Title (en)
Vaccine Based on Recombinant Fusion Protein Combining Hepatitis B Virus PreS with SARS-CoV-2 Wild-Type- and Omicron-Derived Receptor Binding Domain Strongly Induces Omicron-Neutralizing Antibodies in a Murine Model
Language
English
Description (en)
COVID-19, caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), has become a recurrent endemic disease affecting the whole world. Since November 2021, Omicron and its subvariants have dominated in the spread of the disease. In order to prevent severe courses of disease, vaccines are needed to boost and maintain antibody levels capable of neutralizing Omicron. Recently, we produced and characterized a SARS-CoV-2 vaccine based on a recombinant fusion protein consisting of hepatitis B virus (HBV)-derived PreS and two SARS-CoV-2 wild-type RBDs.To develop a PreS-RBD vaccine which induces high levels of Omicron-specific neutralizing antibodies.We designed, produced, characterized and compared strain-specific (wild-type: W-PreS-W; Omicron: O-PreS-O), bivalent (mix of W-PreS-W and O-PreS-O) and chimeric (i.e., W-PreS-O) SARS-CoV-2 protein subunit vaccines. Immunogens were characterized in vitro using protein chemical methods, mass spectrometry, and circular dichroism in combination with thermal denaturation and immunological methods. In addition, BALB/c mice were immunized with aluminum-hydroxide-adsorbed proteins and aluminum hydroxide alone (i.e., placebo) to study the specific antibody and cytokine responses, safety and Omicron neutralization.Defined and pure immunogens could be produced in significant quantities as secreted and folded proteins in mammalian cells. The antibodies induced after vaccination with different doses of strain-specific, bivalent and chimeric PreS-RBD fusion proteins reacted with wild-type and Omicron RBD in a dose-dependent manner and resulted in a mixed Th1/Th2 immune response. Interestingly, the RBD-specific IgG levels induced with the different vaccines were comparable, but the W-PreS-O-induced virus neutralization titers against Omicron (median VNT50: 5000) were seven- and twofold higher than the W-PreS-W- and O-PreS-O-specific ones, respectively, and they were six-fold higher than those of the bivalent vaccine.Among the tested immunogens, the chimeric PreS-RBD subunit vaccine, W-PreS-O, induced the highest neutralizing antibody titers against Omicron. Thus, W-PreS-O seems to be a highly promising COVID-19 vaccine candidate for further preclinical and clinical evaluation.
Keywords (en)
SARS-CoV-2; COVID-19; Omicron; vaccine; neutralizing antibodies
DOI
10.3390/vaccines12030229
Author of the digital object
Pia Gattinger  (Medical University of Vienna)
Rudolf Valenta  (Medical University of Vienna / Karl Landsteiner University of Health Sciences)
Winfried F. Pickl  (Medical University of Vienna)
Hannes Stockinger  (Medical University of Vienna)
Sandra Högler  (University of Veterinary Medicine Vienna)
Walter Keller  (University of Graz)
Lukas Petrowitsch  (University of Graz)
Verena Fuhrmann  (Medical University of Vienna)
Mirjam Schaar  (Medical University of Vienna)
Margarete Focke-Tejkl  (Medical University of Vienna / Karl Landsteiner University of Health Sciences)
Gabor Tajti  (Medical University of Vienna)
Laura Gebetsberger  (Medical University of Vienna)
Anna Ohradanova-Repic  (Medical University of Vienna)
Bernhard Kratzer  (Medical University of Vienna)
Al Nasar Ahmed Sehgal  (Medical University of Vienna)
Format
application/pdf
Size
2.4 MB
Licence Selected
Type of publication
Article
Name of Publication (en)
Vaccines
Pages or Volume
15
Volume
12
Number
3
Publisher
MDPI
Publication Date
2024