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  4. TNF-α-induced protein 3 is a key player in childhood asthma development and environment-mediated protection
 
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TNF-α-induced protein 3 is a key player in childhood asthma development and environment-mediated protection

Date Issued
2019-01-01
Author(s)
Krusche, Johanna
Twardziok, Monika
Rehbach, Katharina
Böck, Andreas
Tsang, Miranda S.
Schröder, Paul C.
Kumbrink, Jörg
Kirchner, Thomas
Xing, Yuhan
Riedler, Josef
Dalphin, Jean-Charles
Pekkanen, Juha
Lauener, Roger
Roponen, Marjut
Li, Jing
Wong, Chun K.
Wong, Gary W. K.
Schaub, Bianca
Pasture, study group
DOI
10.1016/j.jaci.2019.07.029
Abstract
Childhood asthma prevalence is significantly greater in urban areas compared with rural/farm environments. Murine studies have shown that TNF-α-induced protein 3 (TNFAIP3; A20), an anti-inflammatory regulator of nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) signaling, mediates environmentally induced asthma protection.; We aimed to determine the role of TNFAIP3 for asthma development in childhood and the immunomodulatory effects of environmental factors.; In a representative selection of 250 of 2168 children from 2 prospective birth cohorts and 2 cross-sectional studies, we analyzed blood cells of healthy and asthmatic children from urban and rural/farm environments from Europe and China. PBMCs were stimulated ex vivo with dust from "asthma-protective" farms or LPS. NF-κB signaling-related gene and protein expression was assessed in PBMCs and multiplex gene expression assays (NanoString Technologies) in isolated dendritic cells of schoolchildren and in cord blood mononuclear cells from newborns.; Anti-inflammatory TNFAIP3 gene and protein expression was consistently decreased, whereas proinflammatory Toll-like receptor 4 expression was increased in urban asthmatic patients (P < .05), reflecting their increased inflammatory status. Ex vivo farm dust or LPS stimulation restored TNFAIP3 expression to healthy levels in asthmatic patients and shifted NF-κB signaling-associated gene expression toward an anti-inflammatory state (P < .001). Farm/rural children had lower expression, indicating tolerance induction by continuous environmental exposure. Newborns with asthma at school age had reduced TNFAIP3 expression at birth, suggesting TNFAIP3 as a possible biomarker predicting subsequent asthma.; Our data indicate TNFAIP3 as a key regulator during childhood asthma development and its environmentally mediated protection. Because environmental dust exposure conferred the anti-inflammatory effects, it might represent a promising future agent for asthma prevention and treatment.
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