<HashMap><database>ENA</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><center_name>COLUMBIA UNIVERSITY HEALTH SCIENCES</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA950542</full_dataset_link><scientific_name>Homo sapiens</scientific_name><long_description>We conducted a prospective cohort study of adults (RESERVE-U-C19) admitted to Entebbe Regional Referral Hospital (ERRH), a national COVID-19 referral center, across three viral variant-driven phases of the pandemic in Uganda. In this cohort, which reflects the entire spectrum of SARS-CoV-2 infection, we integrated clinical data with serum proteomics (N=306) and whole-blood transcriptomics (N=100) to determine a range of host responses associated with COVID-19 severity, SARS-CoV-2/HIV co-infection, and circulating viral variants. Beyond the prognostic importance of myeloid cell-driven immune activation and lymphopenia, we show that multifaceted impairment of host protein synthesis and extensive redox imbalance define core metabolic signatures of severe COVID-19, with central roles for IL... (for more see dbGaP study page.)</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Multimodal immune profiling to determine mechanisms of COVID-19 clinical trajectory in Uganda</name><description>Multimodal immune profiling to determine mechanisms of COVID-19 clinical trajectory in Uganda</description><dates><last_updated>2025-09-24</last_updated><first_public>2023-04-13</first_public></dates><accession>PRJNA950542</accession><cross_references><taxon>9606</taxon></cross_references></HashMap>