原发性胆汁性肝硬化患者的口服耐受性和丙酮酸脱氢酶。

Ayako Suzuki, Judy Van de Water, M Eric Gershwin, Roberta Jorgensen, Paul Angulo, Keith Lindor
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引用次数: 8

摘要

原发性胆汁性肝硬化(PBC)是一种慢性胆汁淤积性肝病,其特征是小叶内胆管的免疫破坏和血清抗线粒体抗体(AMA)。基于先前的口服耐受性和自身免疫的研究,我们假设喂养PBC线粒体自身抗原会改变临床病程和抗线粒体抗体水平。对6例早期PBC患者纯化牛丙酮酸脱氢酶复合物(PDC),并将其5 mg用明胶胶囊喂养6个月。每3个月检测一次抗线粒体抗体和肝脏生化指标,持续12个月。除1例患者在治疗期间出现原有皮疹恶化外,其余患者均完成了临床试验,该皮疹在停止治疗后2周内消失。然而,1年后,这种治疗既没有显著改变AMAs滴度,也没有显著改变肝脏生化。这是第一个测试口服耐药诱导PBC疗效的试验。然而,范围有限的数据并未显示出有效性,进一步强调了在自身免疫中显示耐受性诱导的持续证据的困难。
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Oral tolerance and pyruvate dehydrogenase in patients with primary biliary cirrhosis.

Primary biliary cirrhosis (PBC) is a chronic cholestatic liver disease characterized by the immunological destruction of intralobular bile ducts and serum anti-mitochondrial antibodies (AMA). Based upon previous work of oral tolerance and autoimmunity, we hypothesized that feeding the mitochondrial autoantigens of PBC would alter the clinical course and the level of antimitochondrial antibodies. The bovine pyruvate dehydrogenase complex (PDC) was purified and 5 mg fed in gelatin capsules to 6 patients with early stage PBC for 6 months. Antimitochondrial antibodies and liver biochemistries were measured at every 3 months for 12 months. The clinical trial was completed for all patients except for 1 who showed deterioration of pre-existing skin rash during treatment, which disappeared within 2 weeks after treatment was discontinued. However, after 1 year, neither the titers of AMAs nor liver biochemistries were significantly changed by this treatment. This is the first trial to test the efficacy of oral tolerance induction in PBC. However, the data, which limited in scope, did not demonstrate efficacy and further highlights the difficulties in showing continuing evidence of tolerance induction in autoimmunity.

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