A multi-scale immuno-epidemiological behavioral model for influenza-like illness: connecting scales through symptom scores
Abstract
For many infectious diseases, behavior change is not a population-level reaction to rising case counts, but a personal one, triggered by how sick an individual feels. Yet most models fail to capture how illness severity drives this response. Multi-scale models that link the immunological scale to the epidemiological scale seem well-suited for capturing this behavior. Most multi-scale models link within-host viral load to population-level transmission rates through linking functions that are a function of viral load. However, viral load is often misaligned with symptom severity and thus possibly ill-suited for the purpose of informing behavior at a population level. We present a novel multi-scale model in which symptomatic individuals dynamically modify their transmission based on systemic symptom scores (a composite measure of muscle ache, fatigue, headache, and feverishness informed by within-host immune dynamics) while asymptomatic individuals do not change behavior. We find that stronger illness-driven behavior change delays and lowers the epidemic peak. Moreover, the resulting epidemic trajectory remains qualitatively similar to that of a standard SEIR model without behavior change, across several distinct choices of linking functions connecting the two scales. This stands in contrast to models where behavior change is driven by population-level feedback (e.g., reported cases or deaths), which can produce qualitatively distinct signatures such as plateaus, shoulders, or an elongated epidemic decline. In the case when an exponential function of symptom score is used as a linking function, we show that the standard SEIR model can closely reproduce the total number of infectious individuals at a given point in time generated through the multi-scale level.
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BibTeX
@misc{pant2026multiscale,
title = {{A multi-scale immuno-epidemiological behavioral model for influenza-like illness: connecting scales through symptom scores}},
author = {Binod Pant and Summer Atkins and Necibe Tuncer and Hana M. Dobrovolny},
howpublished = {arXiv},
year = {2026},
month = oct,
doi = {10.48550/arxiv.2610.00862},
eprint = {2610.00862},
archivePrefix = {arXiv},
url = {https://arxiv.org/abs/2610.00862},
note = {CC BY 4.0},
}
RIS
TY - UNPB
TI - A multi-scale immuno-epidemiological behavioral model for influenza-like illness: connecting scales through symptom scores
AU - Binod Pant
AU - Summer Atkins
AU - Necibe Tuncer
AU - Hana M. Dobrovolny
PY - 2026
DA - 2026/10/01
PB - arXiv
DO - 10.48550/arxiv.2610.00862
UR - https://arxiv.org/abs/2610.00862
AB - For many infectious diseases, behavior change is not a population-level reaction to rising case counts, but a personal one, triggered by how sick an individual feels. Yet most models fail to capture how illness severity drives this response. Multi-scale models that link the immunological scale to the epidemiological scale seem well-suited for capturing this behavior. Most multi-scale models link within-host viral load to population-level transmission rates through linking functions that are a function of viral load. However, viral load is often misaligned with symptom severity and thus possibly ill-suited for the purpose of informing behavior at a population level. We present a novel multi-scale model in which symptomatic individuals dynamically modify their transmission based on systemic symptom scores (a composite measure of muscle ache, fatigue, headache, and feverishness informed by within-host immune dynamics) while asymptomatic individuals do not change behavior. We find that stronger illness-driven behavior change delays and lowers the epidemic peak. Moreover, the resulting epidemic trajectory remains qualitatively similar to that of a standard SEIR model without behavior change, across several distinct choices of linking functions connecting the two scales. This stands in contrast to models where behavior change is driven by population-level feedback (e.g., reported cases or deaths), which can produce qualitatively distinct signatures such as plateaus, shoulders, or an elongated epidemic decline. In the case when an exponential function of symptom score is used as a linking function, we show that the standard SEIR model can closely reproduce the total number of infectious individuals at a given point in time generated through the multi-scale level.
ER -