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Antibody longevity and cross-neutralizing activity following SARS-CoV-2 wave 1 and B.1.1.7 infections.

Authors :
Dupont L
Snell LB
Graham C
Seow J
Merrick B
Lechmere T
Hallett SR
Charalampous T
Alcolea-Medina A
Huettner I
Maguire TJA
Acors S
Almeida N
Cox D
Dickenson RE
Galao RP
Jimenez-Guardeño JM
Kouphou N
Lista MJ
Pickering S
Ortega-Prieto AM
Wilson H
Winstone H
Fairhead C
Su J
Nebbia G
Batra R
Neil S
Shankar-Hari M
Edgeworth JD
Malim MH
Doores KJ
Source :
MedRxiv : the preprint server for health sciences [medRxiv] 2021 Jun 08. Date of Electronic Publication: 2021 Jun 08.
Publication Year :
2021

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.

Details

Language :
English
Database :
MEDLINE
Journal :
MedRxiv : the preprint server for health sciences
Accession number :
34127977
Full Text :
https://doi.org/10.1101/2021.06.07.21258351