<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Dobano C</submitter><pubmed_abstract>COVID-19 affects children to a lesser extent than adults but they can still get infected and transmit SARS-CoV-2 to their contacts. Field deployable non-invasive sensitive diagnostic techniques are needed to evaluate the infectivity dynamics of SARS-CoV-2 in pediatric populations and guide public health interventions, particularly if this population is not fully vaccinated. We evaluated the utility of high-throughput Luminex assays to quantify saliva IgM, IgA and IgG antibodies against five SARS-CoV-2 spike (S) and nucleocapsid (N) antigens in a contacts and infectivity longitudinal study in 122 individuals (52 children and 70 adults). We compared saliva versus serum/plasma samples in infected children and adults diagnosed by weekly RT-PCR over 35 days (n=62), and those who consistently te</pubmed_abstract><journal>Frontiers in immunology</journal><pagination>751705</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8828491</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Multiplex Antibody Analysis of IgM, IgA and IgG to SARS-CoV-2 in Saliva and Serum From Infected Children and Their Close Contacts.</pubmed_title><pmcid>PMC8828491</pmcid><pubmed_authors>Gratacos E</pubmed_authors><pubmed_authors>Fernandez de Sevilla M</pubmed_authors><pubmed_authors>Alonso S</pubmed_authors><pubmed_authors>Moncunill G</pubmed_authors><pubmed_authors>Garcia-Miquel A</pubmed_authors><pubmed_authors>Codina A</pubmed_authors><pubmed_authors>Rodrigo Melero N</pubmed_authors><pubmed_authors>Rubio R</pubmed_authors><pubmed_authors>Puyol L</pubmed_authors><pubmed_authors>Balanza N</pubmed_authors><pubmed_authors>Aguilar R</pubmed_authors><pubmed_authors>Santano R</pubmed_authors><pubmed_authors>Pons Tomas G</pubmed_authors><pubmed_authors>Jordan I</pubmed_authors><pubmed_authors>Carolis C</pubmed_authors><pubmed_authors>Baro B</pubmed_authors><pubmed_authors>Fumado V</pubmed_authors><pubmed_authors>Cubells M</pubmed_authors><pubmed_authors>Garcia-Garcia JJ</pubmed_authors><pubmed_authors>Dobano C</pubmed_authors><pubmed_authors>Bassat Q</pubmed_authors><pubmed_authors>Izquierdo L</pubmed_authors><pubmed_authors>Fortuny C</pubmed_authors><pubmed_authors>Claverol J</pubmed_authors><pubmed_authors>Jimenez A</pubmed_authors><pubmed_authors>Girona-Alarcon M</pubmed_authors><pubmed_authors>Arias S</pubmed_authors><pubmed_authors>Munoz-Almagro C</pubmed_authors><pubmed_authors>Millat-Martinez P</pubmed_authors><pubmed_authors>Mele Casas M</pubmed_authors><pubmed_authors>Barrios D</pubmed_authors><pubmed_authors>Hernandez Garcia M</pubmed_authors><pubmed_authors>Bonet-Carne E</pubmed_authors><pubmed_authors>Vidal M</pubmed_authors><pubmed_authors>Ajanovic S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Multiplex Antibody Analysis of IgM, IgA and IgG to SARS-CoV-2 in Saliva and Serum From Infected Children and Their Close Contacts.</name><description>COVID-19 affects children to a lesser extent than adults but they can still get infected and transmit SARS-CoV-2 to their contacts. Field deployable non-invasive sensitive diagnostic techniques are needed to evaluate the infectivity dynamics of SARS-CoV-2 in pediatric populations and guide public health interventions, particularly if this population is not fully vaccinated. We evaluated the utility of high-throughput Luminex assays to quantify saliva IgM, IgA and IgG antibodies against five SARS-CoV-2 spike (S) and nucleocapsid (N) antigens in a contacts and infectivity longitudinal study in 122 individuals (52 children and 70 adults). We compared saliva versus serum/plasma samples in infected children and adults diagnosed by weekly RT-PCR over 35 days (n=62), and those who consistently te</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-26T02:01:42.38Z</modification><creation>2025-02-19T01:34:24.872Z</creation></dates><accession>S-EPMC8828491</accession><cross_references><pubmed>35154094</pubmed><doi>10.3389/fimmu.2022.751705</doi></cross_references></HashMap>