<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Giroux NS</submitter><funding>NIAID NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>NIGMS NIH HHS</funding><pubmed_abstract>SARS-CoV-2 infection triggers profound and variable immune responses in human hosts. Chromatin remodeling has been observed in individuals severely ill or convalescing with COVID-19, but chromatin remodeling early in disease prior to anti-spike protein IgG seroconversion has not been defined. We performed the Assay for Transposase-Accessible Chromatin using sequencing (ATAC-seq) and RNA-seq on peripheral blood mononuclear cells (PBMCs) from outpatients with mild or moderate symptom severity at different stages of clinical illness. Early in the disease course prior to IgG seroconversion, modifications in chromatin accessibility associate with mild or moderate symptoms are already robust and include severity-associated changes in accessibility of genes in interleukin signaling, regulation of</pubmed_abstract><journal>Research square</journal><pagination>rs.3.rs-1479864</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8996625</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Differential chromatin accessibility in peripheral blood mononuclear cells underlies COVID-19 disease severity prior to seroconversion.</pubmed_title><pmcid>PMC8996625</pmcid><funding_grant_id>R35 GM122465</funding_grant_id><funding_grant_id>K08 HL130557</funding_grant_id><funding_grant_id>UC6 AI058607</funding_grant_id><funding_grant_id>75N93019C00015</funding_grant_id><pubmed_authors>Satterwhite LL</pubmed_authors><pubmed_authors>Rivera GO</pubmed_authors><pubmed_authors>Bose S</pubmed_authors><pubmed_authors>Henao R</pubmed_authors><pubmed_authors>Ginsburg GS</pubmed_authors><pubmed_authors>Tsalik EL</pubmed_authors><pubmed_authors>Wang E</pubmed_authors><pubmed_authors>Nicholson BP</pubmed_authors><pubmed_authors>Xi R</pubmed_authors><pubmed_authors>De Ussel MI</pubmed_authors><pubmed_authors>Burke TW</pubmed_authors><pubmed_authors>Chung HA</pubmed_authors><pubmed_authors>Sempowski GD</pubmed_authors><pubmed_authors>Giroux NS</pubmed_authors><pubmed_authors>Kraft BD</pubmed_authors><pubmed_authors>Ding S</pubmed_authors><pubmed_authors>Ko ER</pubmed_authors><pubmed_authors>Woods C</pubmed_authors><pubmed_authors>Petzold E</pubmed_authors><pubmed_authors>Rotstein T</pubmed_authors><pubmed_authors>McClain MT</pubmed_authors><pubmed_authors>Denny TN</pubmed_authors><pubmed_authors>Shen X</pubmed_authors><pubmed_authors>Chen T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Differential chromatin accessibility in peripheral blood mononuclear cells underlies COVID-19 disease severity prior to seroconversion.</name><description>SARS-CoV-2 infection triggers profound and variable immune responses in human hosts. Chromatin remodeling has been observed in individuals severely ill or convalescing with COVID-19, but chromatin remodeling early in disease prior to anti-spike protein IgG seroconversion has not been defined. We performed the Assay for Transposase-Accessible Chromatin using sequencing (ATAC-seq) and RNA-seq on peripheral blood mononuclear cells (PBMCs) from outpatients with mild or moderate symptom severity at different stages of clinical illness. Early in the disease course prior to IgG seroconversion, modifications in chromatin accessibility associate with mild or moderate symptoms are already robust and include severity-associated changes in accessibility of genes in interleukin signaling, regulation of</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2025-04-04T08:52:59.458Z</modification><creation>2025-04-04T08:52:59.458Z</creation></dates><accession>S-EPMC8996625</accession><cross_references><pubmed>35411343</pubmed><doi>10.21203/rs.3.rs-1479864/v1</doi></cross_references></HashMap>