Immunogenicity and Protective Efficacy of a Single Intranasal Dose Vectored Vaccine Based on Sendai Virus (Moscow Strain) against SARS-CoV-2 Variant of Concern.
Galina V KochnevaGleb A KudrovSergei S ZainutdinovIrina S ShulginaAndrei V ShipovalovAnna V ZaykovskayaMaria Borisovna BorgoyakovaEkaterina V StarostinaSergei A BodnevGalina F SivolobovaAntonina A GrazhdantsevaDaria I IvkinaAlexey M ZadorozhnyLarisa Ivanovna KarpenkoOleg V P'yankovPublished in: Vaccines (2024)
The mouse paramyxovirus Sendai, which is capable of limited replication in human bronchial epithelial cells without causing disease, is well suited for the development of vector-based intranasal vaccines against respiratory infections, including SARS-CoV-2. Using the Moscow strain of the Sendai virus, we developed a vaccine construct, Sen-Sdelta(M), which expresses the full-length spike (S) protein of the SARS-CoV-2 delta variant. A single intranasal delivery of Sen-Sdelta(M) to Syrian hamsters and BALB/c mice induced high titers of virus-neutralizing antibodies specific to the SARS-CoV-2 delta variant. A significant T-cell response, as determined by IFN-γ ELISpot and ICS methods, was also demonstrated in the mouse model. Mice and hamsters vaccinated with Sen-Sdelta(M) were well protected against SARS-CoV-2 challenge. The viral load in the lungs and nasal turbinates, measured by RT-qPCR and TCID 50 assay, decreased dramatically in vaccinated groups. The most prominent effect was revealed in a highly sensitive hamster model, where no tissue samples contained detectable levels of infectious SARS-CoV-2. These results indicate that Sen-Sdelta(M) is a promising candidate as a single-dose intranasal vaccine against SARS-CoV-2, including variants of concern.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- mouse model
- endothelial cells
- dna methylation
- type diabetes
- high fat diet induced
- skeletal muscle
- metabolic syndrome
- insulin resistance
- adipose tissue
- binding protein
- zika virus
- high resolution
- stress induced
- amino acid
- tandem mass spectrometry
- drug induced
- induced pluripotent stem cells