<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Salgado BB</submitter><funding>São Paulo Research Foundation</funding><funding>WHO by the COVID-19 Solidarity Response Fund and the German Federal Ministry of Health (BMG)</funding><funding>WHO Unity Studies</funding><funding>National Council for Scientific and Technological Development</funding><funding>ILMD/Fiocruz Amazônia</funding><funding>Fundo de Apoio ao Ensino, Pesquisa e Extensão from UNICAMP</funding><funding>Fundação de Amparo à Pesquisa do Estado do Amazonas</funding><funding>Inova Fiocruz/Fundação Oswaldo Cruz grant</funding><pagination>1018</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10143282</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>15(4)</volume><pubmed_abstract>Numerous studies have focused on inflammation-related markers to understand COVID-19. In this study, we performed a comparative analysis of spike (S) and nucleocapsid (N) protein-specific IgA, total IgG and IgG subclass response in COVID-19 patients and compared this to their disease outcome. We observed that the SARS-CoV-2 infection elicits a robust IgA and IgG response against the N-terminal (N1) and C-terminal (N3) region of the N protein, whereas we failed to detect IgA antibodies and observed a weak IgG response against the disordered linker region (N2) in COVID-19 patients. N and S protein-specific IgG1, IgG2 and IgG3 response was significantly elevated in hospitalized patients with severe disease compared to outpatients with non-severe disease. IgA and total IgG antibody reactivity </pubmed_abstract><journal>Viruses</journal><pubmed_title>Antigen-Specific Antibody Signature Is Associated with COVID-19 Outcome.</pubmed_title><pmcid>PMC10143282</pmcid><funding_grant_id>305628/2020-8</funding_grant_id><funding_grant_id>2016/00194-8</funding_grant_id><funding_grant_id>2266/20</funding_grant_id><funding_grant_id>48402179682401</funding_grant_id><funding_grant_id>2020/04558-0</funding_grant_id><funding_grant_id>2023-2025</funding_grant_id><funding_grant_id>062.00967/2020</funding_grant_id><funding_grant_id>48401556406778</funding_grant_id><pubmed_authors>Pinto KR</pubmed_authors><pubmed_authors>Nogueira PA</pubmed_authors><pubmed_authors>Salgado BB</pubmed_authors><pubmed_authors>Forato J</pubmed_authors><pubmed_authors>Pereira Filho IV</pubmed_authors><pubmed_authors>Correia IS</pubmed_authors><pubmed_authors>Carvalho NO</pubmed_authors><pubmed_authors>Proenca-Modena JL</pubmed_authors><pubmed_authors>Jordao MF</pubmed_authors><pubmed_authors>Assuncao EN</pubmed_authors><pubmed_authors>Toledo-Teixeira DA</pubmed_authors><pubmed_authors>Salgado Sobrinho WB</pubmed_authors><pubmed_authors>Melo GC</pubmed_authors><pubmed_authors>Sampaio VS</pubmed_authors><pubmed_authors>Monteiro WM</pubmed_authors><pubmed_authors>Barbosa PP</pubmed_authors><pubmed_authors>Souza Neto JN</pubmed_authors><pubmed_authors>Cordeiro IB</pubmed_authors><pubmed_authors>Lalwani JDB</pubmed_authors><pubmed_authors>Granja F</pubmed_authors><pubmed_authors>da Silva DSS</pubmed_authors><pubmed_authors>Lacerda MVG</pubmed_authors><pubmed_authors>Astolfi Filho S</pubmed_authors><pubmed_authors>Lalwani P</pubmed_authors><pubmed_authors>de Morais TBDN</pubmed_authors><pubmed_authors>Souza WM</pubmed_authors><pubmed_authors>Dos Santos RO</pubmed_authors><pubmed_authors>Val FFA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Antigen-Specific Antibody Signature Is Associated with COVID-19 Outcome.</name><description>Numerous studies have focused on inflammation-related markers to understand COVID-19. In this study, we performed a comparative analysis of spike (S) and nucleocapsid (N) protein-specific IgA, total IgG and IgG subclass response in COVID-19 patients and compared this to their disease outcome. We observed that the SARS-CoV-2 infection elicits a robust IgA and IgG response against the N-terminal (N1) and C-terminal (N3) region of the N protein, whereas we failed to detect IgA antibodies and observed a weak IgG response against the disordered linker region (N2) in COVID-19 patients. N and S protein-specific IgG1, IgG2 and IgG3 response was significantly elevated in hospitalized patients with severe disease compared to outpatients with non-severe disease. IgA and total IgG antibody reactivity </description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Apr</publication><modification>2026-04-07T20:57:40.94Z</modification><creation>2024-11-12T07:06:55.724Z</creation></dates><accession>S-EPMC10143282</accession><cross_references><pubmed>37112998</pubmed><doi>10.3390/v15041018</doi></cross_references></HashMap>