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Antibody longevity and cross-neutralizing activity following SARS-CoV-2 wave 1 and B.1.1.7 infections.
Dupont, Liane; Snell, Luke B; Graham, Carl; Seow, Jeffrey; Merrick, Blair; Lechmere, Thomas; Hallett, Sadie R; Charalampous, Themoula; Alcolea-Medina, Adela; Huettner, Isabella; Maguire, Thomas J A; Acors, Sam; Almeida, Nathalia; Cox, Daniel; Dickenson, Ruth E; Galao, Rui Pedro; Jimenez-Guardeño, Jose M; Kouphou, Neophytos; Lista, Marie Jose; Pickering, Suzanne; Ortega-Prieto, Ana Maria; Wilson, Harry; Winstone, Helena; Fairhead, Cassandra; Su, Jia; Nebbia, Gaia; Batra, Rahul; Neil, Stuart; Shankar-Hari, Manu; Edgeworth, Jonathan D; Malim, Michael H; Doores, Katie J.
Afiliação
  • Dupont L; Department of Infectious Diseases, School of Immunology & Microbial Sciences, King's College London, London, UK.
  • Snell LB; Centre for Clinical Infection and Diagnostics Research, Department of Infectious Diseases, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Graham C; Department of Infectious Diseases, School of Immunology & Microbial Sciences, King's College London, London, UK.
  • Seow J; Department of Infectious Diseases, School of Immunology & Microbial Sciences, King's College London, London, UK.
  • Merrick B; Centre for Clinical Infection and Diagnostics Research, Department of Infectious Diseases, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Lechmere T; Department of Infectious Diseases, School of Immunology & Microbial Sciences, King's College London, London, UK.
  • Hallett SR; Department of Infectious Diseases, School of Immunology & Microbial Sciences, King's College London, London, UK.
  • Charalampous T; Centre for Clinical Infection and Diagnostics Research, Department of Infectious Diseases, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Alcolea-Medina A; Centre for Clinical Infection and Diagnostics Research, Department of Infectious Diseases, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Huettner I; Department of Infectious Diseases, School of Immunology & Microbial Sciences, King's College London, London, UK.
  • Maguire TJA; Department of Infectious Diseases, School of Immunology & Microbial Sciences, King's College London, London, UK.
  • Acors S; Department of Infectious Diseases, School of Immunology & Microbial Sciences, King's College London, London, UK.
  • Almeida N; Department of Infectious Diseases, School of Immunology & Microbial Sciences, King's College London, London, UK.
  • Cox D; Department of Infectious Diseases, School of Immunology & Microbial Sciences, King's College London, London, UK.
  • Dickenson RE; Department of Infectious Diseases, School of Immunology & Microbial Sciences, King's College London, London, UK.
  • Galao RP; Department of Infectious Diseases, School of Immunology & Microbial Sciences, King's College London, London, UK.
  • Jimenez-Guardeño JM; Department of Infectious Diseases, School of Immunology & Microbial Sciences, King's College London, London, UK.
  • Kouphou N; Department of Infectious Diseases, School of Immunology & Microbial Sciences, King's College London, London, UK.
  • Lista MJ; Department of Infectious Diseases, School of Immunology & Microbial Sciences, King's College London, London, UK.
  • Pickering S; Department of Infectious Diseases, School of Immunology & Microbial Sciences, King's College London, London, UK.
  • Ortega-Prieto AM; Department of Infectious Diseases, School of Immunology & Microbial Sciences, King's College London, London, UK.
  • Wilson H; Department of Infectious Diseases, School of Immunology & Microbial Sciences, King's College London, London, UK.
  • Winstone H; Department of Infectious Diseases, School of Immunology & Microbial Sciences, King's College London, London, UK.
  • Fairhead C; Centre for Clinical Infection and Diagnostics Research, Department of Infectious Diseases, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Su J; Centre for Clinical Infection and Diagnostics Research, Department of Infectious Diseases, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Nebbia G; Centre for Clinical Infection and Diagnostics Research, Department of Infectious Diseases, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Batra R; Centre for Clinical Infection and Diagnostics Research, Department of Infectious Diseases, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Neil S; Department of Infectious Diseases, School of Immunology & Microbial Sciences, King's College London, London, UK.
  • Shankar-Hari M; Department of Infectious Diseases, School of Immunology & Microbial Sciences, King's College London, London, UK.
  • Edgeworth JD; Centre for Clinical Infection and Diagnostics Research, Department of Infectious Diseases, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Malim MH; Department of Infectious Diseases, School of Immunology & Microbial Sciences, King's College London, London, UK.
  • Doores KJ; Department of Infectious Diseases, School of Immunology & Microbial Sciences, King's College London, London, UK.
medRxiv ; 2021 Jun 08.
Article em En | MEDLINE | ID: mdl-34127977
ABSTRACT
As SARS-CoV-2 variants continue to emerge globally, a major challenge for COVID-19 vaccination is the generation of a durable antibody response with cross-neutralizing activity against both current and newly emerging viral variants. Cross-neutralizing activity against major variants of concern (B.1.1.7, P.1 and B.1.351) has been observed following vaccination, albeit at a reduced potency, but whether vaccines based on the Spike glycoprotein of these viral variants will produce a superior cross-neutralizing antibody response has not been fully investigated. Here, we used sera from individuals infected in wave 1 in the UK to study the long-term cross-neutralization up to 10 months post onset of symptoms (POS), as well as sera from individuals infected with the B.1.1.7 variant to compare cross-neutralizing activity profiles. We show that neutralizing antibodies with cross-neutralizing activity can be detected from wave 1 up to 10 months POS. Although neutralization of B.1.1.7 and B.1.351 is lower, the difference in neutralization potency decreases at later timepoints suggesting continued antibody maturation and improved tolerance to Spike mutations. Interestingly, we found that B.1.1.7 infection also generates a cross-neutralizing antibody response, which, although still less potent against B.1.351, can neutralize parental wave 1 virus to a similar degree as B.1.1.7. These findings have implications for the optimization of vaccines that protect against newly emerging viral variants.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2021 Tipo de documento: Article