B-lymphocyte Subpopulations in Patients with Selective IgA Deficiency

[1]  N. Rezaei,et al.  Analysis of Switched Memory B Cells in Patients with IgA Deficiency , 2011, International Archives of Allergy and Immunology.

[2]  M. Vlková,et al.  Antibody forming cells and plasmablasts in peripheral blood in CVID patients after vaccination. , 2011, Vaccine.

[3]  C. Cunningham-Rundles,et al.  Complement receptor 2/CD21- human naive B cells contain mostly autoreactive unresponsive clones. , 2010, Blood.

[4]  J. Litzman,et al.  Change in Referral Diagnoses and Diagnostic Delay in Hypogammaglobulinaemic Patients during 28 Years in a Single Referral Centre , 2010, International Archives of Allergy and Immunology.

[5]  U. Wagner,et al.  Interleukin-21 restores immunoglobulin production ex vivo in patients with common variable immunodeficiency and selective IgA deficiency. , 2009, Blood.

[6]  K. Schwarz,et al.  Circulating CD21low B cells in common variable immunodeficiency resemble tissue homing, innate-like B cells , 2009, Proceedings of the National Academy of Sciences.

[7]  C. Cunningham-Rundles,et al.  Update in understanding common variable immunodeficiency disorders (CVIDs) and the management of patients with these conditions , 2009, British journal of haematology.

[8]  K. Warnatz,et al.  Flowcytometric phenotyping of common variable immunodeficiency , 2008, Cytometry. Part B, Clinical cytometry.

[9]  T. Lebien,et al.  B lymphocytes: how they develop and function. , 2008, Blood.

[10]  S. Tangye,et al.  IL-21-Induced Isotype Switching to IgG and IgA by Human Naive B Cells Is Differentially Regulated by IL-41 , 2008, The Journal of Immunology.

[11]  Lennart Hammarstrom,et al.  Progression of Selective IgA Deficiency to Common Variable Immunodeficiency , 2008, International Archives of Allergy and Immunology.

[12]  A. Cerutti.  The regulation of IgA class switching , 2008, Nature Reviews Immunology.

[13]  Eren,et al.  The EUROclass trial: defining subgroups in common variable immunodeficiency. , 2008, Blood.

[14]  M. Vlková,et al.  T and B lymphocyte subpopulations and activation/differentiation markers in patients with selective IgA deficiency , 2006, Clinical and experimental immunology.

[15]  L. Notarangelo,et al.  Combined decrease of defined B and T cell subsets in a group of common variable immunodeficiency patients. , 2006, Clinical immunology.

[16]  A. Durandy,et al.  Memory switched B cell percentage and not serum immunoglobulin concentration is associated with clinical complications in children and adults with specific antibody deficiency and common variable immunodeficiency. , 2006, Clinical immunology.

[17]  L. Hummelshoj,et al.  Class switch recombination in selective IgA‐deficient subjects , 2006, Clinical and experimental immunology.

[18]  M. Vlková,et al.  Age dependency and mutual relations in T and B lymphocyte abnormalities in common variable immunodeficiency patients , 2006, Clinical and experimental immunology.

[19]  C. Cunningham-Rundles,et al.  Immune competence and switched memory B cells in common variable immunodeficiency. , 2005, Clinical immunology.

[20]  B. Ferry,et al.  Measurement of peripheral B cell subpopulations in common variable immunodeficiency (CVID) using a whole blood method , 2005, Clinical and experimental immunology.

[21]  H. Eibel,et al.  A new CD21low B cell population in the peripheral blood of patients with SLE. , 2004, Clinical immunology.

[22]  A. Webster.  Clinical and Immunological Spectrum of Common Variable Immunodeficiency (CVID). , 2004, Iranian journal of allergy, asthma, and immunology.

[23]  A. Denz,et al.  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. , 2002, Blood.

[24]  J. Litzman,et al.  IgA Deficiency in Czech Healthy Individuals and Selected Patient Groups , 2000, International Archives of Allergy and Immunology.

[25]  B. Royer,et al.  Study of the B cell memory compartment in common variable immunodeficiency , 2000, European journal of immunology.

[26]  L. Notarangelo,et al.  Diagnostic Criteria for Primary Immunodeficiencies , 1999 .

[27]  C. Cunningham-Rundles,et al.  Common variable immunodeficiency: clinical and immunological features of 248 patients. , 1999, Clinical immunology.

[28]  L. Notarangelo,et al.  Diagnostic criteria for primary immunodeficiencies. Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies). , 1999, Clinical immunology.

[29]  I. Caragol,et al.  Development of a common variable immunodeficiency in IgA-deficient patients. , 1996, Clinical immunology and immunopathology.

[30]  I. Vořechovský,et al.  Family and linkage study of selective IgA deficiency and common variable immunodeficiency. , 1995, Clinical immunology and immunopathology.

[31]  C. Snapper,et al.  Novel in vitro model for high-rate IgA class switching. , 1995, Journal of immunology.

[32]  R. Liblau,et al.  Selective IgA deficiency and autoimmunity. , 1992, International archives of allergy and immunology.

[33]  T. Waldmann,et al.  Characterization of common variable immunodeficiency: identification of a subset of patients with distinctive immunophenotypic and clinical features. , 1990, Blood.