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恰加斯病化疗的现状与新策略:建议。

Present situation and new strategies for Chagas disease chemotherapy: a proposal.

机构信息

Laboratório de Doenças Parasitárias, Instituto Oswaldo Cruz, Fiocruz, Rio de Janeiro 21040-360, Brasil.

出版信息

Mem Inst Oswaldo Cruz. 2009 Jul;104(4):549-54. doi: 10.1590/s0074-02762009000400002.

Abstract

Treatments for Chagas disease have been administered since the first attempts by Mayer & Rocha Lima (1912, 1914) and up to the drugs currently in use (nifurtimox and benznidazole), along with potential drugs such as allopurinol and first, second and third-generation antifungal agents (imidazoles and triazoles), in separate form. Several diseases such as tuberculosis, leprosy and AIDS only came under control after they were treated with associations of drugs with different mechanisms of action. This not only boosts the action of the different compounds, but also may avoid the development of parasite resistance .To this end, over the short term, we propose experimental studies on laboratory animals and clinical trials with the following associations: (i) nifurtimox (8 mg/kg/day) + benznidazole (5 mg/kg/day) x 60 consecutive days; (ii) nifurtimox (8 mg/kg/day) or benznidazole (5 mg/kg/day) + allopurinol (8-10 mg/kg/day) x 60 days and (iii) nifurtimox (8 mg/kg/day) or benznidazole (5 mg/kg/day) + ketoconazole, fluconazole or itraconazole (5-6 mg/kg/day) x 60 consecutive days. The doses of the drugs and the treatment schedules for the clinical trials must be adapted according to the side effects. From these, other double or triple associations could be made, using drugs with different mechanisms of action. This proposal does not exclude investigations on new drugs over the median and long terms, targeting other aspects of the metabolism of Trypanosoma cruzi. Until such time as the ideal drug for specific treatment of Chagas disease might be discovered, we need to develop new strategies for achieving greater efficacy with the old drugs in associations and to develop rational experimentation with new drugs.

摘要

自 Mayer 和 Rocha Lima(1912 年,1914 年)首次尝试以来,一直有治疗查加斯病的方法,直到目前使用的药物(硝呋替莫和苯并咪唑),以及潜在的药物,如别嘌醇和第一代、第二代和第三代抗真菌药(咪唑和三唑),都是单独使用。结核病、麻风病和艾滋病等几种疾病在使用不同作用机制的药物联合治疗后才得到控制。这不仅增强了不同化合物的作用,而且还可以避免寄生虫耐药性的发展。为此,在短期内,我们建议在实验室动物上进行实验研究,并进行以下联合治疗的临床试验:(i)硝呋替莫(8mg/kg/天)+苯并咪唑(5mg/kg/天)x60 天连续治疗;(ii)硝呋替莫(8mg/kg/天)或苯并咪唑(5mg/kg/天)+别嘌醇(8-10mg/kg/天)x60 天;(iii)硝呋替莫(8mg/kg/天)或苯并咪唑(5mg/kg/天)+酮康唑、氟康唑或伊曲康唑(5-6mg/kg/天)x60 天连续治疗。药物剂量和临床试验治疗方案必须根据副作用进行调整。从这些方案中,可以使用不同作用机制的药物,进行其他双重或三重联合治疗。该方案并不排除在中长期内对新药进行研究,针对克氏锥虫代谢的其他方面。在找到治疗恰加斯病的理想药物之前,我们需要开发新的策略,以提高现有药物联合治疗的疗效,并进行新药物的合理实验。

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