Abstract

Chronic hepatitis B (HBV) infection is a major cause of human suffering, and a number of mathematical models have examined the within-host dynamics of the disease. Most previous models assumed that infected hepatocytes do not proliferate; however, the effect of HBV infection on hepatocyte proliferation is controversial, with conflicting data showing both induction and inhibition of proliferation. With a family of ordinary differential equation (ODE) models, we explored the dynamical impact of proliferation among HBV-infected hepatocytes. Here, we show that infected hepatocyte proliferation in this class of models generates a threshold that divides the dynamics into two categories. Sufficiently compromised proliferation in infected cells produces complex dynamics characterized by oscillating viral loads, whereas higher proliferation generates straightforward dynamics that always results in chronic infection, sometimes with liver failure. A global stability result of the liver failure state was included as it is unique to this class of models. Finally, the model analysis motivated a testable biological hypothesis: Healthy hepatocytes are present in chronic HBV infection if and only if the proliferation of infected hepatocytes is severely impaired.

Highlights

  • Hepatitis B virus (HBV) is a global public health problem

  • Goyal et al [42] suggested that infected hepatocytes proliferating to produce uninfected daughter cells may be an important dynamic in preventing acute HBV infection, which directly affects up to 99% of hepatocytes, from progressing to the chronic state

  • We rigorously explored how adding proliferation in infected hepatocytes, in addition to logistic growth in general and the standard incidence term for viral infection, affects the dynamics of basic chronic HBV models

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Summary

Introduction

Hepatitis B virus (HBV) is a global public health problem. It infects hepatocytes, the main cells found in the liver, and can lead to chronic liver disease, cirrhosis, and liver cancer. We rigorously explored how adding proliferation in infected hepatocytes, in addition to logistic growth in general and the standard incidence term for viral infection, affects the dynamics of basic chronic HBV models. The analysis of these models is not intended to provide evidence as to whether infected hepatocytes proliferate or not, but does yield a testable biological hypothesis: healthy hepatocytes are present in chronic HBV infection if and only if the proliferation of infected hepatocytes is severely impaired.

Model Development and Dynamics
Infected Hepatocytes Proliferating at the Same Rate
Infected Hepatocytes Proliferating at a Different Rate
Global Stability Result for E0
Findings
Discussion
Full Text
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