共 35 条
Oral administration of cyclopentane neuraminidase inhibitors protects ferrets against influenza virus infection
被引:33
作者:

Sweet, C
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Univ Birmingham, Sch Biosci, Birmingham B15 2TT, W Midlands, England Univ Birmingham, Sch Biosci, Birmingham B15 2TT, W Midlands, England

Jakeman, KJ
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机构: Univ Birmingham, Sch Biosci, Birmingham B15 2TT, W Midlands, England

Bush, K
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机构: Univ Birmingham, Sch Biosci, Birmingham B15 2TT, W Midlands, England

Wagaman, PC
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h-index: 0
机构: Univ Birmingham, Sch Biosci, Birmingham B15 2TT, W Midlands, England

Mckown, LA
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h-index: 0
机构: Univ Birmingham, Sch Biosci, Birmingham B15 2TT, W Midlands, England

Streeter, AJ
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h-index: 0
机构: Univ Birmingham, Sch Biosci, Birmingham B15 2TT, W Midlands, England

Desai-Krieger, D
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h-index: 0
机构: Univ Birmingham, Sch Biosci, Birmingham B15 2TT, W Midlands, England

Chand, P
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h-index: 0
机构: Univ Birmingham, Sch Biosci, Birmingham B15 2TT, W Midlands, England

Babu, YS
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h-index: 0
机构: Univ Birmingham, Sch Biosci, Birmingham B15 2TT, W Midlands, England
机构:
[1] Univ Birmingham, Sch Biosci, Birmingham B15 2TT, W Midlands, England
[2] RW Johnson Pharmaceut Res Inst, La Jolla, CA USA
[3] RW Johnson Pharmaceut Res Inst, Raritan, NJ 08869 USA
[4] RW Johnson Pharmaceut Res Inst, Spring House, PA 19477 USA
[5] BioCryst Pharmaceut Inc, Birmingham, AL USA
关键词:
D O I:
10.1128/AAC.46.4.996-1004.2002
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Several cyclopentane inhibitors of influenza virus neuraminidase that have inhibitory activities in tissue culture similar to those of zanamivir and oseltamivir have recently been described. These new inhibitors have been examined for efficacy against a virulent H3N2 influenza virus when administered orally to infected ferrets. Preliminary studies indicated that oral administration of BCX-1923, BCX-1827, or BCX-1812 (RWJ-270201) at a dose of 5 or 25 mg/kg of body weight was active in ferrets in reducing respiratory and constitutional signs and symptoms, but these antivirals affected virus titers in the upper and lower respiratory tracts only marginally. Of the three compounds, BCX-1812 seemed to be the most efficacious and was examined further at higher doses of 30 and 100 mg/kg. These doses significantly reduced peak virus titers in nasal washes and total virus shedding as measured by areas under the curve. Virus titers in lung homogenates were also reduced compared to those in controls, but the difference was not statistically significant. As was observed with BCX-1812 at lower doses, the nasal inflammatory cellular response, fever, and nasal signs were reduced while ferret activity was not, with activity remaining similar to uninfected animals.
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页码:996 / 1004
页数:9
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