CD8+ T Cell Populations in Common Variable Immunodeficiency
Author:
Publisher
Elsevier BV
Subject
Hematology,Immunology,Immunology and Allergy
Reference4 articles.
1. The primary immunodeficiencies;Rosen;N. Engl. J. Med.,1995
2. Common variable immunodeficiency: clinical and immunological features of 248 patients;Cunningham-Rundles;Clin Immunol.,1999
3. The CDSbeta ectodomain contributes to the augmented co receptor function of CD8alphabeta heterodimers relative to CD8alphaalpha homodimers;Witte;Cell. Immunol.,1999
4. Primary defect in CD8+ lymphocytes in the antibody deficiency disease (common variable immunodeficiency): abnormalities in intracellular production of interferon-gamma (IFN-gamma) in CD28+ (‘cytotoxic’) and CD28-(‘suppressor’) CD8+ subsets;North;Clin. Exp. Immunol.,1998
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1. In vitro IL-15-activated human naïve CD8+ T cells down-modulate the CD8β chain and become CD8αα T cells;Frontiers in Immunology;2024-06-05
2. Analysis of bulk and virus-specific CD8+ T cells reveals advanced differentiation of CD8+ T cells in patients with common variable immunodeficiency;Clinical Immunology;2011-11
3. Successful Immunosuppressive Therapy With Cyclosporine A for Posthepatitis B-Cell Deficiency With Activated Cytoplasmic Interferon-γ—Positive T-Lymphocytes;International Journal of Hematology;2002-04
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