Toxic and therapeutic effects of Nifurtimox and Benznidazol on Trypanosoma cruzi ex vivo infection of human placental chorionic villi explants
Author
dc.contributor.author
Rojo, Gemma
Author
dc.contributor.author
Castillo, Christian
es_CL
Author
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Duaso, Juan
es_CL
Author
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Liempi, Ana
es_CL
Author
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Droguett Ossa, Daniel
es_CL
Author
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Galanti Garrone, Norbel
es_CL
Author
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Maya Arango, Juan
es_CL
Author
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López Muñoz, Rodrigo
es_CL
Author
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Kemmerling Weis, Ulrike
es_CL
Admission date
dc.date.accessioned
2015-01-07T19:53:20Z
Available date
dc.date.available
2015-01-07T19:53:20Z
Publication date
dc.date.issued
2014
Cita de ítem
dc.identifier.citation
Acta Tropica 132 (2014) 112–118
en_US
Identifier
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dx.doi.org/10.1016/j.actatropica.2014.01.002
Identifier
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https://repositorio.uchile.cl/handle/2250/129607
General note
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Artículo de publicación ISI
en_US
Abstract
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Nifurtimox (Nfx) and Benznidazole (Bnz) are the only available drugs in use for the treatment of Chagas
disease. These drugs are recommended but not fully validated in evidence-based medicine and reports
about the differential toxicity of both drugs are controversial. Here, we evaluated the toxic and therapeutic
effects of Nfx and Bnz on human placental chorionic villi explants (HPCVE) during ex vivo infection
of Trypanosoma cruzi, performing histopathological, histochemical, immunohistochemical as well as
immunofluorescence analysis of the tissue. Additionally, we determined the effect of both drugs on parasite
load by real time PCR. Bnz prevents the parasite induced tissue damage in ex vivo infected HPCVE
compared to Nfx, which is toxic per se. The presence of T. cruzi antigens and DNA in infected explants
suggests that these drugs do not impair parasite invasion into the HPCVE. Additionally, our results confirm
reports suggesting that Bnz is less toxic than Nfx and support the need for the development of more
effective and better-tolerated drugs.
en_US
Patrocinador
dc.description.sponsorship
This study was supported by grants 1120230 (to UK), 1130113
(to NG), 1130189 (to JM), 11110182 (to RL) from FONDECYT, Chile
and by grant CONICYT-PBCT Anillo ACT 112, Chile.