Immunization of mice with live attenuated encephalomyocarditis virus: local immunity and survival
article
Mice were vaccinated with an attenuated encephalomyocarditis (EMC) virus strain by the intraperitoneal (i.p.) route and by various ways of respiratory administration: aerosol exposure and intratracheal (i.t.) and intranasal (i.n.) instillation. A linear relationship was found between vaccine dose and the resulting serum antibody titer. The effectiveness of the vaccine was determined by measuring the 50% protective doses (ED50 values) after a lethal challenge with live virulent virus given by the i.p. route. For all three methods of respiratory immunization essentially the same ED50 value was found, about 200 plaque forming units (PFU), but i.p. immunization was less effective, the ED50 value being about 600 PFU. To investigate the protective effect of local immunity, mice were vaccinated i.p. or i.n. and challenged by the i.n. route. The same ED50 values were found as after i.p. challenge, indicating that the degree of protection afforded by the vaccine depends only on the route of vaccination and not on the route of challenge. This means that protection depends largely on systemic immunity and that local immunity plays only a minor role in this system. The results are discussed in relation to the feasibility of respiratory immunization against animal viruses.
Chemicals/CAS: Aerosols; Antibodies, Viral; Vaccines, Attenuated; Viral Vaccines
Chemicals/CAS: Aerosols; Antibodies, Viral; Vaccines, Attenuated; Viral Vaccines
Topics
AntibodyVaccineVirus antibodyAntibody blood levelEncephalomyocarditisEncephalomyocarditis virusImmunityImmunizationModelMouseRespiratory systemTheoretical studyAdministration, IntranasalAerosolsAnimalAntibodies, ViralEncephalomyocarditis virusHemagglutination Inhibition TestsImmunizationInjections, IntraperitonealIntubation, IntratrachealMaleMiceVaccines, AttenuatedViral Vaccines
TNO Identifier
227466
ISSN
00199567
Source
Infection and Immunity, 8(4), pp. 528-533.
Pages
528-533
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