Skip to main content

This is a preprint.

It has not yet been peer reviewed by a journal.

The National Library of Medicine is running a pilot to include preprints that result from research funded by NIH in PMC and PubMed.

bioRxiv logoLink to bioRxiv
[Preprint]. 2021 May 10:2021.05.09.443299. [Version 1] doi: 10.1101/2021.05.09.443299

Infection and vaccine-induced neutralizing antibody responses to the SARS-CoV-2 B.1.617.1 variant

Venkata-Viswanadh Edara, Lilin Lai, Malaya K Sahoo, Katharine Floyd, Mamdouh Sibai, Daniel Solis, Maria W Flowers, Laila Hussaini, Caroline Rose Ciric, Sarah Bechnack, Kathy Stephens, Elham Bayat Mokhtari, Prakriti Mudvari, Adrian Creanga, Amarendra Pegu, Alexandrine Derrien-Colemyn, Amy R Henry, Matthew Gagne, Barney S Graham, Jens Wrammert, Daniel C Douek, Eli Boritz, Benjamin A Pinsky, Mehul S Suthar
PMCID: PMC8132229  PMID: 34013272

Abstract

SARS-CoV-2 has caused a devastating global pandemic. The recent emergence of SARS-CoV-2 variants that are less sensitive to neutralization by convalescent sera or vaccine-induced neutralizing antibody responses has raised concerns. A second wave of SARS-CoV-2 infections in India is leading to the expansion of SARS-CoV-2 variants. The B.1.617.1 variant has rapidly spread throughout India and to several countries throughout the world. In this study, using a live virus assay, we describe the neutralizing antibody response to the B.1.617.1 variant in serum from infected and vaccinated individuals. We found that the B.1.617.1 variant is 6.8-fold more resistant to neutralization by sera from COVID-19 convalescent and Moderna and Pfizer vaccinated individuals. Despite this, a majority of the sera from convalescent individuals and all sera from vaccinated individuals were still able to neutralize the B.1.617.1 variant. This suggests that protective immunity by the mRNA vaccines tested here are likely retained against the B.1.617.1 variant. As the B.1.617.1 variant continues to evolve, it will be important to monitor how additional mutations within the spike impact antibody resistance, viral transmission and vaccine efficacy.

Full Text Availability

The license terms selected by the author(s) for this preprint version do not permit archiving in PMC. The full text is available from the preprint server.


Articles from bioRxiv are provided here courtesy of Cold Spring Harbor Laboratory Preprints

RESOURCES