| Literature DB >> 27923702 |
Vassilios Lougaris1, Ornella Patrizi2, Manuela Baronio3, Giovanna Tabellini2, Giacomo Tampella3, Eufemia Damiati3, Natalie Frede4, Jos W M van der Meer5, Manfred Fliegauf4, Bodo Grimbacher4, Silvia Parolini2, Alessandro Plebani3.
Abstract
NFKB1, a component of the canonical NF-κB pathway, was recently reported to be mutated in a limited number of CVID patients. CVID-associated mutations in NFKB2 (non-canonical pathway) have previously been shown to impair NK cell cytotoxic activity. Although a biological function of NFKB1 in non-human NK cells has been reported, the role of NFKB1 mutations for human NK cell biology and disease has not been investigated yet. We decided therefore to evaluate the role of monoallelic NFKB1 mutations in human NK cell maturation and functions. We show that NFKB1 mutated NK cells present impaired maturation, defective cytotoxicity and reduced IFN-γ production upon in vitro stimulation. Furthermore, human IL-2 activated NFKB1 mutated NK cells fail to up-regulate the expression of the activating marker NKp44 and show reduced proliferative capacity. These data suggest that NFKB1 plays an essential novel role for human NK cell maturation and effector functions.Entities:
Keywords: Cytotoxicity; Interferon-γ; NFKB1; Natural killer cells
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Year: 2016 PMID: 27923702 DOI: 10.1016/j.clim.2016.11.012
Source DB: PubMed Journal: Clin Immunol ISSN: 1521-6616 Impact factor: 3.969