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Comparative analysis of ChAdOx1 nCoV-19 and Ad26.COV2.S SARS-CoV-2 vector vaccines
Vector-based SARS-CoV-2 vaccines have been associated with vaccine- induced thrombosis with thrombocytopenia syndrome (VITT/TTS), but the causative factors are still unresolved. We comprehensively analyzed the ChAdOx1 nCoV-19 (AstraZeneca) and Ad26.COV2.S (Johnson & Johnson) vaccines. ChAdOx1 nC...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Fondazione Ferrata Storti
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8968905/ https://www.ncbi.nlm.nih.gov/pubmed/35045692 http://dx.doi.org/10.3324/haematol.2021.280154 |
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author | Michalik, Stephan Siegerist, Florian Palankar, Raghavendra Franzke, Kati Schindler, Maximilian Reder, Alexander Seifert, Ulrike Cammann, Clemens Wesche, Jan Steil, Leif Hentschker, Christian Gesell-Salazar, Manuela Reisinger, Emil Beer, Martin Endlich, Nicole Greinacher, Andreas Völker, Uwe |
author_facet | Michalik, Stephan Siegerist, Florian Palankar, Raghavendra Franzke, Kati Schindler, Maximilian Reder, Alexander Seifert, Ulrike Cammann, Clemens Wesche, Jan Steil, Leif Hentschker, Christian Gesell-Salazar, Manuela Reisinger, Emil Beer, Martin Endlich, Nicole Greinacher, Andreas Völker, Uwe |
author_sort | Michalik, Stephan |
collection | PubMed |
description | Vector-based SARS-CoV-2 vaccines have been associated with vaccine- induced thrombosis with thrombocytopenia syndrome (VITT/TTS), but the causative factors are still unresolved. We comprehensively analyzed the ChAdOx1 nCoV-19 (AstraZeneca) and Ad26.COV2.S (Johnson & Johnson) vaccines. ChAdOx1 nCoV-19 contains significant amounts of host cell protein impurities, including functionally active proteasomes, and adenoviral proteins. A much smaller amount of impurities was found in Ad26.COV2.S. Platelet factor 4 formed complexes with ChAdOx1 nCoV-19 constituents, but not with purified virions from ChAdOx1 nCoV-19 or with Ad26.COV2.S. Vascular hyperpermeability was induced by ChAdOx nCoV-19 but not by Ad26.COV2.S. These differences in impurities together with EDTAinduced capillary leakage might contribute to the higher incidence rate of VITT associated with ChAdOx1 nCoV-19 compared to Ad26.COV2.S. |
format | Online Article Text |
id | pubmed-8968905 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Fondazione Ferrata Storti |
record_format | MEDLINE/PubMed |
spelling | pubmed-89689052022-04-11 Comparative analysis of ChAdOx1 nCoV-19 and Ad26.COV2.S SARS-CoV-2 vector vaccines Michalik, Stephan Siegerist, Florian Palankar, Raghavendra Franzke, Kati Schindler, Maximilian Reder, Alexander Seifert, Ulrike Cammann, Clemens Wesche, Jan Steil, Leif Hentschker, Christian Gesell-Salazar, Manuela Reisinger, Emil Beer, Martin Endlich, Nicole Greinacher, Andreas Völker, Uwe Haematologica Article Vector-based SARS-CoV-2 vaccines have been associated with vaccine- induced thrombosis with thrombocytopenia syndrome (VITT/TTS), but the causative factors are still unresolved. We comprehensively analyzed the ChAdOx1 nCoV-19 (AstraZeneca) and Ad26.COV2.S (Johnson & Johnson) vaccines. ChAdOx1 nCoV-19 contains significant amounts of host cell protein impurities, including functionally active proteasomes, and adenoviral proteins. A much smaller amount of impurities was found in Ad26.COV2.S. Platelet factor 4 formed complexes with ChAdOx1 nCoV-19 constituents, but not with purified virions from ChAdOx1 nCoV-19 or with Ad26.COV2.S. Vascular hyperpermeability was induced by ChAdOx nCoV-19 but not by Ad26.COV2.S. These differences in impurities together with EDTAinduced capillary leakage might contribute to the higher incidence rate of VITT associated with ChAdOx1 nCoV-19 compared to Ad26.COV2.S. Fondazione Ferrata Storti 2022-01-20 /pmc/articles/PMC8968905/ /pubmed/35045692 http://dx.doi.org/10.3324/haematol.2021.280154 Text en Copyright© 2022 Ferrata Storti Foundation https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution Noncommercial License (by-nc 4.0) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Article Michalik, Stephan Siegerist, Florian Palankar, Raghavendra Franzke, Kati Schindler, Maximilian Reder, Alexander Seifert, Ulrike Cammann, Clemens Wesche, Jan Steil, Leif Hentschker, Christian Gesell-Salazar, Manuela Reisinger, Emil Beer, Martin Endlich, Nicole Greinacher, Andreas Völker, Uwe Comparative analysis of ChAdOx1 nCoV-19 and Ad26.COV2.S SARS-CoV-2 vector vaccines |
title | Comparative analysis of ChAdOx1 nCoV-19 and Ad26.COV2.S SARS-CoV-2 vector vaccines |
title_full | Comparative analysis of ChAdOx1 nCoV-19 and Ad26.COV2.S SARS-CoV-2 vector vaccines |
title_fullStr | Comparative analysis of ChAdOx1 nCoV-19 and Ad26.COV2.S SARS-CoV-2 vector vaccines |
title_full_unstemmed | Comparative analysis of ChAdOx1 nCoV-19 and Ad26.COV2.S SARS-CoV-2 vector vaccines |
title_short | Comparative analysis of ChAdOx1 nCoV-19 and Ad26.COV2.S SARS-CoV-2 vector vaccines |
title_sort | comparative analysis of chadox1 ncov-19 and ad26.cov2.s sars-cov-2 vector vaccines |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8968905/ https://www.ncbi.nlm.nih.gov/pubmed/35045692 http://dx.doi.org/10.3324/haematol.2021.280154 |
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