Immune Profile and Clinical Outcome of Breakthrough Cases After Vaccination With an Inactivated SARS-CoV-2 Vaccine
Constant efforts to prevent infections by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are actively carried out around the world. Several vaccines are currently approved for emergency use in the population, while ongoing studies continue to provide information on their safety and eff...
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Frontiers Media S.A.
2021-09-01
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Series: | Frontiers in Immunology |
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Online Access: | https://www.frontiersin.org/articles/10.3389/fimmu.2021.742914/full |
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language |
English |
format |
Article |
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DOAJ |
author |
Luisa F. Duarte Luisa F. Duarte Nicolás M. S. Gálvez Nicolás M. S. Gálvez Carolina Iturriaga Felipe Melo-González Felipe Melo-González Jorge A. Soto Jorge A. Soto Bárbara M. Schultz Bárbara M. Schultz Marcela Urzúa Liliana A. González Liliana A. González Yaneisi Vázquez Yaneisi Vázquez Mariana Ríos Mariana Ríos Roslye V. Berríos-Rojas Roslye V. Berríos-Rojas Daniela Rivera-Pérez Daniela Rivera-Pérez Daniela Moreno-Tapia Daniela Moreno-Tapia Gaspar A. Pacheco Gaspar A. Pacheco Omar P. Vallejos Omar P. Vallejos Guillermo Hoppe-Elsholz Guillermo Hoppe-Elsholz María S. Navarrete Álvaro Rojas Rodrigo A. Fasce Jorge Fernández Judith Mora Eugenio Ramírez Gang Zeng Weining Meng José V. González-Aramundiz Pablo A. González Pablo A. González Katia Abarca Katia Abarca Susan M. Bueno Susan M. Bueno Alexis M. Kalergis Alexis M. Kalergis Alexis M. Kalergis |
spellingShingle |
Luisa F. Duarte Luisa F. Duarte Nicolás M. S. Gálvez Nicolás M. S. Gálvez Carolina Iturriaga Felipe Melo-González Felipe Melo-González Jorge A. Soto Jorge A. Soto Bárbara M. Schultz Bárbara M. Schultz Marcela Urzúa Liliana A. González Liliana A. González Yaneisi Vázquez Yaneisi Vázquez Mariana Ríos Mariana Ríos Roslye V. Berríos-Rojas Roslye V. Berríos-Rojas Daniela Rivera-Pérez Daniela Rivera-Pérez Daniela Moreno-Tapia Daniela Moreno-Tapia Gaspar A. Pacheco Gaspar A. Pacheco Omar P. Vallejos Omar P. Vallejos Guillermo Hoppe-Elsholz Guillermo Hoppe-Elsholz María S. Navarrete Álvaro Rojas Rodrigo A. Fasce Jorge Fernández Judith Mora Eugenio Ramírez Gang Zeng Weining Meng José V. González-Aramundiz Pablo A. González Pablo A. González Katia Abarca Katia Abarca Susan M. Bueno Susan M. Bueno Alexis M. Kalergis Alexis M. Kalergis Alexis M. Kalergis Immune Profile and Clinical Outcome of Breakthrough Cases After Vaccination With an Inactivated SARS-CoV-2 Vaccine Frontiers in Immunology CoronaVac phase 3 clinical trial SARS-CoV-2 COVID-19 vaccines breakthrough cases |
author_facet |
Luisa F. Duarte Luisa F. Duarte Nicolás M. S. Gálvez Nicolás M. S. Gálvez Carolina Iturriaga Felipe Melo-González Felipe Melo-González Jorge A. Soto Jorge A. Soto Bárbara M. Schultz Bárbara M. Schultz Marcela Urzúa Liliana A. González Liliana A. González Yaneisi Vázquez Yaneisi Vázquez Mariana Ríos Mariana Ríos Roslye V. Berríos-Rojas Roslye V. Berríos-Rojas Daniela Rivera-Pérez Daniela Rivera-Pérez Daniela Moreno-Tapia Daniela Moreno-Tapia Gaspar A. Pacheco Gaspar A. Pacheco Omar P. Vallejos Omar P. Vallejos Guillermo Hoppe-Elsholz Guillermo Hoppe-Elsholz María S. Navarrete Álvaro Rojas Rodrigo A. Fasce Jorge Fernández Judith Mora Eugenio Ramírez Gang Zeng Weining Meng José V. González-Aramundiz Pablo A. González Pablo A. González Katia Abarca Katia Abarca Susan M. Bueno Susan M. Bueno Alexis M. Kalergis Alexis M. Kalergis Alexis M. Kalergis |
author_sort |
Luisa F. Duarte |
title |
Immune Profile and Clinical Outcome of Breakthrough Cases After Vaccination With an Inactivated SARS-CoV-2 Vaccine |
title_short |
Immune Profile and Clinical Outcome of Breakthrough Cases After Vaccination With an Inactivated SARS-CoV-2 Vaccine |
title_full |
Immune Profile and Clinical Outcome of Breakthrough Cases After Vaccination With an Inactivated SARS-CoV-2 Vaccine |
title_fullStr |
Immune Profile and Clinical Outcome of Breakthrough Cases After Vaccination With an Inactivated SARS-CoV-2 Vaccine |
title_full_unstemmed |
Immune Profile and Clinical Outcome of Breakthrough Cases After Vaccination With an Inactivated SARS-CoV-2 Vaccine |
title_sort |
immune profile and clinical outcome of breakthrough cases after vaccination with an inactivated sars-cov-2 vaccine |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Immunology |
issn |
1664-3224 |
publishDate |
2021-09-01 |
description |
