Greater Endothelial Activation, Weibel-Palade body Release and Host Inflammatory Response to Plasmodium vivax, Compared with Plasmodium falciparum

A Prospective Study in Papua,Indonesia

Tsin Yeo, Daniel Lampah, Emiliana Tjitra, Kim Piera, Retno Gitawati, Enny Kenangalem, Ric Price, Nicholas Anstey

    Research output: Contribution to journalArticleResearchpeer-review

    Abstract

    Pathogenic mechanisms underlying vivax malaria are poorly understood, with few studies comparing endothelial and inflammatory responses with falciparum malaria. In adults with uncomplicated vivax or falciparum malaria, we compared plasma measurements of endothelial Weibel-Palade body release (angiopoietin-2) and activation (ICAM-1, E-selectin), as well as selected cytokines. Despite a lower median parasite count, angiopoietin-2 concentrations were higher in patients with vivax malaria, compared with falciparum malaria. Per peripheral parasite, median plasma angiopoietin-2, ICAM-1, E-selectin, interleukin-6, and interleukin-10 concentrations were higher in patients with malaria due to Plasmodium vivax. P. vivax induces greater endothelial Weibel-Palade body release and activation and greater host inflammatory responses, compared with Plasmodium falciparum. � 2010 by the Infectious Diseases Society of America. All rights reserved.
    Original languageEnglish
    Pages (from-to)109-112
    Number of pages4
    JournalJournal of Infectious Diseases
    Volume202
    Issue number1
    DOIs
    Publication statusPublished - 1 Jul 2010

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    Weibel-Palade Bodies
    Angiopoietin-2
    Vivax Malaria
    Plasmodium vivax
    Indonesia
    Falciparum Malaria
    Plasmodium falciparum
    E-Selectin
    Prospective Studies
    Intercellular Adhesion Molecule-1
    Parasites
    Interleukin-10
    Malaria
    Interleukin-6
    Cytokines

    Cite this

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    title = "Greater Endothelial Activation, Weibel-Palade body Release and Host Inflammatory Response to Plasmodium vivax, Compared with Plasmodium falciparum: A Prospective Study in Papua,Indonesia",
    abstract = "Pathogenic mechanisms underlying vivax malaria are poorly understood, with few studies comparing endothelial and inflammatory responses with falciparum malaria. In adults with uncomplicated vivax or falciparum malaria, we compared plasma measurements of endothelial Weibel-Palade body release (angiopoietin-2) and activation (ICAM-1, E-selectin), as well as selected cytokines. Despite a lower median parasite count, angiopoietin-2 concentrations were higher in patients with vivax malaria, compared with falciparum malaria. Per peripheral parasite, median plasma angiopoietin-2, ICAM-1, E-selectin, interleukin-6, and interleukin-10 concentrations were higher in patients with malaria due to Plasmodium vivax. P. vivax induces greater endothelial Weibel-Palade body release and activation and greater host inflammatory responses, compared with Plasmodium falciparum. � 2010 by the Infectious Diseases Society of America. All rights reserved.",
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    author = "Tsin Yeo and Daniel Lampah and Emiliana Tjitra and Kim Piera and Retno Gitawati and Enny Kenangalem and Ric Price and Nicholas Anstey",
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    Greater Endothelial Activation, Weibel-Palade body Release and Host Inflammatory Response to Plasmodium vivax, Compared with Plasmodium falciparum : A Prospective Study in Papua,Indonesia. / Yeo, Tsin; Lampah, Daniel; Tjitra, Emiliana; Piera, Kim; Gitawati, Retno; Kenangalem, Enny; Price, Ric; Anstey, Nicholas.

    In: Journal of Infectious Diseases, Vol. 202, No. 1, 01.07.2010, p. 109-112.

    Research output: Contribution to journalArticleResearchpeer-review

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