Vaccinia virus inhibitors as a paradigm for the chemotherapy of poxvirus infections

被引:139
作者
De Clercq, E [1 ]
机构
[1] Katholieke Univ Leuven, Rega Inst Med Res, Dept Microbiol & Immunol, Div Virol & Chemotherapy, B-3000 Louvain, Belgium
关键词
D O I
10.1128/CMR.14.2.382-397.2001
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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.
引用
收藏
页码:382 / +
页数:17
相关论文
共 116 条
[91]  
2-0
[92]   SYNTHESIS AND ANTIVIRAL ACTIVITIES OF 8-ALKYNYL-2'-DEOXYADENOSINE, 8-ALKENYL-2'-DEOXYADENOSINE, AND 8-ALKYL-2'-DEOXYADENOSINE ANALOGS [J].
SAGI, G ;
OTVOS, L ;
IKEDA, S ;
ANDREI, G ;
SNOECK, R ;
DECLERCQ, E .
JOURNAL OF MEDICINAL CHEMISTRY, 1994, 37 (09) :1307-1311
[93]   A MUTATION IN THE GENE ENCODING THE VACCINIA VIRUS 37,000-MR PROTEIN CONFERS RESISTANCE TO AN INHIBITOR OF VIRUS ENVELOPMENT AND RELEASE [J].
SCHMUTZ, C ;
PAYNE, LG ;
GUBSER, J ;
WITTEK, R .
JOURNAL OF VIROLOGY, 1991, 65 (07) :3435-3442
[94]   Sulphated polymers are potent and selective inhibitors of various enveloped viruses, including herpes simplex virus, cytomegalovirus, vesicular stomatitis virus, respiratory syncytial virus, and toga-, arena- and retroviruses [J].
Schols, D. ;
De Ctercq, E. ;
Balzanni, J. ;
Baba, M. ;
Witvrouw, M. ;
Hosoya, M. ;
Andrei, G. ;
Snoeck, R. ;
Neyts, J. ;
Pauwels, R. ;
Nagy, M. ;
Gyorgyi-Edelenyi, J. ;
Machovich, R. ;
Horvath, I ;
Low, M. ;
Gorog, S. .
ANTIVIRAL CHEMISTRY & CHEMOTHERAPY, 1990, 1 (04) :233-240
[95]   Novobiocin inhibits vaccinia virus replication by blocking virus assembly [J].
Sekiguchi, JA ;
Shuman, S .
VIROLOGY, 1997, 235 (01) :129-137
[96]   New neplanocin analogues .6. Synthesis and potent antiviral activity of 6'-homoneplanocin A [J].
Shuto, S ;
Obara, T ;
Saito, Y ;
Andrei, G ;
Snoeck, R ;
DeClercq, E ;
Matsuda, A .
JOURNAL OF MEDICINAL CHEMISTRY, 1996, 39 (12) :2392-2399
[97]   NEW NEPLANOCIN ANALOGS .1. SYNTHESIS OF 6'-MODIFIED NEPLANOCIN-A DERIVATIVES AS BROAD-SPECTRUM ANTIVIRAL AGENTS [J].
SHUTO, S ;
OBARA, T ;
TORIYA, M ;
HOSOYA, M ;
SNOECK, R ;
ANDREI, G ;
BALZARINI, J ;
DECLERCQ, E .
JOURNAL OF MEDICINAL CHEMISTRY, 1992, 35 (02) :324-331
[98]   3-DEAZA-5'-NORARISTEROMYCIN AND 7-DEAZA-5'-NORARISTEROMYCIN AND THEIR ANTIVIRAL PROPERTIES [J].
SIDDIQI, SM ;
CHEN, X ;
RAO, J ;
SCHNELLER, SW ;
IKEDA, S ;
SNOECK, R ;
ANDREI, G ;
BALZARINI, J ;
DECLERCQ, E .
JOURNAL OF MEDICINAL CHEMISTRY, 1995, 38 (06) :1035-1038
[99]   ANTIVIRAL ENANTIOMERIC PREFERENCE FOR 5'-NORARISTEROMYCIN [J].
SIDDIQI, SM ;
CHEN, X ;
SCHNELLER, SW ;
IKEDA, S ;
SNOECK, R ;
ANDREI, G ;
BALZARINI, J ;
DECLERCQ, E .
JOURNAL OF MEDICINAL CHEMISTRY, 1994, 37 (04) :551-554
[100]   AN EPIMER OF 5'-NORARISTEROMYCIN AND ITS ANTIVIRAL PROPERTIES [J].
SIDDIQI, SM ;
CHEN, X ;
SCHNELLER, SW ;
IKEDA, S ;
SNOECK, R ;
ANDREI, G ;
BALZARINI, J ;
DECLERCQ, E .
JOURNAL OF MEDICINAL CHEMISTRY, 1994, 37 (09) :1382-1384