Novavax NVX-COV2373 triggers potent neutralization of Omicron sub-lineages

Bhiman, J. N.; Richardson, S. I.; Lambson, B. E.; Kgagudi, P.; Mzindle, N.; Kaldine, H.; Crowther, C.; Gray, G.; Bekker, L.-G.; Koen, A.; Fairlie, L.; Fouche, L.; Bhorat, Q.; Dheda, K.; Tameris, M.; Masilela, M. S. L.; Hoosain, Z.; Singh, N.; Hanley, S.; Archary, M.; Louw, C.; Grobbelaar, C.; Lalloo, U.; Joseph, N.; Kruger, G.; Shinde, V.; Bennett, C.; Glenn, G.; Madhi, S.; Moore, P. L.

doi:10.1101/2022.07.14.500148

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bioRxiv · 10.1101/2022.07.14.500148

Novavax NVX-COV2373 triggers potent neutralization of Omicron sub-lineages

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Abstract

The SARS-CoV-2 Omicron (B.1.1.529) Variant of Concern (VOC) and its sub-lineages (including BA.2, BA.4/5, BA.2.12.1) contain spike mutations that confer high level resistance to neutralizing antibodies. The NVX-CoV2373 vaccine, a protein nanoparticle vaccine, has value in countries with constrained cold-chain requirements. Here we report neutralizing titers following two or three doses of NVX-CoV2373. We show that after two doses, Omicron sub-lineages BA.1 and BA.4 were resistant to neutralization by 72% (21/29) and 59% (17/29) of samples. However, after a third dose of NVX-CoV2373, we observed high titers against Omicron BA.1 (GMT: 1,197) and BA.4 (GMT: 582), with responses similar in magnitude to those triggered by three doses of an mRNA vaccine. These data are of particular relevance as BA.4 is emerging to become the dominant strain in many locations, and highlight the potential utility of the NVX-CoV2373 vaccine as a booster in resource-limited environments.

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Bhiman, J. N., Richardson, S. I., Lambson, B. E., Kgagudi, P., Mzindle, N., Kaldine, H., Crowther, C., Gray, G., Bekker, L.-G., Koen, A., Fairlie, L., Fouche, L., Bhorat, Q., Dheda, K., Tameris, M., Masilela, M. S. L., Hoosain, Z., Singh, N., Hanley, S., Archary, M., Louw, C., Grobbelaar, C., Lalloo, U., Joseph, N., Kruger, G., Shinde, V., Bennett, C., Glenn, G., Madhi, S., Moore, P. L.. 2022-07-17. Novavax NVX-COV2373 triggers potent neutralization of Omicron sub-lineages. https://doi.org/10.1101/2022.07.14.500148

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