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Protection against anthrax with recombinant virus-expressed protective antigen in experimental animals
L C Iacono-Connors1, S L Welkos, B E Ivins
1Virology Division, U.S. Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland 21702-5011.
Infection and Immunity
|June 1, 1991
Summary
Recombinant protective antigen (PA) from Bacillus anthracis, produced in baculovirus and vaccinia virus systems, showed immunogenicity and potential as a live anthrax vaccine candidate.
Area of Science:
- Microbiology
- Immunology
- Vaccinology
Background:
- Bacillus anthracis infection, or anthrax, poses a significant biodefense threat.
- Development of effective anthrax vaccines is crucial for public health and security.
- Protective antigen (PA) is a key component of anthrax toxins and a target for vaccine development.
Purpose of the Study:
- To clone and express the Bacillus anthracis protective antigen (PA) gene.
- To characterize the antigenicity and immunogenicity of recombinant PA produced in different expression systems.
- To evaluate the protective efficacy of recombinant PA against anthrax challenge.
Main Methods:
- Gene cloning and expression of Bacillus anthracis PA in vaccinia virus and baculovirus vectors.
- Characterization of PA antigenicity and antibody responses in immunized animals.
- Challenge studies in guinea pigs and mice using lethal Bacillus anthracis spores.
Main Results:
- Vaccinia virus-expressed PA (WR-PA) provided partial protection (60% in mice, 50% in guinea pigs) against anthrax challenge.
- Baculovirus-expressed PA, purified and combined with adjuvant, offered partial protection in mice and complete protection in guinea pigs.
- Both recombinant and non-recombinant PA preparations induced high anti-PA antibody titers in guinea pigs and mice.
Conclusions:
- Recombinant baculovirus and vaccinia virus systems successfully produced immunogenic PA.
- Baculovirus-derived PA is a valuable source for generating immunogenic PA.
- Vaccinia virus-PA recombinants show promise as live anthrax vaccine candidates for further development.