A Novel, Heterozygous Three Base-Pair Deletion in CARD11 Results in B Cell Expansion with NF-κB and T Cell Anergy Disease

Adrian M. Shields*, Bradly M. Bauman, Chantal E. Hargreaves, Andrew J. Pollard, Andrew L. Snow, Smita Y. Patel

*Corresponding author for this work

Research output: Contribution to journalLetterpeer-review

13 Scopus citations

Abstract

Germline gain-of-function mutations in CARD11 lead to the primary immunodeficiency, B cell expansion with NF-κB, and T cell anergy (BENTA). Herein, we report the case of a girl, presenting at 2 years of age with lymphocytosis and splenomegaly in whom a novel, in-frame, three base pair deletion in CARD11 was identified resulting in the deletion of a single lysine residue (K215del) from the coiled-coil domain. In vitro functional assays demonstrated that this variant leads to a subtle increase in baseline NF-κB signaling and impaired proliferative responses following T cell receptor and mitogenic stimulation. Previously reported immunological defects associated with BENTA appear mild in our patient who is now 6 years of age; a B cell lymphocytosis and susceptibility to upper respiratory tract infections persist; however, she has broad, sustained responses to protein-polysaccharide conjugate vaccines and displays normal proliferative responses to ex vivo T cell stimulation.

Original languageEnglish
Pages (from-to)406-411
Number of pages6
JournalJournal of Clinical Immunology
Volume40
Issue number2
DOIs
StatePublished - 1 Feb 2020
Externally publishedYes

Keywords

  • BENTA
  • CARD11
  • Primary immunodeficiency

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