A Booster Dose of CoronaVac Increases Neutralizing Antibodies and T Cells that Recognize Delta and Omicron Variants of Concern
Bárbara M. Schultz,
Felipe Melo-González,
Luisa F. Duarte,
Nicolás M. S. Gálvez,
Gaspar A. Pacheco,
Jorge A. Soto,
Roslye V. Berríos-Rojas,
Liliana A. González,
Daniela Moreno-Tapia,
Daniela Rivera-Pérez,
Mariana Ríos,
Yaneisi Vázquez,
Guillermo Hoppe-Elsholz,
Catalina A. Andrade-Parra,
Omar P. Vallejos,
Alejandro Piña-Iturbe,
Carolina Iturriaga,
Marcela Urzua,
María S. Navarrete,
Álvaro Rojas,
Rodrigo Fasce,
Jorge Fernández,
Judith Mora,
Eugenio Ramírez,
Aracelly Gaete-Argel,
Mónica L. Acevedo,
Fernando Valiente-Echeverría,
Ricardo Soto-Rifo,
Daniela Weiskopf,
Alba Grifoni,
Alessandro Sette,
Gang Zeng,
Weining Meng,
José V. González-Aramundiz,
Pablo A. González,
Katia Abarca,
Alexis M. Kalergis,
Susan M. Bueno
Affiliations
Bárbara M. Schultz
Millennium Institute on Immunology and Immunotherapy, Santiago, Chile
Felipe Melo-González
Millennium Institute on Immunology and Immunotherapy, Santiago, Chile
Luisa F. Duarte
Millennium Institute on Immunology and Immunotherapy, Santiago, Chile
Nicolás M. S. Gálvez
Millennium Institute on Immunology and Immunotherapy, Santiago, Chile
Gaspar A. Pacheco
Millennium Institute on Immunology and Immunotherapy, Santiago, Chile
Jorge A. Soto
Millennium Institute on Immunology and Immunotherapy, Santiago, Chile
Roslye V. Berríos-Rojas
Millennium Institute on Immunology and Immunotherapy, Santiago, Chile
Liliana A. González
Millennium Institute on Immunology and Immunotherapy, Santiago, Chile
Daniela Moreno-Tapia
Millennium Institute on Immunology and Immunotherapy, Santiago, Chile
Daniela Rivera-Pérez
Millennium Institute on Immunology and Immunotherapy, Santiago, Chile
Mariana Ríos
Millennium Institute on Immunology and Immunotherapy, Santiago, Chile
Yaneisi Vázquez
Millennium Institute on Immunology and Immunotherapy, Santiago, Chile
Guillermo Hoppe-Elsholz
Millennium Institute on Immunology and Immunotherapy, Santiago, Chile
Catalina A. Andrade-Parra
Millennium Institute on Immunology and Immunotherapy, Santiago, Chile
Omar P. Vallejos
Millennium Institute on Immunology and Immunotherapy, Santiago, Chile
Alejandro Piña-Iturbe
Millennium Institute on Immunology and Immunotherapy, Santiago, Chile
Carolina Iturriaga
Departamento de Enfermedades Infecciosas e Inmunología Pediátrica, División de Pediatría, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile
Marcela Urzua
Departamento de Enfermedades Infecciosas e Inmunología Pediátrica, División de Pediatría, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile
María S. Navarrete
Centro de Investigación Clínica UC, Pontificia Universidad Católica de Chile, Santiago, Chile
Álvaro Rojas
Centro de Investigación Clínica UC, Pontificia Universidad Católica de Chile, Santiago, Chile
Rodrigo Fasce
Departamento de Laboratorio Biomédico, Instituto de Salud Pública de Chile, Santiago, Chile
Jorge Fernández
Departamento de Laboratorio Biomédico, Instituto de Salud Pública de Chile, Santiago, Chile
Judith Mora
Departamento de Laboratorio Biomédico, Instituto de Salud Pública de Chile, Santiago, Chile
Eugenio Ramírez
Departamento de Laboratorio Biomédico, Instituto de Salud Pública de Chile, Santiago, Chile
Aracelly Gaete-Argel
Millennium Institute on Immunology and Immunotherapy, Santiago, Chile
Mónica L. Acevedo
Millennium Institute on Immunology and Immunotherapy, Santiago, Chile
Fernando Valiente-Echeverría
Millennium Institute on Immunology and Immunotherapy, Santiago, Chile
