Leidos, Reston, Virginia, United States of America.
Roche Pharmaceutical Research and Early Development, Pharmaceutical Sciences, Roche Innovation Center, F. Hoffmann-La Roche Ltd, Basel, Switzerland.
PLoS Comput Biol. 2023 Jan 6;19(1):e1010797. doi: 10.1371/journal.pcbi.1010797. eCollection 2023 Jan.
To aid understanding of the effect of antiviral treatment on population-level influenza transmission, we used a novel pharmacokinetic-viral kinetic transmission model to test the correlation between nasal viral load and infectiousness, and to evaluate the impact that timing of treatment with the antivirals oseltamivir or baloxavir has on influenza transmission. The model was run under three candidate profiles whereby infectiousness was assumed to be proportional to viral titer on a natural-scale, log-scale, or dose-response model. Viral kinetic profiles in the presence and absence of antiviral treatment were compared for each individual (N = 1000 simulated individuals); subsequently, viral transmission mitigation was calculated. The predicted transmission mitigation was greater with earlier administration of antiviral treatment, and with baloxavir versus oseltamivir. When treatment was initiated 12-24 hours post symptom onset, the predicted transmission mitigation was 39.9-56.4% for baloxavir and 26.6-38.3% for oseltamivir depending on the infectiousness profile. When treatment was initiated 36-48 hours post symptom onset, the predicted transmission mitigation decreased to 0.8-28.3% for baloxavir and 0.8-19.9% for oseltamivir. Model estimates were compared with clinical data from the BLOCKSTONE post-exposure prophylaxis study, which indicated the log-scale model for infectiousness best fit the observed data and that baloxavir affords greater reductions in secondary case rates compared with neuraminidase inhibitors. These findings suggest a role for baloxavir and oseltamivir in reducing influenza transmission when treatment is initiated within 48 hours of symptom onset in the index patient.
为了帮助理解抗病毒治疗对人群水平流感传播的影响,我们使用了一种新的药代动力学-病毒动力学传播模型,以检验鼻病毒载量与传染性之间的相关性,并评估抗病毒药物奥司他韦或巴洛沙韦治疗时机对流感传播的影响。该模型在三种候选方案下运行,假设传染性与自然标度、对数标度或剂量反应模型上的病毒滴度成正比。对每个个体(模拟个体 1000 个)的存在和不存在抗病毒治疗的病毒动力学特征进行了比较;随后,计算了病毒传播缓解情况。抗病毒治疗的早期给药和使用巴洛沙韦而非奥司他韦,预测传播缓解效果更大。当治疗在症状出现后 12-24 小时开始时,根据传染性特征,巴洛沙韦的预测传播缓解率为 39.9-56.4%,奥司他韦为 26.6-38.3%。当治疗在症状出现后 36-48 小时开始时,巴洛沙韦的预测传播缓解率降至 0.8-28.3%,奥司他韦为 0.8-19.9%。模型估计与 BLOCKSTONE 暴露后预防研究的临床数据进行了比较,结果表明,传染性的对数标度模型最适合观察数据,并且巴洛沙韦比神经氨酸酶抑制剂更能降低继发病例率。这些发现表明,在指数患者症状出现后 48 小时内开始治疗时,巴洛沙韦和奥司他韦在降低流感传播方面发挥作用。