| Literature DB >> 34362897 |
Natalia Ortega1, Marta Ribes1, Marta Vidal1, Rocío Rubio1, Ruth Aguilar1, Sarah Williams1, Diana Barrios1, Selena Alonso1, Pablo Hernández-Luis2,3, Robert A Mitchell1, Chenjerai Jairoce1,4, Angeline Cruz1, Alfons Jimenez1,5, Rebeca Santano1, Susana Méndez1, Montserrat Lamoglia1,6, Neus Rosell1, Anna Llupià1,7, Laura Puyol1, Jordi Chi1, Natalia Rodrigo Melero8, Daniel Parras2, Pau Serra2, Edwards Pradenas9, Benjamin Trinité9, Julià Blanco9,10, Alfredo Mayor1,4,5, Sonia Barroso11, Pilar Varela11, Anna Vilella1,5, Antoni Trilla1,5,12, Pere Santamaria7,13,14, Carlo Carolis8, Marta Tortajada11, Luis Izquierdo1, Ana Angulo2,3, Pablo Engel2,3, Alberto L García-Basteiro1,4,15, Gemma Moncunill16, Carlota Dobaño17,18.
Abstract
Unraveling the long-term kinetics of antibodies to SARS-CoV-2 and the individual characteristics influencing it, including the impact of pre-existing antibodies to human coronaviruses causing common cold (HCoVs), is essential to understand protective immunity to COVID-19 and devise effective surveillance strategies. IgM, IgA and IgG levels against six SARS-CoV-2 antigens and the nucleocapsid antigen of the four HCoV (229E, NL63, OC43 and HKU1) were quantified by Luminex, and antibody neutralization capacity was assessed by flow cytometry, in a cohort of health care workers followed up to 7 months (N = 578). Seroprevalence increases over time from 13.5% (month 0) and 15.6% (month 1) to 16.4% (month 6). Levels of antibodies, including those with neutralizing capacity, are stable over time, except IgG to nucleocapsid antigen and IgM levels that wane. After the peak response, anti-spike antibody levels increase from ~150 days post-symptom onset in all individuals (73% for IgG), in the absence of any evidence of re-exposure. IgG and IgA to HCoV are significantly higher in asymptomatic than symptomatic seropositive individuals. Thus, pre-existing cross-reactive HCoVs antibodies could have a protective effect against SARS-CoV-2 infection and COVID-19 disease.Entities:
Year: 2021 PMID: 34362897 DOI: 10.1038/s41467-021-24979-9
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919