<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Abe K</submitter><funding>National Institute of Allergy and Infectious Diseases</funding><funding>NCATS NIH HHS</funding><funding>NIDA NIH HHS</funding><funding>NIAID NIH HHS</funding><funding>NIH HHS</funding><funding>National Science Foundation</funding><pagination>3310-3320</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12726064</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>214(12)</volume><pubmed_abstract>The National Institutes of Health-funded IMPACC (IMmunoPhenotyping Assessment in a COVID-19 Cohort) evaluated longitudinal clinical and immunological features of human patients hospitalized for COVID-19. This study focuses on comparing the novel NULISAseq assay with the Olink platform using a subset of participants to assess their efficacy in predicting COVID-19 severity and understanding immune response dynamics. Our findings reveal that NULISAseq could provide superior detectability and dynamic range across various targets. Elastic net analysis demonstrated that specific proteins, including amphiregulin, effectively predict COVID-19 severity from sera at admission (samples drawn within 96 h of admission), with a test area under the curve of 0.84. Longitudinal analysis identified signific</pubmed_abstract><journal>Journal of immunology (Baltimore, Md. : 1950)</journal><pubmed_title>Evaluating COVID-19 severity prediction and immune dynamics with NULISAseq: Insights from the IMPACC study.</pubmed_title><pmcid>PMC12726064</pmcid><funding_grant_id>R01AI145835-01A1S1</funding_grant_id><funding_grant_id>R01 AI104870</funding_grant_id><funding_grant_id>UM1 TR004528</funding_grant_id><funding_grant_id>3U01AI167892-01S2</funding_grant_id><funding_grant_id>U19 AI062629</funding_grant_id><funding_grant_id>4U19AI090023-11</funding_grant_id><funding_grant_id>U54 AI142766</funding_grant_id><funding_grant_id>3U01AI167892-03S2</funding_grant_id><funding_grant_id>U19 AI118610</funding_grant_id><funding_grant_id>5U19AI062629-17</funding_grant_id><funding_grant_id>5U19AI118608-04</funding_grant_id><funding_grant_id>3U19AI089992-09</funding_grant_id><funding_grant_id>R01 AI122220</funding_grant_id><funding_grant_id>U19 AI128910</funding_grant_id><funding_grant_id>U19 AI128913</funding_grant_id><funding_grant_id>5R01AI104870-07</funding_grant_id><funding_grant_id>4U19AI118610-06</funding_grant_id><funding_grant_id>5T32DA018926-18</funding_grant_id><funding_grant_id>5U19AI125357-05</funding_grant_id><funding_grant_id>R01 AI135803</funding_grant_id><funding_grant_id>3U19AI077439-13</funding_grant_id><funding_grant_id>3U19AI128913-03</funding_grant_id><funding_grant_id>5U54AI142766-03</funding_grant_id><funding_grant_id>5U19AI128913-03</funding_grant_id><funding_grant_id>T32 DA018926</funding_grant_id><funding_grant_id>U19 AI090023</funding_grant_id><funding_grant_id>U01 AI167892</funding_grant_id><funding_grant_id>5U19AI057229-17</funding_grant_id><funding_grant_id>5U19AI057229-18</funding_grant_id><funding_grant_id>DMS2310836</funding_grant_id><funding_grant_id>R01AI122220</funding_grant_id><funding_grant_id>5U19AI128910-04</funding_grant_id><funding_grant_id>U19 AI077439</funding_grant_id><funding_grant_id>5R01AI135803-03</funding_grant_id><funding_grant_id>U19 AI118608</funding_grant_id><funding_grant_id>R01 AI145835</funding_grant_id><funding_grant_id>U19 AI125357</funding_grant_id><funding_grant_id>U19 AI057229</funding_grant_id><funding_grant_id>UM1TR004528</funding_grant_id><funding_grant_id>U19AI128913-04S1</funding_grant_id><funding_grant_id>3U19AI1289130</funding_grant_id><funding_grant_id>U19 AI089992</funding_grant_id><pubmed_authors>Peters B</pubmed_authors><pubmed_authors>Hafler DA</pubmed_authors><pubmed_authors>Simon V</pubmed_authors><pubmed_authors>Kheradmand F</pubmed_authors><pubmed_authors>Agudelo Higuita NI</pubmed_authors><pubmed_authors>Calfee CS</pubmed_authors><pubmed_authors>Schaenman J</pubmed_authors><pubmed_authors>Augustine AD</pubmed_authors><pubmed_authors>Nguyen TT</pubmed_authors><pubmed_authors>Rouphael N</pubmed_authors><pubmed_authors>Erle DJ</pubmed_authors><pubmed_authors>Kleinstein SH</pubmed_authors><pubmed_authors>Maecker HT</pubmed_authors><pubmed_authors>McComsey GA</pubmed_authors><pubmed_authors>Sekaly RP</pubmed_authors><pubmed_authors>Corry DB</pubmed_authors><pubmed_authors>Davis MM</pubmed_authors><pubmed_authors>Reed EF</pubmed_authors><pubmed_authors>Metcalf JP</pubmed_authors><pubmed_authors>Shaw AC</pubmed_authors><pubmed_authors>Ehrlich LIR</pubmed_authors><pubmed_authors>Messer WB</pubmed_authors><pubmed_authors>Haddad EK</pubmed_authors><pubmed_authors>Diray-Arce J</pubmed_authors><pubmed_authors>Ozonoff A</pubmed_authors><pubmed_authors>Melamed E</pubmed_authors><pubmed_authors>Cairns CB</pubmed_authors><pubmed_authors>Kim-Schulze S</pubmed_authors><pubmed_authors>Baden LR</pubmed_authors><pubmed_authors>Brakenridge SC</pubmed_authors><pubmed_authors>Pulendran B</pubmed_authors><pubmed_authors>Abe K</pubmed_authors><pubmed_authors>Hough CL</pubmed_authors><pubmed_authors>Nadeau KC</pubmed_authors><pubmed_authors>Montgomery RR</pubmed_authors><pubmed_authors>Kraft M</pubmed_authors><pubmed_authors>Holmes TH</pubmed_authors><pubmed_authors>Atkinson MA</pubmed_authors><pubmed_authors>Bime C</pubmed_authors><pubmed_authors>Fernandez-Sesma A</pubmed_authors><pubmed_authors>Becker PM</pubmed_authors><pubmed_authors>Levy O</pubmed_authors><pubmed_authors>IMPACC Network</pubmed_authors></additional><is_claimable>false</is_claimable><name>Evaluating COVID-19 severity prediction and immune dynamics with NULISAseq: Insights from the IMPACC study.</name><description>The National Institutes of Health-funded IMPACC (IMmunoPhenotyping Assessment in a COVID-19 Cohort) evaluated longitudinal clinical and immunological features of human patients hospitalized for COVID-19. This study focuses on comparing the novel NULISAseq assay with the Olink platform using a subset of participants to assess their efficacy in predicting COVID-19 severity and understanding immune response dynamics. Our findings reveal that NULISAseq could provide superior detectability and dynamic range across various targets. Elastic net analysis demonstrated that specific proteins, including amphiregulin, effectively predict COVID-19 severity from sera at admission (samples drawn within 96 h of admission), with a test area under the curve of 0.84. Longitudinal analysis identified signific</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-06T09:51:07.181Z</modification><creation>2026-05-28T03:12:47.853Z</creation></dates><accession>S-EPMC12726064</accession><cross_references><pubmed>41166719</pubmed><doi>10.1093/jimmun/vkaf263</doi></cross_references></HashMap>