Identification of Key Determinants of Cerebral Malaria Development and Inhibition Pathways

dc.contributor.authorCha, Sung-Jae
dc.contributor.authorYu, Xiang
dc.contributor.authorGregory, Brian D.
dc.contributor.authorLee, Yong Seok
dc.contributor.authorIshino, Tomoko
dc.contributor.authorOpoka, Robert O.
dc.contributor.authorJohn, Chandy C.
dc.contributor.authorJacobs-Lorena, Marcelo
dc.contributor.departmentPediatrics, School of Medicineen_US
dc.date.accessioned2023-05-15T10:51:24Z
dc.date.available2023-05-15T10:51:24Z
dc.date.issued2022
dc.description.abstractCerebral 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.en_US
dc.eprint.versionFinal published versionen_US
dc.identifier.citationCha SJ, Yu X, Gregory BD, et al. Identification of Key Determinants of Cerebral Malaria Development and Inhibition Pathways. mBio. 2022;13(1):e0370821. doi:10.1128/mbio.03708-21en_US
dc.identifier.urihttps://hdl.handle.net/1805/32954
dc.language.isoen_USen_US
dc.publisherAmerican Society for Microbiologyen_US
dc.relation.isversionof10.1128/mbio.03708-21en_US
dc.relation.journalmBioen_US
dc.rightsAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourcePMCen_US
dc.subjectIGF1en_US
dc.subjectBiomarkeren_US
dc.subjectCerebral malariaen_US
dc.subjectSporozoiteen_US
dc.subjectVascular injuryen_US
dc.titleIdentification of Key Determinants of Cerebral Malaria Development and Inhibition Pathwaysen_US
dc.typeArticleen_US
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