<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Gebo KA</submitter><funding>HHS | NIH | National Institute of Allergy and Infectious Diseases Division of Intramural Research</funding><funding>HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases</funding><funding>HHS | NIH | National Institute on Drug Abuse</funding><funding>U.S. Department of Defense</funding><funding>HHS | NIH | National Institute of Allergy and Infectious Diseases</funding><funding>HHS | NIH | National Center for Advancing Translational Sciences</funding><pubmed_abstract>Post-COVID conditions (PCCs) are common and have significant morbidity. Risk factors for PCC include advancing age, female sex, obesity, and diabetes mellitus. Little is known about treatment, inflammation, and PCC. Among 882 individuals with confirmed SARS-CoV-2 infection participating in a randomized trial of COVID-19 convalescent plasma (CCP) vs control plasma with available biospecimens and symptom data, the association between early CCP treatment, cytokine levels, and PCC was evaluated. Cytokine and chemokine levels were assessed at baseline, day 14, and day 90 using a multiplexed sandwich immunoassay (Meso Scale Discovery). Presence of any self-reported PCC symptoms was assessed at day 90. Associations between CCP treatment, cytokine levels, and PCC were examined using multivariate l</pubmed_abstract><journal>mBio</journal><pagination>e0061823</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10653913</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Early antibody treatment, inflammation, and risk of post-COVID conditions.</pubmed_title><pmcid>PMC10653913</pmcid><funding_grant_id>U24TR001609</funding_grant_id><funding_grant_id>W911QY2090012</funding_grant_id><funding_grant_id>R01AI120938S1</funding_grant_id><funding_grant_id>F31DA054849</funding_grant_id><funding_grant_id>R01AI152078</funding_grant_id><funding_grant_id>R01DK131926</funding_grant_id><pubmed_authors>Gebo KA</pubmed_authors><pubmed_authors>Huaman MA</pubmed_authors><pubmed_authors>Ruff J</pubmed_authors><pubmed_authors>Patel B</pubmed_authors><pubmed_authors>Habtehyimer F</pubmed_authors><pubmed_authors>McBee NA</pubmed_authors><pubmed_authors>Hanley D</pubmed_authors><pubmed_authors>Das P</pubmed_authors><pubmed_authors>Blair JE</pubmed_authors><pubmed_authors>Lane K</pubmed_authors><pubmed_authors>Baksh S</pubmed_authors><pubmed_authors>Sutcliffe CG</pubmed_authors><pubmed_authors>Hammitt LL</pubmed_authors><pubmed_authors>Shade D</pubmed_authors><pubmed_authors>Mosnaim GS</pubmed_authors><pubmed_authors>Paxton JH</pubmed_authors><pubmed_authors>Cachay ER</pubmed_authors><pubmed_authors>Currier JS</pubmed_authors><pubmed_authors>Ram M</pubmed_authors><pubmed_authors>Casadevall A</pubmed_authors><pubmed_authors>CSSC-004 Consortium</pubmed_authors><pubmed_authors>Klein SL</pubmed_authors><pubmed_authors>Kassaye S</pubmed_authors><pubmed_authors>Pekosz A</pubmed_authors><pubmed_authors>Gniadek T</pubmed_authors><pubmed_authors>Levine A</pubmed_authors><pubmed_authors>Heath SL</pubmed_authors><pubmed_authors>Bloch EM</pubmed_authors><pubmed_authors>Patel EU</pubmed_authors><pubmed_authors>Tobian AAR</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>Meisenberg B</pubmed_authors><pubmed_authors>Anjan S</pubmed_authors><pubmed_authors>Raval JS</pubmed_authors><pubmed_authors>Fukuta Y</pubmed_authors><pubmed_authors>Fernandez RE</pubmed_authors><pubmed_authors>Shoham S</pubmed_authors><pubmed_authors>Forthal DN</pubmed_authors><pubmed_authors>Abraham AG</pubmed_authors><pubmed_authors>Zhu X</pubmed_authors><pubmed_authors>Gerber JM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Early antibody treatment, inflammation, and risk of post-COVID conditions.</name><description>Post-COVID conditions (PCCs) are common and have significant morbidity. Risk factors for PCC include advancing age, female sex, obesity, and diabetes mellitus. Little is known about treatment, inflammation, and PCC. Among 882 individuals with confirmed SARS-CoV-2 infection participating in a randomized trial of COVID-19 convalescent plasma (CCP) vs control plasma with available biospecimens and symptom data, the association between early CCP treatment, cytokine levels, and PCC was evaluated. Cytokine and chemokine levels were assessed at baseline, day 14, and day 90 using a multiplexed sandwich immunoassay (Meso Scale Discovery). Presence of any self-reported PCC symptoms was assessed at day 90. Associations between CCP treatment, cytokine levels, and PCC were examined using multivariate l</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Sep</publication><modification>2025-04-19T16:15:46.782Z</modification><creation>2024-11-21T03:37:43.67Z</creation></dates><accession>S-EPMC10653913</accession><cross_references><pubmed>37724870</pubmed><doi>10.1128/mbio.00618-23</doi></cross_references></HashMap>