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Efficacy assessment of a triple anthrax chimeric antigen as a vaccine candidate in guinea pigs: challenge test with Bacillus anthracis 17 JB strain spores

Authors :
Sadegh Hasannia
Seyed-Shahryar Arab
Masoud Abdous
Ali Hatef Salmanian
Source :
Immunopharmacology and Immunotoxicology. 43:495-502
Publication Year :
2021
Publisher :
Informa UK Limited, 2021.

Abstract

Context Bacillus anthracis secretes a tripartite toxin comprising protective antigen (PA), edema factor (EF), and lethal factor (LF). The human anthrax vaccine is mainly composed of the anthrax protective antigen (PA). Considerable efforts are being directed towards improving the efficacy of vaccines because the use of commercial anthrax vaccines (human/veterinary) is associated with several limitations. Objective In this study, a triple chimeric antigen referred to as ELP (gene accession no: MT590758) comprising highly immunogenic domains of PA, LF, and EF was designed, constructed, and assessed for the immunization capacity against anthrax in a guinea pig model. Materials and methods Immunization was carried out considering antigen titration and immunization protocol. The immunoprotective efficacy of the ELP was evaluated in guinea pigs and compared with the potency of veterinary anthrax vaccine using a challenge test with B. anthracis 17JB strain spores. Results The results demonstrated that the ELP antigen induced strong humoral responses. The T-cell response of the ELP was found to be similar to PA, and showed that the ELP could protect 100%, 100%, 100%, 80% and 60% of the animals from 50, 70, 90, 100 and 120 times the minimum lethal dose (MLD, equal 5 × 105 spore/ml), respectively, which killed control animals within 48 h. Discussion and conclusions It is concluded that the ELP antigen has the necessary requirement for proper immunization against anthrax and it can be used to develop an effective recombinant vaccine candidate against anthrax.

Details

ISSN :
15322513 and 08923973
Volume :
43
Database :
OpenAIRE
Journal :
Immunopharmacology and Immunotoxicology
Accession number :
edsair.doi...........0a2983babd8d12a29be925c0e3c61917
Full Text :
https://doi.org/10.1080/08923973.2021.1945087