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Emergence of SARS‐CoV‐2 spike protein at the vaccination site

BACKGROUND: The anti‐coronavirus disease 2019 (COVID‐19) vaccines are of paramount importance in the fight against the COVID‐19 pandemic. Both viral vector‐ and nucleic acid‐based vaccines are known to effectively induce protection against the severe acute respiratory syndrome coronavirus 2 (SARS‐Co...

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Autores principales: Beck, Annika, Dietenberger, Hanna, Kunz, Sebastian N., Mellert, Kevin, Möller, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10052447/
https://www.ncbi.nlm.nih.gov/pubmed/36988249
http://dx.doi.org/10.1002/iid3.827
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author Beck, Annika
Dietenberger, Hanna
Kunz, Sebastian N.
Mellert, Kevin
Möller, Peter
author_facet Beck, Annika
Dietenberger, Hanna
Kunz, Sebastian N.
Mellert, Kevin
Möller, Peter
author_sort Beck, Annika
collection PubMed
description BACKGROUND: The anti‐coronavirus disease 2019 (COVID‐19) vaccines are of paramount importance in the fight against the COVID‐19 pandemic. Both viral vector‐ and nucleic acid‐based vaccines are known to effectively induce protection against the severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) virus by generating high antibody titers and effective T‐cell responses to the spike protein they encode. Although these vaccines are being applied worldwide and have been extensively investigated, the immunomorphological events at the vaccination site with respect to SARS‐CoV‐2 spike protein expression have not yet been described. METHODS: We had the opportunity to examine the deltoid muscles of three men who died shortly after vaccination for unrelated reasons. We examined the vaccination sites histologically and immunohistochemically with various antibodies. Furthermore we incubated two different cell lines with one vaccine and examined the expression of the spike protein. RESULTS: The vaccination sites show a dense lymphohistiocytic interstitial infiltrate which surrounds the small vessels and extends into the perimysium. The spike protein is expressed by histiocytic cells with a dendritic shape that are CD68‐positive and CD207‐negative, fibrocytes, and very rare S100‐positive cells. Interestingly, the skeletal muscle, being constitutively human leukocyte antigen (HLA)‐A,B,C‐negative, is induced at different levels in each specimen. In a cell culture experiment, we confirmed the ability of fibroblasts and interdigitating dendritic sarcoma cells to express spike protein in vitro after incubation with the Comirnaty vaccine. CONCLUSIONS: Histiocytic cells and fibrocytes are the heralds of spike protein synthesis at the vaccination site. The underlying cause of this apparent cell specifity is unknown. This needs to be investigated in future experiments, for example in an animal model.
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spelling pubmed-100524472023-03-30 Emergence of SARS‐CoV‐2 spike protein at the vaccination site Beck, Annika Dietenberger, Hanna Kunz, Sebastian N. Mellert, Kevin Möller, Peter Immun Inflamm Dis Short Reports BACKGROUND: The anti‐coronavirus disease 2019 (COVID‐19) vaccines are of paramount importance in the fight against the COVID‐19 pandemic. Both viral vector‐ and nucleic acid‐based vaccines are known to effectively induce protection against the severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) virus by generating high antibody titers and effective T‐cell responses to the spike protein they encode. Although these vaccines are being applied worldwide and have been extensively investigated, the immunomorphological events at the vaccination site with respect to SARS‐CoV‐2 spike protein expression have not yet been described. METHODS: We had the opportunity to examine the deltoid muscles of three men who died shortly after vaccination for unrelated reasons. We examined the vaccination sites histologically and immunohistochemically with various antibodies. Furthermore we incubated two different cell lines with one vaccine and examined the expression of the spike protein. RESULTS: The vaccination sites show a dense lymphohistiocytic interstitial infiltrate which surrounds the small vessels and extends into the perimysium. The spike protein is expressed by histiocytic cells with a dendritic shape that are CD68‐positive and CD207‐negative, fibrocytes, and very rare S100‐positive cells. Interestingly, the skeletal muscle, being constitutively human leukocyte antigen (HLA)‐A,B,C‐negative, is induced at different levels in each specimen. In a cell culture experiment, we confirmed the ability of fibroblasts and interdigitating dendritic sarcoma cells to express spike protein in vitro after incubation with the Comirnaty vaccine. CONCLUSIONS: Histiocytic cells and fibrocytes are the heralds of spike protein synthesis at the vaccination site. The underlying cause of this apparent cell specifity is unknown. This needs to be investigated in future experiments, for example in an animal model. John Wiley and Sons Inc. 2023-03-29 /pmc/articles/PMC10052447/ /pubmed/36988249 http://dx.doi.org/10.1002/iid3.827 Text en © 2023 The Authors. Immunity, Inflammation and Disease published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Reports
Beck, Annika
Dietenberger, Hanna
Kunz, Sebastian N.
Mellert, Kevin
Möller, Peter
Emergence of SARS‐CoV‐2 spike protein at the vaccination site
title Emergence of SARS‐CoV‐2 spike protein at the vaccination site
title_full Emergence of SARS‐CoV‐2 spike protein at the vaccination site
title_fullStr Emergence of SARS‐CoV‐2 spike protein at the vaccination site
title_full_unstemmed Emergence of SARS‐CoV‐2 spike protein at the vaccination site
title_short Emergence of SARS‐CoV‐2 spike protein at the vaccination site
title_sort emergence of sars‐cov‐2 spike protein at the vaccination site
topic Short Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10052447/
https://www.ncbi.nlm.nih.gov/pubmed/36988249
http://dx.doi.org/10.1002/iid3.827
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