poster abstractChronic granulomatous disease (CGD) is an inherited immunodeficiency associated with defects in
NADPH oxidase, an enzyme that produces oxygen radicals necessary to kill bacterial and fungal
pathogens. NADPH oxidase, made up of six subunits, is located in endosomal and plasma membranes of
immune cells. Although best studied in macrophages and neutrophils, the oxidase is expressed in B cells
where we have shown its link to adaptive immunity and antigen presentation. Here, NADPH oxidase
function was disrupted by mutations or gene knockdown in human B cells, and the role of the oxidase in
innate immunity specifically Toll-like receptor (TLR) signaling tested. TLR7 and 9, which recognize viral
single-stranded RNA and unmethylated CpG DNA respectively, potentially share an endosomal
compartment with the oxidase in B cells. In this project, B cells were stimulated for 24 hours with TLR7
and 9 ligands along with a costimulator PMA. TLR7 signaling was significantly enhanced in oxidase
deficient B cell lines compared with their respective control cells as evidenced by increased IL-6
secretion detected by an ELISA. CGD patients are incapable of producing oxygen radicals rendering them
immunodeficient in terms of pathogen infection. Yet these patients also develop many autoimmune
disorders associated with hyperactivation of the immune system. Thus, our studies on TLR activation
using CGD cell lines may explain in part the development of autoimmunity in individuals with CGD.
Additional studies are underway to examine the regulation of TLR including receptor expression levels
and the subcellular localization of the NADPH oxidase in these B cells from CGD patients. This work has
not yet been published and was supported by NIH 3R01AI079065-03S1
