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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Intensity of Humoral Immune Responses, Adverse Reactions, and Post-Vaccination Morbidity after Adenovirus Vector-Based and mRNA Anti-COVID-19 Vaccines

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Συγγραφέας
Voulgaridi I., Sarrou S., Dadouli A., Peristeri A.-M., Nasika A., Onoufriadis I., Kyritsi M.A., Anagnostopoulos L., Theodoridou A., Avakian I., Pappa D., Konstantinou A.-K., Papadamou G., Mouchtouri V.A., Petinaki E., Speletas M., Hadjichristodoulou C.
Ημερομηνία
2022
Γλώσσα
en
DOI
10.3390/vaccines10081268
Λέξη-κλειδί
ad26.cov2.s vaccine
novokinin
synthetic peptide
tozinameran
unclassified drug
vaxzevria
alternative medicine
animal experiment
animal model
antibody response
antibody titer
antiinflammatory activity
antioxidant activity
article
Article
binding affinity
chemoluminescence
column chromatography
drug efficacy
drug metabolism
drug therapy
enzyme linked immunosorbent assay
food frequency questionnaire
gene expression
high performance liquid chromatography
humoral immunity
immunogenicity
limit of quantitation
liquid chromatography
liquid chromatography-mass spectrometry
low drug dose
mass spectrometry
morbidity
mouse
multiple reaction monitoring
Mycobacterium butyricum
neurite outgrowth
nonhuman
particle size
peptide synthesis
phytochemistry
protein expression
protein purification
public health
rheumatoid arthritis
scoring system
Severe acute respiratory syndrome coronavirus 2
spike
sustained drug release
vaccination
Western blotting
MDPI
Εμφάνιση Μεταδεδομένων
Επιτομή
The aim of the study was to compare mRNA vaccine BNT162b2 with adenovirus vector- based vaccines in terms of presence of adverse reactions, immunogenicity, and protection against COVID-19. A total of 270 individuals were enrolled, of which 135 were vaccinated with adenovirus vector-based vaccines and compared with 135 age- and sex-matched participants who received the BNT162b2 mRNA vaccine. Serum sampling was performed on all participants on days 21, 42, 90, and 180 following the first dose, to evaluate anti-spike IgG and IgA responses. Antibodies were quantified by chemiluminescent microplate and ELISA assays. We demonstrate that both mRNA and adenovirus vector-based vaccines caused mild side-effects and were effective in inducing adequate antibody responses against SARS-CoV-2, although BNT162b2 was superior concerning the intensity of antibody responses and protection against severe COVID-19. Moreover, we identify that IgG and IgA responses depended primarily on both history of previous COVID-19 infection and vaccination platform used, with individuals immunized with a single-dose vaccine having lower antibody titers over time. Lastly, all vaccine platforms had limited side-effects, with the most frequent pain at the injection site. Our results provide useful information regarding antibody responses after vaccination with different vaccine platforms, which can be useful for public health vaccination strategies. © 2022 by the authors.
URI
http://hdl.handle.net/11615/80751
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