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Serum Neutralizing Activity of mRNA-1273 against SARS-CoV-2 Variants

Angela Choi, Matthew Koch, Kai Wu, Groves Dixon, Judy Oestreicher, Holly Legault, Guillaume B.E. Stewart□Jones, Tonya Colpitts, Rolando Pajon, Hamilton Bennett, Andrea Carfi, Darin K. Edwards
doi: https://doi.org/10.1101/2021.06.28.449914
Angela Choi
1Moderna Inc., 200 Technology Square, Cambridge, Massachusetts, 02139, USA
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Matthew Koch
1Moderna Inc., 200 Technology Square, Cambridge, Massachusetts, 02139, USA
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Kai Wu
1Moderna Inc., 200 Technology Square, Cambridge, Massachusetts, 02139, USA
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Groves Dixon
1Moderna Inc., 200 Technology Square, Cambridge, Massachusetts, 02139, USA
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Judy Oestreicher
1Moderna Inc., 200 Technology Square, Cambridge, Massachusetts, 02139, USA
MS
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Holly Legault
1Moderna Inc., 200 Technology Square, Cambridge, Massachusetts, 02139, USA
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Guillaume B.E. Stewart□Jones
1Moderna Inc., 200 Technology Square, Cambridge, Massachusetts, 02139, USA
PhD
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Tonya Colpitts
1Moderna Inc., 200 Technology Square, Cambridge, Massachusetts, 02139, USA
PhD
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Rolando Pajon
1Moderna Inc., 200 Technology Square, Cambridge, Massachusetts, 02139, USA
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Hamilton Bennett
1Moderna Inc., 200 Technology Square, Cambridge, Massachusetts, 02139, USA
MS
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Andrea Carfi
1Moderna Inc., 200 Technology Square, Cambridge, Massachusetts, 02139, USA
PhD
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  • For correspondence: [email protected] [email protected]
Darin K. Edwards
1Moderna Inc., 200 Technology Square, Cambridge, Massachusetts, 02139, USA
PhD
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  • For correspondence: [email protected] [email protected]
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ABSTRACT

The emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants has led to growing concerns over increased transmissibility and the ability of some variants to partially escape immunity. Sera from participants immunized on a prime-boost schedule with the mRNA-1273 COVID-19 vaccine were tested for neutralizing activity against several SARS-CoV-2 variants, including variants of concern (VOCs) and variants of interest (VOIs), compared to neutralization of the wild-type SARS-CoV-2 virus (designated as D614G). Results showed minimal effects on neutralization titers against the B.1.1.7 (Alpha) variant (1.2-fold reduction compared with D614G); other VOCs such as B.1.351 (Beta, including B.1.351-v1, B.1.351-v2, and B.1.351-v3), B.1.617.2 (Delta), and P.1 (Gamma) showed decreased neutralization titers ranging from 2.1-fold to 8.4-fold reductions compared with D614G, although all remained susceptible to mRNA-1273–elicited serum neutralization.

Competing Interest Statement

A.C., M.K., K.W., G.D, J.O., H.L., G.S.-J., T.C., R.P. H.B., A.C. and D.K.E. are employed by Moderna Inc. and hold equities from the company.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission.
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Posted June 28, 2021.
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Serum Neutralizing Activity of mRNA-1273 against SARS-CoV-2 Variants
Angela Choi, Matthew Koch, Kai Wu, Groves Dixon, Judy Oestreicher, Holly Legault, Guillaume B.E. Stewart□Jones, Tonya Colpitts, Rolando Pajon, Hamilton Bennett, Andrea Carfi, Darin K. Edwards
bioRxiv 2021.06.28.449914; doi: https://doi.org/10.1101/2021.06.28.449914
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Serum Neutralizing Activity of mRNA-1273 against SARS-CoV-2 Variants
Angela Choi, Matthew Koch, Kai Wu, Groves Dixon, Judy Oestreicher, Holly Legault, Guillaume B.E. Stewart□Jones, Tonya Colpitts, Rolando Pajon, Hamilton Bennett, Andrea Carfi, Darin K. Edwards
bioRxiv 2021.06.28.449914; doi: https://doi.org/10.1101/2021.06.28.449914

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