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Omicron BA.1 neutralizing antibody response following Delta breakthrough infection compared with booster vaccination of BNT162b2
BACKGROUND: Longitudinal data are lacking to compare booster effects of Delta breakthrough infection versus third vaccine dose on neutralizing antibodies (NAb) against Omicron. METHODS: Participants were the staff of a national research and medical institution in Tokyo who attended serological surve...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10157119/ https://www.ncbi.nlm.nih.gov/pubmed/37142992 http://dx.doi.org/10.1186/s12879-023-08272-2 |
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author | Yamamoto, Shohei Matsuda, Kouki Maeda, Kenji Oshiro, Yusuke Inamura, Natsumi Mizoue, Tetsuya Konishi, Maki Takeuchi, Junko S. Horii, Kumi Ozeki, Mitsuru Sugiyama, Haruhito Mitsuya, Hiroaki Sugiura, Wataru Ohmagari, Norio |
author_facet | Yamamoto, Shohei Matsuda, Kouki Maeda, Kenji Oshiro, Yusuke Inamura, Natsumi Mizoue, Tetsuya Konishi, Maki Takeuchi, Junko S. Horii, Kumi Ozeki, Mitsuru Sugiyama, Haruhito Mitsuya, Hiroaki Sugiura, Wataru Ohmagari, Norio |
author_sort | Yamamoto, Shohei |
collection | PubMed |
description | BACKGROUND: Longitudinal data are lacking to compare booster effects of Delta breakthrough infection versus third vaccine dose on neutralizing antibodies (NAb) against Omicron. METHODS: Participants were the staff of a national research and medical institution in Tokyo who attended serological surveys on June 2021 (baseline) and December 2021 (follow-up); in between, the Delta-dominant epidemic occurred. Of 844 participants who were infection-naïve and had received two doses of BNT162b2 at baseline, we identified 11 breakthrough infections during follow-up. One control matched to each case was selected from boosted and unboosted individuals. We compared live-virus NAb against Wild-type, Delta, and Omicron BA.1 across groups. RESULTS: Breakthrough infection cases showed marked increases in NAb titers against Wild-type (4.1-fold) and Delta (5.5-fold), and 64% had detectable NAb against Omicron BA.1 at follow-up, although the NAb against Omicron after breakthrough infection was 6.7- and 5.2-fold lower than Wild-type and Delta, respectively. The increase was apparent only in symptomatic cases and as high as in the third vaccine recipients. CONCLUSIONS: Symptomatic Delta breakthrough infection increased NAb against Wild-type, Delta, and Omicron BA.1, similar to the third vaccine. Given the much lower NAb against Omicron BA.1, infection prevention measures must be continued irrespective of vaccine and infection history while the immune evasive variants are circulating. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-023-08272-2. |
format | Online Article Text |
id | pubmed-10157119 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-101571192023-05-05 Omicron BA.1 neutralizing antibody response following Delta breakthrough infection compared with booster vaccination of BNT162b2 Yamamoto, Shohei Matsuda, Kouki Maeda, Kenji Oshiro, Yusuke Inamura, Natsumi Mizoue, Tetsuya Konishi, Maki Takeuchi, Junko S. Horii, Kumi Ozeki, Mitsuru Sugiyama, Haruhito Mitsuya, Hiroaki Sugiura, Wataru Ohmagari, Norio BMC Infect Dis Research BACKGROUND: Longitudinal data are lacking to compare booster effects of Delta breakthrough infection versus third vaccine dose on neutralizing antibodies (NAb) against Omicron. METHODS: Participants were the staff of a national research and medical institution in Tokyo who attended serological surveys on June 2021 (baseline) and December 2021 (follow-up); in between, the Delta-dominant epidemic occurred. Of 844 participants who were infection-naïve and had received two doses of BNT162b2 at baseline, we identified 11 breakthrough infections during follow-up. One control matched to each case was selected from boosted and unboosted individuals. We compared live-virus NAb against Wild-type, Delta, and Omicron BA.1 across groups. RESULTS: Breakthrough infection cases showed marked increases in NAb titers against Wild-type (4.1-fold) and Delta (5.5-fold), and 64% had detectable NAb against Omicron BA.1 at follow-up, although the NAb against Omicron after breakthrough infection was 6.7- and 5.2-fold lower than Wild-type and Delta, respectively. The increase was apparent only in symptomatic cases and as high as in the third vaccine recipients. CONCLUSIONS: Symptomatic Delta breakthrough infection increased NAb against Wild-type, Delta, and Omicron BA.1, similar to the third vaccine. Given the much lower NAb against Omicron BA.1, infection prevention measures must be continued irrespective of vaccine and infection history while the immune evasive variants are circulating. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12879-023-08272-2. BioMed Central 2023-05-04 /pmc/articles/PMC10157119/ /pubmed/37142992 http://dx.doi.org/10.1186/s12879-023-08272-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Yamamoto, Shohei Matsuda, Kouki Maeda, Kenji Oshiro, Yusuke Inamura, Natsumi Mizoue, Tetsuya Konishi, Maki Takeuchi, Junko S. Horii, Kumi Ozeki, Mitsuru Sugiyama, Haruhito Mitsuya, Hiroaki Sugiura, Wataru Ohmagari, Norio Omicron BA.1 neutralizing antibody response following Delta breakthrough infection compared with booster vaccination of BNT162b2 |
title | Omicron BA.1 neutralizing antibody response following Delta breakthrough infection compared with booster vaccination of BNT162b2 |
title_full | Omicron BA.1 neutralizing antibody response following Delta breakthrough infection compared with booster vaccination of BNT162b2 |
title_fullStr | Omicron BA.1 neutralizing antibody response following Delta breakthrough infection compared with booster vaccination of BNT162b2 |
title_full_unstemmed | Omicron BA.1 neutralizing antibody response following Delta breakthrough infection compared with booster vaccination of BNT162b2 |
title_short | Omicron BA.1 neutralizing antibody response following Delta breakthrough infection compared with booster vaccination of BNT162b2 |
title_sort | omicron ba.1 neutralizing antibody response following delta breakthrough infection compared with booster vaccination of bnt162b2 |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10157119/ https://www.ncbi.nlm.nih.gov/pubmed/37142992 http://dx.doi.org/10.1186/s12879-023-08272-2 |
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