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International Immunology, Vol. 13, No. 7, 871-876, July 2001
© 2001 Japanese Society for Immunology

B cell co-receptors regulating T cell-dependent antibody production in common variable immunodeficiency: CD27 pathway defects identify subsets of severely immuno-compromised patients

Serge Jacquot, Laëtitia Maçon-Lemaître, Estelle Paris, Tetsuji Kobata1, Yuetsu Tanaka2, Chikao Morimoto3, Stuart F. Schlossman3 and François Tron INSERM U519, IFRMP 23, Laboratoire d'Immunopathologie Clinique et Expérimentale, CHU Charles Nicolle, Faculté de Médecine et de Pharmacie, 22 boulevard Gambetta, 76183 Rouen Cedex, France
1 Division of Immunology, Institute for Medical Science, Dokkyo University School of Medicine, Tochigi 321-0293, Japan
2 Department of Infectious Disease and Immunology, Okinawa-Asia Research Center of Medical Science, University of the Ryukyus School of Medicine, Okinawa 903-0215, Japan
3 Division of Tumor Immunology, Department of Cancer Immunology and AIDS, Dana-Farber Cancer Institute; Department of Medicine, Harvard Medical School, Boston, MA 02115, USA

Correspondence to: S. Jacquot

CD27 and CD134 ligand (CD134L) are two B cell co-receptors for Th cell activation-induced ligands (i.e. CD70 and CD134) that promote differentiation of B cells into plasma cells and high-rate antibody production respectively. We explored the CD27 pathway and T cell CD134 expression in common variable immunodeficiency (CVID), a disease characterized by a lack of plasma cells and low Ig serum levels. Twelve patients were compared to seven healthy controls. We found a low percentage of circulating CD27+ B cells in seven patients and B cell CD27 expression was not up-regulated by in vitro activation in two of them. Importantly, the number of circulating CD27+ B cells was correlated with the severity of the disease—the patients with the lowest CD27+ B cell counts having the lowest serum Ig concentrations and the lowest total peripheral blood B cell counts. In contrast, CD70 and CD134 were normally expressed on in vitro activated T cells. CD134L was not detected on patient and control B cells in our activation conditions. Functional studies of in vitro Ig production demonstrated an absence of B cell response to CD27 cross-linking, in particular in a patient with normal CD27 expression. Our results indicate that a defect in CD27 expression or function contributes to the pathogenesis of certain severe forms of CVID.

Keywords: memory B cells, T-B interactions, tumor necrosis factor receptor family

Transmitting editor: S. Izui


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