Memory switched B cell percentage and not serum immunoglobulin concentration is associated with clinical complications in children and adults with specific antibody deficiency and common variable immunodeficiency

Hana Alachkar, Nadine Taubenheim, Mansel R. Haeney, Anne Durandy, Peter D. Arkwright

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Although idiopathic humoral immunodeficiencies are arbitrarily classified into specific antibody deficiency (SAD) or common variable immunodeficiency (CVID), this distinction does not accurately predict the risk of the bronchiectasis, one of the major long-term clinical complications in these patients. In this study, clinical complications were compared with laboratory markers of cellular and humoral immunity in fifty-five consecutive patients (27 children and 28 adults) attending regional immunology clinics in Manchester, United Kingdom. Reduced CD19+CD27+IgD- B cell percentage but not serum immunoglobulin levels or classification of patients into SAD and CVID was associated with a significantly higher prevalence of bronchiectasis (OR 0.4 (0.2-0.8), P = 0.001), splenomegaly (OR 0.2 (0.1-0.5), P = 0.001) and autoimmunity (OR 0.4 (0.2-0.7), P = 0.003). We conclude that in patients with idiopathic humoral immunodeficiencies assessment of B cell switching more accurately predicts clinical prognosis than either classification of patients into SAD and CVID or serum immunoglobulin concentrations. © 2006 Elsevier Inc. All rights reserved.
    Original languageEnglish
    Pages (from-to)310-318
    Number of pages8
    JournalClinical Immunology
    Volume120
    Issue number3
    DOIs
    Publication statusPublished - Sept 2006

    Keywords

    • B cell switching
    • Bronchiectasis
    • CVID
    • Specific antibody immunodeficiency
    • Splenomegaly

    Fingerprint

    Dive into the research topics of 'Memory switched B cell percentage and not serum immunoglobulin concentration is associated with clinical complications in children and adults with specific antibody deficiency and common variable immunodeficiency'. Together they form a unique fingerprint.

    Cite this