Overcoming Trypanosoma cruzi persistence with a mechanistically distinct drug combination

Infections with the protozoan parasite Trypanosoma cruzi are widespread in the Americas and can lead to severe cardiac and/or gastrointestinal pathology. Current treatments are limited to monotherapies characterised by prolonged dosing regimens, disputed efficacy and toxic side-effects. Sterile cure is often confounded by persistence of a small sub-population of parasites that display increased drug tolerance. Here, we demonstrate that short duration co-administration of well-tolerated sub-efficacious oral doses of the parasite-selective proteasome inhibitor GNF6702 and the pro-drug benznidazole produce parasitological cure in an experimental model of chronic Chagas disease.

Authors

Institutions

Publication Details

Journal
npj Antimicrobials and Resistance
Published
2026-04-30
DOI
https://doi.org/10.1038/s44259-026-00205-8
Primary Topic
Trypanosoma species research and implications
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Overcoming Trypanosoma cruzi persistence with a mechanistically distinct drug combination

Fanny Escudié, Amanda Fortes Francisco, Eric Chatelain, John M Kelly et al.
npj Antimicrobials and Resistance
Trypanosoma species research and implications
article

Overcoming Trypanosoma cruzi persistence with a mechanistically distinct drug combination

Fanny Escudié, Amanda Fortes Francisco, Eric Chatelain, John M Kelly, Francisco Olmo
article en

Abstract

Infections with the protozoan parasite Trypanosoma cruzi are widespread in the Americas and can lead to severe cardiac and/or gastrointestinal pathology. Current treatments are limited to monotherapies characterised by prolonged dosing regimens, disputed efficacy and toxic side-effects. Sterile cure is often confounded by persistence of a small sub-population of parasites that display increased drug tolerance. Here, we demonstrate that short duration co-administration of well-tolerated sub-efficacious oral doses of the parasite-selective proteasome inhibitor GNF6702 and the pro-drug benznidazole produce parasitological cure in an experimental model of chronic Chagas disease.

npj Antimicrobials and ResistanceVol. 4(1)
Drugs for Neglected Diseases Initiative (CH), Universidad de Granada (ES), London School of Hygiene & Tropical Medicine (GB)
Fundación Ramón Areces, Universidad de Granada, Drugs for Neglected Diseases initiative, Medical Research Council
Good health and well-being
Openalex Percentile: Top 15%
Trypanosoma species research and implications
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Overcoming Trypanosoma cruzi persistence with a mechanistically distinct drug combination — Fanny Escudié, Amanda Fortes Francisco, et al. · npj Antimicrobials and Resistance (2026) | TGRS Research Map | TGRS