| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 3393814 | Acta Tropica | 2014 | 7 Pages |
•Bnz prevents the parasite induced tissue damage in ex vivo infected human placenta.•Nfx is toxic per se.•Bnz and Nfx do not impair parasite invasion into human placenta.
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.
Graphical abstractBnz prevents the parasite induced tissue damage in ex vivo infected placenta compared to Nfx, which is toxic per se. However, these drugs do not impair parasite invasion into the tissue. Arrows show parasite antigen in the placental tissue.Figure optionsDownload full-size imageDownload as PowerPoint slide
