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. 2023 Mar 10;14:1309. doi: 10.1038/s41467-023-36908-z

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© The Author(s) 2023

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 2 — Pseudovirus-neutralizing antibody against a the prototype D614G, variants of concern b Beta, c Delta, and d Omicron (BA.1), and e SARS-CoV-1 were assessed up to D176 (mRNA-primed macaques, n = 4) or day 178 (protein-primed macaques, n = 5) post-booster with ancestral D614 vaccine, Beta vaccine, or bivalent ancestral + Beta vaccine. Individual macaque data are shown. Connecting lines represent geometric mean titers (GMTs). Horizontal dotted lines represent the limit of quantification of the assay. *Timepoints relative to booster injection day.