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Similarly efficacious anti-malarial drugs SJ733 and pyronaridine differ in their ability to remove circulating parasites in mice

BACKGROUND: Artemisinin-based combination therapy (ACT) has been a mainstay for malaria prevention and treatment. However, emergence of drug resistance has incentivised development of new drugs. Defining the kinetics with which circulating parasitized red blood cells (pRBC) are lost after drug treat...

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Autores principales: SheelaNair, Arya, Romanczuk, Aleksandra S., Aogo, Rosemary A., Haldar, Rohit Nemai, Lansink, Lianne I. M., Cromer, Deborah, Salinas, Yandira G., Guy, R. Kiplin, McCarthy, James S., Davenport, Miles P., Haque, Ashraful, Khoury, David S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8848794/
https://www.ncbi.nlm.nih.gov/pubmed/35172826
http://dx.doi.org/10.1186/s12936-022-04075-z
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author SheelaNair, Arya
Romanczuk, Aleksandra S.
Aogo, Rosemary A.
Haldar, Rohit Nemai
Lansink, Lianne I. M.
Cromer, Deborah
Salinas, Yandira G.
Guy, R. Kiplin
McCarthy, James S.
Davenport, Miles P.
Haque, Ashraful
Khoury, David S.
author_facet SheelaNair, Arya
Romanczuk, Aleksandra S.
Aogo, Rosemary A.
Haldar, Rohit Nemai
Lansink, Lianne I. M.
Cromer, Deborah
Salinas, Yandira G.
Guy, R. Kiplin
McCarthy, James S.
Davenport, Miles P.
Haque, Ashraful
Khoury, David S.
author_sort SheelaNair, Arya
collection PubMed
description BACKGROUND: Artemisinin-based combination therapy (ACT) has been a mainstay for malaria prevention and treatment. However, emergence of drug resistance has incentivised development of new drugs. Defining the kinetics with which circulating parasitized red blood cells (pRBC) are lost after drug treatment, referred to as the “parasite clearance curve”, has been critical for assessing drug efficacy; yet underlying mechanisms remain partly unresolved. The clearance curve may be shaped both by the rate at which drugs kill parasites, and the rate at which drug-affected parasites are removed from circulation. METHODS: In this context, two anti-malarials, SJ733, and an ACT partner drug, pyronaridine were compared against sodium artesunate in mice infected with Plasmodium berghei (strain ANKA). To measure each compound’s capacity for pRBC removal in vivo, flow cytometric monitoring of a single cohort of fluorescently-labelled pRBC was employed, and combined with ex vivo parasite culture to assess parasite maturation and replication. RESULTS: These three compounds were found to be similarly efficacious in controlling established infection by reducing overall parasitaemia. While sodium artesunate acted relatively consistently across the life-stages, single-dose SJ733 elicited a biphasic effect, triggering rapid, partly phagocyte-dependent removal of trophozoites and schizonts, followed by arrest of residual ring-stages. In contrast, pyronaridine abrogated maturation of younger parasites, with less pronounced effects on mature parasites, while modestly increasing pRBC removal. CONCLUSIONS: Anti-malarials SJ733 and pyronaridine, though similarly efficacious in reducing overall parasitaemia in mice, differed markedly in their capacity to arrest replication and remove pRBC from circulation. Thus, similar parasite clearance curves can result for anti-malarials with distinct capacities to inhibit, kill and clear parasites.
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spelling pubmed-88487942022-02-18 Similarly efficacious anti-malarial drugs SJ733 and pyronaridine differ in their ability to remove circulating parasites in mice SheelaNair, Arya Romanczuk, Aleksandra S. Aogo, Rosemary A. Haldar, Rohit Nemai Lansink, Lianne I. M. Cromer, Deborah Salinas, Yandira G. Guy, R. Kiplin McCarthy, James S. Davenport, Miles P. Haque, Ashraful Khoury, David S. Malar J Research BACKGROUND: Artemisinin-based combination therapy (ACT) has been a mainstay for malaria prevention and treatment. However, emergence of drug resistance has incentivised development of new drugs. Defining the kinetics with which circulating parasitized red blood cells (pRBC) are lost after drug treatment, referred to as the “parasite clearance curve”, has been critical for assessing drug efficacy; yet underlying mechanisms remain partly unresolved. The clearance curve may be shaped both by the rate at which drugs kill parasites, and the rate at which drug-affected parasites are removed from circulation. METHODS: In this context, two anti-malarials, SJ733, and an ACT partner drug, pyronaridine were compared against sodium artesunate in mice infected with Plasmodium berghei (strain ANKA). To measure each compound’s capacity for pRBC removal in vivo, flow cytometric monitoring of a single cohort of fluorescently-labelled pRBC was employed, and combined with ex vivo parasite culture to assess parasite maturation and replication. RESULTS: These three compounds were found to be similarly efficacious in controlling established infection by reducing overall parasitaemia. While sodium artesunate acted relatively consistently across the life-stages, single-dose SJ733 elicited a biphasic effect, triggering rapid, partly phagocyte-dependent removal of trophozoites and schizonts, followed by arrest of residual ring-stages. In contrast, pyronaridine abrogated maturation of younger parasites, with less pronounced effects on mature parasites, while modestly increasing pRBC removal. CONCLUSIONS: Anti-malarials SJ733 and pyronaridine, though similarly efficacious in reducing overall parasitaemia in mice, differed markedly in their capacity to arrest replication and remove pRBC from circulation. Thus, similar parasite clearance curves can result for anti-malarials with distinct capacities to inhibit, kill and clear parasites. BioMed Central 2022-02-16 /pmc/articles/PMC8848794/ /pubmed/35172826 http://dx.doi.org/10.1186/s12936-022-04075-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
SheelaNair, Arya
Romanczuk, Aleksandra S.
Aogo, Rosemary A.
Haldar, Rohit Nemai
Lansink, Lianne I. M.
Cromer, Deborah
Salinas, Yandira G.
Guy, R. Kiplin
McCarthy, James S.
Davenport, Miles P.
Haque, Ashraful
Khoury, David S.
Similarly efficacious anti-malarial drugs SJ733 and pyronaridine differ in their ability to remove circulating parasites in mice
title Similarly efficacious anti-malarial drugs SJ733 and pyronaridine differ in their ability to remove circulating parasites in mice
title_full Similarly efficacious anti-malarial drugs SJ733 and pyronaridine differ in their ability to remove circulating parasites in mice
title_fullStr Similarly efficacious anti-malarial drugs SJ733 and pyronaridine differ in their ability to remove circulating parasites in mice
title_full_unstemmed Similarly efficacious anti-malarial drugs SJ733 and pyronaridine differ in their ability to remove circulating parasites in mice
title_short Similarly efficacious anti-malarial drugs SJ733 and pyronaridine differ in their ability to remove circulating parasites in mice
title_sort similarly efficacious anti-malarial drugs sj733 and pyronaridine differ in their ability to remove circulating parasites in mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8848794/
https://www.ncbi.nlm.nih.gov/pubmed/35172826
http://dx.doi.org/10.1186/s12936-022-04075-z
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