Common variable immunodeficiency and idiopathic primary hypogammaglobulinemia: two different conditions within the same disease spectrum

Gertjan J Driessen, Virgil A S H Dalm, P Martin van Hagen, H. Anne Grashoff, Nico G. Hartwig, Annemarie M C van Rossum, Adilia Warris, Esther de Vries, Barbara H Barendregt, Ingrid Pico, Sandra Posthumus, Menno C van Zelm, Jacques J M van Dongen, Mirjam van der Burg

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Abstract

Patients with hypogammaglobulinemia who do not fulfill all the classical diagnostic criteria for common variable immunodeficiency (reduction of two immunoglobulin isotypes and a reduced response to vaccination) constitute a diagnostic and therapeutic dilemma, because information concerning the clinical and immunological characteristics of these patients with idiopathic primary hypogammaglobulinemia is not available. In 44 common variable immunodeficiency and 21 idiopathic primary hypogammaglobulinemia patients we determined the clinical phenotypes and performed flow cytometric immunophenotyping to assess the pathophysiological B-cell patterns and memory B-cell subset counts. Age-matched B-cell subset reference values of 130 healthy donors were generated. Severe pneumonia and bronchiectasis occurred at similar frequencies in idiopathic primary hypogammaglobulinemia and common variable immunodeficiency. Although IgG levels were only moderately reduced compared to common variable immunodeficiency, 12 of 21 idiopathic primary hypogammaglobulinemia patients required immunoglobulin replacement. Non-infectious disease-related clinical phenotypes (autoimmune cytopenia, polyclonal lymphocytic proliferation and persistent unexplained enteropathy) were exclusively observed in common variable immunodeficiency and were associated with early peripheral B-cell maturation defects or B-cell survival defects. T-cell dependent memory B-cell formation was more severely affected in common variable immunodeficiency. Furthermore, 14 of 21 idiopathic primary hypogammaglobulinemia patients showed normal peripheral B-cell subset counts, suggestive for a plasma cell defect. In conclusion, idiopathic primary hypogammaglobulinemia patients who do not fulfill all diagnostic criteria of common variable immunodeficiency have moderately decreased immunoglobulin levels and often a normal peripheral B-cell subset distribution, but still suffer from serious infectious complications.

Original languageEnglish
Pages (from-to)1617-1623
Number of pages7
JournalHaematologica
Volume98
Issue number10
DOIs
Publication statusPublished - Oct 2013

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Common Variable Immunodeficiency
Agammaglobulinemia
B-Lymphocyte Subsets
B-Lymphocytes
Immunoglobulins
Cell Count
Phenotype
Immunophenotyping
Bronchiectasis
Immunoglobulin Isotypes
Plasma Cells
Cell Survival
Pneumonia
Reference Values
Vaccination
Immunoglobulin G
Tissue Donors
T-Lymphocytes

Cite this

Driessen, G. J., Dalm, V. A. S. H., van Hagen, P. M., Grashoff, H. A., Hartwig, N. G., van Rossum, A. M. C., ... van der Burg, M. (2013). Common variable immunodeficiency and idiopathic primary hypogammaglobulinemia: two different conditions within the same disease spectrum. Haematologica, 98(10), 1617-1623. https://doi.org/10.3324/haematol.2013.085076

Common variable immunodeficiency and idiopathic primary hypogammaglobulinemia : two different conditions within the same disease spectrum. / Driessen, Gertjan J; Dalm, Virgil A S H; van Hagen, P Martin; Grashoff, H. Anne; Hartwig, Nico G.; van Rossum, Annemarie M C; Warris, Adilia; de Vries, Esther; Barendregt, Barbara H; Pico, Ingrid; Posthumus, Sandra; van Zelm, Menno C; van Dongen, Jacques J M; van der Burg, Mirjam.

In: Haematologica, Vol. 98, No. 10, 10.2013, p. 1617-1623.

