VIOLIN Logo
VO Banner
Search: for Help
About
Introduction
Statistics
VIOLIN News
Your VIOLIN
Register or Login
Submission
Tutorial
Vaccine & Components
Vaxquery
Vaxgen
VBLAST
Protegen
VirmugenDB
DNAVaxDB
CanVaxKB
Vaxjo
Vaxvec
Vevax
Huvax
Cov19VaxKB
Host Responses
VaximmutorDB
VIGET
Vaxafe
Vaxar
Vaxism
Vaccine Literature
VO-SciMiner
Litesearch
Vaxmesh
Vaxlert
Vaccine Design
Vaxign2
Vaxign
Community Efforts
Vaccine Ontology
ICoVax 2012
ICoVax 2013
Advisory Committee
Vaccine Society
Vaxperts
VaxPub
VaxCom
VaxLaw
VaxMedia
VaxMeet
VaxFund
VaxCareer
Data Exchange
V-Utilities
VIOLINML
Help & Documents
Publications
Documents
FAQs
Links
Acknowledgements
Disclaimer
Contact Us
UM Logo

Vaccine Detail

Recombinant vesicular stomatitis virus encoding HA from Influenza A virus (A/WSN/1933(H1N1))
Vaccine Information
  • Vaccine Name: Recombinant vesicular stomatitis virus encoding HA from Influenza A virus (A/WSN/1933(H1N1))
  • Target Pathogen: Influenza virus
  • Target Disease: Influenza (flu)
  • Vaccine Ontology ID: VO_0004168
  • Type: Recombinant vector vaccine
  • Status: Clinical trial
  • Antigen: Influenza A virus (A/WSN/1933(H1N1)) HA hemagglutinin
  • HA from Influenza A virus (A/WSN/1933(H1N1)) gene engineering:
    • Type: Recombinant vector construction
    • Description: Recombinant vesicular stomatitis virus (VSV) expressing an influenza virus hemagglutinin (HA) protein (Roberts et al., 1999)
    • Detailed Gene Information: Click Here.
  • Immunization Route: Intranasal
Host Response

Mouse Response

  • Host Strain: BALB/c
  • Vaccination Protocol: Five- to 6-week-old female BALB/c mice from Charles River Laboratories were housed in filter-isolette cages upon arrival. The mice were inoculated no earlier than 4 days after arrival. Prior to inoculation (day 0), the mice were lightly anesthetized with Methoxyflurane (Mallinckrodt Veterinary, Inc., Mundelein, Ill.) and marked by ear punch. Twenty-five microliters of inoculum were delivered intranasally by 200-μl pipette to the anesthetized mice, and the mice were weighed in a plastic beaker to ±0.02 g. Boosts were administered in an identical fashion with viruses of equal kind, titer, and volume on day 21, unless otherwise indicated (Roberts et al., 1999).
  • Challenge Protocol: Challenge was administered in a total volume of 50 μl per mouse on day 35 (Roberts et al., 1999) .
  • Efficacy: A nonpathogenic vector of the cytoplasmic domain of the VSV G protein and expressing influenza virus HA (derived from Influenza A virus (A/WSN/1933(H1N1))) provides complete protection from lethal influenza virus challenge after intranasal administration. A second vector with VSV G deleted and expressing HA (DeltaG-HA) is also protective and nonpathogenic and has the advantage of not inducing neutralizing antibodies to the vector itself (Roberts et al., 1999).
References
Roberts et al., 1999: Roberts A, Buonocore L, Price R, Forman J, Rose JK. Attenuated vesicular stomatitis viruses as vaccine vectors. Journal of virology. 1999; 73(5); 3723-3732. [PubMed: 10196265].