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A CARD9 Founder Mutation Disrupts NF-κB Signaling by Inhibiting BCL10 and MALT1 Recruitment and Signalosome Formation
Background: Inherited CARD9 deficiency constitutes a primary immunodeficiency predisposing uniquely to chronic and invasive fungal infections. Certain mutations are shown to negatively impact CARD9 protein expression and/or NF-κB activation, but the underlying biochemical mechanism remains to be ful...
Autores principales: | De Bruyne, Marieke, Hoste, Levi, Bogaert, Delfien J., Van den Bossche, Lien, Tavernier, Simon J., Parthoens, Eef, Migaud, Mélanie, Konopnicki, Deborah, Yombi, Jean Cyr, Lambrecht, Bart N., van Daele, Sabine, Alves de Medeiros, Ana Karina, Brochez, Lieve, Beyaert, Rudi, De Baere, Elfride, Puel, Anne, Casanova, Jean-Laurent, Goffard, Jean-Christophe, Savvides, Savvas N., Haerynck, Filomeen, Staal, Jens, Dullaers, Melissa |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6220056/ https://www.ncbi.nlm.nih.gov/pubmed/30429846 http://dx.doi.org/10.3389/fimmu.2018.02366 |
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