Preclinical evaluation of PHH-1V vaccine candidate against SARS-CoV-2 in non-human primates
SARS-CoV-2 emerged in December 2019 and quickly spread worldwide, continuously striking with an unpredictable evolution. Despite the success in vaccine production and mass vaccination programs, the situation is not still completely controlled, and therefore accessible second-generation vaccines are...
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Veröffentlicht in: | iScience 2023-07, Vol.26 (7), p.107224-107224, Article 107224 |
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Sprache: | eng |
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Zusammenfassung: | SARS-CoV-2 emerged in December 2019 and quickly spread worldwide, continuously striking with an unpredictable evolution. Despite the success in vaccine production and mass vaccination programs, the situation is not still completely controlled, and therefore accessible second-generation vaccines are required to mitigate the pandemic. We previously developed an adjuvanted vaccine candidate coded PHH-1V, based on a heterodimer fusion protein comprising the RBD domain of two SARS-CoV-2 variants. Here, we report data on the efficacy, safety, and immunogenicity of PHH-1V in cynomolgus macaques. PHH-1V prime-boost vaccination induces high levels of RBD-specific IgG binding and neutralizing antibodies against several SARS-CoV-2 variants, as well as a balanced Th1/Th2 cellular immune response. Remarkably, PHH-1V vaccination prevents SARS-CoV-2 replication in the lower respiratory tract and significantly reduces viral load in the upper respiratory tract after an experimental infection. These results highlight the potential use of the PHH-1V vaccine in humans, currently undergoing Phase III clinical trials.
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•PHH-1V vaccine is safe and well-tolerated in non-human primates•PHH-1V elicits neutralizing antibodies and T-cells against various SARS-CoV-2 variants•PHH-1V vaccination prevents SARS-CoV-2 replication in the lower respiratory tract•PHH-1V vaccination reduces the SARS-CoV-2 infective viral load in the upper airways
Health sciences; Immunology; Immune response; Microbiology |
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ISSN: | 2589-0042 2589-0042 |
DOI: | 10.1016/j.isci.2023.107224 |