Evaluation of the Immune Response Induced by CoronaVac 28-Day Schedule Vaccination in a Healthy Population Group

CoronaVac vaccine from Sinovac Life Science is currently being used in several countries. In Chile, the effectiveness of preventing hospitalization is higher than 80% with a vaccination schedule. However, to date, there are no data about immune response induction or specific memory. For this reason,...

Full description

Saved in:
Bibliographic Details
Published inFrontiers in immunology Vol. 12; p. 766278
Main Authors Escobar, Alejandro, Reyes-López, Felipe E, Acevedo, Mónica L, Alonso-Palomares, Luis, Valiente-Echeverría, Fernando, Soto-Rifo, Ricardo, Portillo, Hugo, Gatica, Jimena, Flores, Ivan, Nova-Lamperti, Estefanía, Barrera-Avalos, Carlos, Bono, María Rosa, Vargas, Leonardo, Simon, Valeska, Leiva-Salcedo, Elias, Vial, Cecilia, Hormazabal, Juan, Cortes, Lina Jimena, Valdés, Daniel, Sandino, Ana M, Imarai, Mónica, Acuña-Castillo, Claudio
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 31.01.2022
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:CoronaVac vaccine from Sinovac Life Science is currently being used in several countries. In Chile, the effectiveness of preventing hospitalization is higher than 80% with a vaccination schedule. However, to date, there are no data about immune response induction or specific memory. For this reason, we recruited 15 volunteers without previous suspected/diagnosed COVID-19 and with negative PCR over time to evaluate the immune response to CoronaVac 28 and 90 days after the second immunization (dpi). The CoronaVac administration induces total and neutralizing anti-spike antibodies in all vaccinated volunteers at 28 and 90 dpi. Furthermore, using ELISpot analysis to assay cellular immune responses against SARS-CoV-2 spike protein, we found an increase in IFN-gamma- and Granzyme B-producing cells in vaccinated volunteers at 28 and 90 dpi. Together, our results indicate that CoronaVac induces a robust humoral immune response and cellular immune memory of at least 90 dpi.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
Edited by: Arun Kumar, Coalition for Epidemic Preparedness Innovations (CEPI), Norway
Reviewed by: Rupsa Basu, Helaina Inc., United States; Abhishek Mishra, Lala Lajpat Rai Memorial Medical College, India
These authors have contributed equally to this work
This article was submitted to Vaccines and Molecular Therapeutics, a section of the journal Frontiers in Immunology
ISSN:1664-3224
1664-3224
DOI:10.3389/fimmu.2021.766278