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Clusters of SARS-CoV-2 Lineage B.1.1.7 Infection after Vaccination with Adenovirus-Vectored and Inactivated Vaccines.
de Souza, William M; Muraro, Stéfanie P; Souza, Gabriela F; Amorim, Mariene R; Sesti-Costa, Renata; Mofatto, Luciana S; Forato, Julia; Barbosa, Priscilla P; Toledo-Teixeira, Daniel A; Bispo-Dos-Santos, Karina; Parise, Pierina L; Brunetti, Natalia S; Moreira, Joselia C O; Costa, Vitor A; Cardozo, Daniela M; Moretti, Maria L; Barros-Mazon, Silvia; Marchesi, Gabriela F; Ambrosio, Christiane; Spilki, Fernando R; Almeida, Valeria C; Vieira, Andre S; Zambon, Lair; Farias, Alessandro S; Addas-Carvalho, Marcelo; Benites, Bruno D; Marques, Rafael E; Sabino, Ester C; Zuben, Andrea B Von; Weaver, Scott C; Faria, Nuno R; Granja, Fabiana; Angerami, Rodrigo N; Proença-Módena, José Luiz.
  • de Souza WM; Virology Research Centre, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto 14049-900, Brazil.
  • Muraro SP; Department of Microbiology and Immunology, University of Texas Medical Branch, Galveston, TX 77555, USA.
  • Souza GF; Laboratory of Emerging Viruses, Department of Genetics, Microbiology and Immunology, Institute of Biology, University of Campinas, Campinas 13083-862, Brazil.
  • Amorim MR; Laboratory of Emerging Viruses, Department of Genetics, Microbiology and Immunology, Institute of Biology, University of Campinas, Campinas 13083-862, Brazil.
  • Sesti-Costa R; Laboratory of Emerging Viruses, Department of Genetics, Microbiology and Immunology, Institute of Biology, University of Campinas, Campinas 13083-862, Brazil.
  • Mofatto LS; Brazilian Biosciences National Laboratory, Brazilian Centre for Research in Energy and Materials, Campinas 13083-100, Brazil.
  • Forato J; Hematology and Hemotherapy Center, University of Campinas, Campinas 13083-862, Brazil.
  • Barbosa PP; Laboratory of Emerging Viruses, Department of Genetics, Microbiology and Immunology, Institute of Biology, University of Campinas, Campinas 13083-862, Brazil.
  • Toledo-Teixeira DA; Laboratory of Emerging Viruses, Department of Genetics, Microbiology and Immunology, Institute of Biology, University of Campinas, Campinas 13083-862, Brazil.
  • Bispo-Dos-Santos K; Laboratory of Emerging Viruses, Department of Genetics, Microbiology and Immunology, Institute of Biology, University of Campinas, Campinas 13083-862, Brazil.
  • Parise PL; Laboratory of Emerging Viruses, Department of Genetics, Microbiology and Immunology, Institute of Biology, University of Campinas, Campinas 13083-862, Brazil.
  • Brunetti NS; Laboratory of Emerging Viruses, Department of Genetics, Microbiology and Immunology, Institute of Biology, University of Campinas, Campinas 13083-862, Brazil.
  • Moreira JCO; Laboratory of Emerging Viruses, Department of Genetics, Microbiology and Immunology, Institute of Biology, University of Campinas, Campinas 13083-862, Brazil.
  • Costa VA; Autoimmune Research Laboratory, Department of Genetics, Microbiology and Immunology, Institute of Biology, University of Campinas, Campinas 13083-862, Brazil.
  • Cardozo DM; Department of Structural and Functional Biology, Institute of Biology, University of Campinas, Campinas 13083-862, Brazil.
  • Moretti ML; Hematology and Hemotherapy Center, University of Campinas, Campinas 13083-862, Brazil.
  • Barros-Mazon S; Department of Clinical Pathology, School of Medical Sciences, University of Campinas, Campinas 13083-862, Brazil.
