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Monocyte derived dendritic cell responses in common variable immunodeficiency
Author(s) -
SCOTTTAYLOR T. H.,
GREEN M. R. J.,
EREN E.,
WEBSTER A. D. B.
Publication year - 2004
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1111/j.1365-2249.2004.02640.x
Subject(s) - common variable immunodeficiency , immunology , cd86 , antigen presentation , biology , monocyte , antigen , dendritic cell , major histocompatibility complex , mhc class ii , immune system , t cell , antibody
SUMMARY The phenotype and function of monocyte derived dendritic cells (MdDC) were investigated in 25 patients with common variable immunodeficiency (CVID) to test for abnormalities that might help explain the failure of antibody production. Using MHC class II DR and CD86 as markers of maturation, DCs from the majority of CVID patients were normal. However 5 patients, the majority of whom had affected family members who had previously been shown to have a susceptibility genetic locus in the MHC region, expressed abnormally low levels of DR on repeated testing, in some cases associated with a reduced capacity to support antigen stimulated T cell proliferation; nevertheless costimulatory molecules for production of IL‐13, IL‐10 and IFN‐ γ from T cells were intact. In contrast to DCs from healthy donors, DCs from many CVID patients had high spontaneous production of IL‐8 and lipopolysaccharide stimulation often caused a reduction in DR expression. Expression of other cytokines (IL‐1a, IL‐6 and IL‐12), either before or after LPS stimulation, was normal. The data suggests there is a fundamental defect in the maturation of MdDCs in a subset of CVID patients that may compromise antigen presentation and subsequent antibody production.

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