorably influence the course of primary biliary cirrhosis by its immunologic action in addition to its copper-chelating action.

摘要

青霉胺在体内和体外均对免疫复合物和免疫球蛋白有作用。因此,我们研究了青霉胺对原发性胆汁性肝硬化患者免疫复合物和免疫球蛋白的影响。28例患者被随机分为接受600至900毫克青霉胺治疗的治疗组或对照组,随访最长24个月。12个月和24个月后,与对照组相比,治疗组患者血清免疫复合物显著下降(P<0.05,P<0.01)。治疗使IgA、IgG和IgM浓度降低,6个月、12个月和24个月时IgM与对照组有显著差异(P<0.01)。在24个月期间,治疗组患者血清天冬氨酸转氨酶水平下降,而对照组上升(P<0.01)。治疗组患者胆红素浓度升高速度较慢。青霉胺除了具有铜螯合作用外,还可能通过其免疫作用对原发性胆汁性肝硬化的病程产生有利影响。

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