4.7 Article

Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations

Journal

JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY
Volume 146, Issue 4, Pages 901-911

Publisher

MOSBY-ELSEVIER
DOI: 10.1016/j.jaci.2019.11.051

Keywords

NFKB1 variant; NFKB1 mutation; common variable immunodeficiency; reduced penetrance; NF-kappa B1-related phenotype; autosomal dominant

Funding

  1. German Research Foundation (DFG) [SFB1160]
  2. Germany's Excellence Strategy [EXC-2189, 390939984, EXC 2155, 39087428]
  3. E-rare program of the European Union [GR1617/14-1]
  4. Netzwerke Seltener Erkrankungen of the German Ministry of Education and Research (BMBF) [GAIN_ 01GM1910A]
  5. German Ministry of Education and Research (BMBF) [01E01303, 01ZX1306F]
  6. MRC [MR/L006197/1, MR/K020919/1] Funding Source: UKRI

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Background: An increasing number of NFKB1 variants are being identified in patients with heterogeneous immunologic phenotypes. Objective: To characterize the clinical and cellular phenotype as well as the management of patients with heterozygous NFKB1 mutations. Methods: In a worldwide collaborative effort, we evaluated 231 individuals harboring 105 distinct heterozygous NFKB1 variants. To provide evidence for pathogenicity, each variant was assessed in silico; in addition, 32 variants were assessed by functional in vitro testing of nuclear factor of kappa light polypeptide gene enhancer in B cells (NF-kappa B) signaling. Results: We classified 56 of the 105 distinct NFKB1 variants in 157 individuals from 68 unrelated families as pathogenic. Incomplete clinical penetrance (70%) and age-dependent severity of NFKB1-related phenotypes were observed. The phenotype included hypogammaglobulinemia (88.9%), reduced switched memory B cells (60.3%), and respiratory (83%) and gastrointestinal (28.6%) infections, thus characterizing the disorder as primary immunodeficiency. However, the high frequency of autoimmunity (57.4%), lymphoproliferation (52.4%), noninfectious enteropathy (23.1%), opportunistic infections (15.7%), autoinflammation (29.6%), and malignancy (16.8%) identified NF-kappa B1-related disease as an inborn error of immunity with immune dysregulation, rather than a mere primary immunodeficiency. Current treatment includes immunoglobulin replacement and immunosuppressive agents. Conclusions: We present a comprehensive clinical overview of the NF-kappa B1-related phenotype, which includes immunodeficiency, autoimmunity, autoinflammation, and cancer. Because of its multisystem involvement, clinicians from each and every medical discipline need to be made aware of this autosomal-dominant disease. Hematopoietic stem cell transplantation and NF-kappa B1 pathway-targeted therapeutic strategies should be considered in the future.

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