dc.contributor.authorLee, Wenn-Chyau
dc.contributor.authorMalleret, Benoit
dc.contributor.authorLau, Yee-Ling
dc.contributor.authorMauduit, Marjorie
dc.contributor.authorFong, Mun-Yik
dc.contributor.authorCho, Jee Sun
dc.contributor.authorSuwanarusk, Rossarin
dc.contributor.authorZhang, Rou
dc.contributor.authorAlbrecht, Letusa
dc.contributor.authorCosta, Fabio T. M.
dc.contributor.authorPreiser, Peter
dc.contributor.authorMcGready, Rose
dc.contributor.authorRenia, Laurent
dc.contributor.authorNosten, Francois
dc.contributor.authorRussell, Bruce
dc.identifier.citationLee, W.-C., Malleret, B., Lau, Y.-L., Mauduit, M., Fong, M.-Y., Cho, J. S., et al. (2014). Glycophorin C (CD236R) mediates vivax malaria parasite rosetting to normocytes. Blood, 123(18), e100-e109.en_US
dc.description.abstractRosetting phenomenon has been linked to malaria pathogenesis. While rosetting occurs in all causes of human malaria, most data on this subject has been derived from Plasmodium falciparum. Here we investigate the function and factors affecting rosette formation in Plasmodium vivax. To achieve this, we utilised a range of novel ex vivo protocols to study fresh and cryopreserved P. vivax (n=135) and P. falciparum (n=77) isolates from Thailand. Rosetting is more common in vivax than falciparum malaria, both in terms of incidence in patient samples and percentage of infected erythrocytes forming rosettes. Rosetting to P. vivax asexual and sexual stages was evident 20 hrs post reticulocyte invasion, reaching a plateau after 30 hrs. Host ABO blood group, reticulocyte count and parasitemia were not correlated with P. vivax rosetting. Importantly, mature erythrocytes (normocytes) rather than reticulocytes preferentially form rosetting complexes, indicating this process is unlikely to directly facilitate merozoite invasion. While antibodies against host erythrocyte receptors CD235a and CD35 had no effect; Fab against the BRIC 4 region of CD236R significantly inhibited rosette formation. Rosetting assays using CD236R knock down normocytes derived from hematopoietic stem cells, further supports the role of Glycophorin C as a receptor in P. vivax rosette formation.en_US
dc.description.sponsorshipASTAR (Agency for Sci., Tech. and Research, S’pore)
dc.rights© 2014 American Society of Hematology.en_US
dc.subjectDRNTU::Science::Biological sciences
dc.titleGlycophorin C (CD236R) mediates vivax malaria parasite rosetting to normocytesen_US
dc.typeJournal Article
dc.contributor.schoolSchool of Biological Sciencesen_US

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