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KAF156 Is an Antimalarial Clinical Candidate with Potential for Use in Prophylaxis, Treatment, and Prevention of Disease Transmission
Renewed global efforts toward malaria eradication have highlighted the need for novel antimalarial agents with activity against multiple stages of the parasite life cycle. We have previously reported the discovery of a novel class of antimalarial compounds in the imidazolopiperazine series that have...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4135840/ https://www.ncbi.nlm.nih.gov/pubmed/24913172 http://dx.doi.org/10.1128/AAC.02727-13 |
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author | Kuhen, Kelli L. Chatterjee, Arnab K. Rottmann, Matthias Gagaring, Kerstin Borboa, Rachel Buenviaje, Jennifer Chen, Zhong Francek, Carolyn Wu, Tao Nagle, Advait Barnes, S. Whitney Plouffe, David Lee, Marcus C. S. Fidock, David A. Graumans, Wouter van de Vegte-Bolmer, Marga van Gemert, Geert J. Wirjanata, Grennady Sebayang, Boni Marfurt, Jutta Russell, Bruce Suwanarusk, Rossarin Price, Ric N. Nosten, Francois Tungtaeng, Anchalee Gettayacamin, Montip Sattabongkot, Jetsumon Taylor, Jennifer Walker, John R. Tully, David Patra, Kailash P. Flannery, Erika L. Vinetz, Joseph M. Renia, Laurent Sauerwein, Robert W. Winzeler, Elizabeth A. Glynne, Richard J. Diagana, Thierry T. |
author_facet | Kuhen, Kelli L. Chatterjee, Arnab K. Rottmann, Matthias Gagaring, Kerstin Borboa, Rachel Buenviaje, Jennifer Chen, Zhong Francek, Carolyn Wu, Tao Nagle, Advait Barnes, S. Whitney Plouffe, David Lee, Marcus C. S. Fidock, David A. Graumans, Wouter van de Vegte-Bolmer, Marga van Gemert, Geert J. Wirjanata, Grennady Sebayang, Boni Marfurt, Jutta Russell, Bruce Suwanarusk, Rossarin Price, Ric N. Nosten, Francois Tungtaeng, Anchalee Gettayacamin, Montip Sattabongkot, Jetsumon Taylor, Jennifer Walker, John R. Tully, David Patra, Kailash P. Flannery, Erika L. Vinetz, Joseph M. Renia, Laurent Sauerwein, Robert W. Winzeler, Elizabeth A. Glynne, Richard J. Diagana, Thierry T. |
author_sort | Kuhen, Kelli L. |
collection | PubMed |
description | Renewed global efforts toward malaria eradication have highlighted the need for novel antimalarial agents with activity against multiple stages of the parasite life cycle. We have previously reported the discovery of a novel class of antimalarial compounds in the imidazolopiperazine series that have activity in the prevention and treatment of blood stage infection in a mouse model of malaria. Consistent with the previously reported activity profile of this series, the clinical candidate KAF156 shows blood schizonticidal activity with 50% inhibitory concentrations of 6 to 17.4 nM against P. falciparum drug-sensitive and drug-resistant strains, as well as potent therapeutic activity in a mouse models of malaria with 50, 90, and 99% effective doses of 0.6, 0.9, and 1.4 mg/kg, respectively. When administered prophylactically in a sporozoite challenge mouse model, KAF156 is completely protective as a single oral dose of 10 mg/kg. Finally, KAF156 displays potent Plasmodium transmission blocking activities both in vitro and in vivo. Collectively, our data suggest that KAF156, currently under evaluation in clinical trials, has the potential to treat, prevent, and block the transmission of malaria. |
format | Online Article Text |
