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Original Article

 

Cytokine Production by Activated T Cells in Common Variable Immunodeficiency

 

N Rezaei,1,2 A Aghamohammadi,1 M Nourizadeh,3 GA Kardar,3 Z Pourpak,3 A Zare,3 RC Read2

1Research Group for Immunodeficiencies, Pediatrics Center of Excellence, Children’s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
2Department of Infection and Immunity, School of Medicine and Biomedical Sciences, The University of Sheffield, Sheffield, United Kingdom
3Immunology, Asthma and Allergy Research Institute, Tehran University of Medical Sciences, Tehran, Iran

J Investig Allergol Clin Immunol 2010; Vol. 20(3): 244-251

 

 Abstract


Background: Common variable immunodeficiency (CVID) is the most common symptomatic antibody defi ciency. It is characterized by hypogammaglobulinemia, increased susceptibility to recurrent infections, autoimmunity, and malignancies.
Objectives: To determine whether patients with CVID have cytokine production defects after T-cell activation and to assess whether or not these are correlated with markers of severe disease.

Methods: Twenty-seven patients with CVID and 17 healthy volunteers were investigated. Peripheral blood mononuclear cells were cultured under standard conditions in the presence and absence of phytohemaglutinin. Subsequent cell proliferation and cytokine release were measured and compared between stimulated and unstimulated cells.

Results: A general enhancement in cytokine production was observed in both CVID patients and controls after stimulation. However, we detected a lower production of interferon-γ in CVID patients than in controls (P=.026). A production defect for at least 1 cytokine wasobserved in 12 patients. Ten of these failed to generate protective titers in response to the polysaccharide vaccine, and the frequency of bronchiectasis in this group of patients was 91.7%. Cytokine release correlated strongly with cell proliferation.

Conclusions: This study indicates that some CVID patients have T-cell proliferation and secretory defects and that these may be associated with severe manifestations of disease. Screening for such defects could permit more effective monitoring and therapeutic strategies for CVID patients.

Key words: Common variable immunodeficiency. Cytokine. Proliferation. T cell.