Molecular mechanisms responsible for SARS-CoV-2 antibody waning and vaccine escape in Omicron sublineages BA.4 and BA.5

Mutations in the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) genome continue to threaten the global landscape of the coronavirus disease 2019 (COVID-19) pandemic. The Omicron variant (B.1.1.529) rapidly displaced previous ‘variants of concern’ (VoC) in 2021 due to its high rate of...

وصف كامل

التفاصيل البيبلوغرافية
الحاوية / القاعدة:Journal of Infection in Developing Countries
المؤلفون الرئيسيون: Benjamin Hewins, Christopher Richardson, Salvatore Rubino, Alyson Kelvin, Ali Toloue Ostadgavahi, David J Kelvin
التنسيق: مقال
اللغة:الإنجليزية
منشور في: The Journal of Infection in Developing Countries 2022-07-01
الموضوعات:
الوصول للمادة أونلاين:https://jidc.org/index.php/journal/article/view/17010
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author Benjamin Hewins
Christopher Richardson
Salvatore Rubino
Alyson Kelvin
Ali Toloue Ostadgavahi
David J Kelvin
author_facet Benjamin Hewins
Christopher Richardson
Salvatore Rubino
Alyson Kelvin
Ali Toloue Ostadgavahi
David J Kelvin
author_sort Benjamin Hewins
collection DOAJ
container_title Journal of Infection in Developing Countries
description Mutations in the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) genome continue to threaten the global landscape of the coronavirus disease 2019 (COVID-19) pandemic. The Omicron variant (B.1.1.529) rapidly displaced previous ‘variants of concern’ (VoC) in 2021 due to its high rate of transmissibility and multitude of mutations. This global influx of infections saturated healthcare systems, overwhelmed testing capacity and case reporting, and increased the COVID-19 death toll. Global health leaders are now being faced with the most transmissible COVID-19 variants yet, the Omicron sublineages BA.4 and BA.5, which contain additional spike protein (S) mutations from previous Omicron and VoC serotypes. With universally observed antibody waning, increasing vaccine-variant mismatch, and resuming international travel, the stage is set for unprecedented levels of breakthrough infections and superspreading events. In this paper, we raise awareness to these novel variants and provide context for the high likelihood of an upcoming wave of infection capable of inflicting significant disease burden on a global scale.
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spelling doaj-art-a37fc60c3d8546bb86a5d588df7d22932025-08-20T02:16:06ZengThe Journal of Infection in Developing CountriesJournal of Infection in Developing Countries1972-26802022-07-01160710.3855/jidc.17010Molecular mechanisms responsible for SARS-CoV-2 antibody waning and vaccine escape in Omicron sublineages BA.4 and BA.5Benjamin Hewins0Christopher Richardson1Salvatore Rubino2Alyson Kelvin3Ali Toloue Ostadgavahi4David J Kelvin5Department of Microbiology and Immunology, Canadian Centre for Vaccinology CCfV, Faculty of Medicine, Dalhousie University, Halifax, CanadaDepartment of Microbiology and Immunology, Canadian Centre for Vaccinology CCfV, Faculty of Medicine, Dalhousie University, Halifax, CanadaDepartment of Biomedical Sciences, University of Sassari, Sassari, ItalyDepartment of Microbiology and Immunology, Canadian Centre for Vaccinology CCfV, Faculty of Medicine, Dalhousie University, Halifax, CanadaDepartment of Microbiology and Immunology, Canadian Centre for Vaccinology CCfV, Faculty of Medicine, Dalhousie University, Halifax, CanadaDepartment of Microbiology and Immunology, Canadian Centre for Vaccinology CCfV, Faculty of Medicine, Dalhousie University, Halifax, Canada Mutations in the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) genome continue to threaten the global landscape of the coronavirus disease 2019 (COVID-19) pandemic. The Omicron variant (B.1.1.529) rapidly displaced previous ‘variants of concern’ (VoC) in 2021 due to its high rate of transmissibility and multitude of mutations. This global influx of infections saturated healthcare systems, overwhelmed testing capacity and case reporting, and increased the COVID-19 death toll. Global health leaders are now being faced with the most transmissible COVID-19 variants yet, the Omicron sublineages BA.4 and BA.5, which contain additional spike protein (S) mutations from previous Omicron and VoC serotypes. With universally observed antibody waning, increasing vaccine-variant mismatch, and resuming international travel, the stage is set for unprecedented levels of breakthrough infections and superspreading events. In this paper, we raise awareness to these novel variants and provide context for the high likelihood of an upcoming wave of infection capable of inflicting significant disease burden on a global scale. https://jidc.org/index.php/journal/article/view/17010Vaccination fatiguevaccine-variant mismatchantibody escapevariants of concern (VoCs)breakthrough infection
spellingShingle Benjamin Hewins
Christopher Richardson
Salvatore Rubino
Alyson Kelvin
Ali Toloue Ostadgavahi
David J Kelvin
Molecular mechanisms responsible for SARS-CoV-2 antibody waning and vaccine escape in Omicron sublineages BA.4 and BA.5
Vaccination fatigue
vaccine-variant mismatch
antibody escape
variants of concern (VoCs)
breakthrough infection
title Molecular mechanisms responsible for SARS-CoV-2 antibody waning and vaccine escape in Omicron sublineages BA.4 and BA.5
title_full Molecular mechanisms responsible for SARS-CoV-2 antibody waning and vaccine escape in Omicron sublineages BA.4 and BA.5
title_fullStr Molecular mechanisms responsible for SARS-CoV-2 antibody waning and vaccine escape in Omicron sublineages BA.4 and BA.5
title_full_unstemmed Molecular mechanisms responsible for SARS-CoV-2 antibody waning and vaccine escape in Omicron sublineages BA.4 and BA.5
title_short Molecular mechanisms responsible for SARS-CoV-2 antibody waning and vaccine escape in Omicron sublineages BA.4 and BA.5
title_sort molecular mechanisms responsible for sars cov 2 antibody waning and vaccine escape in omicron sublineages ba 4 and ba 5
topic Vaccination fatigue
vaccine-variant mismatch
antibody escape
variants of concern (VoCs)
breakthrough infection
url https://jidc.org/index.php/journal/article/view/17010
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