Abstract |
A rapid, peripheral disease model utilizing the Bunyavirus, Caraparu, was established in mice for the evaluation of antiviral therapy with immunomodulators. 4-6-week-old B6C3F1 female mice, inoculated intraperitoneally with virus, developed coagulative liver necrosis and died between 4-6 days after infection. This Caraparu disease model was relatively resistant to treatment with immunomodulators, such as ABMP, Ampligen, alpha-interferon (IFN-alpha) or beta-interferon (IFN-beta). However, a significant increase in median survival time (MST) was consistently observed upon treatment with gamma-interferon (IFN-gamma). The nucleoside analog-- ribavirin--was highly effective against Caraparu virus in repeated treatment schedules begun on either day -1, day 0, or day +1 of infection. Ribavirin gave little protection when initiation of treatment was delayed until day +2. However, combined treatment with IFN-gamma, starting on day 0 and ribavirin starting on day +2, significantly reduced mortality.
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Authors | M A Brinton, E I Gavin, W K Lo, A J Pinto, P S Morahan |
Journal | Antiviral research
(Antiviral Res)
Vol. 20
Issue 2
Pg. 155-71
(Feb 1993)
ISSN: 0166-3542 [Print] Netherlands |
PMID | 8460932
(Publication Type: Journal Article, Research Support, U.S. Gov't, Non-P.H.S.)
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Chemical References |
- Adjuvants, Immunologic
- Antiviral Agents
- Recombinant Proteins
- Ribavirin
- Interferon-gamma
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Topics |
- Adjuvants, Immunologic
(pharmacology, therapeutic use)
- Animals
- Antiviral Agents
(pharmacology, therapeutic use)
- Bunyaviridae Infections
(drug therapy, microbiology)
- Female
- Interferon-gamma
(pharmacology)
- Liver
(pathology)
- Liver Diseases
(drug therapy, microbiology, pathology)
- Mice
- Mice, Inbred Strains
- Microscopy, Electron
- Orthobunyavirus
(drug effects)
- Recombinant Proteins
- Ribavirin
(pharmacology)
- Virus Replication
(drug effects)
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