Nilius R, Schentke U, Otto L, Teichmann W, Zipprich B, Schmidt W, Brügmann E, Busse H J
Hepatogastroenterology. 1983 Jun;30(3):90-2.
The effectiveness of levamisole in the immunmodulatory treatment of chronic hepatitis was assessed in a multicentric double blind trial. Twenty patients received in the first week 50 mg, in the second 100 mg and thereafter 150 mg, levamisole on two days every week for 6 months, 20 others received a placebo. Five patients dropped out (non-compliance 1, pregnancy 1, adverse effects 3). The diagnoses were confirmed by clinical, biochemical immunological and histological data. After 6 months 26 subjects allowed us to take a control liver biopsy. The results showed that the rate of improved, unchanged and impaired cases was not significantly different in the levamisole and placebo groups. No correlation was found between etiology, activity or histological type of chronic hepatitis, skin test reactivity (DNCB, PPD, Streptokinase) and therapeutic effect, respectively. Clinical improvement was not associated with the elimination of HBs antigen. In general levamisole was well tolerated, but we saw one case of severe agranulocytosis.
在一项多中心双盲试验中评估了左旋咪唑对慢性肝炎免疫调节治疗的有效性。20名患者在第一周接受50毫克,第二周接受100毫克,此后每周两次,每次150毫克左旋咪唑,持续6个月,另外20名患者接受安慰剂。5名患者退出(不依从1例,妊娠1例,不良反应3例)。通过临床、生化、免疫学和组织学数据确诊。6个月后,26名受试者接受了对照肝活检。结果显示,左旋咪唑组和安慰剂组中病情改善、无变化和恶化的病例比例无显著差异。慢性肝炎的病因、活动度或组织学类型、皮肤试验反应性(二硝基氯苯、结核菌素纯蛋白衍生物、链激酶)与治疗效果之间均未发现相关性。临床改善与乙肝表面抗原的清除无关。总体而言,左旋咪唑耐受性良好,但我们观察到1例严重粒细胞缺乏症。