CoviVac vaccination induces production of neutralizing antibodies against Delta and Omicron variants of SARS-CoV-2
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Abstract
Vaccines are proven to be an effective tool in prophylaxis of severe COVID-19, but emerging mutated SARS-CoV-2 variants constantly challenge vaccines’ protectivity. We have evaluated the ability of the sera from individuals vaccinated with two variants of inactivated vaccine CoviVac and COVID-19 convalescents (May-December 2020) to neutralize SARS-CoV-2 variants Delta and Omicron. Four groups of serum samples (CoviVac vaccinees; COVID-19 convalescents; mice immunized with CoviVac preparations based on prototype B.1.1 strain and Delta variant) were evaluated in virus neutralization test against SARS-CoV-2 heterologous B.1.1 virus, Delta and Omicron variants. CoviVac preparations based on B.1.1 and Delta induced neutralizing antibodies against SARS-CoV-2 B.1.1 and two variants of concern. We observed a decrease in neutralization capacity in the sera from CoviVac (based on B.1.1 strain) vaccinees: 57.1% samples had detectable neutralizing antibodies against Delta and 61.9% against Omicron variants. Sera samples of all (100%) mice immunized with a candidate vaccine based on the SARS-CoV-2 Delta variant strain had neutralizing antibodies against all tested strains.
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SciScore for 10.1101/2022.02.10.22270781: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Ethics Field Sample Permit: COVID-19 convalescent sera samples were collected in Russia from May to December 2020 from convalescent donors according to the state program of plasma collection to be used for treatment. Sex as a biological variable not detected. Randomization not detected. Blinding not detected. Power Analysis not detected. Cell Line Authentication not detected. Table 2: Resources
Antibodies Sentences Resources Serum samples: Serum samples were collected from Phase I/II Clinical trials participants, who tested negative for SARS-CoV-2 antibodies in NT and in ELISA before the trials (ClinicalTrials.gov, NCT05046548) and were vaccinated with CoviVac (0.5 ml) intramuscularly twice with 14 days period. S…SciScore for 10.1101/2022.02.10.22270781: (What is this?)
Please note, not all rigor criteria are appropriate for all manuscripts.
Table 1: Rigor
Ethics Field Sample Permit: COVID-19 convalescent sera samples were collected in Russia from May to December 2020 from convalescent donors according to the state program of plasma collection to be used for treatment. Sex as a biological variable not detected. Randomization not detected. Blinding not detected. Power Analysis not detected. Cell Line Authentication not detected. Table 2: Resources
Antibodies Sentences Resources Serum samples: Serum samples were collected from Phase I/II Clinical trials participants, who tested negative for SARS-CoV-2 antibodies in NT and in ELISA before the trials (ClinicalTrials.gov, NCT05046548) and were vaccinated with CoviVac (0.5 ml) intramuscularly twice with 14 days period. SARS-CoV-2suggested: NoneExperimental Models: Cell Lines Sentences Resources After 3-5 passages in Vero cells, viruses were stored as infected cell suspension at –70°C. 2.2. Verosuggested: CLS Cat# 605372/p622_VERO, RRID:CVCL_0059)Experimental Models: Organisms/Strains Sentences Resources BALB/c mice were vaccinated with CoviVac preparation based on B.1.1 strain (GISAID EPI_ISL_428851) intramuscularly (0.5 ml) twice with 14 days interval, serum samples were collected 7 days after the last immunization for vaccine immunogenicity testing as described previously [7]. BALB/csuggested: NoneSoftware and Algorithms Sentences Resources The CoviVac candidate vaccine based on Delta variant was prepared using the Delta variant strain (GISAID EPI_ISL_8799478) by the same technology as CoviVac [7]. CoviVacsuggested: NoneResults from OddPub: We did not detect open data. We also did not detect open code. Researchers are encouraged to share open data when possible (see Nature blog).
Results from LimitationRecognizer: An explicit section about the limitations of the techniques employed in this study was not found. We encourage authors to address study limitations.Results from TrialIdentifier: We found the following clinical trial numbers in your paper:
Identifier Status Title NCT05046548 Completed This is a Double-blind, Placebo-controlled, Randomized Study… Results from Barzooka: We did not find any issues relating to the usage of bar graphs.
Results from JetFighter: We did not find any issues relating to colormaps.
Results from rtransparent:- Thank you for including a conflict of interest statement. Authors are encouraged to include this statement when submitting to a journal.
- Thank you for including a funding statement. Authors are encouraged to include this statement when submitting to a journal.
- No protocol registration statement was detected.
Results from scite Reference Check: We found no unreliable references.
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