<HashMap><database>ENA</database><scores/><additional><omics_type>Genomics</omics_type><center_name>NIAID</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA1308187</full_dataset_link><scientific_name>Homo sapiens</scientific_name><long_description>T cells play a central role in host protection against respiratory pathogens, but maladaptive T cell responses can lead to pulmonary diseases. Defining the biology of protective versus pathogenic T cell responses in the lungs of humans will be critical to nominate novel approaches to improve respiratory health. Previous studies have examined T cells from the lungs captured via bronchoalveolar lavage (BAL), endobronchial brushings, or biopsies. However, whether these different approaches are capturing distinct T cell phenotypes and/or clonotypes remains unclear. We aimed to evaluate and compare the transcriptional signatures of T cells isolated via BAL versus endobronchial brushings in healthy controls (HCs) and allergic asthmatics (AAs). The most significant difference in T cell subsets... (for more see dbGaP study page.)</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Distinct phenotypes and repertoires of bronchoalveolar and airway mucosal T cells in health and allergic asthma</name><description>Distinct phenotypes and repertoires of bronchoalveolar and airway mucosal T cells in health and allergic asthma</description><dates><last_updated>2025-09-24</last_updated><first_public>2025-09-08</first_public></dates><accession>PRJNA1308187</accession><cross_references><taxon>9606</taxon></cross_references></HashMap>