Emergency response for evaluating SARS-CoV-2 immune status, seroprevalence and convalescent plasma in Argentina.
Adult
Aged
Antibodies, Neutralizing
/ immunology
Antibodies, Viral
/ immunology
Antibody Formation
Argentina
/ epidemiology
COVID-19
/ epidemiology
Enzyme-Linked Immunosorbent Assay
/ methods
Female
Humans
Immunoglobulin G
/ immunology
Immunoglobulin M
/ immunology
Longitudinal Studies
Male
Middle Aged
Pandemics
SARS-CoV-2
/ immunology
Seroepidemiologic Studies
Spike Glycoprotein, Coronavirus
/ immunology
Journal
PLoS pathogens
ISSN: 1553-7374
Titre abrégé: PLoS Pathog
Pays: United States
ID NLM: 101238921
Informations de publication
Date de publication:
01 2021
01 2021
Historique:
received:
15
10
2020
accepted:
13
11
2020
entrez:
14
1
2021
pubmed:
15
1
2021
medline:
29
1
2021
Statut:
epublish
Résumé
We report the emergency development and application of a robust serologic test to evaluate acute and convalescent antibody responses to SARS-CoV-2 in Argentina. The assays, COVIDAR IgG and IgM, which were produced and provided for free to health authorities, private and public health institutions and nursing homes, use a combination of a trimer stabilized spike protein and the receptor binding domain (RBD) in a single enzyme-linked immunosorbent assay (ELISA) plate. Over half million tests have already been distributed to detect and quantify antibodies for multiple purposes, including assessment of immune responses in hospitalized patients and large seroprevalence studies in neighborhoods, slums and health care workers, which resulted in a powerful tool for asymptomatic detection and policy making in the country. Analysis of antibody levels and longitudinal studies of symptomatic and asymptomatic SARS-CoV-2 infections in over one thousand patient samples provided insightful information about IgM and IgG seroconversion time and kinetics, and IgM waning profiles. At least 35% of patients showed seroconversion within 7 days, and 95% within 45 days of symptoms onset, with simultaneous or close sequential IgM and IgG detection. Longitudinal studies of asymptomatic cases showed a wide range of antibody responses with median levels below those observed in symptomatic patients. Regarding convalescent plasma applications, a protocol was standardized for the assessment of end point IgG antibody titers with COVIDAR with more than 500 plasma donors. The protocol showed a positive correlation with neutralizing antibody titers, and was used for clinical trials and therapies across the country. Using this protocol, about 80% of convalescent donor plasmas were potentially suitable for therapies. Here, we demonstrate the importance of providing a robust and specific serologic assay for generating new information about antibody kinetics in infected individuals and mitigation policies to cope with pandemic needs.
Identifiants
pubmed: 33444413
doi: 10.1371/journal.ppat.1009161
pii: PPATHOGENS-D-20-02254
pmc: PMC7808630
doi:
Substances chimiques
Antibodies, Neutralizing
0
Antibodies, Viral
0
Immunoglobulin G
0
Immunoglobulin M
0
Spike Glycoprotein, Coronavirus
0
spike protein, SARS-CoV-2
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e1009161Subventions
Organisme : NIAID NIH HHS
ID : F31 AI154739
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI095175
Pays : United States
Déclaration de conflit d'intérêts
The authors have declared that no competing interests exist.
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