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Clusters of SARS-CoV-2 Lineage B.1.1.7 Infection after Vaccination with Adenovirus-Vectored and Inactivated Vaccines.

William M de SouzaStefanie Primon MuraroGabriela F SouzaMariene Ribeiro AmorimRenata Sesti-CostaLuciana S MofattoJulia ForatoPriscilla P BarbosaDaniel Augusto de Toledo-TeixeiraKarina Bispo-Dos-SantosPierina Lorencini PariseNatalia S BrunettiJoselia C O MoreiraVitor A CostaDaniela M CardozoMaria L MorettiSilvia Barros-MazonGabriela F MarchesiChristiane AmbrosioFernando Rosado SpilkiValéria Correia de AlmeidaAndre S VieiraLair ZambonAlessandro S FariasMarcelo Addas-CarvalhoBruno Deltreggia BenitesRafael Elias MarquesEster C SabinoAndrea B Von ZubenScott C WeaverNuno R FariaFabiana GranjaRodrigo Nogueira AngeramiJosé Luis Proença Modena
Published in: Viruses (2021)
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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