id | pubmed-4135840 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-41358402014-09-24 KAF156 Is an Antimalarial Clinical Candidate with Potential for Use in Prophylaxis, Treatment, and Prevention of Disease Transmission Kuhen, Kelli L. Chatterjee, Arnab K. Rottmann, Matthias Gagaring, Kerstin Borboa, Rachel Buenviaje, Jennifer Chen, Zhong Francek, Carolyn Wu, Tao Nagle, Advait Barnes, S. Whitney Plouffe, David Lee, Marcus C. S. Fidock, David A. Graumans, Wouter van de Vegte-Bolmer, Marga van Gemert, Geert J. Wirjanata, Grennady Sebayang, Boni Marfurt, Jutta Russell, Bruce Suwanarusk, Rossarin Price, Ric N. Nosten, Francois Tungtaeng, Anchalee Gettayacamin, Montip Sattabongkot, Jetsumon Taylor, Jennifer Walker, John R. Tully, David Patra, Kailash P. Flannery, Erika L. Vinetz, Joseph M. Renia, Laurent Sauerwein, Robert W. Winzeler, Elizabeth A. Glynne, Richard J. Diagana, Thierry T. Antimicrob Agents Chemother Experimental Therapeutics Renewed global efforts toward malaria eradication have highlighted the need for novel antimalarial agents with activity against multiple stages of the parasite life cycle. We have previously reported the discovery of a novel class of antimalarial compounds in the imidazolopiperazine series that have activity in the prevention and treatment of blood stage infection in a mouse model of malaria. Consistent with the previously reported activity profile of this series, the clinical candidate KAF156 shows blood schizonticidal activity with 50% inhibitory concentrations of 6 to 17.4 nM against P. falciparum drug-sensitive and drug-resistant strains, as well as potent therapeutic activity in a mouse models of malaria with 50, 90, and 99% effective doses of 0.6, 0.9, and 1.4 mg/kg, respectively. When administered prophylactically in a sporozoite challenge mouse model, KAF156 is completely protective as a single oral dose of 10 mg/kg. Finally, KAF156 displays potent Plasmodium transmission blocking activities both in vitro and in vivo. Collectively, our data suggest that KAF156, currently under evaluation in clinical trials, has the potential to treat, prevent, and block the transmission of malaria. American Society for Microbiology 2014-09 /pmc/articles/PMC4135840/ /pubmed/24913172 http://dx.doi.org/10.1128/AAC.02727-13 Text en Copyright © 2014 Kuhen et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 3.0 Unported license (http://creativecommons.org/licenses/by/3.0/) . |
spellingShingle | Experimental Therapeutics Kuhen, Kelli L. Chatterjee, Arnab K. Rottmann, Matthias Gagaring, Kerstin Borboa, Rachel Buenviaje, Jennifer Chen, Zhong Francek, Carolyn Wu, Tao Nagle, Advait Barnes, S. Whitney Plouffe, David Lee, Marcus C. S. Fidock, David A. Graumans, Wouter van de Vegte-Bolmer, Marga van Gemert, Geert J. Wirjanata, Grennady Sebayang, Boni Marfurt, Jutta Russell, Bruce Suwanarusk, Rossarin Price, Ric N. Nosten, Francois Tungtaeng, Anchalee Gettayacamin, Montip Sattabongkot, Jetsumon Taylor, Jennifer Walker, John R. Tully, David Patra, Kailash P. Flannery, Erika L. Vinetz, Joseph M. Renia, Laurent Sauerwein, Robert W. Winzeler, Elizabeth A. Glynne, Richard J. Diagana, Thierry T. KAF156 Is an Antimalarial Clinical Candidate with Potential for Use in Prophylaxis, Treatment, and Prevention of Disease Transmission |
title | KAF156 Is an Antimalarial Clinical Candidate with Potential for Use in Prophylaxis, Treatment, and Prevention of Disease Transmission |
title_full | KAF156 Is an Antimalarial Clinical Candidate with Potential for Use in Prophylaxis, Treatment, and Prevention of Disease Transmission |
title_fullStr | KAF156 Is an Antimalarial Clinical Candidate with Potential for Use in Prophylaxis, Treatment, and Prevention of Disease Transmission |
title_full_unstemmed | KAF156 Is an Antimalarial Clinical Candidate with Potential for Use in Prophylaxis, Treatment, and Prevention of Disease Transmission |
title_short | KAF156 Is an Antimalarial Clinical Candidate with Potential for Use in Prophylaxis, Treatment, and Prevention of Disease Transmission |
title_sort | kaf156 is an antimalarial clinical candidate with potential for use in prophylaxis, treatment, and prevention of disease transmission |
topic | Experimental Therapeutics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4135840/ https://www.ncbi.nlm.nih.gov/pubmed/24913172 http://dx.doi.org/10.1128/AAC.02727-13 |
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