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Development and evaluation of candidate subunit vaccine and novel antitoxin against botulinum neurotoxin serotype E.

Authors :
Shi DY
Liu FJ
Mao YY
Cui RT
Lu JS
Yu YZ
Dong XJ
Yang ZX
Sun ZW
Pang XB
Source :
Human vaccines & immunotherapeutics [Hum Vaccin Immunother] 2020; Vol. 16 (1), pp. 100-108. Date of Electronic Publication: 2019 Jul 26.
Publication Year :
2020

Abstract

Botulinum neurotoxins (BoNTs) are among the most toxic proteins. Vaccination is an effective strategy to prevent botulism. To generate a vaccine suitable for human use, a recombinant non-His-tagged isoform of the Hc domain of botulinum neurotoxin serotype E (rEHc) was expressed in Escherichia coli and purified by sequential chromatography. The immunogenicity of rEHc was evaluated in mice and dose- and time-dependent immune responses were observed in both antibody titers and protective potency. Then, the pilot-scale expression and purification of rEHc were performed, and its immunological activity was characterized. Our results showed rEHc has good immunogenicity and can elicit strong protective potency against botulinum neurotoxin serotype E (BoNT/E) in mice, indicating that rEHc is an effective botulism vaccine candidate. Further, we developed a novel antitoxin against BoNT/E by purifying F(ab') <subscript>2</subscript> from pepsin-digested serum IgG of rEHc-inoculated horses. The protective effect of the F(ab') <subscript>2</subscript> antitoxin was determined in vitro and in vivo . The results showed that our F(ab') <subscript>2</subscript> antitoxin can prevent botulism in BoNT/E-challenged mice and effectively alleviate the progression of paralysis caused by BoNT/E to achieve therapeutic effects. Therefore, our results provide valuable experimental data for the production of a novel antitoxin, which is a promising candidate for the treatment of BoNT/E-induced botulism.

Details

Language :
English
ISSN :
2164-554X
Volume :
16
Issue :
1
Database :
MEDLINE
Journal :
Human vaccines & immunotherapeutics
Publication Type :
Academic Journal
Accession number :
31210561
Full Text :
https://doi.org/10.1080/21645515.2019.1633878