Gabaldón-Figueira Juan Carlos, Martinez-Peinado Nieves, Escabia Elisa, Ros-Lucas Albert, Chatelain Eric, Scandale Ivan, Gascon Joaquim, Pinazo María-Jesús, Alonso-Padilla Julio
Barcelona Institute for Global Health (ISGlobal), Hospital Clínic-University of Barcelona, Barcelona, Spain.
CIBER de Enfermedades Infecciosas, Instituto de Salud Carlos III (CIBERINFEC, ISCIII), Madrid, Spain.
Res Rep Trop Med. 2023 Jun 14;14:1-19. doi: 10.2147/RRTM.S415273. eCollection 2023.
Chagas disease is the most important protozoan infection in the Americas, and constitutes a significant public health concern throughout the world. Development of new medications against its etiologic agent, , has been traditionally slow and difficult, lagging in comparison with diseases caused by other kinetoplastid parasites. Among the factors that explain this are the incompletely understood mechanisms of pathogenesis of infection and its complex set of interactions with the host in the chronic stage of the disease. These demand the performance of a variety of in vitro and in vivo assays as part of any drug development effort. In this review, we discuss recent breakthroughs in the understanding of the parasite's life cycle and their implications in the search for new chemotherapeutics. For this, we present a framework to guide drug discovery efforts against Chagas disease, considering state-of-the-art preclinical models and recently developed tools for the identification and validation of molecular targets.
恰加斯病是美洲最重要的原生动物感染疾病,也是全球重大的公共卫生问题。传统上,针对其病原体开发新药物进展缓慢且困难,与其他动基体寄生虫引起的疾病相比滞后。造成这种情况的因素包括对感染发病机制的理解不完整,以及在疾病慢性阶段病原体与宿主之间复杂的相互作用。这些因素要求在任何药物研发工作中都要进行各种体外和体内试验。在本综述中,我们讨论了在理解寄生虫生命周期方面的最新突破及其对寻找新化疗药物的影响。为此,我们提出了一个指导恰加斯病药物研发工作的框架,考虑了最先进的临床前模型以及最近开发的用于分子靶点鉴定和验证的工具。