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甲型 H1N1-2009 流感大流行期间奥司他韦化学预防失败原因的调查。

Investigation of causes of oseltamivir chemoprophylaxis failures during influenza A (H1N1-2009) outbreaks.

机构信息

Biodefence Centre, Ministry of Defence, Singapore.

出版信息

J Clin Virol. 2011 Feb;50(2):104-8. doi: 10.1016/j.jcv.2010.10.004. Epub 2010 Nov 19.

DOI:10.1016/j.jcv.2010.10.004
PMID:21094080
Abstract

BACKGROUND

Antiviral post-exposure prophylaxis with oseltamivir has been used as a strategy in mitigating the Influenza A (H1N1-2009) pandemic. There have been few reports of well-documented prophylaxis failures and the reasons for failure.

OBJECTIVES

We report herein a series of 10 cases of prophylaxis failures and explore the reasons behind their prophylaxis failure.

STUDY DESIGN

In the early pandemic phase, the military employed oseltamivir post-exposure ring-prophylaxis of affected units. From June 22 to July 30, 2009, cases of laboratory-confirmed prophylaxis failures were identified. Nasopharyngeal swabs were collected and tested by PCR. Samples with sufficient RNA material were sent for whole genome sequencing, and screened for mutations that confer oseltamivir resistance, especially the H275Y mutation.

RESULTS

Ten cases of laboratory-confirmed prophylaxis failure were identified, with a mean age of 22.3 years. One case was asymptomatic; the remaining 9 had fever or cough but without severe complications. The mean duration of exposure before starting oseltamivir was 1.9 days (SD 0.9), while the mean duration of oseltamivir consumption before symptom onset was 1.9 days (SD 1.4). None of the samples had the H275Y mutation or other known mutations that confer resistance. From the whole genome sequencing, several mutations at the HA (T220S, E275V, T333A, D239G); PB2 (K660R, L607V, V292I); NS1 (F103S), and NP (W104G) gene segments were detected, but none of them were likely to result in anti-viral resistance.

CONCLUSIONS

Primary prophylaxis failures exhibited mild symptoms without complications; all did not have the H275Y mutation and were unlikely to result from other mutations.

摘要

背景

抗病毒暴露后用奥司他韦预防已被用作减轻甲型流感(H1N1-2009)大流行的策略。有少数关于记录完善的预防失败和失败原因的报告。

目的

我们在此报告一系列 10 例预防失败病例,并探讨其预防失败的原因。

研究设计

在大流行早期阶段,军方对受影响的单位采用奥司他韦暴露后环式预防。从 2009 年 6 月 22 日至 7 月 30 日,确定了实验室确诊的预防失败病例。采集鼻咽拭子并通过 PCR 检测。收集有足够 RNA 物质的样本进行全基因组测序,并筛选出赋予奥司他韦耐药性的突变,特别是 H275Y 突变。

结果

确定了 10 例实验室确诊的预防失败病例,平均年龄为 22.3 岁。有 1 例为无症状病例;其余 9 例有发热或咳嗽,但无严重并发症。开始使用奥司他韦前的暴露平均持续时间为 1.9 天(标准差为 0.9),而在出现症状前使用奥司他韦的平均持续时间为 1.9 天(标准差为 1.4)。所有样本均未发现 H275Y 突变或其他已知的耐药性突变。从全基因组测序中检测到 HA(T220S、E275V、T333A、D239G);PB2(K660R、L607V、V292I);NS1(F103S)和 NP(W104G)基因片段的几个突变,但没有一个可能导致抗病毒耐药性。

结论

初级预防失败表现为轻度症状,无并发症;均未发现 H275Y 突变,不太可能是其他突变所致。

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