Year: 2026
Type: article
Abstract: NFKB1 encodes the p105/p50 NF-κB1 transcription factor. Heterozygous mutations in NFKB1 may lead to NFKB1 insufficiency affecting multiple organ systems. This study aimed to develop an NFKB1-Disease-Activity-Score (NFKB1-DAS), serving as a tool in future clinical trials. Based on published phenotypic data from 179 patients with 77 distinct NFKB1 variants, we drafted an initial score consisting of 42 parameters. This draft was subsequently analyzed in a multicenter cohort of 41 patients with 22 distinct pathogenic NFKB1 variants. Using a Leave-One-Out (LOO) analysis (cutoff differential value: 23.07), we identified the 21 most relevant parameters to construct the final NFKB1-DAS. Calculation of the NFKB1-DAS in 31 CTLA4-deficient patients as a comparison cohort showed higher scores in NFKB1-insufficient patients (p = 0.03 (95% CI [-0.16, -0.01]) and the NFKB1-DAS correlated with hospitalization (p = 0.01; OR 2.07 (95% CI [1.18; 3.62]). However, given the optimism bias occurring when testing the score in the cohort it was developed with and the limited case numbers, validation of the NFKB1-DAS in an unrelated cohort remains essential. Analysis of the NFKB1-DAS in patients with variants of unknown significance (VUS) in NFKB1 (n = 14) showed individual patients reaching high scores. Future studies could evaluate a possible utility of the score in assessing VUS pathogenicity. Ultimately, the proposed NFKB1-DAS represents a first step toward monitoring disease activity and treatment response in future clinical trials in NFKB1 insufficiency.
Source: Journal of Clinical Immunology
Authors: Katharina Thoma, Pia Hassunah, Manfred Fliegauf, Gabriele Müller, Andres Caballero Garcia de Oteyza, Pavla Mrovecova, Helene Kraus, Prerana Agarwal, Maximilian Frederik Russe, Birgit Sawitzki, Lev Petrov, Katrin Vogt, Nadezhda Camacho Ordonez, Aleksandra Hirsch, Christoph B. Geier, Máté Krausz, Sigune Goldacker, Natalie Frede, Stephan Ehl, Sarah Salou, Ansgar Schulz, Shahrzad Bakhtiar, Maria Fasshauer, Oliver Hausmann, Anja-Dorothee Hüfner, Martin Stanulla, Anna Luijendijk, Faranaz Atschekzei, Georgios Sogkas, Ulrich Salzer, Baerbel Keller, Michele Proietti, Klaus Warnatz, Bodo Grimbacher
Institutions: University of Freiburg, University Medical Center Freiburg, Berlin Institute of Health at Charité - Universitätsmedizin Berlin, Charité – Universitätsmedizin Berlin, Carl von Ossietzky Universität Oldenburg, University Hospital Ulm, Goethe University Frankfurt, Klinikum St. Georg, University Medical Center Hamburg-Eppendorf, Medizinische Hochschule Hannover, Haukeland University Hospital, German Center for Infection Research
Language: English
Subfield: Immunology
Field: Immunology and Microbiology
Domain: Life Sciences
Open Access status: hybrid
Estimated APC paid: $4,990
Awards: G1078610655, Funktion und Bedeutung des Transkriptionsfaktors ZNF341 in Lymphozyten, G259924242, G3523822304, G4206229305, EXC 2155: RESIST Resolving Infection Susceptibility, EXC 2189: CIBSS Centre for Integrative Biological Signalling Studies, G5171826047, G5186833673, G6160902421, G6351858858, G7833425038, GAIN - Deutsches Netzwerk für die Erforschung und Therapieoptimierung von Patienten mit genetischen Multi-Organ-Autoimmunerkrankungen: Koordination, Patientenregister, Forschung zu verschiedenen Immundefekten (CTLA4, FKB1, STAT3-GOF), epidemiologische Studie zur Verbesserung der Versorgung und Lebensqualität
OpenAlex ID: W7222949528