Short report: Childhood coinfections with Plasmodium falciparum and Schistosoma mansoni result in lower percentages of activated T cells and T regulatory memory cells than schistosomiasis only

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dc.contributor.author Ng'ang'a, Zipporah W.
dc.contributor.author Muok, Erick M. O.
dc.contributor.author Colley, Daniel G.
dc.contributor.author Karanja, Diana M. S.
dc.contributor.author Secor, W. Evan
dc.contributor.author Gicheru, Michael M.
dc.contributor.author Carter, Jennifer M.
dc.contributor.author Black, Carla L.
dc.contributor.author Mwinzi, Pauline N. M.
dc.date.accessioned 2014-12-03T11:50:21Z
dc.date.available 2014-12-03T11:50:21Z
dc.date.issued 2009
dc.identifier.citation Am J Trop Med Hyg 2009 Mar;80(3):475-8 en_US
dc.identifier.uri http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2821587/
dc.identifier.uri http://hdl.handle.net/123456789/316
dc.description.abstract Flow cytometric analyses were performed to evaluate HLA-DR+ activated T lymphocytes (Tact; CD3+/CD4+/CD25medium) and T regulatory cells (Treg; CD3+/CD4+/CD25high) in the circulation of children 8–10 years of age living in an area endemic for both Plasmodium falciparum and Schistosoma mansoni in western Kenya. Those children with only S. mansoni had a higher mean percentage of HLA-DR+ Tact than those who were co-infected with these two intravascular parasites. The proportion of circulating Treg was comparable in children with only schistosomiasis and both schistosomiasis and malaria. However, the mean level of memory Treg (Treg expressing CD45RO+) in those with dual infections was lower than in children with schistosomiasis alone. These imbalances in Tact and Treg memory subsets in children infected with both schistosomiasis and malaria may be related to the differential morbidity or course of infection attributed to coinfections with these parasites. en_US
dc.language.iso en en_US
dc.publisher American Society of Tropical Medicine and Hygiene
dc.title Short report: Childhood coinfections with Plasmodium falciparum and Schistosoma mansoni result in lower percentages of activated T cells and T regulatory memory cells than schistosomiasis only en_US
dc.type Article en_US


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