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. 2024 Jul 31;15:6085. doi: 10.1038/s41467-024-49634-x

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© The Author(s) 2024

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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 1 — Vertical lines depict 95% CIs; these are not visible when they are very narrow. There were no AMI events during weeks 13–26 after mRNA-1273 booster vaccination, so follow-up is grouped as 1–4 and 5–26 weeks post-vaccination. The number of people eligible for first, second, and booster dose analyses were 45,673,965; 37,249,850 and 35,853,120, respectively. The number of people who received a first dose of ChAdOx1, BNT-162b2 and mRNA-1273 were 19,317,985, 16,846,995, and 1,084,865, respectively; a second dose of ChAdOx1, BNT-162b2 and mRNA-1273 were 18,920,225, 15,961,330, and 971,565, respectively; a booster dose of BNT-162b2 and mRNA-1273 following a primary course of ChAdOx1 were 11,964,635and 4,153,760 respectively; a booster dose of BNT-162b2 and mRNA-1273 following a primary course of BNT-162b2 were 9,821,835 and 1,914,925, respectively. The numerical values of hazard ratios and 95% CIs are displayed in Supplementary Tables 8, 9, 11, 12, 14, 15, 17 and 18.