<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Davis SK</submitter><funding>Paul Ramsay Foundation</funding><funding>Howard Hughes Medical Institute</funding><funding>National Health and Medical Research Council</funding><funding>Wellcome Trust</funding><funding>Australian Research Council</funding><pagination>e1424</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9588388</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(10)</volume><pubmed_abstract>&lt;h4>Objectives&lt;/h4>Following infection with SARS-CoV-2, virus-specific antibodies are generated, which can both neutralise virions and clear infection via Fc effector functions. The importance of IgG antibodies for protection and control of SARS-CoV-2 has been extensively reported. By comparison, other antibody isotypes including IgA have been poorly characterised.&lt;h4>Methods&lt;/h4>Here, we characterised plasma IgA from 41 early convalescent COVID-19 subjects for neutralisation and Fc effector functions.&lt;h4>Results&lt;/h4>Convalescent plasma IgA from > 60% of the cohort had the capacity to inhibit the interaction between wild-type RBD and ACE2. Furthermore, a third of the cohort induced stronger IgA-mediated ACE2 inhibition than matched IgG when tested at equivalent concentrations. Plasma IgA a</pubmed_abstract><journal>Clinical &amp; translational immunology</journal><pubmed_title>Heterologous SARS-CoV-2 IgA neutralising antibody responses in convalescent plasma.</pubmed_title><pmcid>PMC9588388</pmcid><funding_grant_id>208693/Z/17/Z</funding_grant_id><pubmed_authors>Godfrey DI</pubmed_authors><pubmed_authors>Pymm P</pubmed_authors><pubmed_authors>Redmond SJ</pubmed_authors><pubmed_authors>Kent SJ</pubmed_authors><pubmed_authors>Adair A</pubmed_authors><pubmed_authors>Haycroft ER</pubmed_authors><pubmed_authors>Davis SK</pubmed_authors><pubmed_authors>Wheatley AK</pubmed_authors><pubmed_authors>Chung AW</pubmed_authors><pubmed_authors>Selva KJ</pubmed_authors><pubmed_authors>Lopez E</pubmed_authors><pubmed_authors>Tham WH</pubmed_authors><pubmed_authors>Lee WS</pubmed_authors><pubmed_authors>Juno JA</pubmed_authors><pubmed_authors>Gherardin NA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Heterologous SARS-CoV-2 IgA neutralising antibody responses in convalescent plasma.</name><description>&lt;h4>Objectives&lt;/h4>Following infection with SARS-CoV-2, virus-specific antibodies are generated, which can both neutralise virions and clear infection via Fc effector functions. The importance of IgG antibodies for protection and control of SARS-CoV-2 has been extensively reported. By comparison, other antibody isotypes including IgA have been poorly characterised.&lt;h4>Methods&lt;/h4>Here, we characterised plasma IgA from 41 early convalescent COVID-19 subjects for neutralisation and Fc effector functions.&lt;h4>Results&lt;/h4>Convalescent plasma IgA from > 60% of the cohort had the capacity to inhibit the interaction between wild-type RBD and ACE2. Furthermore, a third of the cohort induced stronger IgA-mediated ACE2 inhibition than matched IgG when tested at equivalent concentrations. Plasma IgA a</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2026-04-12T19:28:02.853Z</modification><creation>2025-04-05T10:06:46.456Z</creation></dates><accession>S-EPMC9588388</accession><cross_references><pubmed>36299410</pubmed><doi>10.1002/cti2.1424</doi></cross_references></HashMap>