Why the study?
Does multiple doses of polyriboinosinic-polyribocytidylic acid improve survival in mice infected with encephalomyocarditis virus?
Does multiple doses of polyriboinosinic-polyribocytidylic acid improve survival in mice infected with encephalomyocarditis virus?
In mice infected with encephalomyocarditis virus, polyriboinosinic-polyribocytidylic acid therapy is only effective if it suppresses viremia before central nervous system seeding occurs.
Answers are grounded in this paper and cite their sources.
May require pre-CNS seeding intervention for efficacy in EMCV models; leaves open translation to human neurotropic infections.
These studies were designed to evaluate the therapeutic efficacy of multiple doses of an interferon inducer, polyriboinosinic-polyribocytidylic acid, in encephalomyocarditis virus infection of mice. The results indicated that suppression of a detectable viremia was essential to the successful protection of mice from the lethal consequences of infection. The viremic phase of the infection could be delayed or partially suppressed without protection. The data strongly suggest that once the central nervous system had been seeded and virus replication had begun, inducer therapy was ineffective in altering the outcome of infection. This fact could be attributed in part to the low levels of interferon found in brain tissue after intraperitoneal administration of polyriboinosinic-polyribocytidylic acid. Also, animals that received the most effective regimen of the interferon inducer and that survived the infection were not protected against a second infection with the same virus, an observation suggesting that the incidence of circulating antibody to encephalomyocarditis virus is reduced after the initial infection.
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Stringfellow et al. (1974) studied this question.
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