Burden of copy number variation in common variable immunodeficiency

M. Keller, J. Glessner, E. Resnick, E. Perez, H. Chapel, M. Lucas, K. E. Sullivan, C. Cunningham-Rundles, J. S. Orange, H. Hakonarson

Research output: Contribution to journalArticle

13 Scopus citations

Abstract

Common variable immunodeficiency (CVID) has been associated recently with a dramatic increase in total copy number variation burden, the cause of which is unclear. In order to explore further the origin and clinical relevance of this finding, we quantified the total genomic copy number variation (CNV) burden in affected patients and evaluated clinical details in relationship to total CNV burden. No correlation was found between total CNV burden and either patient age or time elapsed since symptom onset, and higher total burden did not correlate with incidence of malignancy or other subphenotypes. These findings suggest that the increased CNV burden is static and intrinsic to CVID as a disease.

Original languageEnglish (US)
Pages (from-to)269-271
Number of pages3
JournalClinical and Experimental Immunology
Volume177
Issue number1
DOIs
StatePublished - Jul 1 2014

Keywords

  • Copy number variation
  • CVID
  • Immunodeficiency
  • Immunoglobulin

ASJC Scopus subject areas

  • Immunology
  • Immunology and Allergy

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    Keller, M., Glessner, J., Resnick, E., Perez, E., Chapel, H., Lucas, M., Sullivan, K. E., Cunningham-Rundles, C., Orange, J. S., & Hakonarson, H. (2014). Burden of copy number variation in common variable immunodeficiency. Clinical and Experimental Immunology, 177(1), 269-271. https://doi.org/10.1111/cei.12255