{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Martino D"],"funding":["NIAID NIH HHS","National Institutes of Health","NIH HHS"],"pagination":["85"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC11223352"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["16(1)"],"pubmed_abstract":["Background
Infants with frequent viral and bacterial respiratory infections exhibit compromised immunity to routine immunizations. They are also more likely to develop chronic respiratory diseases in later childhood. This study investigated the feasibility of epigenetic profiling to reveal endotype-specific molecular pathways with potential for early identification and immuno-modulation. Peripheral blood mononuclear cells from respiratory infection allergy/asthma-prone (IAP) infants and non-infection allergy/asthma prone (NIAP) were retrospectively selected for genome-wide DNA methylation and single nucleotide polymorphism analysis. The IAP infants were enriched for the low vaccine responsiveness (LVR) phenotype (Fisher's exact p-value = 0.02).Results
An endotype signature "],"journal":["Clinical epigenetics"],"pubmed_title":["Respiratory infection- and asthma-prone, low vaccine responder children demonstrate distinct mononuclear cell DNA methylation pathways."],"pmcid":["PMC11223352"],"funding_grant_id":["U19 AI168643","U19AI168643"],"pubmed_authors":["Kresoje N","in association with the IDEAL Consortium","Martino D","Diray-Arce J","Su JL","Schultz N","Hoch A","Pichichero M","Kaur R","Levy O","van Haren SD"],"additional_accession":[]},"is_claimable":false,"name":"Respiratory infection- and asthma-prone, low vaccine responder children demonstrate distinct mononuclear cell DNA methylation pathways.","description":"Background
Infants with frequent viral and bacterial respiratory infections exhibit compromised immunity to routine immunizations. They are also more likely to develop chronic respiratory diseases in later childhood. This study investigated the feasibility of epigenetic profiling to reveal endotype-specific molecular pathways with potential for early identification and immuno-modulation. Peripheral blood mononuclear cells from respiratory infection allergy/asthma-prone (IAP) infants and non-infection allergy/asthma prone (NIAP) were retrospectively selected for genome-wide DNA methylation and single nucleotide polymorphism analysis. The IAP infants were enriched for the low vaccine responsiveness (LVR) phenotype (Fisher's exact p-value = 0.02).Results
An endotype signature ","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 Jul","modification":"2025-04-04T19:23:37.489Z","creation":"2025-04-04T19:23:37.489Z"},"accession":"S-EPMC11223352","cross_references":{"pubmed":["38961479"],"doi":["10.1186/s13148-024-01703-0"]}}