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Evidence for in vitro and in vivo activity of the antimalarial pyronaridine against Schistosoma
BACKGROUND: Schistosomiasis is highly prevalent in Africa. Praziquantel is effective against adult schistosomes but leaves prepatent stages unaffected—which is a limit to patient management and elimination. Given the large-scale use of praziquantel, development of drug resistance by Schistosoma is f...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8263063/ https://www.ncbi.nlm.nih.gov/pubmed/34166393 http://dx.doi.org/10.1371/journal.pntd.0009511 |
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author | Koehne, Erik Zander, Nina Rodi, Miriam Held, Jana Hoffmann, Wolfgang Zoleko-Manego, Rella Ramharter, Michael Mombo-Ngoma, Ghyslain Kremsner, Peter G. Kreidenweiss, Andrea |
author_facet | Koehne, Erik Zander, Nina Rodi, Miriam Held, Jana Hoffmann, Wolfgang Zoleko-Manego, Rella Ramharter, Michael Mombo-Ngoma, Ghyslain Kremsner, Peter G. Kreidenweiss, Andrea |
author_sort | Koehne, Erik |
collection | PubMed |
description | BACKGROUND: Schistosomiasis is highly prevalent in Africa. Praziquantel is effective against adult schistosomes but leaves prepatent stages unaffected—which is a limit to patient management and elimination. Given the large-scale use of praziquantel, development of drug resistance by Schistosoma is feared. Antimalarials are promising drugs for alternative treatment strategies of Schistosoma infections. Development of drugs with activity against both malaria and schistosomiasis is particularly appealing as schistosome infections often occur concomitantly with malaria parasites in sub-Saharan Africa. Therefore, antiplasmodial compounds were progressively tested against Schistosoma in vitro, in mice, and in a clinical study. RESULTS: Amongst 16 drugs and 1 control tested, pyronaridine, methylene blue and 5 other antimalarials were highly active in vitro against larval stage schistosomula with a 50% inhibitory concentration below 10 μM. Both drugs were lethal to ex vivo adult worms tested at 30 μM with methylene blue also active at 10 μM. Pyronaridine treatment of mice infected with S. mansoni at the prepatent stage reduced worm burden by 82% and cured 7 out of 12 animals, however in mice adult stages remained viable. In contrast, methylene blue inhibited adult worms by 60% but cure was not achieved. In an observational pilot trial in Gabon in children, the antimalarial drug combination pyronaridine-artesunate (Pyramax) reduced S. haematobium egg excretion from 10/10 ml urine to 0/10 ml urine, and 3 out of 4 children were cured. CONCLUSION: Pyronaridine and methylene blue warrant further investigation as candidates for schistosomiasis treatment. Both compounds are approved for human use and evidence for their potential as antischistosomal compounds can be obtained directly from clinical testing. Particularly, pyronaridine-artesunate, already available as an antimalarial drug, calls for further clinical evaluation. TRIAL REGISTRATION: ClinicalTrials.gov Identifier NCT03201770. |
format | Online Article Text |
id | pubmed-8263063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-82630632021-07-19 Evidence for in vitro and in vivo activity of the antimalarial pyronaridine against Schistosoma Koehne, Erik Zander, Nina Rodi, Miriam Held, Jana Hoffmann, Wolfgang Zoleko-Manego, Rella Ramharter, Michael Mombo-Ngoma, Ghyslain Kremsner, Peter G. Kreidenweiss, Andrea PLoS Negl Trop Dis Research Article BACKGROUND: Schistosomiasis is highly prevalent in Africa. Praziquantel is effective against adult schistosomes but leaves prepatent stages unaffected—which is a limit to patient management and elimination. Given the large-scale use of praziquantel, development of drug resistance by Schistosoma is feared. Antimalarials are promising drugs for alternative treatment strategies of Schistosoma infections. Development of drugs with activity against both malaria and schistosomiasis is particularly appealing as schistosome infections often occur concomitantly with malaria parasites in sub-Saharan Africa. Therefore, antiplasmodial compounds were progressively tested against Schistosoma in vitro, in mice, and in a clinical study. RESULTS: Amongst 16 drugs and 1 control tested, pyronaridine, methylene blue and 5 other antimalarials were highly active in vitro against larval stage schistosomula with a 50% inhibitory concentration below 10 μM. Both drugs were lethal to ex vivo adult worms tested at 30 μM with methylene blue also active at 10 μM. Pyronaridine treatment of mice infected with S. mansoni at the prepatent stage reduced worm burden by 82% and cured 7 out of 12 animals, however in mice adult stages remained viable. In contrast, methylene blue inhibited adult worms by 60% but cure was not achieved. In an observational pilot trial in Gabon in children, the antimalarial drug combination pyronaridine-artesunate (Pyramax) reduced S. haematobium egg excretion from 10/10 ml urine to 0/10 ml urine, and 3 out of 4 children were cured. CONCLUSION: Pyronaridine and methylene blue warrant further investigation as candidates for schistosomiasis treatment. Both compounds are approved for human use and evidence for their potential as antischistosomal compounds can be obtained directly from clinical testing. Particularly, pyronaridine-artesunate, already available as an antimalarial drug, calls for further clinical evaluation. TRIAL REGISTRATION: ClinicalTrials.gov Identifier NCT03201770. Public Library of Science 2021-06-24 /pmc/articles/PMC8263063/ /pubmed/34166393 http://dx.doi.org/10.1371/journal.pntd.0009511 Text en © 2021 Koehne et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Koehne, Erik Zander, Nina Rodi, Miriam Held, Jana Hoffmann, Wolfgang Zoleko-Manego, Rella Ramharter, Michael Mombo-Ngoma, Ghyslain Kremsner, Peter G. Kreidenweiss, Andrea Evidence for in vitro and in vivo activity of the antimalarial pyronaridine against Schistosoma |
title | Evidence for in vitro and in vivo activity of the antimalarial pyronaridine against Schistosoma |
title_full | Evidence for in vitro and in vivo activity of the antimalarial pyronaridine against Schistosoma |
title_fullStr | Evidence for in vitro and in vivo activity of the antimalarial pyronaridine against Schistosoma |
title_full_unstemmed | Evidence for in vitro and in vivo activity of the antimalarial pyronaridine against Schistosoma |
title_short | Evidence for in vitro and in vivo activity of the antimalarial pyronaridine against Schistosoma |
title_sort | evidence for in vitro and in vivo activity of the antimalarial pyronaridine against schistosoma |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8263063/ https://www.ncbi.nlm.nih.gov/pubmed/34166393 http://dx.doi.org/10.1371/journal.pntd.0009511 |
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