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Neuraminidase Inhibitor Resistance in Influenza: Assessing the Danger of Its Generation and Spread

机译:流感中神经氨酸酶抑制剂的耐药性:评估其产生和扩散的危险

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摘要

Neuraminidase Inhibitors (NI) are currently the most effective drugs against influenza. Recent cases of NI resistance are a cause for concern. To assess the danger of NI resistance, a number of studies have reported the fraction of treated patients from which resistant strains could be isolated. Unfortunately, those results strongly depend on the details of the experimental protocol. Additionally, knowing the fraction of patients harboring resistance is not too useful by itself. Instead, we want to know how likely it is that an infected patient can generate a resistant infection in a secondary host, and how likely it is that the resistant strain subsequently spreads. While estimates for these parameters can often be obtained from epidemiological data, such data is lacking for NI resistance in influenza. Here, we use an approach that does not rely on epidemiological data. Instead, we combine data from influenza infections of human volunteers with a mathematical framework that allows estimation of the parameters that govern the initial generation and subsequent spread of resistance. We show how these parameters are influenced by changes in drug efficacy, timing of treatment, fitness of the resistant strain, and details of virus and immune system dynamics. Our study provides estimates for parameters that can be directly used in mathematical and computational models to study how NI usage might lead to the emergence and spread of resistance in the population. We find that the initial generation of resistant cases is most likely lower than the fraction of resistant cases reported. However, we also show that the results depend strongly on the details of the within-host dynamics of influenza infections, and most importantly, the role the immune system plays. Better knowledge of the quantitative dynamics of the immune response during influenza infections will be crucial to further improve the results.
机译:神经氨酸酶抑制剂(NI)是目前最有效的抗流感药物。最近的NI抵抗病例令人担忧。为了评估NI抵抗的危险性,许多研究报告了可以从中分离出耐药菌株的接受治疗的患者比例。不幸的是,这些结果在很大程度上取决于实验方案的细节。另外,仅了解患者自身抵抗力的比例并不太有用。相反,我们想知道被感染的患者在继发宿主中产生抗药性感染的可能性有多大,以及抗药性菌株随后传播的可能性有多大。尽管通常可以从流行病学数据中获得这些参数的估计值,但缺乏此类数据可用于流感中的NI抵抗力。在这里,我们使用的方法不依赖流行病学数据。相反,我们将来自人类志愿者的流感感染的数据与一个数学框架相结合,该数学框架可以估计控制抗药性的初始产生和随后传播的参数。我们展示了这些参数如何受到药物功效,治疗时机,耐药菌株适应性以及病毒和免疫系统动力学细节的影响。我们的研究提供了可以直接在数学和计算模型中使用的参数估计值,以研究NI的使用如何导致抗药性在人群中的出现和扩散。我们发现,抗药性病例的最初产生很可能低于所报道的抗药性病例的比例。但是,我们还表明,结果在很大程度上取决于流感病毒感染宿主内部动态的细节,最重要的是,免疫系统所发挥的作用。更好地了解流感感染期间免疫反应的定量动力学知识,对于进一步改善结果至关重要。

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