<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Pickering H</submitter><funding>BLRD VA</funding><funding>NCATS NIH HHS</funding><funding>NIAID NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>U.S. Department of Health &amp;amp; Human Services | NIH | National Heart, Lung, and Blood Institute</funding><funding>U.S. Department of Health &amp; Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI)</funding><pagination>586</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11723965</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(1)</volume><pubmed_abstract>Coronavirus disease 2019 (COVID-19) poses significant risks for solid organ transplant recipients, who have atypical but poorly characterized immune responses to infection. We aim to understand the host immunologic and microbial features of COVID-19 in transplant recipients by leveraging a prospective multicenter cohort of 86 transplant recipients age- and sex-matched with 172 non-transplant controls. We find that transplant recipients have higher nasal SARS-CoV-2 viral abundance and impaired viral clearance, and lower anti-spike IgG levels. In addition, transplant recipients exhibit decreased plasmablasts and transitional B cells, and increased senescent T cells. Blood and nasal transcriptional profiling demonstrate unexpected upregulation of innate immune signaling pathways and increased</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Host-microbe multiomic profiling identifies distinct COVID-19 immune dysregulation in solid organ transplant recipients.</pubmed_title><pmcid>PMC11723965</pmcid><funding_grant_id>R01 AI135803</funding_grant_id><funding_grant_id>R01 AI104870</funding_grant_id><funding_grant_id>U19 AI090023</funding_grant_id><funding_grant_id>U19 AI062629</funding_grant_id><funding_grant_id>UL1 TR001863</funding_grant_id><funding_grant_id>U54 AI142766</funding_grant_id><funding_grant_id>U19 AI118610</funding_grant_id><funding_grant_id>R01 HL155418</funding_grant_id><funding_grant_id>U19 AI077439</funding_grant_id><funding_grant_id>P01 AI153559</funding_grant_id><funding_grant_id>I01 BX005023</funding_grant_id><funding_grant_id>R01 AI145835</funding_grant_id><funding_grant_id>U19 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recipients, who have atypical but poorly characterized immune responses to infection. We aim to understand the host immunologic and microbial features of COVID-19 in transplant recipients by leveraging a prospective multicenter cohort of 86 transplant recipients age- and sex-matched with 172 non-transplant controls. We find that transplant recipients have higher nasal SARS-CoV-2 viral abundance and impaired viral clearance, and lower anti-spike IgG levels. In addition, transplant recipients exhibit decreased plasmablasts and transitional B cells, and increased senescent T cells. Blood and nasal transcriptional profiling demonstrate unexpected upregulation of innate immune signaling pathways and increased</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jan</publication><modification>2026-06-01T05:06:26.889Z</modification><creation>2026-04-08T09:26:09.781Z</creation></dates><accession>S-EPMC11723965</accession><cross_references><pubmed>39794319</pubmed><doi>10.1038/s41467-025-55823-z</doi></cross_references></HashMap>