Comparative analysis of ChAdOx1 nCoV-19 and Ad26.COV2.S SARS-CoV-2 vector vaccines.


Journal

Haematologica
ISSN: 1592-8721
Titre abrégé: Haematologica
Pays: Italy
ID NLM: 0417435

Informations de publication

Date de publication:
01 04 2022
Historique:
received: 05 10 2021
pubmed: 21 1 2022
medline: 5 4 2022
entrez: 20 1 2022
Statut: epublish

Résumé

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 and 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.

Identifiants

pubmed: 35045692
doi: 10.3324/haematol.2021.280154
pmc: PMC8968905
doi:

Substances chimiques

Ad26COVS1 JT2NS6183B
COVID-19 Vaccines 0
Vaccines 0
ChAdOx1 nCoV-19 B5S3K2V0G8

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

947-957

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Auteurs

Stephan Michalik (S)

Interfaculty Institute of Genetics and Functional Genomics, Department Functional Genomics, University Medicine Greifswald, Greifswald, Germany.

Florian Siegerist (F)

Institute for Anatomy and Cell Biology, University Medicine Greifswald, Greifswald, Germany.

Raghavendra Palankar (R)

Institute of Transfusion Medicine, University Medicine Greifswald, Greifswald, Germany.

Kati Franzke (K)

Institute of Infectiology, Friedrich-Loeffler-Institut, Greifswald-Insel Riems, Germany.

Maximilian Schindler (M)

Institute for Anatomy and Cell Biology, University Medicine Greifswald, Greifswald, Germany.

Alexander Reder (A)

Interfaculty Institute of Genetics and Functional Genomics, Department Functional Genomics, University Medicine Greifswald, Greifswald, Germany.

Ulrike Seifert (U)

Friedrich Loeffler-Institute of Medical Microbiology-Virology, University Medicine Greifswald, Greifswald, Germany..

Clemens Cammann (C)

Friedrich Loeffler-Institute of Medical Microbiology-Virology, University Medicine Greifswald, Greifswald, Germany..

Jan Wesche (J)

Institute of Transfusion Medicine, University Medicine Greifswald, Greifswald, Germany.

Leif Steil (L)

Interfaculty Institute of Genetics and Functional Genomics, Department Functional Genomics, University Medicine Greifswald, Greifswald, Germany.

Christian Hentschker (C)

Interfaculty Institute of Genetics and Functional Genomics, Department Functional Genomics, University Medicine Greifswald, Greifswald, Germany.

Manuela Gesell-Salazar (M)

Interfaculty Institute of Genetics and Functional Genomics, Department Functional Genomics, University Medicine Greifswald, Greifswald, Germany.

Emil Reisinger (E)

Division of Tropical Medicine and Infectious Diseases, Center of Internal Medicine II, Rostock University Medical Center, Rostock, Germany.

Martin Beer (M)

Institute of Diagnostic Virology, Friedrich-Loeffler-Institut, Greifswald-Insel Riems, Germany.

Nicole Endlich (N)

Institute for Anatomy and Cell Biology, University Medicine Greifswald, Greifswald, Germany.

Andreas Greinacher (A)

Institute of Transfusion Medicine, University Medicine Greifswald, Greifswald, Germany. andreas.greinacher@med.unigreifswald.

Uwe Völker (U)

Interfaculty Institute of Genetics and Functional Genomics, Department Functional Genomics, University Medicine Greifswald, Greifswald, Germany. voelker@uni-greifswald.de.

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Classifications MeSH