The T cell response to persistent herpes virus infections in common variable immunodeficiency
Author(s) -
Raeiszadeh M.,
Kopycinski J.,
Paston S. J.,
Diss T.,
Lowdell M.,
Hardy G. A. D.,
Hislop A. D.,
Workman S.,
Dodi A.,
Emery V.,
Webster A. D.
Publication year - 2006
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.1365-2249.2006.03209.x
Subject(s) - common variable immunodeficiency , immunology , enteropathy , cd8 , perforin , cytomegalovirus , antigen , biology , immune system , cellular immunity , virology , cytotoxic t cell , t cell , virus , medicine , disease , antibody , herpesviridae , viral disease , biochemistry , in vitro
Summary We show that at least half of patients with common variable immunodeficiency (CVID) have circulating CD8 + T cells specific for epitopes derived from cytomegalovirus (CMV) and/or the Epstein–Barr virus (EBV). Compared to healthy age‐matched subjects, more CD8 + T cells in CVID patients were committed to CMV. Despite previous reports of defects in antigen presentation and cellular immunity in CVID, specific CD4 + and CD8 + T cells produced interferon (IFN)‐γ after stimulation with CMV peptides, and peripheral blood mononuclear cells secreted perforin in response to these antigens. In CVID patients we found an association between a high percentage of circulating CD8 + CD57 + T cells containing perforin, CMV infection and a low CD4/CD8 ratio, suggesting that CMV may have a major role in the T cell abnormalities described previously in this disease. We also show preliminary evidence that CMV contributes to the previously unexplained severe enteropathy that occurs in about 5% of patients.
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