<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Cervia C</submitter><funding>Schweizerische Akademie der Medizinischen Wissenschaften</funding><funding>Swiss National Science Foundation</funding><funding>Gottfried und Julia Bangerter-Rhyner-Stiftung (Bangerter-Stiftung)</funding><funding>Schweizerische Akademie der Medizinischen Wissenschaften (Swiss Academy of Medical Sciences)</funding><funding>University of Zurich (UZH Forschungskredit Candoc</funding><funding>Gottfried und Julia Bangerter-Rhyner-Stiftung</funding><funding>Clinical Research Priority Program CYTIMM-Z of University of Zurich (UZH), Pandemic Fund of University of Zurich (UZH), Innovation grant of University Hospital Zurich</funding><pagination>446</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8789854</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(1)</volume><pubmed_abstract>Following acute infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) a significant proportion of individuals develop prolonged symptoms, a serious condition termed post-acute coronavirus disease 2019 (COVID-19) syndrome (PACS) or long COVID. Predictors of PACS are needed. In a prospective multicentric cohort study of 215 individuals, we study COVID-19 patients during primary infection and up to one year later, compared to healthy subjects. We discover an immunoglobulin (Ig) signature, based on total IgM and IgG3 levels, which - combined with age, history of asthma bronchiale, and five symptoms during primary infection - is able to predict the risk of PACS independently of timepoint of blood sampling. We validate the score in an independent cohort of 395 individuals w</pubmed_abstract><journal>Nature communications</journal><pubmed_title>Immunoglobulin signature predicts risk of post-acute COVID-19 syndrome.</pubmed_title><pmcid>PMC8789854</pmcid><funding_grant_id>323530-177975</funding_grant_id><funding_grant_id>310030-200669</funding_grant_id><funding_grant_id>YTCR 32/18</funding_grant_id><funding_grant_id>NRP 78 Implementation Programme</funding_grant_id><funding_grant_id>323530-191220</funding_grant_id><funding_grant_id>323530-191230</funding_grant_id><funding_grant_id>4078P0-198431</funding_grant_id><pubmed_authors>Rudiger A</pubmed_authors><pubmed_authors>Menges D</pubmed_authors><pubmed_authors>Bachli E</pubmed_authors><pubmed_authors>Nilsson J</pubmed_authors><pubmed_authors>Zurbuchen Y</pubmed_authors><pubmed_authors>Taeschler P</pubmed_authors><pubmed_authors>Raeber ME</pubmed_authors><pubmed_authors>Adamo S</pubmed_authors><pubmed_authors>Held U</pubmed_authors><pubmed_authors>Boyman O</pubmed_authors><pubmed_authors>Huber LC</pubmed_authors><pubmed_authors>Puhan MA</pubmed_authors><pubmed_authors>Cervia C</pubmed_authors><pubmed_authors>Hasler S</pubmed_authors><pubmed_authors>Stussi-Helbling M</pubmed_authors><pubmed_authors>Ballouz T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Immunoglobulin signature predicts risk of post-acute COVID-19 syndrome.</name><description>Following acute infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) a significant proportion of individuals develop prolonged symptoms, a serious condition termed post-acute coronavirus disease 2019 (COVID-19) syndrome (PACS) or long COVID. Predictors of PACS are needed. In a prospective multicentric cohort study of 215 individuals, we study COVID-19 patients during primary infection and up to one year later, compared to healthy subjects. We discover an immunoglobulin (Ig) signature, based on total IgM and IgG3 levels, which - combined with age, history of asthma bronchiale, and five symptoms during primary infection - is able to predict the risk of PACS independently of timepoint of blood sampling. We validate the score in an independent cohort of 395 individuals w</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Jan</publication><modification>2025-04-04T14:59:05.409Z</modification><creation>2025-04-04T14:59:05.409Z</creation></dates><accession>S-EPMC8789854</accession><cross_references><pubmed>35078982</pubmed><doi>10.1038/s41467-021-27797-1</doi></cross_references></HashMap>