Constant efforts to prevent infections by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are actively carried out around the world. Several vaccines are currently approved for emergency use in the population, while ongoing studies continue to provide information on their safety and effectiveness. CoronaVac is an inactivated SARS-CoV-2 vaccine with a good safety and immunogenicity profile as seen in phase 1, 2, and 3 clinical trials around the world, with an effectiveness of 65.9% for symptomatic cases. Although vaccination reduces the risk of disease, infections can still occur during or after completion of the vaccination schedule (breakthrough cases). This report describes the clinical and immunological profile of vaccine breakthrough cases reported in a clinical trial in progress in Chile that is evaluating the safety, immunogenicity, and efficacy of two vaccination schedules of CoronaVac (clinicaltrials.gov NCT04651790). Out of the 2,263 fully vaccinated subjects, at end of June 2021, 45 have reported symptomatic SARS-CoV-2 infection 14 or more days after the second dose (1.99% of fully vaccinated subjects). Of the 45 breakthrough cases, 96% developed mild disease; one case developed a moderate disease; and one developed a severe disease and required mechanical ventilation. Both cases that developed moderate and severe disease were adults over 60 years old and presented comorbidities. The immune response before and after SARS-CoV-2 infection was analyzed in nine vaccine breakthrough cases, revealing that six of them exhibited circulating anti-S1-RBD IgG antibodies with neutralizing capacities after immunization, which showed a significant increase 2 and 4 weeks after symptoms onset. Two cases exhibited low circulating anti-S1-RBD IgG and almost non-existing neutralizing capacity after either vaccination or infection, although they developed a mild disease. An increase in the number of interferon-γ-secreting T cells specific for SARS-CoV-2 was detected 2 weeks after the second dose in seven cases and after symptoms onset. In conclusion, breakthrough cases were mostly mild and did not necessarily correlate with a lack of vaccine-induced immunity, suggesting that other factors, to be defined in future studies, could lead to symptomatic infection after vaccination with CoronaVac. |
topic |
CoronaVac phase 3 clinical trial SARS-CoV-2 COVID-19 vaccines breakthrough cases |
url |
https://www.frontiersin.org/articles/10.3389/fimmu.2021.742914/full |
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doaj-4e8fbbc37cb647b0bcc16a6cfa23cc352021-09-29T05:47:28ZengFrontiers Media S.A.Frontiers in Immunology1664-32242021-09-011210.3389/fimmu.2021.742914742914Immune Profile and Clinical Outcome of Breakthrough Cases After Vaccination With an Inactivated SARS-CoV-2 VaccineLuisa F. Duarte0Luisa F. Duarte1Nicolás M. S. Gálvez2Nicolás M. S. Gálvez3Carolina Iturriaga4Felipe Melo-González5Felipe Melo-González6Jorge A. Soto7Jorge A. Soto8Bárbara M. Schultz9Bárbara M. Schultz10Marcela Urzúa11Liliana A. González12Liliana A. González13Yaneisi Vázquez14Yaneisi Vázquez15Mariana Ríos16Mariana Ríos17Roslye V. Berríos-Rojas18Roslye V. Berríos-Rojas19Daniela Rivera-Pérez20Daniela Rivera-Pérez21Daniela Moreno-Tapia22Daniela Moreno-Tapia23Gaspar A. Pacheco24Gaspar A. Pacheco25Omar P. Vallejos26Omar P. Vallejos27Guillermo Hoppe-Elsholz28Guillermo Hoppe-Elsholz29María S. Navarrete30Álvaro Rojas31Rodrigo A. Fasce32Jorge Fernández33Judith Mora34Eugenio Ramírez35Gang Zeng36Weining Meng37José V. González-Aramundiz38Pablo A. González39Pablo A. González40Katia Abarca41Katia Abarca42Susan M. Bueno43Susan M. Bueno44Alexis M. Kalergis45Alexis M. Kalergis46Alexis M. Kalergis47Millennium Institute on Immunology and Immunotherapy, Santiago, ChileDepartamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, ChileMillennium Institute on Immunology and Immunotherapy, Santiago, ChileDepartamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, ChileDepartamento de Enfermedades Infecciosas e Inmunología Pediátricas, División de Pediatría, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, ChileMillennium Institute on Immunology and Immunotherapy, Santiago, ChileDepartamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, ChileMillennium Institute on Immunology and Immunotherapy, Santiago, ChileDepartamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, ChileMillennium Institute on Immunology and Immunotherapy, Santiago, ChileDepartamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, ChileDepartamento de Enfermedades Infecciosas e Inmunología Pediátricas, División de Pediatría, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, ChileMillennium Institute on Immunology and Immunotherapy, Santiago, ChileDepartamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, ChileMillennium Institute on Immunology and Immunotherapy, Santiago, ChileDepartamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, ChileMillennium Institute on Immunology and Immunotherapy, Santiago, ChileDepartamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, ChileMillennium