| Literature DB >> 27622939 |
Valentina Perri1, Elena Gianchecchi1, Riccardo Scarpa2, Mariella Valenzise3, Maria Manuela Rosado4, Ezio Giorda5, Antonino Crinò6, Marco Cappa6, Susi Barollo2, Silvia Garelli2, Corrado Betterle2, Alessandra Fierabracci7.
Abstract
APECED is a T-cell mediated disease with increased frequencies of CD8+ effector and reduction of FoxP3+ T regulatory cells. Antibodies against affected organs and neutralizing to cytokines are found in the peripheral blood. The contribution of B cells to multiorgan autoimmunity in Aire-/- mice was reported opening perspectives on the utility of anti-B cell therapy. We aimed to analyse the B cell phenotype of APECED patients compared to age-matched controls. FACS analysis was conducted on PBMC in basal conditions and following CpG stimulation. Total B and switched memory (SM) B cells were reduced while IgM memory were increased in patients. In those having more than 15 years from the first clinical manifestation the defect included also mature and transitional B cells; total memory B cells were increased, while SM were unaffected. In patients with shorter disease duration, total B cells were unaltered while SM and IgM memory behaved as in the total group. A defective B cell proliferation was detected after 4day-stimulation. In conclusion APECED patients show, in addition to a significant alteration of the B cell phenotype, a dysregulation of the B cell function involving peripheral innate immune mechanisms particularly those with longer disease duration.Entities:
Keywords: AIRE gene; Adaptive immunity; B cell phenotype; Innate immunity; Type 1 autoimmune polyglandular syndrome
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Year: 2016 PMID: 27622939 DOI: 10.1016/j.imbio.2016.09.001
Source DB: PubMed Journal: Immunobiology ISSN: 0171-2985 Impact factor: 3.144