1992
DOI: 10.1128/cmr.5.2.146-182.1992
|View full text |Cite
|
Sign up to set email alerts
|

Antiviral therapy: current concepts and practices.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...

Citation Types

0
2
0

Year Published

1995
1995
2013
2013

Publication Types

Select...
2

Relationship

0
2

Authors

Journals

citations
Cited by 2 publications
(2 citation statements)
references
References 250 publications
(283 reference statements)
0
2
0
Order By: Relevance
“…Ribavirin (1-b-D-ribofuranosyl-1,2,4-triazole-3-carboxamide) is a synthetic nucleotide analogue [1] that has a broad spectrum of antiviral activity [2][3][4][5][6][7][8][9][10]. Various mechanisms of action were suggested to explain antiviral activity, including enzyme suppression [10][11][12][13][14][15] and the 'error catastrophe' effect in which a lethal accumulation of minor mutations leads to a stop in viral replication [16,17]. Although highly effective in vitro, ribavirin's therapeutic efficacy remains controversial and even conflicting clinical results are often seen with the same viral infection, such as with hantavirus [18,19].…”
mentioning
confidence: 99%
“…Ribavirin (1-b-D-ribofuranosyl-1,2,4-triazole-3-carboxamide) is a synthetic nucleotide analogue [1] that has a broad spectrum of antiviral activity [2][3][4][5][6][7][8][9][10]. Various mechanisms of action were suggested to explain antiviral activity, including enzyme suppression [10][11][12][13][14][15] and the 'error catastrophe' effect in which a lethal accumulation of minor mutations leads to a stop in viral replication [16,17]. Although highly effective in vitro, ribavirin's therapeutic efficacy remains controversial and even conflicting clinical results are often seen with the same viral infection, such as with hantavirus [18,19].…”
mentioning
confidence: 99%
“…The human immunodeficiency viruses, human immunodeficiency virus type 1 (HIV-1) and HIV-2, cause AIDS, which leads to a progressive destruction of the immune system with a prominent loss of circulating CD4 ϩ cells (2,14,33). A variety of drugs which interfere with the viral replication cycle has been evaluated, including both nucleoside and nonnucleoside reverse transcriptase inhibitors and protease inhibitors (3). The rapid development of resistance and the cytotoxicity of the chemical compounds, together with inefficient immune responses to heterologous virus in vaccination trials, are at present the major drawbacks in the fight against AIDS.…”
mentioning
confidence: 99%