| Literature DB >> 23773925 |
Kabir Matharu1, Kol A Zarember, Beatriz E Marciano, Douglas B Kuhns, Christine Spalding, Mary Garofalo, Thomas Dimaggio, Tyra Estwick, Chiung-Yu Huang, Danielle Fink, Debra L Priel, Thomas A Fleisher, Steven M Holland, Harry L Malech, John I Gallin.
Abstract
Chronic Granulomatous Disease (CGD) is an inherited defect in superoxide production leading to life-threatening infections, granulomas, and, possibly, abnormal immunoglobulin concentrations. We investigated whether factors controlling antibody production, such as B-cell activating factor (BAFF), were altered in CGD. CGD subjects had significantly increased mean (2.3-fold, p < 0.0001) plasma concentrations of BAFF compared to healthy donors. Patients on IFN-γ treatment had significantly higher BAFF concentrations compared with CGD patients not taking IFN-γ (1.6-fold, p < 0.005). Leukocytes from CGD subjects produced normal amounts of BAFF in response to IFN-γ or G-CSF in vitro. Expression of BAFF-R and TACI was significantly reduced on CGD B cells. Elevated BAFF in CGD correlated with CRP (R = 0.44), ESR (R = 0.49), and IgM (R = 0.47) and increased rapidly in healthy subjects following intravenous endotoxin administration. These findings suggest that elevated BAFF in CGD subjects and healthy donors is a consequence of acute and chronic inflammation. Published by Elsevier Inc.Entities:
Keywords: B cell activating factor; B cell receptor; B-cell activating factor; BAFF; BCR; CGD; Chronic Granulomatous Disease; Inflammation; TACI; transmembrane activator and CAML-interactor.
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Year: 2013 PMID: 23773925 PMCID: PMC3774275 DOI: 10.1016/j.clim.2013.05.007
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969