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Five doses of the mRNA vaccination potentially suppress ancestral-strain stimulated SARS-CoV2-specific cellular immunity: a cohort study from the Fukushima vaccination community survey, Japan
The bivalent mRNA vaccine is recommended to address coronavirus disease variants, with additional doses suggested for high-risk groups. However, the effectiveness, optimal frequency, and number of doses remain uncertain. In this study, we examined the long-term cellular and humoral immune responses...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10469480/ https://www.ncbi.nlm.nih.gov/pubmed/37662950 http://dx.doi.org/10.3389/fimmu.2023.1240425 |
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author | Tani, Yuta Takita, Morihito Wakui, Masatoshi Saito, Hiroaki Nishiuchi, Takamitsu Zhao, Tianchen Yamamoto, Chika Kawamura, Takeshi Sugiyama, Akira Nakayama, Aya Kaneko, Yudai Kodama, Tatsuhiko Shinaha, Ryuzaburo Tsubokura, Masaharu |
author_facet | Tani, Yuta Takita, Morihito Wakui, Masatoshi Saito, Hiroaki Nishiuchi, Takamitsu Zhao, Tianchen Yamamoto, Chika Kawamura, Takeshi Sugiyama, Akira Nakayama, Aya Kaneko, Yudai Kodama, Tatsuhiko Shinaha, Ryuzaburo Tsubokura, Masaharu |
author_sort | Tani, Yuta |
collection | PubMed |
description | The bivalent mRNA vaccine is recommended to address coronavirus disease variants, with additional doses suggested for high-risk groups. However, the effectiveness, optimal frequency, and number of doses remain uncertain. In this study, we examined the long-term cellular and humoral immune responses following the fifth administration of the mRNA severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine in patients undergoing hemodialysis. To our knowledge, this is the first study to monitor long-term data on humoral and cellular immunity dynamics in high-risk populations after five doses of mRNA vaccination, including the bivalent mRNA vaccine. Whereas most patients maintained humoral immunity throughout the observation period, we observed reduced cellular immune reactivity as measured by the ancestral-strain-stimulated ELISpot assay in a subset of patients. Half of the individuals (50%; 14/28) maintained cellular immunity three months after the fifth dose, despite acquiring humoral immunity. The absence of a relationship between positive controls and T-Spot reactivity suggests that these immune alterations were specific to SARS-CoV-2. In multivariable analysis, participants aged ≥70 years showed a marginally significant lower likelihood of having reactive results. Notably, among the 14 individuals who received heterologous vaccines, 13 successfully acquired cellular immunity, supporting the effectiveness of this administration strategy. These findings provide valuable insights for future vaccination strategies in vulnerable populations. However, further research is needed to evaluate the involvement of immune tolerance and exhaustion through repeated vaccination to optimize immunization strategies. |
format | Online Article Text |
id | pubmed-10469480 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-104694802023-09-01 Five doses of the mRNA vaccination potentially suppress ancestral-strain stimulated SARS-CoV2-specific cellular immunity: a cohort study from the Fukushima vaccination community survey, Japan Tani, Yuta Takita, Morihito Wakui, Masatoshi Saito, Hiroaki Nishiuchi, Takamitsu Zhao, Tianchen Yamamoto, Chika Kawamura, Takeshi Sugiyama, Akira Nakayama, Aya Kaneko, Yudai Kodama, Tatsuhiko Shinaha, Ryuzaburo Tsubokura, Masaharu Front Immunol Immunology The bivalent mRNA vaccine is recommended to address coronavirus disease variants, with additional doses suggested for high-risk groups. However, the effectiveness, optimal frequency, and number of doses remain uncertain. In this study, we examined the long-term cellular and humoral immune responses following the fifth administration of the mRNA severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccine in patients undergoing hemodialysis. To our knowledge, this is the first study to monitor long-term data on humoral and cellular immunity dynamics in high-risk populations after five doses of mRNA vaccination, including the bivalent mRNA vaccine. Whereas most patients maintained humoral immunity throughout the observation period, we observed reduced cellular immune reactivity as measured by the ancestral-strain-stimulated ELISpot assay in a subset of patients. Half of the individuals (50%; 14/28) maintained cellular immunity three months after the fifth dose, despite acquiring humoral immunity. The absence of a relationship between positive controls and T-Spot reactivity suggests that these immune alterations were specific to SARS-CoV-2. In multivariable analysis, participants aged ≥70 years showed a marginally significant lower likelihood of having reactive results. Notably, among the 14 individuals who received heterologous vaccines, 13 successfully acquired cellular immunity, supporting the effectiveness of this administration strategy. These findings provide valuable insights for future vaccination strategies in vulnerable populations. However, further research is needed to evaluate the involvement of immune tolerance and exhaustion through repeated vaccination to optimize immunization strategies. Frontiers Media S.A. 2023-08-16 /pmc/articles/PMC10469480/ /pubmed/37662950 http://dx.doi.org/10.3389/fimmu.2023.1240425 Text en Copyright © 2023 Tani, Takita, Wakui, Saito, Nishiuchi, Zhao, Yamamoto, Kawamura, Sugiyama, Nakayama, Kaneko, Kodama, Shinaha and Tsubokura https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Tani, Yuta Takita, Morihito Wakui, Masatoshi Saito, Hiroaki Nishiuchi, Takamitsu Zhao, Tianchen Yamamoto, Chika Kawamura, Takeshi Sugiyama, Akira Nakayama, Aya Kaneko, Yudai Kodama, Tatsuhiko Shinaha, Ryuzaburo Tsubokura, Masaharu Five doses of the mRNA vaccination potentially suppress ancestral-strain stimulated SARS-CoV2-specific cellular immunity: a cohort study from the Fukushima vaccination community survey, Japan |
title | Five doses of the mRNA vaccination potentially suppress ancestral-strain stimulated SARS-CoV2-specific cellular immunity: a cohort study from the Fukushima vaccination community survey, Japan |
title_full | Five doses of the mRNA vaccination potentially suppress ancestral-strain stimulated SARS-CoV2-specific cellular immunity: a cohort study from the Fukushima vaccination community survey, Japan |
title_fullStr | Five doses of the mRNA vaccination potentially suppress ancestral-strain stimulated SARS-CoV2-specific cellular immunity: a cohort study from the Fukushima vaccination community survey, Japan |
title_full_unstemmed | Five doses of the mRNA vaccination potentially suppress ancestral-strain stimulated SARS-CoV2-specific cellular immunity: a cohort study from the Fukushima vaccination community survey, Japan |
title_short | Five doses of the mRNA vaccination potentially suppress ancestral-strain stimulated SARS-CoV2-specific cellular immunity: a cohort study from the Fukushima vaccination community survey, Japan |
title_sort | five doses of the mrna vaccination potentially suppress ancestral-strain stimulated sars-cov2-specific cellular immunity: a cohort study from the fukushima vaccination community survey, japan |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10469480/ https://www.ncbi.nlm.nih.gov/pubmed/37662950 http://dx.doi.org/10.3389/fimmu.2023.1240425 |
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