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SARS-CoV-2 501Y.V2 (B.1.351) elicits cross-reactive neutralizing antibodies
Thandeka Moyo-Gwete; Mashudu Madzivhandila; Zanele Makhado; Frances Ayres; Donald Mhlanga; Brent Oosthuysen; Bronwen Lambson; Prudence Kgagudi; Houriiyah Tegally; Arash Iranzadeh; Deelan Doolabh; Lynn Tyers; Lionel Chinhoyi; Mathilda Mennen; Sango Skelem; Gert Marais; Constantinos Kurt Wibmer; Jinal Bhiman; Veronica Ueckermann; Theresa Rossouw; Michael Boswell; Tulio de Oliveira; Carolyn Williamson; Wendy Burgers; Ntobeko Ntusi; Lynn Morris; Penny Moore.
Affiliation
  • Thandeka Moyo-Gwete; National Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg, South Africa
  • Mashudu Madzivhandila; National Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg, South Africa
  • Zanele Makhado; National Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg, South Africa
  • Frances Ayres; National Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg, South Africa
  • Donald Mhlanga; National Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg, South Africa
  • Brent Oosthuysen; National Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg, South Africa
  • Bronwen Lambson; National Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg, South Africa
  • Prudence Kgagudi; National Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg, South Africa
  • Houriiyah Tegally; KwaZulu-Natal Research Innovation and Sequencing Platform (KRISP), Department of Laboratory Medicine & Medical Sciences, University of KwaZulu-Natal, Durban, So
  • Arash Iranzadeh; nstitute of Infectious Disease and Molecular Medicine, Division of Medical Virology, Department of Pathology, University of Cape Town, Cape Town, South Africa
  • Deelan Doolabh; nstitute of Infectious Disease and Molecular Medicine, Division of Medical Virology, Department of Pathology, University of Cape Town, Cape Town, South Africa
  • Lynn Tyers; Institute of Infectious Disease and Molecular Medicine, Division of Medical Virology, Department of Pathology, University of Cape Town, Cape Town, South Africa
  • Lionel Chinhoyi; Wellcome Centre for Infectious Diseases Research in Africa, University of Cape Town, Cape Town, South Afric
  • Mathilda Mennen; Wellcome Centre for Infectious Diseases Research in Africa, University of Cape Town, Cape Town, South Afric
  • Sango Skelem; Wellcome Centre for Infectious Diseases Research in Africa, University of Cape Town, Cape Town, South Afric
  • Gert Marais; University of Cape Town
  • Constantinos Kurt Wibmer; National Institute for Communicable Diseases
  • Jinal Bhiman; National Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg, South Africa
  • Veronica Ueckermann; Division for Infectious Diseases, Department of Internal Medicine, Steve Biko Academic Hospital and University of Pretoria, Pretoria, South Africa
  • Theresa Rossouw; Department of Immunology, Faculty of Health Sciences, University of Pretoria, Pretoria, South Africa.
  • Michael Boswell; Division for Infectious Diseases, Department of Internal Medicine, Steve Biko Academic Hospital and University of Pretoria, Pretoria, South Africa
  • Tulio de Oliveira; University of KwaZulu-Natal
  • Carolyn Williamson; Institute of Infectious Disease and Molecular Medicine, Division of Medical Virology, Department of Pathology, University of Cape Town, Cape Town, South Africa
  • Wendy Burgers; University of Cape Town
  • Ntobeko Ntusi; Wellcome Centre for Infectious Diseases Research in Africa, University of Cape Town, Cape Town, South Africa
  • Lynn Morris; National Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg, South Africa
  • Penny Moore; National Institute for Communicable Diseases of the National Health Laboratory Service, Johannesburg, South Africa
Preprint in En | PREPRINT-BIORXIV | ID: ppbiorxiv-434193
ABSTRACT
Neutralization escape by SARS-CoV-2 variants, as has been observed in the 501Y.V2 (B.1.351) variant, has impacted the efficacy of first generation COVID-19 vaccines. Here, the antibody response to the 501Y.V2 variant was examined in a cohort of patients hospitalized with COVID-19 in early 2021 - when over 90% of infections in South Africa were attributed to 501Y.V2. Robust binding and neutralizing antibody titers to the 501Y.V2 variant were detected and these binding antibodies showed high levels of cross-reactivity for the original variant, from the first wave. In contrast to an earlier study where sera from individuals infected with the original variant showed dramatically reduced potency against 501Y.V2, sera from 501Y.V2-infected patients maintained good cross-reactivity against viruses from the first wave. Furthermore, sera from 501Y.V2-infected patients also neutralized the 501Y.V3 (P.1) variant first described in Brazil, and now circulating globally. Collectively these data suggest that the antibody response in patients infected with 501Y.V2 has a broad specificity and that vaccines designed with the 501Y.V2 sequence may elicit more cross-reactive responses.
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Full text: 1 Collection: 09-preprints Database: PREPRINT-BIORXIV Type of study: Cohort_studies / Diagnostic_studies / Observational_studies / Prognostic_studies / Rct Language: En Year: 2021 Document type: Preprint
Full text: 1 Collection: 09-preprints Database: PREPRINT-BIORXIV Type of study: Cohort_studies / Diagnostic_studies / Observational_studies / Prognostic_studies / Rct Language: En Year: 2021 Document type: Preprint