Vaccinia Virus Inhibitors as a Paradigm for the Chemotherapy of Poxvirus Infections
Author:
Open Access
- 1 April 2001
- journal article
- review article
- Published by American Society for Microbiology in Clinical Microbiology Reviews
- Vol. 14 (2) , 382-397
Abstract
SUMMARY: Poxviruses continue to pose a major threat to human health. Monkeypox is endemic in central Africa, and the discontinuation of the vaccination (with vaccinia virus) has rendered most humans vulnerable to variola virus, the etiologic agent of smallpox, should this virus be used in biological warfare or terrorism. However, a large variety of compounds have been described that are potent inhibitors of vaccinia virus replication and could be expected to be active against other poxviruses as well. These compounds could be grouped in different classes: (i) IMP dehydrogenase inhibitors (e.g., EICAR); (ii) SAH hydrolase inhibitors (e.g., 5′-noraristeromycin, 3-deazaneplanocin A, and various neplanocin A derivatives); (iii) OMP decarboxylase inhibitors (e.g., pyrazofurin) and CTP synthetase inhibitors (e.g., cyclopentenyl cytosine); (iv) thymidylate synthase inhibitors (e.g., 5-substituted 2′-deoxyuridines); (v) nucleoside analogues that are targeted at viral DNA synthesis (e.g., Ara-A); (vi) acyclic nucleoside phosphonates [e.g., (S)-HPMPA and (S)-HPMPC (cidofovir)]; and (vii) polyanionic substances (e.g., polyacrylic acid). All these compounds could be considered potential candidate drugs for the therapy and prophylaxis of poxvirus infections at large. Some of these compounds, in particular polyacrylic acid and cidofovir, were found to generate, on single-dose administration, a long-lasting protective efficacy against vaccinia virus infection in vivo. Cidofovir, which has been approved for the treatment of cytomegalovirus retinitis in immunocompromised patients, was also found to protect mice, again when given as a single dose, against a lethal aerosolized or intranasal cowpox virus challenge. In a biological warfare scenario, it would be advantageous to be able to use a single treatment for an individual exposed to an aerosolized poxvirus. Cidofovir thus holds great promise for treating human smallpox, monkeypox, and other poxvirus infections. Anecdotal experience points to the efficacy of cidofovir in the treatment of the poxvirus infections molluscum contagiosum and orf (ecthyma contagiosum) in immunosuppressed patients.Keywords
This publication has 119 references indexed in Scilit:
- Synthesis and Antiviral Evaluation of Analogs of Adenosine-N1-Oxide and 1-(Benzyloxy)AdenosineNucleosides and Nucleotides, 1998
- Antiviral Agents That Are Active against CMV: Potential of Cidofovir for the Treatment of CMV and Other Virus Infections1997
- Antiviral Activity Spectrum and Target of Action of Different Classes of Nucleoside AnaloguesNucleosides and Nucleotides, 1994
- Synthesis of 3-deazaneplanocin A, a powerful inhibitor of S-adenosylhomocysteine hydrolase with potent and selective in vitro and in vivo antiviral activitiesJournal of Medicinal Chemistry, 1989
- Cyclopentenylcytosine. A carbocyclic nucleoside with antitumor and antiviral propertiesJournal of Medicinal Chemistry, 1988
- Antiviral potency of adenosine analogues: Correlation with inhibition of S-adenosylhomocysteine hydrolaseBiochemical and Biophysical Research Communications, 1985
- Fluoroimidazoles as antiviral agents and inhibitors of polynucleotide biosynthesisLife Sciences, 1975
- Rifampicin inhibits the Growth of Some Mammalian VirusesNature, 1969
- Branched-chain sugar nucleosides. V. Synthesis and antiviral properties of several branched-chain sugar nucleosidesJournal of Medicinal Chemistry, 1969
- PROPHYLACTIC TREATMENT OF SMALLPOX CONTACTS WITH N-METHYLISATIN β-THIOSEMICARBAZONE (COMPOUND 33T57, MARBORAN)The Lancet, 1963