A spatial model of the efficiency of T cell search in the influenza-infected lung
Authored by Soumya Banerjee, Melanie Moses, Stephanie Forrest, Drew Levin, Candice Clay, Judy Cannon, Frederick Koster
Date Published: 2016
DOI: 10.1016/j.jtbi.2016.02.022
Sponsors:
No sponsors listed
Platforms:
CyCells
Model Documentation:
Other Narrative
Mathematical description
Model Code URLs:
Model code not found
Abstract
Emerging strains of influenza, such as avian H5N1 and 2009 pandemic
H1N1, are more virulent than seasonal H1N1 influenza, yet the underlying
mechanisms for these differences are not well understood. Subtle
differences in how a given strain interacts with the immune system are
likely a key factor in determining virulence. One aspect of the
interaction is the ability of T cells to locate the foci of the
infection in time to prevent uncontrolled expansion. Here, we develop an
agent based spatial model to focus on T cell migration from lymph nodes
through the vascular system to sites of infection. We use our model to
investigate whether different strains of influenza modulate this
process.
We calibrate the model using viral and chemokine secretion rates we
measure in vitro together with values taken from literature. The spatial
nature of the model reveals unique challenges for T cell recruitment
that are not apparent in standard differential equation models. In this
model comparing three influenza viruses, plaque expansion is governed
primarily by the replication rate of the virus strain, and the
efficiency of the T cell search-and-kill is limited by the density of
infected epithelial cells in each plaque. Thus for each virus there is a
different threshold of T cell search time above which recruited T cells
are unable to control further expansion. Future models could use this
relationship to more accurately predict control of the infection. (C)
2016 Elsevier Ltd. All rights reserved.
Tags
Dendritic cells
Central-nervous-system
A virus-infection
Antigen presentation
Bronchial epithelial-cells
Adaptive immune-response
Inflammatory response
Chemokine expression
Human alveolar
Lymph-node