| Literature DB >> 25812841 |
Todd G Smith1, Marina Siirin2, Xianfu Wu3, Cathleen A Hanlon3, Victor Bronshtein2.
Abstract
A rabies vaccine that is thermostable over a range of ambient environmental temperatures would be highly advantageous, especially for tropical regions with challenging cold-chain storage where canine rabies remains enzootic resulting in preventable human mortality. Live attenuated rabies virus (RABV) strain ERAG333 (R333E) was preserved by vaporization (PBV) in a dry, stable foam. RABV stabilized using this process remains viable for at least 23 months at 22°C, 15 months at 37°C, and 3h at 80°C. An antigen capture assay revealed RABV PBV inactivated by irradiation contained similar levels of antigen as a commercial vaccine. Viability and antigen capture testing confirmed that the PBV process stabilized RABV with no significant loss in titer or antigen content. Live attenuated and inactivated RABV PBV both effectively induced RABV neutralizing antibodies and protected mice from peripheral RABV challenge. These results demonstrate that PBV is an efficient method for RABV stabilization. Published by Elsevier Ltd.Entities:
Keywords: Efficacy; Immunogenicity; Preservation by vaporization; Rabies virus; Stability
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Year: 2015 PMID: 25812841 PMCID: PMC4398650 DOI: 10.1016/j.vaccine.2015.03.025
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641