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Vaccination-infection interval determines cross-neutralization potency to SARS-CoV-2 Omicron after breakthrough infection by other variants

BACKGROUND: The immune profile against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has dramatically diversified due to a complex combination of exposure to vaccines and infection by various lineages/variants, likely generating a heterogeneity in protective immunity in a given popula...

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Autores principales: Miyamoto, Sho, Arashiro, Takeshi, Adachi, Yu, Moriyama, Saya, Kinoshita, Hitomi, Kanno, Takayuki, Saito, Shinji, Katano, Harutaka, Iida, Shun, Ainai, Akira, Kotaki, Ryutaro, Yamada, Souichi, Kuroda, Yudai, Yamamoto, Tsukasa, Ishijima, Keita, Park, Eun-Sil, Inoue, Yusuke, Kaku, Yoshihiro, Tobiume, Minoru, Iwata-Yoshikawa, Naoko, Shiwa-Sudo, Nozomi, Tokunaga, Kenzo, Ozono, Seiya, Hemmi, Takuya, Ueno, Akira, Kishida, Noriko, Watanabe, Shinji, Nojima, Kiyoko, Seki, Yohei, Mizukami, Takuo, Hasegawa, Hideki, Ebihara, Hideki, Maeda, Ken, Fukushi, Shuetsu, Takahashi, Yoshimasa, Suzuki, Tadaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8894731/
https://www.ncbi.nlm.nih.gov/pubmed/35261995
http://dx.doi.org/10.1016/j.medj.2022.02.006
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author Miyamoto, Sho
Arashiro, Takeshi
Adachi, Yu
Moriyama, Saya
Kinoshita, Hitomi
Kanno, Takayuki
Saito, Shinji
Katano, Harutaka
Iida, Shun
Ainai, Akira
Kotaki, Ryutaro
Yamada, Souichi
Kuroda, Yudai
Yamamoto, Tsukasa
Ishijima, Keita
Park, Eun-Sil
Inoue, Yusuke
Kaku, Yoshihiro
Tobiume, Minoru
Iwata-Yoshikawa, Naoko
Shiwa-Sudo, Nozomi
Tokunaga, Kenzo
Ozono, Seiya
Hemmi, Takuya
Ueno, Akira
Kishida, Noriko
Watanabe, Shinji
Nojima, Kiyoko
Seki, Yohei
Mizukami, Takuo
Hasegawa, Hideki
Ebihara, Hideki
Maeda, Ken
Fukushi, Shuetsu
Takahashi, Yoshimasa
Suzuki, Tadaki
author_facet Miyamoto, Sho
Arashiro, Takeshi
Adachi, Yu
Moriyama, Saya
Kinoshita, Hitomi
Kanno, Takayuki
Saito, Shinji
Katano, Harutaka
Iida, Shun
Ainai, Akira
Kotaki, Ryutaro
Yamada, Souichi
Kuroda, Yudai
Yamamoto, Tsukasa
Ishijima, Keita
Park, Eun-Sil
Inoue, Yusuke
Kaku, Yoshihiro
Tobiume, Minoru
Iwata-Yoshikawa, Naoko
Shiwa-Sudo, Nozomi
Tokunaga, Kenzo
Ozono, Seiya
Hemmi, Takuya
Ueno, Akira
Kishida, Noriko
Watanabe, Shinji
Nojima, Kiyoko
Seki, Yohei
Mizukami, Takuo
Hasegawa, Hideki
Ebihara, Hideki
Maeda, Ken
Fukushi, Shuetsu
Takahashi, Yoshimasa
Suzuki, Tadaki
author_sort Miyamoto, Sho
collection PubMed
description BACKGROUND: The immune profile against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has dramatically diversified due to a complex combination of exposure to vaccines and infection by various lineages/variants, likely generating a heterogeneity in protective immunity in a given population. To further complicate this, the Omicron variant, with numerous spike mutations, has emerged. These circumstances have created the need to assess the potential of immune evasion by Omicron in individuals with various immune histories. METHODS: The neutralization susceptibility of the variants, including Omicron and their ancestors, was comparably assessed using a panel of plasma/serum derived from individuals with divergent immune histories. Blood samples were collected from either mRNA vaccinees or from those who suffered from breakthrough infections of Alpha/Delta with multiple time intervals following vaccination. FINDINGS: Omicron was highly resistant to neutralization in fully vaccinated individuals without a history of breakthrough infections. In contrast, robust cross-neutralization against Omicron was induced in vaccinees that experienced breakthrough infections. The time interval between vaccination and infection, rather than the variant types of infection, was significantly correlated with the magnitude and potency of Omicron-neutralizing antibodies. CONCLUSIONS: Immune histories with breakthrough infections can overcome the resistance to infection by Omicron, with the vaccination-infection interval being the key determinant of the magnitude and breadth of neutralization. The diverse exposure history in each individual warrants a tailored and cautious approach to understanding population immunity against Omicron and future variants. FUNDING: This study was supported by grants from the Japan Agency for Medical Research and Development (AMED).
