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Booster Vaccination with BNT162b2 Improves Cellular and Humoral Immune Response in the Pediatric Population Immunized
Diego A Díaz-Dinamarca1, Simone Cárdenas-Cáceres2, Nicolás A Muena2
1Subdepartamento Innovación y Desarrollo, Departamento Agencia Nacional de Dispositivos Médicos, Innovación y Desarrollo, Instituto de Salud Pública de Chile, Santiago 7780050, Chile.
Insights
Booster vaccinations with BNT162b2 significantly enhance immune responses against the Omicron variant in children compared to CoronaVac alone. Three doses of BNT162b2 provided the strongest protection against SARS-CoV-2 Omicron.
Area of Science:
- Immunology
- Virology
- Pediatric Medicine
Background:
- The SARS-CoV-2 Omicron variant causes significant pediatric COVID-19 hospitalizations globally.
- BNT162b2 and CoronaVac are primary pediatric vaccines in Chile, with limited data on Wuhan-Hu-1 strain-based vaccines in this age group.
- Booster vaccinations are crucial for maintaining immunity against emerging SARS-CoV-2 Omicron sublineages.
Purpose of the Study:
- To characterize the humoral and cellular immune responses against the Omicron BA.1 variant in a pediatric cohort.
- To compare the immunogenicity of different vaccination schedules involving CoronaVac and BNT162b2 boosters.
- To assess the effectiveness of heterologous vaccination strategies in children aged 10-16 years.
Main Methods:
- A pediatric cohort (10-16 years) received varying vaccination schedules: 2 doses CoronaVac, 2x CoronaVac + 1x BNT162b2, 2x CoronaVac + 2x BNT162b2, or 3x BNT162b2.
- Humoral immunity was assessed via anti-S1 and neutralizing antibody titers against Omicron BA.1.
- Cellular immunity was evaluated by measuring specific CD4 and CD8 T cell responses.
Main Results:
- The [CoronaVac(2x) + BNT162b2 (2x)] schedule induced higher anti-S1 and neutralizing antibody titers than 2x CoronaVac alone.
- Enhanced CD4 and CD8 T cell immunity specific to Omicron was observed in the heterologous vaccination groups.
- The highest immunity against Omicron was achieved in the group receiving three doses of BNT162b2.
Conclusions:
- Booster vaccination with BNT162b2 significantly improves protective immunity against Omicron in children compared to two CoronaVac doses.
- Heterologous vaccination strategies, particularly with multiple BNT162b2 boosters, enhance pediatric immune responses to SARS-CoV-2 Omicron.
- BNT162b2 vaccination, especially in a three-dose regimen, offers superior protection against Omicron in the pediatric population.
Abstract:
The SARS-CoV-2 Omicron variant and its sublineages continue to cause COVID-19-associated pediatric hospitalizations, severe disease, and death globally. BNT162b2 and CoronaVac are the main vaccines used in Chile. Much less is known about the Wuhan-Hu-1 strain-based vaccines in the pediatric population compared to adults. Given the worldwide need for booster vaccinations to stimulate the immune response against new Omicron variants of SARS-CoV-2, we characterized the humoral and cellular immune response against Omicron variant BA.1 in a pediatric cohort aged 10 to 16 years who received heterologous vaccination based on two doses of CoronaVac, two doses of CoronaVac (2x) plus one booster dose of BNT162b2 [CoronaVac(2x) + BNT162b2 (1x)], two doses of CoronaVac plus two booster doses of BNT162b2 [CoronaVac(2x) + BNT162b2 (2x)], and three doses of BNT162b2. We observed that the [CoronaVac(2x) + BNT162b2 (2x)] vaccination showed higher anti-S1 and neutralizing antibody titers and CD4 and CD8 T cell immunity specific to the Omicron variant compared to immunization with two doses of CoronaVac alone. Furthermore, from all groups tested, immunity against Omicron was highest in individuals who received three doses of BNT162b2. We conclude that booster vaccination with BNT162b2, compared to two doses of CoronaVac alone, induces a greater protective immunity.
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