%0 Journal Article
%T Suppression of circulating IgD+CD27+ memory B cells in infants living in a malaria-endemic region of Kenya
%A Amolo S Asito
%A Erwan Piriou
%A Walter GZO Jura
%A Collins Ouma
%A Peter S Odada
%A Sidney Ogola
%A Nancy Fiore
%A Rosemary Rochford
%J Malaria Journal
%D 2011
%I BioMed Central
%R 10.1186/1475-2875-10-362
%X To evaluate the impact of exposure to P. falciparum on B cell development in infants, flow cytometry was used to analyse the distribution and phenotypic characteristic of B cell subsets in infant cohorts prospectively followed at 12, 18 and 24 months from two geographically proximate regions in western Kenya with divergent malaria exposure i.e. Kisumu (malaria-endemic, n = 24) and Nandi (unstable malaria transmission, n = 21).There was significantly higher frequency and absolute cell numbers of CD19+ B cells in Kisumu relative to Nandi at 12(p = 0.0440), 18(p = 0.0210) and 24 months (p = 0.0493). No differences were observed between the infants from the two sites in frequencies of na£żve B cells (IgD+CD27-) or classical memory B cells (IgD-CD27+). However, immature transitional B cells (CD19+CD10+CD34-) were higher in Kisumu relative to Nandi at all three ages. In contrast, the levels of non-class switched memory B cells (CD19+IgD+CD27+) were significantly lower overall in Kisumu relative to Nandi at significantly at 12 (p = 0.0144), 18 (p = 0.0013) and 24 months (p = 0.0129).These data suggest that infants living in malaria endemic regions have altered B cell subset distribution. Further studies are needed to understand the functional significance of these changes and long-term impact on ability of these infants to develop antibody responses to P. falciparum and heterologous infections.Development of immunity is dependent on both exposures to pathogens as well as age of the host. Children living in malaria endemic regions of sub-Saharan Africa have the burden of both early age of exposure and repeated exposure to malaria while their immune system is developing. That this is problematic is evidenced by the fact that not only do children under 5 years of age suffer the highest morbidity and mortality due to Plasmodium falciparum infection, they also have the highest all-cause mortality of any age group living in malaria endemic regions. Several reasons have been propo
%K B cells
%K Infant immunity
%K Plasmodium falciparum
%U http://www.malariajournal.com/content/10/1/362