  • Marchesi GF; Department of Internal Medicine, School of Medical Sciences, University of Campinas, Campinas 13083-862, Brazil.
  • Ambrosio C; Department of Clinical Pathology, School of Medical Sciences, University of Campinas, Campinas 13083-862, Brazil.
  • Spilki FR; Campinas Department of Public Health Surveillance, Campinas 13015-904, Brazil.
  • Almeida VC; Campinas Department of Public Health Surveillance, Campinas 13015-904, Brazil.
  • Vieira AS; One Health Laboratory, Feevale University, Novo Hamburgo 93510-235, Brazil.
  • Zambon L; Campinas Department of Public Health Surveillance, Campinas 13015-904, Brazil.
  • Farias AS; Department of Structural and Functional Biology, Institute of Biology, University of Campinas, Campinas 13083-862, Brazil.
  • Addas-Carvalho M; Department of Internal Medicine, School of Medical Sciences, University of Campinas, Campinas 13083-862, Brazil.
  • Benites BD; Autoimmune Research Laboratory, Department of Genetics, Microbiology and Immunology, Institute of Biology, University of Campinas, Campinas 13083-862, Brazil.
  • Marques RE; Obesity and Comorbidities Research Center, University of Campinas, Campinas 13083-862, Brazil.
  • Sabino EC; Experimental Medicine Research Cluster, University of Campinas, Campinas 13083-862, Brazil.
  • Zuben ABV; Hematology and Hemotherapy Center, University of Campinas, Campinas 13083-862, Brazil.
  • Weaver SC; Hematology and Hemotherapy Center, University of Campinas, Campinas 13083-862, Brazil.
  • Faria NR; Brazilian Biosciences National Laboratory, Brazilian Centre for Research in Energy and Materials, Campinas 13083-100, Brazil.
  • Granja F; Tropical Medicine Institute, Medical School, University of São Paulo, São Paulo 05403-907, Brazil.
  • Angerami RN; Department of Infectious and Parasitic Disease, Medical School, University of São Paulo, São Paulo 05403-000, Brazil.
  • Proença-Módena JL; Campinas Department of Public Health Surveillance, Campinas 13015-904, Brazil.
Viruses ; 13(11)2021 10 22.
Article in English | MEDLINE | ID: covidwho-1481018
ABSTRACT
A SARS-CoV-2 B.1.1.7 variant of concern (VOC) has been associated with increased transmissibility, hospitalization, and mortality. This study aimed to explore the factors associated with B.1.1.7 VOC infection in the context of vaccination. On March 2021, we detected SARS-CoV-2 RNA in nasopharyngeal samples from 14 of 22 individuals vaccinated with a single-dose of ChAdOx1 (outbreak A, n = 26), and 22 of 42 of individuals with two doses of the CoronaVac vaccine (outbreak B, n = 52) for breakthrough infection rates for ChAdOx1 of 63.6% and 52.4% for CoronaVac. The outbreaks were caused by two independent clusters of the B.1.1.7 VOC. The serum of PCR-positive symptomatic SARS-CoV-2-infected individuals had ~1.8-3.4-fold more neutralizing capacity against B.1.1.7 compared to the serum of asymptomatic individuals. These data based on exploratory analysis suggest that the B.1.1.7 variant can infect individuals partially immunized with a single dose of an adenovirus-vectored vaccine or fully immunized with two doses of an inactivated vaccine, although the vaccines were able to reduce the risk of severe disease and death caused by this VOC, even in the elderly.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Vaccination / COVID-19 Vaccines / SARS-CoV-2 / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines / Variants Limits: Adult / Aged / Female / Humans / Male / Middle aged / Young adult Country/Region as subject: South America / Brazil Language: English Year: 2021 Document Type: Article Affiliation country: V13112127

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Vaccination / COVID-19 Vaccines / SARS-CoV-2 / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines / Variants Limits: Adult / Aged / Female / Humans / Male / Middle aged / Young adult Country/Region as subject: South America / Brazil Language: English Year: 2021 Document Type: Article Affiliation country: V13112127