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Modeling The Lifecycle Of Ebola Virus Under Biosafety Level 2 Conditions With Virus-like Particles Containing Tetracistronic Minigenomes
Published on: September 27, 2014
Prospects for immunisation against Marburg and Ebola viruses
Thomas W Geisbert1, Daniel G Bausch, Heinz Feldmann
1Galveston National Laboratory1 and Department of Microbiology and Immunology2, University of Texas Medical Branch, 301 University Blvd., Galveston, TX, USA. twgeisbe@utmb.edu
Abstract:
For more than 30 years the filoviruses, Marburg virus and Ebola virus, have been associated with periodic outbreaks of hemorrhagic fever that produce severe and often fatal disease. The filoviruses are endemic primarily in resource-poor regions in Central Africa and are also potential agents of bioterrorism. Although no vaccines or antiviral drugs for Marburg or Ebola are currently available, remarkable progress has been made over the last decade in developing candidate preventive vaccines against filoviruses in nonhuman primate models. Due to the generally remote locations of filovirus outbreaks, a single-injection vaccine is desirable. Among the prospective vaccines that have shown efficacy in nonhuman primate models of filoviral hemorrhagic fever, two candidates, one based on a replication-defective adenovirus serotype 5 and the other on a recombinant VSV (rVSV), were shown to provide complete protection to nonhuman primates when administered as a single injection. The rVSV-based vaccine has also shown utility when administered for postexposure prophylaxis against filovirus infections. A VSV-based Ebola vaccine was recently used to manage a potential laboratory exposure.
Insights
Developing effective vaccines against filoviruses like Marburg and Ebola is crucial. Promising single-injection vaccines, particularly a recombinant VSV (rVSV) candidate, show complete protection in nonhuman primates and potential for post-exposure use.
Area of Science:
- Virology
- Vaccinology
- Public Health
Background:
- Filoviruses, including Marburg and Ebola viruses, cause severe hemorrhagic fever outbreaks in Central Africa.
- These viruses pose significant public health risks and are potential bioterrorism agents.
- Current treatments are limited, highlighting the need for effective vaccines.
Purpose of the Study:
- To review progress in developing preventive vaccines against filoviruses.
- To identify promising vaccine candidates for filoviral hemorrhagic fever.
- To assess the potential for single-injection vaccines suitable for remote outbreak locations.
Main Methods:
- Evaluation of candidate vaccines in nonhuman primate models of filoviral hemorrhagic fever.
- Assessment of vaccine efficacy following single-dose administration.
- Review of postexposure prophylaxis strategies and real-world applications.
Main Results:
- Significant progress has been made in developing filovirus vaccines over the last decade.
- Two vaccine candidates, one adenovirus serotype 5-based and one recombinant VSV (rVSV)-based, demonstrated complete protection in nonhuman primates after a single injection.
- The rVSV-based vaccine also proved effective for postexposure prophylaxis and was used in a recent laboratory exposure incident.
Conclusions:
- Single-injection vaccines are highly desirable for filovirus outbreaks due to remote locations.
- The rVSV-based vaccine represents a promising candidate for both prevention and postexposure prophylaxis of filovirus infections.
- Continued research and development of these vaccines are critical for global health security.
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