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spelling pubmed-88947312022-03-04 Vaccination-infection interval determines cross-neutralization potency to SARS-CoV-2 Omicron after breakthrough infection by other variants Miyamoto, Sho Arashiro, Takeshi Adachi, Yu Moriyama, Saya Kinoshita, Hitomi Kanno, Takayuki Saito, Shinji Katano, Harutaka Iida, Shun Ainai, Akira Kotaki, Ryutaro Yamada, Souichi Kuroda, Yudai Yamamoto, Tsukasa Ishijima, Keita Park, Eun-Sil Inoue, Yusuke Kaku, Yoshihiro Tobiume, Minoru Iwata-Yoshikawa, Naoko Shiwa-Sudo, Nozomi Tokunaga, Kenzo Ozono, Seiya Hemmi, Takuya Ueno, Akira Kishida, Noriko Watanabe, Shinji Nojima, Kiyoko Seki, Yohei Mizukami, Takuo Hasegawa, Hideki Ebihara, Hideki Maeda, Ken Fukushi, Shuetsu Takahashi, Yoshimasa Suzuki, Tadaki Med Clinical and Translational Report BACKGROUND: The immune profile against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has dramatically diversified due to a complex combination of exposure to vaccines and infection by various lineages/variants, likely generating a heterogeneity in protective immunity in a given population. To further complicate this, the Omicron variant, with numerous spike mutations, has emerged. These circumstances have created the need to assess the potential of immune evasion by Omicron in individuals with various immune histories. METHODS: The neutralization susceptibility of the variants, including Omicron and their ancestors, was comparably assessed using a panel of plasma/serum derived from individuals with divergent immune histories. Blood samples were collected from either mRNA vaccinees or from those who suffered from breakthrough infections of Alpha/Delta with multiple time intervals following vaccination. FINDINGS: Omicron was highly resistant to neutralization in fully vaccinated individuals without a history of breakthrough infections. In contrast, robust cross-neutralization against Omicron was induced in vaccinees that experienced breakthrough infections. The time interval between vaccination and infection, rather than the variant types of infection, was significantly correlated with the magnitude and potency of Omicron-neutralizing antibodies. CONCLUSIONS: Immune histories with breakthrough infections can overcome the resistance to infection by Omicron, with the vaccination-infection interval being the key determinant of the magnitude and breadth of neutralization. The diverse exposure history in each individual warrants a tailored and cautious approach to understanding population immunity against Omicron and future variants. FUNDING: This study was supported by grants from the Japan Agency for Medical Research and Development (AMED). Elsevier Inc. 2022-04-08 2022-03-04 /pmc/articles/PMC8894731/ /pubmed/35261995 http://dx.doi.org/10.1016/j.medj.2022.02.006 Text en © 2022 Elsevier Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Clinical and Translational Report
Miyamoto, Sho
Arashiro, Takeshi
Adachi, Yu
Moriyama, Saya
Kinoshita, Hitomi
Kanno, Takayuki
Saito, Shinji
Katano, Harutaka
Iida, Shun
Ainai, Akira
Kotaki, Ryutaro
Yamada, Souichi
Kuroda, Yudai
Yamamoto, Tsukasa
Ishijima, Keita
Park, Eun-Sil
Inoue, Yusuke
Kaku, Yoshihiro
Tobiume, Minoru
Iwata-Yoshikawa, Naoko
Shiwa-Sudo, Nozomi
Tokunaga, Kenzo
Ozono, Seiya
Hemmi, Takuya
Ueno, Akira
Kishida, Noriko
Watanabe, Shinji
Nojima, Kiyoko
Seki, Yohei
Mizukami, Takuo
Hasegawa, Hideki
Ebihara, Hideki
Maeda, Ken
Fukushi, Shuetsu
Takahashi, Yoshimasa
Suzuki, Tadaki
Vaccination-infection interval determines cross-neutralization potency to SARS-CoV-2 Omicron after breakthrough infection by other variants
title Vaccination-infection interval determines cross-neutralization potency to SARS-CoV-2 Omicron after breakthrough infection by other variants
title_full Vaccination-infection interval determines cross-neutralization potency to SARS-CoV-2 Omicron after breakthrough infection by other variants
title_fullStr Vaccination-infection interval determines cross-neutralization potency to SARS-CoV-2 Omicron after breakthrough infection by other variants
title_full_unstemmed Vaccination-infection interval determines cross-neutralization potency to SARS-CoV-2 Omicron after breakthrough infection by other variants
title_short Vaccination-infection interval determines cross-neutralization potency to SARS-CoV-2 Omicron after breakthrough infection by other variants
title_sort vaccination-infection interval determines cross-neutralization potency to sars-cov-2 omicron after breakthrough infection by other variants
topic Clinical and Translational Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8894731/
https://www.ncbi.nlm.nih.gov/pubmed/35261995
http://dx.doi.org/10.1016/j.medj.2022.02.006
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