Abstract |
An inbred murine model (BALB/c) was utilized to assess the protective effect of the immunomodulator methyl inosine 5'-monophosphate ( MIMP) against infection with influenza A/PR/8/34 (H1N1) virus. Contrary to the data reported for outbred mice (NMRI) infected with the aerosolized virus (Masihi, Hadden, 2003. J. Int. Immunopharmacol. 3, 1205-1215), there were no improvements in the outcomes of infection in the inbred animals treated with MIMP intranasally 1 day before the challenge and/or orally after the challenge for 5 days (up to 10 mg/kg/day). Nevertheless, complete protection against lethality was afforded by the treatment with the neuraminidase inhibitor peramivir given once daily for 5 days after the challenge (10 mg/kg/day). We speculate that the rapid progression of the disease in inbred mice caused by the intranasal challenge may render the MIMP-treatment ineffective. Our results emphasize the need for careful consideration of murine strains and routes of virus challenge in the design of experiments utilizing lethal influenza virus infection.
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Authors | Vasiliy P Mishin, Frederick G Hayden, Kathy L Signorelli, Larisa V Gubareva |
Journal | Antiviral research
(Antiviral Res)
Vol. 71
Issue 1
Pg. 64-8
(Aug 2006)
ISSN: 0166-3542 [Print] Netherlands |
PMID | 16581141
(Publication Type: Journal Article, Research Support, N.I.H., Extramural)
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Chemical References |
- Acids, Carbocyclic
- Antiviral Agents
- Cyclopentanes
- Guanidines
- Inosine Monophosphate
- methyl inosine monophosphate
- peramivir
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Topics |
- Acids, Carbocyclic
- Age Factors
- Animals
- Antiviral Agents
(pharmacology)
- Body Weight
- Cyclopentanes
(pharmacology)
- Disease Models, Animal
- Female
- Guanidines
(pharmacology)
- Influenza A Virus, H1N1 Subtype
(growth & development)
- Inosine Monophosphate
(analogs & derivatives, pharmacology)
- Mice
- Mice, Inbred BALB C
- Orthomyxoviridae Infections
(drug therapy, virology)
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