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受感染细胞中 SHIV 的产生持续时间不是呈指数分布的:对感染参数和抗病毒疗效估计的影响。

Duration of SHIV production by infected cells is not exponentially distributed: Implications for estimates of infection parameters and antiviral efficacy.

机构信息

Department of Physics, Ryerson University, Toronto, M5B 2K3, Canada.

Interdisciplinary Theoretical Science (iTHES) Research Group, RIKEN, Wako, 351-0198, Japan.

出版信息

Sci Rep. 2017 Feb 16;7:42765. doi: 10.1038/srep42765.

Abstract

The duration of the eclipse phase, from cell infection to the production and release of the first virion progeny, immediately followed by the virus-production phase, from the first to the last virion progeny, are important steps in a viral infection, by setting the pace of infection progression and modulating the response to antiviral therapy. Using a mathematical model (MM) and data for the infection of HSC-F cells with SHIV in vitro, we reconfirm our earlier finding that the eclipse phase duration follows a fat-tailed distribution, lasting 19 h (18-20 h). Most importantly, for the first time, we show that the virus-producing phase duration, which lasts 11 h (9.8-12 h), follows a normal-like distribution, and not an exponential distribution as is typically assumed. We explore the significance of this finding and its impact on analysis of plasma viral load decays in HIV patients under antiviral therapy. We find that incorrect assumptions about the eclipse and virus-producing phase distributions can lead to an overestimation of antiviral efficacy. Additionally, our predictions for the rate of plasma HIV decay under integrase inhibitor therapy offer an opportunity to confirm whether HIV production duration in vivo also follows a normal distribution, as demonstrated here for SHIV infections in vitro.

摘要

从细胞感染到第一个病毒子代的产生和释放的潜伏期,紧接着是病毒产生期,从第一个到最后一个病毒子代,是病毒感染的重要步骤,它设定了感染进展的速度,并调节了对抗病毒治疗的反应。我们使用数学模型 (MM) 和体外感染 HSC-F 细胞的 SHIV 数据,重新证实了我们之前的发现,即潜伏期持续时间遵循长尾分布,持续 19 小时(18-20 小时)。最重要的是,我们首次表明,病毒产生期持续 11 小时(9.8-12 小时),遵循正态分布,而不是通常假设的指数分布。我们探讨了这一发现的意义及其对分析接受抗病毒治疗的 HIV 患者血浆病毒载量衰减的影响。我们发现,对潜伏期和病毒产生期分布的不正确假设会导致抗病毒疗效的高估。此外,我们对整合酶抑制剂治疗下血浆 HIV 衰减率的预测提供了一个机会,可以确认体内 HIV 产生持续时间是否也遵循正态分布,正如我们在这里对体外 SHIV 感染所展示的那样。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9bde/5311941/6e67b48125ff/srep42765-f1.jpg

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