TY - JOUR
T1 - Humoral immunity against SARS-CoV-2 evoked by heterologous vaccination groups using the CoronaVac (Sinovac) and BNT162b2 (Pfizer/BioNTech) vaccines in Chile
AU - Díaz-Dinamarca, Diego A.
AU - Díaz, Pablo
AU - Barra, Gisselle
AU - Puentes, Rodrigo
AU - Arata, Loredana
AU - Grossolli, Jonnathan
AU - Riveros-Rodriguez, Boris
AU - Ardiles, Luis
AU - Santelises, Julio
AU - Vasquez-Saez, Valeria
AU - Escobar, Daniel F.
AU - Soto, Daniel
AU - Canales, Cecilia
AU - Díaz, Janepsy
AU - Lamperti, Liliana
AU - Castillo, Daniela
AU - Urra, Mychel
AU - Zuñiga, Felipe
AU - Ormazabal, Valeska
AU - Nova-Lamperti, Estefanía
AU - Benítez, Rosana
AU - Rivera, Alejandra
AU - Cortes, Claudia P.
AU - Valenzuela, María Teresa
AU - García-Escorza, Heriberto E.
AU - Vasquez, Abel E.
N1 - Publisher Copyright:
Copyright © 2023 Díaz-Dinamarca, Díaz, Barra, Puentes, Arata, Grossolli, Riveros-Rodriguez, Ardiles, Santelises, Vasquez-Saez, Escobar, Soto, Canales, Díaz, Lamperti, Castillo, Urra, Zuñiga, Ormazabal, Nova-Lamperti, Benítez, Rivera, Cortes, Valenzuela, García-Escorza and Vasquez.
PY - 2023/8/23
Y1 - 2023/8/23
N2 - Introduction: Severe acute respiratory syndrome virus 2 (SARS-CoV-2) has caused over million deaths worldwide, with more than 61,000 deaths in Chile. The Chilean government has implemented a vaccination program against SARS-CoV-2, with over 17.7 million people receiving a complete vaccination scheme. The final target is 18 million individuals. The most common vaccines used in Chile are CoronaVac (Sinovac) and BNT162b2 (Pfizer-Biotech). Given the global need for vaccine boosters to combat the impact of emerging virus variants, studying the immune response to SARS-CoV-2 is crucial. In this study, we characterize the humoral immune response in inoculated volunteers from Chile who received vaccination schemes consisting of two doses of CoronaVac [CoronaVac (2x)], two doses of CoronaVac plus one dose of BNT162b2 [CoronaVac (2x) + BNT162b2 (1x)], and three doses of BNT162b2 [BNT162b2 (3x)]. Methods: We recruited 469 participants from Clínica Dávila in Santiago and the Health Center Víctor Manuel Fernández in the city of Concepción, Chile. Additionally, we included participants who had recovered from COVID-19 but were not vaccinated (RCN). We analyzed antibodies, including anti-N, anti-S1-RBD, and neutralizing antibodies against SARS-CoV-2. Results: We found that antibodies against the SARS-CoV-2 nucleoprotein were significantly higher in the CoronaVac (2x) and RCN groups compared to the CoronaVac (2x) + BNT162b2 (1x) or BNT162b2 (3x) groups. However, the CoronaVac (2x) + BNT162b2 (1x) and BNT162b2 (3x) groups exhibited a higher concentration of S1-RBD antibodies than the CoronaVac (2x) group and RCN group. There were no significant differences in S1-RBD antibody titers between the CoronaVac (2x) + BNT162b2 (1x) and BNT162b2 (3x) groups. Finally, the group immunized with BNT162b2 (3x) had higher levels of neutralizing antibodies compared to the RCN group, as well as the CoronaVac (2x) and CoronaVac (2x) + BNT162b2 (1x) groups. Discussion: These findings suggest that vaccination induces the secretion of antibodies against SARS-CoV-2, and a booster dose of BNT162b2 is necessary to generate a protective immune response. In the current state of the pandemic, these data support the Ministry of Health of the Government of Chile’s decision to promote heterologous vaccination as they indicate that a significant portion of the Chilean population has neutralizing antibodies against SARS-CoV-2.
AB - Introduction: Severe acute respiratory syndrome virus 2 (SARS-CoV-2) has caused over million deaths worldwide, with more than 61,000 deaths in Chile. The Chilean government has implemented a vaccination program against SARS-CoV-2, with over 17.7 million people receiving a complete vaccination scheme. The final target is 18 million individuals. The most common vaccines used in Chile are CoronaVac (Sinovac) and BNT162b2 (Pfizer-Biotech). Given the global need for vaccine boosters to combat the impact of emerging virus variants, studying the immune response to SARS-CoV-2 is crucial. In this study, we characterize the humoral immune response in inoculated volunteers from Chile who received vaccination schemes consisting of two doses of CoronaVac [CoronaVac (2x)], two doses of CoronaVac plus one dose of BNT162b2 [CoronaVac (2x) + BNT162b2 (1x)], and three doses of BNT162b2 [BNT162b2 (3x)]. Methods: We recruited 469 participants from Clínica Dávila in Santiago and the Health Center Víctor Manuel Fernández in the city of Concepción, Chile. Additionally, we included participants who had recovered from COVID-19 but were not vaccinated (RCN). We analyzed antibodies, including anti-N, anti-S1-RBD, and neutralizing antibodies against SARS-CoV-2. Results: We found that antibodies against the SARS-CoV-2 nucleoprotein were significantly higher in the CoronaVac (2x) and RCN groups compared to the CoronaVac (2x) + BNT162b2 (1x) or BNT162b2 (3x) groups. However, the CoronaVac (2x) + BNT162b2 (1x) and BNT162b2 (3x) groups exhibited a higher concentration of S1-RBD antibodies than the CoronaVac (2x) group and RCN group. There were no significant differences in S1-RBD antibody titers between the CoronaVac (2x) + BNT162b2 (1x) and BNT162b2 (3x) groups. Finally, the group immunized with BNT162b2 (3x) had higher levels of neutralizing antibodies compared to the RCN group, as well as the CoronaVac (2x) and CoronaVac (2x) + BNT162b2 (1x) groups. Discussion: These findings suggest that vaccination induces the secretion of antibodies against SARS-CoV-2, and a booster dose of BNT162b2 is necessary to generate a protective immune response. In the current state of the pandemic, these data support the Ministry of Health of the Government of Chile’s decision to promote heterologous vaccination as they indicate that a significant portion of the Chilean population has neutralizing antibodies against SARS-CoV-2.
KW - BNT162b2 (Pfizer-BioNTech)
KW - COVID19
KW - Chilean vaccination
KW - CoronaVac vaccine
KW - SARS-CoV-2
KW - SARS-CoV-2 neutralizing antibodies
KW - heterologous vaccination
KW - immunization schedules
UR - http://www.scopus.com/inward/record.url?scp=85169920178&partnerID=8YFLogxK
U2 - 10.3389/fpubh.2023.1229045
DO - 10.3389/fpubh.2023.1229045
M3 - Article
AN - SCOPUS:85169920178
SN - 2296-2565
VL - 11
SP - 1
EP - 15
JO - Frontiers in Public Health
JF - Frontiers in Public Health
M1 - 1229045
ER -