Institute on Immunology and Immunotherapy, Santiago, ChileDepartamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, ChileMillennium Institute on Immunology and Immunotherapy, Santiago, ChileDepartamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, ChileMillennium Institute on Immunology and Immunotherapy, Santiago, ChileDepartamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, ChileMillennium Institute on Immunology and Immunotherapy, Santiago, ChileDepartamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, ChileMillennium Institute on Immunology and Immunotherapy, Santiago, ChileDepartamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, ChileMillennium Institute on Immunology and Immunotherapy, Santiago, ChileDepartamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, ChileDepartamento de Enfermedades Infecciosas del Adulto, División de Medicina, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, ChileDepartamento de Enfermedades Infecciosas del Adulto, División de Medicina, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, ChileDepartamento de Laboratorio Biomédico, Instituto de Salud Pública de Chile, Santiago, ChileDepartamento de Laboratorio Biomédico, Instituto de Salud Pública de Chile, Santiago, ChileDepartamento de Laboratorio Biomédico, Instituto de Salud Pública de Chile, Santiago, ChileDepartamento de Laboratorio Biomédico, Instituto de Salud Pública de Chile, Santiago, ChileSinovac Biotech, Beijing, ChinaSinovac Biotech, Beijing, ChinaDepartamento de Farmacia, Facultad de Química y de Farmacia, Pontificia Universidad Católica de Chile, Santiago, ChileMillennium Institute on Immunology and Immunotherapy, Santiago, ChileDepartamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, ChileMillennium Institute on Immunology and Immunotherapy, Santiago, ChileDepartamento de Enfermedades Infecciosas e Inmunología Pediátricas, División de Pediatría, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, ChileMillennium Institute on Immunology and Immunotherapy, Santiago, ChileDepartamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, ChileMillennium Institute on Immunology and Immunotherapy, Santiago, ChileDepartamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, ChileDepartamento de Endocrinología, Facultad de Medicina, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, ChileConstant efforts to prevent infections by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are actively carried out around the world. Several vaccines are currently approved for emergency use in the population, while ongoing studies continue to provide information on their safety and effectiveness. CoronaVac is an inactivated SARS-CoV-2 vaccine with a good safety and immunogenicity profile as seen in phase 1, 2, and 3 clinical trials around the world, with an effectiveness of 65.9% for symptomatic cases. Although vaccination reduces the risk of disease, infections can still occur during or after completion of the vaccination schedule (breakthrough cases). This report describes the clinical and immunological profile of vaccine breakthrough cases reported in a clinical trial in progress in Chile that is evaluating the safety, immunogenicity, and efficacy of two vaccination schedules of CoronaVac (clinicaltrials.gov NCT04651790). Out of the 2,263 fully vaccinated subjects, at end of June 2021, 45 have reported symptomatic SARS-CoV-2 infection 14 or more days after the second dose (1.99% of fully vaccinated subjects). Of the 45 breakthrough cases, 96% developed mild disease; one case developed a moderate disease; and one developed a severe disease and required mechanical ventilation. Both cases that developed moderate and severe disease were adults over 60 years old and presented comorbidities. The immune response before and after SARS-CoV-2 infection was analyzed in nine vaccine breakthrough cases, revealing that six of them exhibited circulating anti-S1-RBD IgG antibodies with neutralizing capacities after immunization, which showed a significant increase 2 and 4 weeks after symptoms onset. Two cases exhibited low circulating anti-S1-RBD IgG and almost non-existing neutralizing capacity after either vaccination or infection, although they developed a mild disease. An increase in the number of interferon-γ-secreting T cells specific for SARS-CoV-2 was detected 2 weeks after the second dose in seven cases and after symptoms onset. In conclusion, breakthrough cases were mostly mild and did not necessarily correlate with a lack of vaccine-induced immunity, suggesting that other factors, to be defined in future studies, could lead to symptomatic infection after vaccination with CoronaVac.https://www.frontiersin.org/articles/10.3389/fimmu.2021.742914/fullCoronaVacphase 3 clinical trialSARS-CoV-2COVID-19vaccinesbreakthrough cases |