Suppr超能文献

临床试验中 IV 扎那米韦耐药分析的启示。

Lessons from resistance analysis in clinical trials of IV zanamivir.

机构信息

GlaxoSmithKline, Stevenage, United Kingdom.

GlaxoSmithKline, Stevenage, United Kingdom.

出版信息

Virus Res. 2023 Feb;325:199039. doi: 10.1016/j.virusres.2023.199039. Epub 2023 Jan 4.

Abstract

Influenza infection causes substantial morbidity and mortality during seasonal epidemics and pandemics. Antivirals, including neuraminidase inhibitors, play an important role in the treatment of severely ill patients infected with influenza. Resistance is a key factor that can affect the efficacy of neuraminidase inhibitors (NAIs). It is a recommendation by regulatory authorities to monitor for resistance during the development of anti-influenza medications. An additional requirement by regulators is to examine amino acid sequences for minority species harbouring resistance substitutions. In a Phase III study of intravenous (IV) zanamivir respiratory samples were analysed for the presence of resistant quasi species using Next Generation Sequencing (NGS). In this study ten resistance substitutions, two of which were treatment emergent, were detected by NGS that otherwise would not have been detectable by Sanger sequencing. None of the substitutions were present at any other timepoints analysed. The effect these mutations have on clinical response is difficult to characterize; in fact, all patients from which these variants were isolated had a successful clinical outcome and the effect on clinical response was therefore likely minimal. Although NGS is becoming a routine method for nucleic acid sequencing and will detect substitutions previously undetected by Sanger sequencing, the value of this technique in identifying minority species with resistance substitutions that are clinically meaningful remains to be demonstrated, particularly with acute infections such as influenza.

摘要

流感感染在季节性流行和大流行期间会导致大量发病率和死亡率。抗病毒药物,包括神经氨酸酶抑制剂,在治疗感染流感的重症患者方面发挥着重要作用。耐药性是一个关键因素,会影响神经氨酸酶抑制剂(NAIs)的疗效。监管机构建议在开发抗流感药物期间监测耐药性。监管机构的另一项要求是检查携带耐药性替代物的少数物种的氨基酸序列。在一项静脉注射(IV)扎那米韦的 III 期研究中,使用下一代测序(NGS)分析了呼吸道样本中是否存在耐药准种。在这项研究中,通过 NGS 检测到了 10 种耐药替换,其中两种是治疗后出现的,而通过 Sanger 测序则无法检测到。在分析的任何其他时间点均未发现这些替换。这些突变对临床反应的影响难以确定;实际上,从这些变体中分离出的所有患者都有成功的临床结果,因此对临床反应的影响可能很小。尽管 NGS 正在成为核酸测序的常规方法,并将检测到以前通过 Sanger 测序无法检测到的替换,但该技术在识别具有临床意义的耐药替换少数物种方面的价值仍有待证明,特别是对于流感等急性感染。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/025d/10194138/74b16238bca5/gr1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验