Research output: Contribution to journalArticle

Driessen, GJ, Dalm, VASH, van Hagen, PM, Grashoff, HA, Hartwig, NG, van Rossum, AMC, Warris, A, de Vries, E, Barendregt, BH, Pico, I, Posthumus, S, van Zelm, MC, van Dongen, JJM & van der Burg, M 2013, 'Common variable immunodeficiency and idiopathic primary hypogammaglobulinemia: two different conditions within the same disease spectrum', Haematologica, vol. 98, no. 10, pp. 1617-1623. https://doi.org/10.3324/haematol.2013.085076
Driessen, Gertjan J ; Dalm, Virgil A S H ; van Hagen, P Martin ; Grashoff, H. Anne ; Hartwig, Nico G. ; van Rossum, Annemarie M C ; Warris, Adilia ; de Vries, Esther ; Barendregt, Barbara H ; Pico, Ingrid ; Posthumus, Sandra ; van Zelm, Menno C ; van Dongen, Jacques J M ; van der Burg, Mirjam. / Common variable immunodeficiency and idiopathic primary hypogammaglobulinemia : two different conditions within the same disease spectrum. In: Haematologica. 2013 ; Vol. 98, No. 10. pp. 1617-1623.
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abstract = "Patients with hypogammaglobulinemia who do not fulfill all the classical diagnostic criteria for common variable immunodeficiency (reduction of two immunoglobulin isotypes and a reduced response to vaccination) constitute a diagnostic and therapeutic dilemma, because information concerning the clinical and immunological characteristics of these patients with idiopathic primary hypogammaglobulinemia is not available. In 44 common variable immunodeficiency and 21 idiopathic primary hypogammaglobulinemia patients we determined the clinical phenotypes and performed flow cytometric immunophenotyping to assess the pathophysiological B-cell patterns and memory B-cell subset counts. Age-matched B-cell subset reference values of 130 healthy donors were generated. Severe pneumonia and bronchiectasis occurred at similar frequencies in idiopathic primary hypogammaglobulinemia and common variable immunodeficiency. Although IgG levels were only moderately reduced compared to common variable immunodeficiency, 12 of 21 idiopathic primary hypogammaglobulinemia patients required immunoglobulin replacement. Non-infectious disease-related clinical phenotypes (autoimmune cytopenia, polyclonal lymphocytic proliferation and persistent unexplained enteropathy) were exclusively observed in common variable immunodeficiency and were associated with early peripheral B-cell maturation defects or B-cell survival defects. T-cell dependent memory B-cell formation was more severely affected in common variable immunodeficiency. Furthermore, 14 of 21 idiopathic primary hypogammaglobulinemia patients showed normal peripheral B-cell subset counts, suggestive for a plasma cell defect. In conclusion, idiopathic primary hypogammaglobulinemia patients who do not fulfill all diagnostic criteria of common variable immunodeficiency have moderately decreased immunoglobulin levels and often a normal peripheral B-cell subset distribution, but still suffer from serious infectious complications.",
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N2 - Patients with hypogammaglobulinemia who do not fulfill all the classical diagnostic criteria for common variable immunodeficiency (reduction of two immunoglobulin isotypes and a reduced response to vaccination) constitute a diagnostic and therapeutic dilemma, because information concerning the clinical and immunological characteristics of these patients with idiopathic primary hypogammaglobulinemia is not available. In 44 common variable immunodeficiency and 21 idiopathic primary hypogammaglobulinemia patients we determined the clinical phenotypes and performed flow cytometric immunophenotyping to assess the pathophysiological B-cell patterns and memory B-cell subset counts. Age-matched B-cell subset reference values of 130 healthy donors were generated. Severe pneumonia and bronchiectasis occurred at similar frequencies in idiopathic primary hypogammaglobulinemia and common variable immunodeficiency. Although IgG levels were only moderately reduced compared to common variable immunodeficiency, 12 of 21 idiopathic primary hypogammaglobulinemia patients required immunoglobulin replacement. Non-infectious disease-related clinical phenotypes (autoimmune cytopenia, polyclonal lymphocytic proliferation and persistent unexplained enteropathy) were exclusively observed in common variable immunodeficiency and were associated with early peripheral B-cell maturation defects or B-cell survival defects. T-cell dependent memory B-cell formation was more severely affected in common variable immunodeficiency. Furthermore, 14 of 21 idiopathic primary hypogammaglobulinemia patients showed normal peripheral B-cell subset counts, suggestive for a plasma cell defect. In conclusion, idiopathic primary hypogammaglobulinemia patients who do not fulfill all diagnostic criteria of common variable immunodeficiency have moderately decreased immunoglobulin levels and often a normal peripheral B-cell subset distribution, but still suffer from serious infectious complications.

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