Clinical and virologic characterization of acyclovir-resistant varicella-zoster viruses isolated from 11 patients with acquired immunodeficiency syndrome

被引:36
作者
Saint-Léger, E
Caumes, E
Breton, G
Douard, D
Saiag, P
Huraux, JM
Bricaire, F
Agut, H
Fillet, AM
机构
[1] Hop La Pitie Salpetriere, Assistance Publ Hop Paris, Dept Virol, Paris, France
[2] Hop La Pitie Salpetriere, Assistance Publ Hop Paris, Dept Infect & Trop Dis, Paris, France
[3] Pellegrin Hosp, Dept Pediat, Bordeaux, France
[4] Hop Ambroise Pare, Assistance Publ Hop Paris, Dept Dermatol, Boulogne, France
关键词
D O I
10.1086/324503
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We studied the clinical resistance to acyclovir of infections with varicella-zoster viruses (VZV) in patients with acquired immunodeficiency syndrome, and we correlated it to virologic analyses. Eleven patients with VZV infections (treated with acyclovir, 30 mg/kg/day, given intravenously, or 4 g/day, given orally) were included in the study because of the failure of 10 days of acyclovir therapy. Susceptibility of VZV isolates to acyclovir was tested using a plaque reduction assay to determine the 50% inhibitory concentration (IC50) of acyclovir and the SI50 (IC50 of the patient isolate/IC50 of the reference strain) to acyclovir. The thymidine kinase (TK) gene, which supports the resistance, was sequenced on amplified products. Only 3 patients had a significant increase in the IC50, as compared with the IC50 of the reference strain (SI50 of greater than or equal to4), and a mutation in the TK gene. For the other 8 patients, the clinical resistance was not confirmed by the virologic results: the SI50 was <4, and no mutation was detected in the TK gene. Because no acyclovir-resistant strain appeared during a shorter period of time, we suggest an increase in the duration of the treatment to 21 days before acyclovir resistance is suspected.
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页码:2061 / 2067
页数:7
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