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<jats:title>Abstract</jats:title><jats:sec> <jats:title>Background</jats:title> <jats:p>Pneumococcal infections are a major cause of morbidity and mortality in young children and immaturity of the immune system partly underlies poor vaccine responses seen in the young. Emerging evidence suggests a key role for epigenetics in the maturation and regulation of the immune system in health and disease. The study aimed to investigate epigenetic changes in early life and to understand the relationship between the epigenome and antigen-specific antibody responses to pneumococcal vaccination.</jats:p> </jats:sec><jats:sec> <jats:title>Methods</jats:title> <jats:p>The epigenetic profiles from 24 healthy children were analyzed at 12 months prior to a booster dose of the 13-valent pneumococcal conjugate vaccine (PCV-13), and at 24 months of age, using the Illumina Methylation 450 K assay and assessed for differences over time and between high and low vaccine responders.</jats:p> </jats:sec><jats:sec> <jats:title>Results</jats:title> <jats:p>Our analysis revealed 721 significantly differentially methylated positions between 12 and 24 months (FDR < 0.01), with significant enrichment in pathways involved in the regulation of cell–cell adhesion and T cell activation. Comparing high and low vaccine responders, we identified differentially methylated CpG sites (<jats:italic>P</jats:italic> value < 0.01) associated with <jats:italic>HLA-DPB1</jats:italic> and <jats:italic>IL6</jats:italic>.</jats:p> </jats:sec><jats:sec> <jats:title>Conclusion</jats:title> <jats:p>These data imply that epigenetic changes that occur during early childhood may be associated with antigen-specific antibody responses to pneumococcal vaccines.</jats:p> </jats:sec>

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Journal article


Clinical Epigenetics


Springer Science and Business Media LLC

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