Association between Fcγ receptor IIA, IIIA and IIIB genetic polymorphisms and susceptibility to severe malaria anemia in children in western Kenya
dc.contributor.author | Munde, Elly O | |
dc.contributor.author | Okeyo, Winnie A | |
dc.contributor.author | Raballah, Evans | |
dc.contributor.author | Anyona, Samuel B | |
dc.contributor.author | Were, Tom | |
dc.contributor.author | Ong’echa, John M | |
dc.contributor.author | Perkins, Douglas J | |
dc.contributor.author | Ouma, Collins | |
dc.date.accessioned | 2018-01-19T13:31:12Z | |
dc.date.available | 2018-01-19T13:31:12Z | |
dc.date.issued | 2017-04-20 | |
dc.identifier.uri | https://repository.maseno.ac.ke/handle/123456789/154 | |
dc.description.abstract | Background Naturally-acquired immunity to Plasmodium falciparum malaria develops after several episodes of infection. Fc gamma receptors (FcγRs) bind to immunoglobulin G (IgG) antibodies and mediate phagocytosis of opsonized microbes, thereby, linking humoral and cellular immunity. FcγR polymorphisms influence binding affinity to IgGs and consequently, can influence clinical malaria outcomes. Specifically, variations in FcγRIIA-131Arg/His, FcγRIIIA-176F/V and FcγRIIIB-NA1/NA2 modulate immune responses through altered binding preferences to IgGs and immune complexes. Differential binding, in turn, changes ability of immune cells to respond to infection through production of inflammatory mediators during P. falciparum infection. Methods We determined the association between haplotypes of FcγRIIA-131Arg/His, FcγRIIIA-176F/V and FcγRIIIB-NA1/NA2 variants and severe … | en_US |
dc.publisher | BioMed Central | en_US |
dc.title | Association between Fcγ receptor IIA, IIIA and IIIB genetic polymorphisms and susceptibility to severe malaria anemia in children in western Kenya | en_US |
dc.type | Article | en_US |
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