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SARS-CoV-2 Omicron triggers cross-reactive neutralization and Fc effector functions in previously vaccinated, but not unvaccinated individuals
Simone I Richardson; Vimbai Sharon Madzorera; Holly Spencer; Nelia P Manamela; Mieke van der Mescht; Bronwen E Lambson; Brent Oosthuysen; Frances Ayres; Zanele Makhado; Thandeka Moyo-Gwete; Nonkululeko Mzindle; Thopisang Motlou; Amy Strydom; Adriano Mendes; Houriiyah Tegally; Zelda de Beer; Talita Roma de Villiers; Annie Bodenstein; Gretha van den Berg; Marietjie Venter; Tulio de Oliviera; Veronica Ueckermann; Theresa M Rossouw; Michael T Boswell; Penny L Moore.
Afiliação
  • Simone I Richardson; National Institute for Communicable Diseases of the National Health Laboratory Services
  • Vimbai Sharon Madzorera; National Institute for Communicable Diseases of the National Health Laboratory Services
  • Holly Spencer; National Institute for Communicable Diseases of the National Health Laboratory Services
  • Nelia P Manamela; National Institute for Communicable Diseases of the National Health Laboratory Services
  • Mieke van der Mescht; Department of Immunology, Faculty of Health Sciences, University of Pretoria, Pretoria, South Africa
  • Bronwen E Lambson; National Institute for Communicable Diseases of the National Health Laboratory Services, Johannesburg, South Africa
  • Brent Oosthuysen; National Institute for Communicable Diseases of the National Health Laboratory Services
  • Frances Ayres; National Institute for Communicable Diseases of the National Health Laboratory Services
  • Zanele Makhado; National Institute for Communicable Diseases of the National Health Laboratory Services
  • Thandeka Moyo-Gwete; National Institute for Communicable Diseases of the National Health Laboratory Services
  • Nonkululeko Mzindle; National Institute for Communicable Diseases of the National Health Laboratory Services, Johannesburg, South Africa
  • Thopisang Motlou; National Institute for Communicable Diseases of the National Health Laboratory Services, Johannesburg, South Africa
  • Amy Strydom; Zoonotic Arbo and Respiratory Virus Program, Centre for Viral Zoonoses, Department of Medical Virology, University of Pretoria, Pretoria, South Africa.
  • Adriano Mendes; Zoonotic Arbo and Respiratory Virus Program, Centre for Viral Zoonoses, Department of Medical Virology, University of Pretoria, Pretoria, South Africa.
  • Houriiyah Tegally; KwaZulu-Natal Research Innovation and Sequencing Platform, Durban, South Africa
  • Zelda de Beer; Tshwane District Hospital, Pretoria, South Africa
  • Talita Roma de Villiers; Tshwane District Hospital, Pretoria, South Africa
  • Annie Bodenstein; Tshwane District Hospital, Pretoria, South Africa.
  • Gretha van den Berg; Tshwane District Hospital, Pretoria, South Africa.
  • Marietjie Venter; Zoonotic Arbo and Respiratory Virus Program, Centre for Viral Zoonoses, Department of Medical Virology, University of Pretoria, Pretoria, South Africa
  • Tulio de Oliviera; Zoonotic Arbo and Respiratory Virus Program, Centre for Viral Zoonoses, Department of Medical Virology, University of Pretoria, Pretoria, South Africa.
  • Veronica Ueckermann; Division for Infectious Diseases, Department of Internal Medicine, Steve Biko Academic Hospital and University of Pretoria, Pretoria, South Africa
  • Theresa M Rossouw; Department of Immunology, Faculty of Health Sciences, University of Pretoria, Pretoria, South Africa
  • Michael T Boswell; Division for Infectious Diseases, Department of Internal Medicine, Steve Biko Academic Hospital and University of Pretoria, Pretoria, South Africa
  • Penny L Moore; National Institute for Communicable Diseases of the National Health Laboratory Services, Johannesburg, South Africa
Preprint em Inglês | medRxiv | ID: ppmedrxiv-22270789
ABSTRACT
The SARS-CoV-2 Omicron variant escapes neutralizing antibodies elicited by vaccines or infection. However, whether Omicron triggers cross-reactive humoral responses to other variants of concern (VOCs) remains unknown. We use plasma from 20 unvaccinated and seven vaccinated individuals infected by Omicron BA.1 to test binding, Fc effector function and neutralization against VOCs. In unvaccinated individuals, Fc effector function and binding antibodies target Omicron and other VOCs at comparable levels. However, Omicron BA.1-triggered neutralization is not extensively cross-reactive for VOCs (14 to 31-fold titer reduction) and we observe 4-fold decreased titers against Omicron BA.2. In contrast, vaccination followed by breakthrough Omicron infection was associated with improved cross-neutralization of VOCs, with titers exceeding 12,100. This has important implications for vulnerability of unvaccinated Omicron-infected individuals to reinfection by circulating and emerging VOCs. While Omicron-based immunogens may be adequate boosters, they are unlikely to be superior to existing vaccines for priming in SARS-CoV-2 naive individuals.
Licença
cc_by_nc_nd
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Experimental_studies / Rct Idioma: Inglês Ano de publicação: 2022 Tipo de documento: Preprint
Texto completo: Disponível Coleções: Preprints Base de dados: medRxiv Tipo de estudo: Experimental_studies / Rct Idioma: Inglês Ano de publicação: 2022 Tipo de documento: Preprint
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