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Vulnerability to Meningococcal Disease in Immunodeficiency Due to a Novel Pathogenic Missense Variant in NFKB1

NF-κB1 deficiency is suggested to be the most common cause of common variable immunodeficiency (CVID). NFKB1 encodes for the p105 precursor protein of NF-κB1, which is converted into the active transcriptional subunit p50 through proteasomal processing of its C-terminal half upon stimulation and is...

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Autores principales: Anim, Manfred, Sogkas, Georgios, Schmidt, Gunnar, Dubrowinskaja, Natalia, Witte, Torsten, Schmidt, Reinhold Ernst, Atschekzei, Faranaz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8738076/
https://www.ncbi.nlm.nih.gov/pubmed/35003082
http://dx.doi.org/10.3389/fimmu.2021.767188
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author Anim, Manfred
Sogkas, Georgios
Schmidt, Gunnar
Dubrowinskaja, Natalia
Witte, Torsten
Schmidt, Reinhold Ernst
Atschekzei, Faranaz
author_facet Anim, Manfred
Sogkas, Georgios
Schmidt, Gunnar
Dubrowinskaja, Natalia
Witte, Torsten
Schmidt, Reinhold Ernst
Atschekzei, Faranaz
author_sort Anim, Manfred
collection PubMed
description NF-κB1 deficiency is suggested to be the most common cause of common variable immunodeficiency (CVID). NFKB1 encodes for the p105 precursor protein of NF-κB1, which is converted into the active transcriptional subunit p50 through proteasomal processing of its C-terminal half upon stimulation and is implicated in the canonical NF-kB pathway. Rare monoallelic NFKB1 variants have been shown to cause (haplo) insufficiency. Our report describes a novel NFKB1 missense variant (c.691C>T, p.R230C; allele frequency 0.00004953) in a family vulnerable to meningitis, sepsis, and late-onset hypogammaglobulinemia. We investigated the pathogenic relevance of this variant by lymphocyte stimulation, immunophenotyping, overexpression study and immunoblotting. The ectopic expression of p50 for c.691 C>T restricted transcriptionally active p50 in the cytoplasm, and immunoblotting revealed reduced p105/50 expression. This study shows that the deleterious missense variant in NFKB1 adversely affects the transcriptional and translational activity of NFκB1, impairing its function. Patients immunological parameters show a progressive course of hypogammaglobulinemia, which may partially account for the incomplete disease penetrance and suggest the need for closer immunological monitoring of those mutation carriers.
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spelling pubmed-87380762022-01-08 Vulnerability to Meningococcal Disease in Immunodeficiency Due to a Novel Pathogenic Missense Variant in NFKB1 Anim, Manfred Sogkas, Georgios Schmidt, Gunnar Dubrowinskaja, Natalia Witte, Torsten Schmidt, Reinhold Ernst Atschekzei, Faranaz Front Immunol Immunology NF-κB1 deficiency is suggested to be the most common cause of common variable immunodeficiency (CVID). NFKB1 encodes for the p105 precursor protein of NF-κB1, which is converted into the active transcriptional subunit p50 through proteasomal processing of its C-terminal half upon stimulation and is implicated in the canonical NF-kB pathway. Rare monoallelic NFKB1 variants have been shown to cause (haplo) insufficiency. Our report describes a novel NFKB1 missense variant (c.691C>T, p.R230C; allele frequency 0.00004953) in a family vulnerable to meningitis, sepsis, and late-onset hypogammaglobulinemia. We investigated the pathogenic relevance of this variant by lymphocyte stimulation, immunophenotyping, overexpression study and immunoblotting. The ectopic expression of p50 for c.691 C>T restricted transcriptionally active p50 in the cytoplasm, and immunoblotting revealed reduced p105/50 expression. This study shows that the deleterious missense variant in NFKB1 adversely affects the transcriptional and translational activity of NFκB1, impairing its function. Patients immunological parameters show a progressive course of hypogammaglobulinemia, which may partially account for the incomplete disease penetrance and suggest the need for closer immunological monitoring of those mutation carriers. Frontiers Media S.A. 2021-12-24 /pmc/articles/PMC8738076/ /pubmed/35003082 http://dx.doi.org/10.3389/fimmu.2021.767188 Text en Copyright © 2021 Anim, Sogkas, Schmidt, Dubrowinskaja, Witte, Schmidt and Atschekzei https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Anim, Manfred
Sogkas, Georgios
Schmidt, Gunnar
Dubrowinskaja, Natalia
Witte, Torsten
Schmidt, Reinhold Ernst
Atschekzei, Faranaz
Vulnerability to Meningococcal Disease in Immunodeficiency Due to a Novel Pathogenic Missense Variant in NFKB1
title Vulnerability to Meningococcal Disease in Immunodeficiency Due to a Novel Pathogenic Missense Variant in NFKB1
title_full Vulnerability to Meningococcal Disease in Immunodeficiency Due to a Novel Pathogenic Missense Variant in NFKB1
title_fullStr Vulnerability to Meningococcal Disease in Immunodeficiency Due to a Novel Pathogenic Missense Variant in NFKB1
title_full_unstemmed Vulnerability to Meningococcal Disease in Immunodeficiency Due to a Novel Pathogenic Missense Variant in NFKB1
title_short Vulnerability to Meningococcal Disease in Immunodeficiency Due to a Novel Pathogenic Missense Variant in NFKB1
title_sort vulnerability to meningococcal disease in immunodeficiency due to a novel pathogenic missense variant in nfkb1
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8738076/
https://www.ncbi.nlm.nih.gov/pubmed/35003082
http://dx.doi.org/10.3389/fimmu.2021.767188
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