<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ren K</submitter><funding>the Precision Medicine Research on the Prevention and Control of Vaccines for Major Infectious Diseases</funding><pagination>10</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12846271</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(1)</volume><pubmed_abstract>It has been demonstrated that infants and young children exhibit immune tolerance as a consequence of immature immune systems, which are characterized by a natural Th2 bias. RSV infection has been reported to result in acute lower respiratory infection (ALRI), while formalin-inactivated vaccination has been observed to exacerbate Th2 responses, consequently leading to enhanced respiratory disease (ERD). Transcriptomic data from three independent cohorts of RSV-infected infants were analyzed (GSE246622 served as the discovery and train set; GSE105450 and GSE188427 were used as validation sets). Immune infiltration analysis revealed immunological characteristics, which were then used to perform unsupervised clustering using feature-related genes. WGCNA was used to identify co-expressed gene </pubmed_abstract><journal>Tropical medicine and infectious disease</journal><pubmed_title>Analysis of the Specific Expression Profile of Immune Cells in Infants and Young Children Infected with RSV and Construction of a Disease Prediction Model.</pubmed_title><pmcid>PMC12846271</pmcid><funding_grant_id>MP-GZNL2023A01005</funding_grant_id><pubmed_authors>Ren K</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Ma K</pubmed_authors><pubmed_authors>Sun H</pubmed_authors><pubmed_authors>Ren T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Analysis of the Specific Expression Profile of Immune Cells in Infants and Young Children Infected with RSV and Construction of a Disease Prediction Model.</name><description>It has been demonstrated that infants and young children exhibit immune tolerance as a consequence of immature immune systems, which are characterized by a natural Th2 bias. RSV infection has been reported to result in acute lower respiratory infection (ALRI), while formalin-inactivated vaccination has been observed to exacerbate Th2 responses, consequently leading to enhanced respiratory disease (ERD). Transcriptomic data from three independent cohorts of RSV-infected infants were analyzed (GSE246622 served as the discovery and train set; GSE105450 and GSE188427 were used as validation sets). Immune infiltration analysis revealed immunological characteristics, which were then used to perform unsupervised clustering using feature-related genes. WGCNA was used to identify co-expressed gene </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-14T03:23:42.849Z</modification><creation>2026-06-14T03:15:07.891Z</creation></dates><accession>S-EPMC12846271</accession><cross_references><pubmed>41591219</pubmed><doi>10.3390/tropicalmed11010010</doi></cross_references></HashMap>