Silent Information Regulator 2 from Trypanosoma cruzi Is a Potential Target to Infection Control

Luís Gaspar, Terry K. Smith, N. Moretti, S. Schenkman, A. Cordeiro-da-Silva
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Abstract

Human trypanosomiasis is a neglected tropical disease caused by protozoan parasites of the genus Trypanosoma . Trypanosoma brucei is responsible for sleeping sickness, also called African trypanosomiasis, while Trypanosoma cruzi causes Chagas disease, or American trypanosomiasis. Together, these diseases are responsible for significant mortality, mor-bidity and lost productivity in the endemic regions. There are no vaccines and treatments rely on drugs with limited efficacy, high cost, serious side effects and long administration periods. Since these diseases affect mostly the poor, there is no economic interest in the development of new drugs by pharmaceutical companies, and hopes for new treatments rely on public initiatives, public-private partnerships or philanthropic programs. The first step in the discovery of new drugs involves the identification of active molecules as starting points for further development, by either employing whole cells or by specific molecular target screenings. Research efforts undertaken by the authors ’ groups have focused on exploiting both strategies in the search for new molecules for trypanosomiasis drug discovery. In this chapter, we focus on Chagas disease and the recently uncovered potential of using sirtuins as targets for infection control. proliferation might be instrumental to mediate tissue integrity during aging.
克氏锥虫沉默信息调控因子2是控制感染的潜在靶点
人类锥虫病是由锥虫属原生动物寄生虫引起的一种被忽视的热带病。布鲁氏锥虫会导致昏睡病,也被称为非洲锥虫病,而克氏锥虫会导致恰加斯病,或美洲锥虫病。这些疾病共同造成流行区域的大量死亡率、发病率和生产力损失。目前没有疫苗,治疗依赖于疗效有限、费用高、副作用严重、给药期长的药物。由于这些疾病主要影响穷人,制药公司开发新药没有经济利益,新疗法的希望依赖于公共倡议、公私合作伙伴关系或慈善项目。发现新药的第一步包括识别活性分子,作为进一步开发的起点,要么利用整个细胞,要么通过特定的分子靶点筛选。作者小组所进行的研究工作集中在利用这两种策略来寻找用于发现锥虫病药物的新分子。在本章中,我们关注恰加斯病和最近发现的使用sirtuins作为感染控制靶点的潜力。细胞增生可能在衰老过程中介导组织完整性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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