Key result
Intra-muscular immunization with live H1N1 influenza A virus protected 100% of highly susceptible DBA/2J mice from a subsequent lethal challenge, compared to 0% survival in non-immunized mice.
Why the study?
Does intra-muscular immunization with live H1N1 influenza A virus protect highly susceptible DBA/2J mice from lethal infection?
Does intra-muscular immunization with live H1N1 influenza A virus protect highly susceptible DBA/2J mice from lethal infection?
DBA/2J mice represent a suitable model to evaluate immunization regimes against human influenza strains without prior adaptation of the virus to the mouse.
Demonstrates proof-of-concept for IM live-virus immunization in susceptible mice; leaves open translation to human influenza protection.
BACKGROUND: The mouse represents an important model system to study the host response to influenza A infections and to evaluate new prevention or treatment strategies. We and others reported that the susceptibility to influenza A virus infections strongly varies among different inbred mouse strains. In particular, DBA/2J mice are highly susceptible to several influenza A subtypes, including human isolates and exhibit severe symptoms after infection with clinical isolates. FINDINGS: Upon intra-muscular immunization with live H1N1 influenza A virus (mouse-adapted PR8M, and 2009 pandemic human HA04), DBA/2J mice mounted virus-specific IgG responses and were protected against a subsequent lethal challenge. The immune response and rescue from death after immunization in DBA/2J was similar to those observed for C57BL/6J mice. CONCLUSIONS: DBA/2J mice represent a suitable mouse model to evaluate virulence and pathogenicity as well as immunization regimes against existing and newly emerging human influenza strains without the need for prior adaptation of the virus to the mouse.
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Dengler et al. (2012) studied Influenza A H1N1 infection. Live H1N1 influenza A virus vaccine vs. Non-immunized mice was evaluated on Survival after lethal challenge. Intra-muscular immunization with live H1N1 influenza A virus protected 100% of highly susceptible DBA/2J mice from a subsequent lethal challenge, compared to 0% survival in non-immunized mice.
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