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Modified vaccinia Ankara vaccine expressing Marburg virus-like particles protects guinea pigs from lethal Marburg virus infection.

Delphine C MalherbeArban DomiMary J HauserMichelle MeyerBronwyn M GunnGalit AlterAlexander BukreyevFarshad Guirakhoo
Published in: NPJ vaccines (2020)
We introduce a new vaccine platform against Marburg virus (MARV) combining the advantages of the immunogenicity of a highly attenuated vaccine vector (Modified Vaccinia Ankara, MVA) with the authentic conformation of virus-like particles (VLPs). Our vaccine, MVA-MARV-VLP, expresses the minimal components of MARV VLPs: the envelope glycoprotein GP and the matrix protein VP40. Electron microscopy confirmed self-assembly and budding of VLPs from infected cells. Prime/boost vaccination of guinea pigs with MVA-MARV-VLP-elicited MARV-specific binding and neutralizing antibody responses. Vaccination also induced Fc-mediated innate immune effector functions including activation of NK cells and antibody-dependent phagocytosis by neutrophils and monocytes. Inoculation of vaccinated animals with guinea pig-adapted MARV demonstrated 100% protection against death and disease with no viremia. Therefore, our vaccine platform, expressing two antigens resulting in assembly of VLPs in the native conformation in vaccinated hosts, can be used as a potent vaccine against MARV.
Keyphrases
  • innate immune
  • induced apoptosis
  • nk cells
  • electron microscopy
  • high throughput
  • small molecule
  • amino acid
  • endothelial cells
  • cell death
  • peripheral blood
  • endoplasmic reticulum stress
  • crystal structure
  • dna binding