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SpiN-Tec: A T cell-based recombinant vaccine that is safe, immunogenic, and shows high efficacy in experimental models challenged with SARS-CoV-2 variants of concern. | LitMetric

AI Article Synopsis

  • New variants of SARS-CoV-2 are emerging, leading experts to believe COVID-19 will become endemic, highlighting the need for booster vaccines to maintain immunity.
  • The SpiN-Tec vaccine, designed to enhance immune response to these variants, showed promising results in mice and hamsters, inducing strong antibody and cell responses against multiple SARS-CoV-2 proteins.
  • Safety tests in rats indicated that SpiN-Tec is safe, paving the way for its approval for phase I/II clinical trials.

Article Abstract

The emergence of new SARS-CoV-2 variants of concern associated with waning immunity induced by natural infection or vaccines currently in use suggests that the COVID-19 pandemic will become endemic. Investing in new booster vaccines using different platforms is a promising way to enhance protection and keep the disease under control. Here, we evaluated the immunogenicity, efficacy, and safety of the SpiN-Tec vaccine, based on a chimeric recombinant protein (SpiN) adjuvanted with CTVad1 (MF59-based adjuvant), aiming at boosting immunity against variants of concern of SARS-CoV-2. Immunization of K18-hACE-2 transgenic mice and hamsters induced high antibody titers and cellular immune response to the SpiN protein as well as to its components, RBD and N proteins. Importantly in a heterologous prime/boost protocol with a COVID-19 vaccine approved for emergency use (ChAdOx1), SpiN-Tec enhanced the level of circulation neutralizing antibodies (nAb). In addition to protection against the Wuhan isolate, protection against the Delta and Omicron variants was also observed as shown by reduced viral load and lung pathology. Toxicity and safety tests performed in rats demonstrated that the SpiN-Tec vaccine was safe and, based on these results, the SpiN-Tec phase I/II clinical trial was approved.

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Source
http://dx.doi.org/10.1016/j.vaccine.2024.126394DOI Listing

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