Random time-shift approximation enables hierarchical Bayesian inference of mechanistic within-host viral dynamics models on large datasets.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 41343660.
- Also identified by DOI 10.1371/journal.pcbi.1013775 and PMC identifier 12688156.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Mechanistic mathematical models of within-host viral dynamics are tools for understanding how a virus' biology and its interaction with the immune system shape the infectivity of a host. The biology of the process is encoded by the structure and parameters of the model that can be inferred statistically by fitting to viral load data. The main drawback of mechanistic models is that this inference is computationally expensive because the model must be repeatedly solved. This limits the size of the datasets that can be considered or the complexity of the models fitted. In this paper we develop a much cheaper inference method for this class of models by implementing a novel approximation of the model dynamics that uses a combination of random and deterministic processes. This approximation also properly accounts for process noise early in the infection when cell and virion numbers are small, which is important for the viral dynamics but often overlooked. Our method runs on a consumer laptop and is fast enough to facilitate a full hierarchical Bayesian treatment of the problem with sharing of information to allow for individual level parameter differences. We apply our method to simulated datasets and a reanalysis of COVID-19 monitoring data in an National Basketball Association cohort of 163 individuals.
Medical subject headings
- Models, Biological
- Host-Pathogen Interactions