Lymphocytes and B-cell abnormalities in patients with common variable immunodeficiency (CVID)

Allergologia et Immunopathologia - Tập 42 - Trang 35-43 - 2014
L. Berrón-Ruiz1,2,3, G. López-Herrera1,2, A. Vargas-Hernández1, D. Mogica-Martínez4, E. García-Latorre3, L. Blancas-Galicia2, F.J. Espinosa-Rosales2, L. Santos-Argumedo1
1Department of Molecular Biomedicine, Center for Research and Advanced Studies, IPN, Avenida Instituto Politécnico Nacional # 2508, Colonia Zacatenco, 07360 Mexico DF, Mexico
2Immunodeficiency Research Unit, National Institute of Pediatrics SSA, Avenida Insurgentes Sur # 3700-C, Colonia Insurgentes Cuicuilco, Mexico City, Mexico
3Laboratory of Immunochemistry I, National School of Biological Sciences, IPN, Carpio y Plan de Ayala s/n, Colonia Santo Tomas, 11340 Mexico DF, Mexico
4Department of Allergy and Clinical Immunology, National Medical Center “La Raza”, IMSS, Avenida Vallejo s/n esquina Jacarandas, Colonia La Raza, 02200 Mexico DF, Mexico

Tài liệu tham khảo

Chapel, 2008, Common variable immunodeficiency disorders: division into distinct clinical phenotypes, Blood, 112, 277, 10.1182/blood-2007-11-124545 Wood, 2009, Primary antibody deficiency syndromes, Ann Clin Biochem, 46, 99, 10.1258/acb.2008.008175 Hammarstrom, 2000, Selective IgA deficiency (SIGAD) and common variable immunodeficiency (CVID), Clin Exp Immunol, 120, 225, 10.1046/j.1365-2249.2000.01131.x Farrington, 1994, Cd40 ligand expression is defective in a subset of patients with common variable immunodeficiency, Proc Natl Acad Sci USA, 91, 1099, 10.1073/pnas.91.3.1099 Agematsu, 2002, Absence of memory B-cells in patients with common variable immunodeficiency, Clin Immunol, 103, 34, 10.1006/clim.2001.5197 van Zelm, 2006, An antibody-deficiency syndrome due to mutations in the CD19 gene, N Engl J Med, 354, 1901, 10.1056/NEJMoa051568 van Zelm, 2010, Cd81 gene defect in humans disrupts CD19 complex formation and leads to antibody deficiency, J Clin Invest, 120, 1265, 10.1172/JCI39748 Sekine, 2007, Role for MSH5 in the regulation of Ig class switch recombination, Proc Natl Acad Sci USA, 104, 7193, 10.1073/pnas.0700815104 Thiel, 2012, Genetic CD21 deficiency is associated with hypogammaglobulinemia, J Allergy Clin Immunol, 129, 801, 10.1016/j.jaci.2011.09.027 Warnatz, 2009, B-cell activating factor receptor deficiency is associated with an adult-onset antibody deficiency syndrome in humans, Proc Natl Acad Sci USA, 106, 13945, 10.1073/pnas.0903543106 Kuijpers, 2010, CD20 deficiency in humans results in impaired T cell-independent antibody responses, J Clin Invest, 120, 214, 10.1172/JCI40231 Castigli, 2005, TACI is mutant in common variable immunodeficiency and IgA deficiency, Nat Genet, 37, 829, 10.1038/ng1601 Grimbacher, 2003, Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency, Nat Immunol, 4, 261, 10.1038/ni902 Warnatz, 2002, Severe deficiency of switched memory B-cells (CD27(+)IgM(−)IgD(−)) in subgroups of patients with common variable immunodeficiency: a new approach to classify a heterogeneous disease, Blood, 99, 1544, 10.1182/blood.V99.5.1544 Piqueras, 2003, Common variable immunodeficiency patient classification based on impaired B cell memory differentiation correlates with clinical aspects, J Clin Immunol, 23, 385, 10.1023/A:1025373601374 Conley, 1999, Diagnostic criteria for primary immunodeficiencies. Representing PAGID (pan-American group for immunodeficiency) and ESID (European Society for Immunodeficiencies), Clin Immunol, 93, 190, 10.1006/clim.1999.4799 Giovannetti, 2007, Unravelling the complexity of t cell abnormalities in common variable immunodeficiency, J Immunol, 178, 3932, 10.4049/jimmunol.178.6.3932 Wright, 1990, Characterization of common variable immunodeficiency: identification of a subset of patients with distinctive immunophenotypic and clinical features, Blood, 76, 2046, 10.1182/blood.V76.10.2046.2046 Vlkova, 2006, Age dependency and mutual relations in T and B lymphocyte abnormalities in common variable immunodeficiency patients, Clin Exp Immunol, 143, 373, 10.1111/j.1365-2249.2006.02999.x Mouillot, 2010, B-cell and T-cell phenotypes in CVID patients correlate with the clinical phenotype of the disease, J Clin Immunol, 30, 746, 10.1007/s10875-010-9424-3 Ozsahin, 1997, Adenosine deaminase deficiency in adults, Blood, 89, 2849, 10.1182/blood.V89.8.2849 Wehr, 2008, The euroclass trial: defining subgroups in common variable immunodeficiency, Blood, 111, 77, 10.1182/blood-2007-06-091744 Oksenhendler, 2008, Infections in 252 patients with common variable immunodeficiency, Clin Infect Dis, 46, 1547, 10.1086/587669 Bacchelli, 2007, Translational mini-review series on immunodeficiency: molecular defects in common variable immunodeficiency, Clin Exp Immunol, 149, 401, 10.1111/j.1365-2249.2007.03461.x Kowalczyk, 2006, The expression of CD40 on monocytes of children with primary humoral immunodeficiencies, Pediatr Res, 59, 816, 10.1203/01.pdr.0000219298.96471.18 Weston, 2001, Assessment of male CVID patients for mutations in the Btk gene: how many have been misdiagnosed?, Clin Exp Immunol, 124, 465, 10.1046/j.1365-2249.2001.01556.x Kanegane, 2000, Detection of Bruton's tyrosine kinase mutations in hypogammaglobulinaemic males registered as common variable immunodeficiency (CVID) in the Japanese immunodeficiency registry, Clin Exp Immunol, 120, 512, 10.1046/j.1365-2249.2000.01244.x Sigmon, 2008, X-linked agammaglobulinemia diagnosed late in life: case report and review of the literature, Clin Mol Allergy, 6, 5, 10.1186/1476-7961-6-5