Development of a Disease Activity Score to Assess Treatment Success in Patients with NFKB1 Mutations

Background NFKB1 encodes for the p105/p50 nuclear factor-kappa-B (NF-kB1) transcription factors. Heterozygous mutations in NFKB1 may lead to NF-kB1 insufficiency, which may result in a multiorgan disease. Here, we aimed to develop a disease activity score to assess treatment success in patients with NF-kB1 insufficiency. Methods Based on phenotypic data of 179 patients with 77 distinct NFKB1 variants and clinical data from 41 patients with 22 distinct pathogenic NFKB1 variants, we identified the most relevant score parameters in a Leave-One-Out (LOO) analysis and developed the NFKB1-DAS. NFKB1-DAS values in patients with pathogenic variants in NFKB1 were compared to those of CTLA4-insufficient patients as a control group. Results Patients who spent at least one day in hospital in the last 6 months had a median NFKB1-DAS of 46% compared to 28% in patients without a hospital stay. In patients with pathogenic NFKB1 variants (n = 41), mean score values were 1.4-fold higher than in patients with CTLA4 deficiency (n = 31). Discussion We found the first indications that the newly developed NFKB1-DAS is able to measure disease activity. In a follow-up study, the NFKB1-DAS will be further validated and used to measure the effectiveness of treatment in a worldwide NFKB1 cohort.

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Journal
Journal of Human Immunity
Published
2026-05-01
DOI
https://doi.org/10.70962/cis2026abstract.47
Primary Topic
NF-κB Signaling Pathways
Type
article
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article

Development of a Disease Activity Score to Assess Treatment Success in Patients with NFKB1 Mutations

Baerbel Keller, Aleksandra Hirsch, Katharina Thoma, Martin Stanulla et al.
Journal of Human Immunity
NF-κB Signaling Pathways
article

Development of a Disease Activity Score to Assess Treatment Success in Patients with NFKB1 Mutations

Baerbel Keller, Aleksandra Hirsch, Katharina Thoma, Martin Stanulla, Faranaz Atschekzei, Maria Faßhauer, Birgit Sawitzki, Máté Krausz, Manfred Fliegauf, Klaus Warnatz, Shahrzad Bakhtiar, Gabriele Müller, Sigune Goldacker, Anja-Dorothee Hüfner, Maximilian Frederik Russe, Georgios Sogkas, Katrin Vogt, Bodo Grimbacher, Ulrich Salzer, Sarah Salou, Christoph B. Geier, Michele Proietti, Natalie Frede, Prerana Agarwal, Helene Kraus, Oliver Hausmann, Stephan Ehl, IPavla Mrovecova, Andres Caballero Garcia de Oteyza, Pia Hassunah, Nadezhda Nadezhda Camacho Ordonez, Lev Petrov, Ansgar Schulz, Anna Luijendijk
article en

Abstract

Background NFKB1 encodes for the p105/p50 nuclear factor-kappa-B (NF-kB1) transcription factors. Heterozygous mutations in NFKB1 may lead to NF-kB1 insufficiency, which may result in a multiorgan disease. Here, we aimed to develop a disease activity score to assess treatment success in patients with NF-kB1 insufficiency. Methods Based on phenotypic data of 179 patients with 77 distinct NFKB1 variants and clinical data from 41 patients with 22 distinct pathogenic NFKB1 variants, we identified the most relevant score parameters in a Leave-One-Out (LOO) analysis and developed the NFKB1-DAS. NFKB1-DAS values in patients with pathogenic variants in NFKB1 were compared to those of CTLA4-insufficient patients as a control group. Results Patients who spent at least one day in hospital in the last 6 months had a median NFKB1-DAS of 46% compared to 28% in patients without a hospital stay. In patients with pathogenic NFKB1 variants (n = 41), mean score values were 1.4-fold higher than in patients with CTLA4 deficiency (n = 31). Discussion We found the first indications that the newly developed NFKB1-DAS is able to measure disease activity. In a follow-up study, the NFKB1-DAS will be further validated and used to measure the effectiveness of treatment in a worldwide NFKB1 cohort.

Journal of Human ImmunityVol. 2(CIS2026)
Goethe University Frankfurt (DE), Universität Hamburg (DE), University of Freiburg (DE), Universität Ulm (DE), Klinikum St. Georg (DE), Haukeland University Hospital (NO), University Medical Center Freiburg (DE), Medizinische Hochschule Hannover (DE), University Medical Center Hamburg-Eppendorf (DE), University of Teacher Education Lucerne (CH), Berlin Institute of Health at Charité - Universitätsmedizin Berlin (DE), University Hospital Ulm (DE)
Good health and well-being
Openalex Percentile: Top 10%
NF-κB Signaling Pathways
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