Emerging Agents for the treatment of Chagas disease: what is in the preclinical and clinical development pipeline?

ntroduction: Chagas disease treatment relies on the lengthy administration of benznidazole and/or nifurtimox, which have frequent toxicity associated. The disease, caused by the parasite Trypanosoma cruzi, is mostly diagnosed at its chronic phase when life-threatening symptomatology manifest in appr...

Descripción completa

Detalles Bibliográficos
Autores: Martinez-Peinado, Nieves, Cortes Serra, Núria, Losada Galván, Irene, Alonso Vega, Cristina, Urbina, Julio A., Rodríguez, Ana, VandeBerg, John L., Pinazo, Maria-Jesus, Gascón i Brustenga, Joaquim, Alonso Padilla, Julio
Tipo de recurso: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2020
País:España
Institución:Universidad de Barcelona
Repositorio:Dipòsit Digital de la UB
OAI Identifier:oai:diposit.ub.edu:2445/211921
Acceso en línea:https://hdl.handle.net/2445/211921
Access Level:acceso abierto
Palabra clave:Malaltia de Chagas
Malalties parasitàries
Chagas' disease
Parasitic diseases
Descripción
Sumario:ntroduction: Chagas disease treatment relies on the lengthy administration of benznidazole and/or nifurtimox, which have frequent toxicity associated. The disease, caused by the parasite Trypanosoma cruzi, is mostly diagnosed at its chronic phase when life-threatening symptomatology manifest in approximately 30% of those infected. Considering that both available drugs have variable efficacy by then, and there are over 6 million people infected, there is a pressing need to find safer, more efficacious drugs. Areas covered: We provide an updated view of the path to achieve the aforementioned goal. From state-of-the-art in vitro and in vivo assays based on genetically engineered parasites that have allowed high throughput screenings of large chemical collections, to the unfulfilled requirement of having treatment-response biomarkers for the clinical evaluation of drugs. In between, we describe the most promising pre-clinical hits and the landscape of clinical trials with new drugs or new regimens of existing ones. Moreover, the use of monkey models to reduce the pre-clinical to clinical attrition rate is discussed. Expert opinion: In addition to the necessary research on new drugs and much awaited biomarkers of treatment efficacy, a key step will be to generalize access to diagnosis and treatment and maximize efforts to impede transmission.