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| Format: | Preprint |
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2025
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| Online Access: | https://arxiv.org/abs/2503.19665 |
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| _version_ | 1866918137880903680 |
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| author | Taye, Mesfin |
| author_facet | Taye, Mesfin |
| contents | Due to the persistence of latently infected CD4$^+$ T cells, achieving a functional cure for HIV-1 remains a significant challenge since the viruses are able to evade immune clearance, which in turn enables post-treatment viral rebound. Because traditional deterministic models assume a constant reactivation rate, they fail to capture the stochastic nature of latency reversal influenced by immune perturbations and ART pharmacokinetics. Thus, in this study, by using a Poisson-driven stochastic framework that incorporates fluctuations in activation rates, we study viral rebound dynamics. Via an exponentially decreasing drug washout model, we accurately quantifies the nonlinear interplay between ART decay and stochastic reactivation, improving the theoretical estimates of post-treatment control. Beyond the introduction of stochasticity, our model establishes a time-dependent viral reactivation framework that integrates periodic and random perturbations in the activation rates. Unlike conventional models that assume uniform (temporally independent reactivation), we show that latency reversal follows structured oscillatory patterns modulated by immune cycles, circadian rhythms, and transient inflammatory episodes. This finding suggests that viral rebound risk is dynamically shaped by immune fluctuations, contrary to the assumption of a constant reactivation probability. We also study the model system by incorporating Gamma-distributed waiting times to account for heterogeneity in reactivation kinetics, which in turn provides a more flexible characterization of reservoir dynamics. We believe that these insights have critical implications for HIV cure strategies. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2503_19665 |
| institution | arXiv |
| publishDate | 2025 |
| record_format | arxiv |
| spellingShingle | Drug Washout and Viral Rebound: Modeling HIV Reactivation Under ART Discontinuation Taye, Mesfin Biological Physics Due to the persistence of latently infected CD4$^+$ T cells, achieving a functional cure for HIV-1 remains a significant challenge since the viruses are able to evade immune clearance, which in turn enables post-treatment viral rebound. Because traditional deterministic models assume a constant reactivation rate, they fail to capture the stochastic nature of latency reversal influenced by immune perturbations and ART pharmacokinetics. Thus, in this study, by using a Poisson-driven stochastic framework that incorporates fluctuations in activation rates, we study viral rebound dynamics. Via an exponentially decreasing drug washout model, we accurately quantifies the nonlinear interplay between ART decay and stochastic reactivation, improving the theoretical estimates of post-treatment control. Beyond the introduction of stochasticity, our model establishes a time-dependent viral reactivation framework that integrates periodic and random perturbations in the activation rates. Unlike conventional models that assume uniform (temporally independent reactivation), we show that latency reversal follows structured oscillatory patterns modulated by immune cycles, circadian rhythms, and transient inflammatory episodes. This finding suggests that viral rebound risk is dynamically shaped by immune fluctuations, contrary to the assumption of a constant reactivation probability. We also study the model system by incorporating Gamma-distributed waiting times to account for heterogeneity in reactivation kinetics, which in turn provides a more flexible characterization of reservoir dynamics. We believe that these insights have critical implications for HIV cure strategies. |
| title | Drug Washout and Viral Rebound: Modeling HIV Reactivation Under ART Discontinuation |
| topic | Biological Physics |
| url | https://arxiv.org/abs/2503.19665 |