<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Park HS</submitter><funding>NCATS</funding><funding>NCATS NIH HHS</funding><funding>NIAID NIH HHS</funding><funding>NHLBI NIH HHS</funding><funding>State of Maryland</funding><funding>Moriah Fund</funding><funding>NIAID</funding><funding>Mental Wellness Foundation</funding><funding>Healthnetwork Foundation</funding><funding>NHLBI</funding><funding>Octapharma</funding><funding>Shear Family Foundation</funding><funding>Bloomberg Philanthropies</funding><funding>NIGMS NIH HHS</funding><funding>Defense Health Agency</funding><pagination>e178460</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11141865</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(8)</volume><pubmed_abstract>BACKGROUNDCOVID-19 convalescent plasma (CCP) virus-specific antibody levels that translate into recipient posttransfusion antibody levels sufficient to prevent disease progression are not defined.METHODSThis secondary analysis correlated donor and recipient antibody levels to hospitalization risk among unvaccinated, seronegative CCP recipients within the outpatient, double-blind, randomized clinical trial that compared CCP to control plasma. The majority of COVID-19 CCP arm hospitalizations (15/17, 88%) occurred in this unvaccinated, seronegative subgroup. A functional cutoff to delineate recipient high versus low posttransfusion antibody levels was established by 2 methods: (i) analyzing virus neutralization-equivalent anti-Spike receptor-binding domain immunoglobulin G (anti-S-RBD IgG) r</pubmed_abstract><journal>JCI insight</journal><pubmed_title>Outpatient COVID-19 convalescent plasma recipient antibody thresholds correlated to reduced hospitalizations within a randomized trial.</pubmed_title><pmcid>PMC11141865</pmcid><funding_grant_id>R01 AI152078</funding_grant_id><funding_grant_id>W911QY2090012</funding_grant_id><funding_grant_id>T32 GM149382</funding_grant_id><funding_grant_id>U24TR001609-S3</funding_grant_id><funding_grant_id>U24 TR001609</funding_grant_id><funding_grant_id>1</funding_grant_id><funding_grant_id>2</funding_grant_id><funding_grant_id>3</funding_grant_id><funding_grant_id>UL1 TR001409</funding_grant_id><funding_grant_id>4</funding_grant_id><funding_grant_id>K23 HL151826</funding_grant_id><funding_grant_id>5</funding_grant_id><funding_grant_id>T32 AI102623</funding_grant_id><funding_grant_id>6</funding_grant_id><funding_grant_id>7</funding_grant_id><funding_grant_id>1K23HL151826NIH</funding_grant_id><funding_grant_id>3R01AI152078-01S1</funding_grant_id><pubmed_authors>Huaman MA</pubmed_authors><pubmed_authors>Gebo KA</pubmed_authors><pubmed_authors>Na YB</pubmed_authors><pubmed_authors>Wu J</pubmed_authors><pubmed_authors>Cluzet VC</pubmed_authors><pubmed_authors>Patel B</pubmed_authors><pubmed_authors>Blair JE</pubmed_authors><pubmed_authors>Lane K</pubmed_authors><pubmed_authors>Arroyo-Curras N</pubmed_authors><pubmed_authors>Rausch W</pubmed_authors><pubmed_authors>Ehrhardt S</pubmed_authors><pubmed_authors>Lee JS</pubmed_authors><pubmed_authors>Park HS</pubmed_authors><pubmed_authors>Sitaras I</pubmed_authors><pubmed_authors>Betenbaugh MJ</pubmed_authors><pubmed_authors>Paxton JH</pubmed_authors><pubmed_authors>Ou J</pubmed_authors><pubmed_authors>Oei K</pubmed_authors><pubmed_authors>Cordisco ME</pubmed_authors><pubmed_authors>Knoll MD</pubmed_authors><pubmed_authors>Currier JS</pubmed_authors><pubmed_authors>Karlen N</pubmed_authors><pubmed_authors>Jabs DA</pubmed_authors><pubmed_authors>Ram M</pubmed_authors><pubmed_authors>Casadevall A</pubmed_authors><pubmed_authors>Pekosz