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Identification of Key Determinants of Cerebral Malaria Development and Inhibition Pathways

Cerebral malaria (CM), coma caused by Plasmodium falciparum-infected red blood cells (iRBCs), is the deadliest complication of malaria. The mechanisms that lead to CM development are incompletely understood. Here we report on the identification of activation and inhibition pathways leading to mouse...

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Autores principales: Cha, Sung-Jae, Yu, Xiang, Gregory, Brian D., Lee, Yong Seok, Ishino, Tomoko, Opoka, Robert O., John, Chandy C., Jacobs-Lorena, Marcelo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8787489/
https://www.ncbi.nlm.nih.gov/pubmed/35073748
http://dx.doi.org/10.1128/mbio.03708-21
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author Cha, Sung-Jae
Yu, Xiang
Gregory, Brian D.
Lee, Yong Seok
Ishino, Tomoko
Opoka, Robert O.
John, Chandy C.
Jacobs-Lorena, Marcelo
author_facet Cha, Sung-Jae
Yu, Xiang
Gregory, Brian D.
Lee, Yong Seok
Ishino, Tomoko
Opoka, Robert O.
John, Chandy C.
Jacobs-Lorena, Marcelo
author_sort Cha, Sung-Jae
collection PubMed
description Cerebral malaria (CM), coma caused by Plasmodium falciparum-infected red blood cells (iRBCs), is the deadliest complication of malaria. The mechanisms that lead to CM development are incompletely understood. Here we report on the identification of activation and inhibition pathways leading to mouse CM with supporting evidence from the analysis of human specimens. We find that CM suppression can be induced by vascular injury when sporozoites exit the circulation to infect the liver and that CM suppression is mediated by the release of soluble factors into the circulation. Among these factors is insulin like growth factor 1 (IGF1), administration of which inhibits CM development in mice.
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spelling pubmed-87874892022-02-07 Identification of Key Determinants of Cerebral Malaria Development and Inhibition Pathways Cha, Sung-Jae Yu, Xiang Gregory, Brian D. Lee, Yong Seok Ishino, Tomoko Opoka, Robert O. John, Chandy C. Jacobs-Lorena, Marcelo mBio Research Article Cerebral malaria (CM), coma caused by Plasmodium falciparum-infected red blood cells (iRBCs), is the deadliest complication of malaria. The mechanisms that lead to CM development are incompletely understood. Here we report on the identification of activation and inhibition pathways leading to mouse CM with supporting evidence from the analysis of human specimens. We find that CM suppression can be induced by vascular injury when sporozoites exit the circulation to infect the liver and that CM suppression is mediated by the release of soluble factors into the circulation. Among these factors is insulin like growth factor 1 (IGF1), administration of which inhibits CM development in mice. American Society for Microbiology 2022-01-25 /pmc/articles/PMC8787489/ /pubmed/35073748 http://dx.doi.org/10.1128/mbio.03708-21 Text en Copyright © 2022 Cha et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Cha, Sung-Jae
Yu, Xiang
Gregory, Brian D.
Lee, Yong Seok
Ishino, Tomoko
Opoka, Robert O.
John, Chandy C.
Jacobs-Lorena, Marcelo
Identification of Key Determinants of Cerebral Malaria Development and Inhibition Pathways
title Identification of Key Determinants of Cerebral Malaria Development and Inhibition Pathways
title_full Identification of Key Determinants of Cerebral Malaria Development and Inhibition Pathways
title_fullStr Identification of Key Determinants of Cerebral Malaria Development and Inhibition Pathways
title_full_unstemmed Identification of Key Determinants of Cerebral Malaria Development and Inhibition Pathways
title_short Identification of Key Determinants of Cerebral Malaria Development and Inhibition Pathways
title_sort identification of key determinants of cerebral malaria development and inhibition pathways
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8787489/
https://www.ncbi.nlm.nih.gov/pubmed/35073748
http://dx.doi.org/10.1128/mbio.03708-21
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