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A clearance test in mice using non-adapted viruses to determine the immunogenicity of influenza strains

Identifieur interne : 001165 ( Istex/Corpus ); précédent : 001164; suivant : 001166

A clearance test in mice using non-adapted viruses to determine the immunogenicity of influenza strains

Auteurs : G. A. Tannock ; Margaret C. Wark ; Linda E. Smith ; Megan M. Sutherland

Source :

RBID : ISTEX:F0D4D1DC0DFA2504515C853FF0A973A8E78C2A37

English descriptors

Abstract

Summary: A test for the immunogenicity of influenza viruses is described, which is based upon the intranasal vaccinating dose required to induce inhibition of multiplication of unadapted influenza viruses in the lungs of mice. This test is more sensitive than an antigen extinction procedure, in which immunogenicity is measured according to the dose required to induce the formation of hemagglutination-inhibition antibody. The clearance test has been used to demonstrate that a) influenza A/Northern Territory/60/68 virus is a better imunogen than A/Victoria/3/75 and both are probably superior to A/U.S.S.R./92/77; b) for A/Northern Territory/60/68, vaccination by the intranasal route in 25 g mice is at least 43,600 times more efficient than by the intraperitoneal route and c) common immunogenic relationships exist between various H3N2 viruses and an H1N1 strain.

Url:
DOI: 10.1007/BF01315003

Links to Exploration step

ISTEX:F0D4D1DC0DFA2504515C853FF0A973A8E78C2A37

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<abstract lang="en">Summary: A test for the immunogenicity of influenza viruses is described, which is based upon the intranasal vaccinating dose required to induce inhibition of multiplication of unadapted influenza viruses in the lungs of mice. This test is more sensitive than an antigen extinction procedure, in which immunogenicity is measured according to the dose required to induce the formation of hemagglutination-inhibition antibody. The clearance test has been used to demonstrate that a) influenza A/Northern Territory/60/68 virus is a better imunogen than A/Victoria/3/75 and both are probably superior to A/U.S.S.R./92/77; b) for A/Northern Territory/60/68, vaccination by the intranasal route in 25 g mice is at least 43,600 times more efficient than by the intraperitoneal route and c) common immunogenic relationships exist between various H3N2 viruses and an H1N1 strain.</abstract>
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