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


Journal

Journal of clinical immunology
ISSN: 1573-2592
Titre abrégé: J Clin Immunol
Pays: Netherlands
ID NLM: 8102137

Informations de publication

Date de publication:
02 2020
Historique:
received: 26 02 2019
accepted: 26 11 2019
pubmed: 4 1 2020
medline: 3 7 2021
entrez: 4 1 2020
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 31897776
doi: 10.1007/s10875-019-00729-x
pii: 10.1007/s10875-019-00729-x
doi:

Substances chimiques

CARD Signaling Adaptor Proteins 0
NF-kappa B 0
CARD11 protein, human EC 4.6.1.2
Guanylate Cyclase EC 4.6.1.2

Types de publication

Case Reports Letter

Langues

eng

Sous-ensembles de citation

IM

Pagination

406-411

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Auteurs

Adrian M Shields (AM)

Clinical Immunology Service, Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, West Midlands, B15 2TT, UK. a.m.shields@bham.ac.uk.

Bradly M Bauman (BM)

Department of Pharmacology and Molecular Therapeutics, Uniformed Services University of the Health Sciences, Bethesda, MD, USA.

Chantal E Hargreaves (CE)

Department of Clinical Immunology, John Radcliffe Hospital, Oxford, OX3 9DU, UK.
NIHR Oxford Biomedical Research Centre, Oxford, UK.

Andrew J Pollard (AJ)

Oxford Vaccine Group, Department of Paediatrics, University of Oxford, Oxford, UK.

Andrew L Snow (AL)

Department of Pharmacology and Molecular Therapeutics, Uniformed Services University of the Health Sciences, Bethesda, MD, USA.

Smita Y Patel (SY)

Department of Clinical Immunology, John Radcliffe Hospital, Oxford, OX3 9DU, UK.
NIHR Oxford Biomedical Research Centre, Oxford, UK.

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Classifications MeSH