Research Article
Efficacy of recombinant anthrax vaccine against Bacillus anthracis aerosol spore challenge: Preclinical evaluation in rabbits and Rhesus monkeys
Article first published online: 18 MAR 2009
DOI: 10.1002/biot.200800213
Copyright © 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Issue

Biotechnology Journal
Special Issue: Biotech in India
Volume 4, Issue 3, pages 391–399, March 2009
Additional Information
How to Cite
Chawla, A., Midha, S. and Bhatnagar, R. (2009), Efficacy of recombinant anthrax vaccine against Bacillus anthracis aerosol spore challenge: Preclinical evaluation in rabbits and Rhesus monkeys. Biotechnology Journal, 4: 391–399. doi: 10.1002/biot.200800213
Publication History
- Issue published online: 18 MAR 2009
- Article first published online: 18 MAR 2009
- Manuscript Accepted: 9 FEB 2009
- Manuscript Revised: 4 FEB 2009
- Manuscript Received: 15 SEP 2008
Funded by
- Department of Biotechnology, Government of India
- Indian Council of Medical Research, New Delhi, India
- Council of Scientific and Industrial Research, New Delhi, India
Vol. 4, Issue 5, 599, Article first published online: 18 MAY 2009
- Abstract
- References
- Cited By
Keywords:
- Anthrax;
- Recombinant vaccine;
- Protective antigen
Abstract
This report describes the immunogenicity and protective efficacy of Escherichia coli-expressed recombinant protective antigen (rPA) in New Zealand White rabbits and Rhesus Macaques against an aerosol challenge with Bacillus anthracis spores (IVRI strain, tox+cap+). A dose-ranging study was performed in which it became evident that the level of anti-PA IgG and toxin-neutralizing antibody titer was directly proportional to the dose of rPA administered. However, the onset time of primary and secondary immune response was not dependent on the dosage. Revaccination of primed animals with the same threshold dose yielded a robust and rapid secondary response. Quantitative differences in peak titers were obtained for both the animal models, in addition to qualitative differences in the immune kinetics. In spite of a weak priming response, the secondary response in rabbits peaked earlier than that in macaques once the booster dose was administered. However, evaluation of the post-challenge quantitative anti-rPA ELISA titer measurements indicated higher titers for non-human primates as compared to the lagomorphs. Importantly, 100% protection was seen for the dosage groups that received ≥25 μg rPA, following a challenge against a target dose of 1000 LD50 of aerosolized spores of Bacillus anthracis.

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