| Literature DB >> 27664934 |
Reza Yazdani1, Mazdak Ganjalikhani-Hakemi2, Mohammad Esmaeili3, Hassan Abolhassani4, Shahram Vaeli3, Abbas Rezaei5, Zohre Sharifi3, Gholamreza Azizi6, Nima Rezaei7, Asghar Aghamohammadi8.
Abstract
Common variable immunodeficiency (CVID) is a heterogeneous group of primary immunodeficiency characterized by recurrent infections. We evaluated whether defective PI3K/Akt/FoxO pathway could influence B-cell fate. Determination of B-cell subsets in CVD patients and healthy donors (HDs) were performed using flow cytometry. We evaluated mRNA and protein expression of PI3K, Akt and FoxO using real-time PCR and flow cytometry, respectively. Moreover, phosphorylated Akt (pAkt) expression in B-cells has been measured by flowcytometry. We identified a significant reduction in the percentage of marginal zone like B-cells, memory B-cells (total, switched and unswitched) and plasmablasts in patients, as these decreased B-cell subsets had a significant negative correlation with increased apoptosis in patients. Surprisingly, we identified decreased pAkt expression in B-cells of patients than HDs. We described for the first time impaired pAkt expression in B-cells of CVID patients that had a significant correlation with antibody response to the vaccine and worse clinical complications.Entities:
Keywords: Antibody response; B-cell; Common variable immunodeficiency; PI3K/Akt/FoxO pathway; Phosphorylated Akt
Mesh:
Substances:
Year: 2016 PMID: 27664934 DOI: 10.1016/j.clim.2016.09.009
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969