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The rapid immunostimulatory properties of recombinant vesicular stomatitis virus (rVSV)-based vaccines make them ideal postexposure treatments against the filoviruses Ebola virus and Marburg virus (MARV); nonetheless, the mechanisms that drive this protection tend to be undefined. Previously, we reported 60-75% success of rhesus macaques addressed with rVSV vectors revealing MARV glycoprotein (GP) 20-30 moments after a decreased dose exposure to the essential pathogenic variation of MARV, Angola. Surviv
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