Ricardo Soto-Rifo
Millennium Institute on Immunology and Immunotherapy, Santiago, Chile
Daniela Weiskopf
Center for Infectious Disease and Vaccine Research, La Jolla Institute for Immunology, La Jolla, California, USA
Alba Grifoni
Center for Infectious Disease and Vaccine Research, La Jolla Institute for Immunology, La Jolla, California, USA
Alessandro Sette
Center for Infectious Disease and Vaccine Research, La Jolla Institute for Immunology, La Jolla, California, USA
Gang Zeng
Sinovac Biotech, Beijing, China
Weining Meng
Sinovac Biotech, Beijing, China
José V. González-Aramundiz
Departamento de Farmacia, Facultad de Química y de Farmacia, Pontificia Universidad Católica de Chile, Santiago, Chile
Pablo A. González
Millennium Institute on Immunology and Immunotherapy, Santiago, Chile
Katia Abarca
Millennium Institute on Immunology and Immunotherapy, Santiago, Chile
Alexis M. Kalergis
Millennium Institute on Immunology and Immunotherapy, Santiago, Chile
Susan M. Bueno
Millennium Institute on Immunology and Immunotherapy, Santiago, Chile
ABSTRACT CoronaVac is an inactivated SARS-CoV-2 vaccine approved by the World Health Organization (WHO). Previous studies reported increased levels of neutralizing antibodies and specific T cells 2 and 4 weeks after two doses of CoronaVac; these levels were significantly reduced at 6 to 8 months after the two doses. Here, we report the effect of a booster dose of CoronaVac on the anti-SARS-CoV-2 immune response generated against the variants of concern (VOCs), Delta and Omicron, in adults participating in a phase III clinical trial in Chile. Volunteers immunized with two doses of CoronaVac in a 4-week interval received a booster dose of the same vaccine between 24 and 30 weeks after the second dose. Neutralization capacities and T cell activation against VOCs Delta and Omicron were assessed 4 weeks after the booster dose. We observed a significant increase in neutralizing antibodies 4 weeks after the booster dose. We also observed a rise in anti-SARS-CoV-2-specific CD4+ T cells over time, and these cells reached a peak 4 weeks after the booster dose. Furthermore, neutralizing antibodies and SARS-CoV-2-specific T cells induced by the booster showed activity against VOCs Delta and Omicron. Our results show that a booster dose of CoronaVac increases adults’ humoral and cellular anti-SARS-CoV-2 immune responses. In addition, immunity induced by a booster dose of CoronaVac is active against VOCs, suggesting adequate protection. IMPORTANCE CoronaVac is an inactivated vaccine against SARS-CoV-2 that has been approved by WHO for emergency use. Phase III clinical trials are in progress in several countries, including China, Brazil, Turkey, and Chile, and have shown safety and immunogenicity after two doses of the vaccine. This report characterizes immune responses induced by two doses of CoronaVac followed by a booster dose 5 months after the second dose in healthy Chilean adults. The data reported here show that a booster dose increased the immune responses against SARS-CoV-2, enhancing levels of neutralizing antibodies against the ancestral strain and VOCs. Similarly, anti-SARS-CoV-2 CD4+ T cell responses were increased following the booster dose. In contrast, levels of gamma interferon secretion and T cell activation against the VOCs Delta and Omicron were not significantly different from those for the ancestral strain. Therefore, a third dose of CoronaVac in a homologous vaccination schedule improves its immunogenicity in healthy volunteers.