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流感病毒中的神经氨酸酶抑制剂耐药性。

Neuraminidase inhibitor resistance in influenza viruses.

作者信息

Reece Phillip Andrew

机构信息

Department of Pharmacology, University of Melbourne, Parkville, VIC, Australia.

出版信息

J Med Virol. 2007 Oct;79(10):1577-86. doi: 10.1002/jmv.20951.

DOI:10.1002/jmv.20951
PMID:17705169
Abstract

Zanamivir and oseltamivir, the currently marketed influenza virus neuraminidase inhibitors (NAIs), are prescribed for the treatment and prophylaxis of influenza and are being stockpiled for pandemic influenza. Oseltamivir resistance has been reported in up to 2% of patients in clinical trials of oseltamivir and in up to 18% of treated children. There are also reports in at least three patients treated with oseltamivir for influenza A (H5N1) infections. At this stage, there are no reports of resistance occurring to zanamivir in immunocompetent patients. Zanamivir and oseltamivir bind differently at the neuraminidase catalytic site and this contributes to different drug resistance profiles. The magnitude and duration of NAI concentrations at the site of infection are also expected to be important factors and are determined by route and timing of drug administration, dose, and pharmacokinetic differences between patients. In addition, the type, strain, and virulence of the influenza strain and the nature of the immune response all appear to play a role in determining the likelihood of drug resistance arising. The clinical significance of a particular NAI-resistant isolate from a patient is often not clear but virus viability and transmissibility are clearly important characteristics. Early initiation of NAI treatment in suspected cases of influenza is important for maximizing efficacy and minimizing the risk of drug resistance. Higher NAI doses and longer periods of treatment may be required for patients with influenza A (H5N1) infections but further work is needed in this area.

摘要

扎那米韦和奥司他韦是目前已上市的流感病毒神经氨酸酶抑制剂(NAIs),用于流感的治疗和预防,并且被储备用于应对大流行性流感。在奥司他韦的临床试验中,高达2%的患者出现了奥司他韦耐药,接受治疗的儿童中这一比例高达18%。也有至少3例甲型H5N1流感感染患者接受奥司他韦治疗后出现耐药的报告。现阶段,免疫功能正常的患者中尚无扎那米韦耐药的报告。扎那米韦和奥司他韦在神经氨酸酶催化位点的结合方式不同,这导致了不同的耐药谱。感染部位NAI浓度的大小和持续时间预计也是重要因素,这取决于给药途径和时间、剂量以及患者之间的药代动力学差异。此外,流感毒株的类型、菌株和毒力以及免疫反应的性质似乎都在决定耐药发生可能性方面发挥作用。从患者分离出的特定NAI耐药株的临床意义通常并不明确,但病毒的生存能力和传播性显然是重要特征。在疑似流感病例中尽早开始NAI治疗对于最大化疗效和最小化耐药风险很重要。甲型H5N1流感感染患者可能需要更高的NAI剂量和更长的治疗时间,但这方面还需要进一步研究。

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