A</pubmed_authors><pubmed_authors>Kassaye SG</pubmed_authors><pubmed_authors>Bloch EM</pubmed_authors><pubmed_authors>Sachithanandham J</pubmed_authors><pubmed_authors>Yoon S</pubmed_authors><pubmed_authors>Hanley DF</pubmed_authors><pubmed_authors>Gniadek TJ</pubmed_authors><pubmed_authors>Li M</pubmed_authors><pubmed_authors>Levine AC</pubmed_authors><pubmed_authors>Meisenberg BR</pubmed_authors><pubmed_authors>Caputo CA</pubmed_authors><pubmed_authors>Ford DE</pubmed_authors><pubmed_authors>Ornelas-Gatdula E</pubmed_authors><pubmed_authors>Ndahiro N</pubmed_authors><pubmed_authors>Shoham S</pubmed_authors><pubmed_authors>Forthal DN</pubmed_authors><pubmed_authors>Spivak ES</pubmed_authors><pubmed_authors>Shade DM</pubmed_authors><pubmed_authors>McBee NA</pubmed_authors><pubmed_authors>Ziman A</pubmed_authors><pubmed_authors>Yin A</pubmed_authors><pubmed_authors>Hammel J</pubmed_authors><pubmed_authors>Sutcliffe CG</pubmed_authors><pubmed_authors>Hammitt LL</pubmed_authors><pubmed_authors>Mosnaim GS</pubmed_authors><pubmed_authors>Jedlicka A</pubmed_authors><pubmed_authors>Cachay ER</pubmed_authors><pubmed_authors>Abinante M</pubmed_authors><pubmed_authors>Zand MS</pubmed_authors><pubmed_authors>Klein SL</pubmed_authors><pubmed_authors>Cruser D</pubmed_authors><pubmed_authors>Heath SL</pubmed_authors><pubmed_authors>Greenblatt B</pubmed_authors><pubmed_authors>Shapiro JR</pubmed_authors><pubmed_authors>Singh A</pubmed_authors><pubmed_authors>Laeyendecker O</pubmed_authors><pubmed_authors>Sullivan DJ</pubmed_authors><pubmed_authors>Baker OR</pubmed_authors><pubmed_authors>Gawad AL</pubmed_authors><pubmed_authors>Barranta C</pubmed_authors><pubmed_authors>Eby Y</pubmed_authors><pubmed_authors>Anjan S</pubmed_authors><pubmed_authors>Appel LJ</pubmed_authors><pubmed_authors>Shenoy AG</pubmed_authors><pubmed_authors>Broderick PB</pubmed_authors><pubmed_authors>Raval JS</pubmed_authors><pubmed_authors>Fernandez RE</pubmed_authors><pubmed_authors>Fukuta Y</pubmed_authors><pubmed_authors>Yarava A</pubmed_authors><pubmed_authors>Petrini JR</pubmed_authors><pubmed_authors>Caturegli P</pubmed_authors><pubmed_authors>Marshall CE</pubmed_authors><pubmed_authors>Gerber JM</pubmed_authors><pubmed_authors>Lau B</pubmed_authors><pubmed_authors>Baksh SN</pubmed_authors><pubmed_authors>Tobian AA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Outpatient COVID-19 convalescent plasma recipient antibody thresholds correlated to reduced hospitalizations within a randomized trial.</name><description>BACKGROUNDCOVID-19 convalescent plasma (CCP) virus-specific antibody levels that translate into recipient posttransfusion antibody levels sufficient to prevent disease progression are not defined.METHODSThis secondary analysis correlated donor and recipient antibody levels to hospitalization risk among unvaccinated, seronegative CCP recipients within the outpatient, double-blind, randomized clinical trial that compared CCP to control plasma. The majority of COVID-19 CCP arm hospitalizations (15/17, 88%) occurred in this unvaccinated, seronegative subgroup. A functional cutoff to delineate recipient high versus low posttransfusion antibody levels was established by 2 methods: (i) analyzing virus neutralization-equivalent anti-Spike receptor-binding domain immunoglobulin G (anti-S-RBD IgG) r</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-04-08T19:51:13.712Z</modification><creation>2026-04-08T14:32:06.92Z</creation></dates><accession>S-EPMC11141865</accession><cross_references><pubmed>38483534</pubmed><doi>10.1172/jci.insight.178460</doi></cross_references></HashMap>