Peer-reviewed veterinary case report
Fozivudine treatment lowers virus levels in cats with early FIV
By Fogle, J E et al.·Published in Journal of veterinary internal medicine·2011·Department of Population Health and Pathobiology, United States·View original on PubMed →
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Original publication title: Fozivudine tidoxil as single-agent therapy decreases plasma and cell-associated viremia during acute feline immunodeficiency virus infection.
- Species:
- cat
Plain-English summary
A group of male, neutered cats around 7 months old were treated with a new antiviral medication called fozivudine tidoxil (FZD) after being infected with feline immunodeficiency virus (FIV). The treatment reduced the amount of virus in their blood during the first two weeks, but it did not prevent the infection, as all the cats were still infected after six weeks. Fortunately, the cats did not experience any negative side effects from the medication. More research is needed to find the best dosage and to compare this treatment with other antiviral options.
People also search for: cat FIV treatment · feline immunodeficiency virus medication · fozivudine for cats
Abstract
BACKGROUND: Feline immunodeficiency virus (FIV) is a lentivirus that infects domestic and wild felidae and the course of disease is similar to that of human immunodeficiency virus infection. The thymidine nucleoside analog fozivudine (FZD) tidoxil is a lipid-zidovudine (ZDV) conjugate and member of the family of nucleoside reverse transcriptase (RT) inhibitors (NRTIs). HYPOTHESIS: FZD administration to cats during acute FIV infection produces antiviral activity with fewer adverse effects than its parent compound ZDV (AZT). ANIMALS: Male, neutered cats approximately 7 months of age (n = 12). METHODS: FZD (45 mg/kg q12h, n = 6) or placebo (n = 6) was administered PO in a nonblinded trial for 6 weeks to cats infected with the NCSU(1) isolate of FIV. Peripheral blood was collected preinfection and at 2, 4, and 6 weeks postinfection for CBC, evaluation of CD4(+) and CD8(+) cell counts by flow cytometry, and quantification of plasma and cell-associated viremia by real time RT-PCR. RESULTS: Treatment of cats with FZD during the acute stage of FIV infection decreased plasma and cell-associated viremia during the first 2 weeks of infection, but was not protective against FIV, as all cats were infected by 6 weeks. CONCLUSIONS: At the dosage used in this study, treatment with FZD results in a short-term decrease in viral load with no adverse effects. Further investigation of FZD is warranted to assess pharmacokinetics, optimal dosage, and to directly compare the antiviral activity of FZD to ZDV in naturally infected cats.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/21457319/