AI Article Synopsis

  • Chikungunya virus (CHIKV) can cause long-lasting joint pain, especially in tropical and subtropical areas, and currently, there are no approved vaccines to prevent it.
  • Researchers are exploring DNA-launched virus-like particle (VLP) vaccines as a safer alternative to traditional vaccines, but there is a lack of comprehensive mouse models that include both sexes for testing.
  • A study evaluated these vaccines using engineered virus strains in male and female mice, revealing the potential effectiveness of DNA-launched VLP vaccines and highlighting gender differences in viral load, which could influence future vaccine development.

Article Abstract

Chikungunya virus (CHIKV) infection can result in chronic and debilitating arthralgia affecting humans in tropical and subtropical regions around the world, yet there are no licensed vaccines to prevent infection. DNA launched virus like particle (VLP) vaccines represent a potentially safer alternative to traditional live-attenuated vaccines; however, fully characterized immunocompetent mouse models which appropriately include both male and female animals for preclinical evaluation of these, and other, vaccine platforms are lacking. Utilizing virus stocks engineered to express mutations reported to enhance CHIKV virulence in mice, infection of male and female immunocompetent mice was evaluated, and the resulting model utilized to assess the efficacy of candidate DNA launched CHIKV VLP vaccines. Results demonstrate the potential utility of DNA launched VLP vaccines in comparison to a live attenuated CHIKV vaccine and identify gender differences in viral RNA loads that impact interpretation of vaccine efficacy and may have important implications for future CHIKV vaccine development.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8067036PMC
http://dx.doi.org/10.3390/vaccines9040345DOI Listing

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