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. 2023 Jul 28;9:78. doi: 10.1038/s41421-023-00581-9

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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. 8 — a–c The NT₅₀ against the indicated S pseudovirions of sera from mice immunized by trimeric SARS-CoV-2 S ectodomain (a), BANAL-20-52 S ectodomain (b), and BANAL-20-236 S ectodomain (c). The numbers above each group indicate the neutralizing GMTs of each group. d The NT₅₀ against WT and Q498H mutant SARS-CoV-2 S pseudovirions of sera from trimeric BANAL-20-52 S ectodomain-immunized mice. e, f The NT₅₀ against the indicated S pseudovirions of sera from mice immunized with trimeric BANAL-20-52 S ectodomain (e) or BANAL-20-236 S ectodomain (f).