Infant RSV immunoprophylaxis changes nasal epithelial DNA methylation at 6 years of age
Xu, Cheng-Jian; Scheltema, Nienke M; Qi, Cancan; Vedder, Rolf; Klein, Laura B C; Nibbelke, Elisabeth E; van der Ent, Cornelis K; Bont, Louis J; Koppelman, Gerard H
(2021) Pediatric Pulmonology, volume 56, issue 12, pp. 3822 - 3831
(Article)
Abstract
BACKGROUND: Respiratory syncytial virus (RSV) infection has been associated with childhood wheeze and asthma, and potential mechanisms include persistent epigenetic effects. METHODS: In the randomized, placebo-controlled MAKI trial, 429 preterm infants randomly received RSV immunoprophylaxis with palivizumab or placebo during their first RSV season. Children were followed until age 6
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for asthma evaluation. DNA methylation in cells obtained by nasal brushes at age 6 was measured by Illumina MethylationEPIC array. RESULTS: RSV immunoprophylaxis in infancy had a significant impact on global methylation patterns in nasal cells at age 6. The first principal component (PC) related to the immunoprophylaxis intervention was enriched for the pathway "detection of chemical stimulus involved in sensory perception of smell" and "T cell differentiation." Subsequent analysis of these PCs indicated an effect of RSV immunoprophylaxis on cell type composition of nasal brushed cells. Three CpG sites, cg18040241, cg08243963, and cg19555973 which are annotated to genes GLB1L2, SC5D, and BPIFB1, were differentially methylated at genome-wide significance, but were not associated with asthma. CONCLUSION: The study provides the first proof of concept that RSV immunoprophylaxis during infancy has long-term effects on nasal epigenetic signatures at age 6, relating to host sensory perception, epidermal growth factor receptor signaling, and adaptive immune responses.
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Keywords: asthma, DNA methylation, epigenetics, RSV immunoprophylaxis, RSV infection, Pulmonary and Respiratory Medicine, Pediatrics, Perinatology, and Child Health, Journal Article
ISSN: 8755-6863
Publisher: John Wiley & Sons Inc.
Note: Funding Information: The authors are indebted to all the participating children and their families for their commitment and participation. The authors thank all members of the MAKI research team, including the staff of the pediatric lung function laboratory, and the laboratory staff. The authors also thank the staff of the Genomics Analysis Facility for providing technical assistance with the methylation analyses of this study. This study was supported by MedImmune Grant ESR‐14‐10006. Funding Information: This study was supported by a grant from MedImmune to LJB and GHK. Funders had no role in design, interpretation, and reporting of this study. LJB reports grants from AbbVie during the conduct of the study and grants from MedImmune, Janssen, MeMed, and the Bill & Melinda Gates Foundation. None of the other authors report competing interests relating to the work presented in this study. Publisher Copyright: © 2021 The Authors. Pediatric Pulmonology published by Wiley Periodicals LLC
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