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Development of a murine nose-only inhalation model of influenza: comparison of disease caused by instilled and inhaled A/PR/8/34

机译:流感的仅鼠鼻吸入模型的建立:滴注和吸入引起的疾病比较A / PR / 8/34

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摘要

Influenza continues to cause widespread disease and death during winter months. In preclinical studies to evaluate the potential efficacy of drugs and vaccines, influenza challenge virus is usually instilled into the noses of animals in the form of large liquid drops. Since inhalation of aerosolized influenza is commonly associated with human transmission, instillation of challenge virus raises uncertainty about the applicability of results. In order to compare the challenge methods, we established conditions to generate influenza aerosols with a mass median aerodynamic diameter (MMAD) of 1 μm that were delivered to mice in a nose-only inhalation system. In this report, we describe the system and compare the 50% lethal dose (LD50) of instilled and inhaled A/PR/8/34 (PR8) in BALB/c mice. The estimated LD50 for inhaled virus was 8.7 plaque forming units (PFU) and the mean time to death was 7.7 days, whereas the estimated LD50 for instilled virus was 51.6 PFU and the mean time to death was 8.2 days. Our results show that mice are more sensitive to inhaled virus than virus delivered by intranasal instillation. The murine nose-only inhalation model of influenza infection can be used to infect large numbers of animals simultaneously with well-characterized, homogenous PR8 bioaerosol in a controlled and reproducible manner. This model provides the means to evaluate the efficacy of drug and vaccine candidates against the relevant route of challenge, thereby providing data that may better predict clinical outcome.
机译:在冬季,流感继续导致广泛的疾病和死亡。在评估药物和疫苗潜在功效的临床前研究中,流感挑战病毒通常以大液滴的形式滴入动物的鼻子中。由于雾化流感的吸入通常与人类传播有关,因此滴注挑战病毒增加了结果适用性的不确定性。为了比较这些挑战性方法,我们建立了条件,以产生质量中位数空气动力学直径(MMAD)为1μm的流感气溶胶,并通过纯鼻吸入系统将其递送给小鼠。在此报告中,我们描述了该系统,并比较了BALB / c小鼠的A / PR / 8/34(PR8)滴注和吸入的50%致死剂量(LD50)。吸入病毒的估计LD50为8.7个噬菌斑形成单位(PFU),平均死亡时间为7.7天,而滴注病毒的估计LD50为51.6 PFU,平均死亡时间为8.2天。我们的结果表明,小鼠对吸入的病毒比鼻内滴注的病毒更敏感。流感感染的仅鼠鼻吸入模型可用于以可控和可重复的方式同时感染特征明确的同质PR8生物气溶胶同时感染大量动物。该模型提供了一种手段,可以评估针对相关挑战途径的候选药物和疫苗的功效,从而提供可以更好地预测临床结果的数据。

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