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Immune Profile and Clinical Outcome of Breakthrough Cases After Vaccination With an Inactivated SARS-CoV-2 Vaccine.
Duarte, Luisa F; Gálvez, Nicolás M S; Iturriaga, Carolina; Melo-González, Felipe; Soto, Jorge A; Schultz, Bárbara M; Urzúa, Marcela; González, Liliana A; Vázquez, Yaneisi; Ríos, Mariana; Berríos-Rojas, Roslye V; Rivera-Pérez, Daniela; Moreno-Tapia, Daniela; Pacheco, Gaspar A; Vallejos, Omar P; Hoppe-Elsholz, Guillermo; Navarrete, María S; Rojas, Álvaro; Fasce, Rodrigo A; Fernández, Jorge; Mora, Judith; Ramírez, Eugenio; Zeng, Gang; Meng, Weining; González-Aramundiz, José V; González, Pablo A; Abarca, Katia; Bueno, Susan M; Kalergis, Alexis M.
  • Duarte LF; Millennium Institute on Immunology and Immunotherapy, Santiago, Chile.
  • Gálvez NMS; Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Iturriaga C; Millennium Institute on Immunology and Immunotherapy, Santiago, Chile.
  • Melo-González F; Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Soto JA; Departamento de Enfermedades Infecciosas e Inmunología Pediátricas, División de Pediatría, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Schultz BM; Millennium Institute on Immunology and Immunotherapy, Santiago, Chile.
  • Urzúa M; Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • González LA; Millennium Institute on Immunology and Immunotherapy, Santiago, Chile.
  • Vázquez Y; Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Ríos M; Millennium Institute on Immunology and Immunotherapy, Santiago, Chile.
  • Berríos-Rojas RV; Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Rivera-Pérez D; Departamento de Enfermedades Infecciosas e Inmunología Pediátricas, División de Pediatría, Escuela de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Moreno-Tapia D; Millennium Institute on Immunology and Immunotherapy, Santiago, Chile.
  • Pacheco GA; Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Vallejos OP; Millennium Institute on Immunology and Immunotherapy, Santiago, Chile.
  • Hoppe-Elsholz G; Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Navarrete MS; Millennium Institute on Immunology and Immunotherapy, Santiago, Chile.
  • Rojas Á; Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Fasce RA; Millennium Institute on Immunology and Immunotherapy, Santiago, Chile.
  • Fernández J; Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Mora J; Millennium Institute on Immunology and Immunotherapy, Santiago, Chile.
  • Ramírez E; Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Zeng G; Millennium Institute on Immunology and Immunotherapy, Santiago, Chile.
  • Meng W; Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • González-Aramundiz JV; Millennium Institute on Immunology and Immunotherapy, Santiago, Chile.
  • González PA; Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Abarca K; Millennium Institute on Immunology and Immunotherapy, Santiago, Chile.
  • Bueno SM; Departamento de Genética Molecular y Microbiología, Facultad de Ciencias Biológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.
  • Kalergis AM; Millennium Institute on Immunology and Immunotherapy, Santiago, Chile.
Front Immunol ; 12: 742914, 2021.
Article in English | MEDLINE | ID: covidwho-1472387
ABSTRACT
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.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: T-Lymphocytes / Vaccines, Inactivated / Antibodies, Neutralizing / COVID-19 Vaccines / SARS-CoV-2 / COVID-19 / Antibodies, Viral Type of study: Experimental Studies / Prognostic study / Randomized controlled trials Topics: Vaccines Limits: Adult / Aged / Female / Humans / Male / Middle aged / Young adult Country/Region as subject: South America / Chile Language: English Journal: Front Immunol Year: 2021 Document Type: Article Affiliation country: Fimmu.2021.742914

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Full text: Available Collection: International databases Database: MEDLINE Main subject: T-Lymphocytes / Vaccines, Inactivated / Antibodies, Neutralizing / COVID-19 Vaccines / SARS-CoV-2 / COVID-19 / Antibodies, Viral Type of study: Experimental Studies / Prognostic study / Randomized controlled trials Topics: Vaccines Limits: Adult / Aged / Female / Humans / Male / Middle aged / Young adult Country/Region as subject: South America / Chile Language: English Journal: Front Immunol Year: 2021 Document Type: Article Affiliation country: Fimmu.2021.742914