Dynamics of killer T cell inflation in viral infections
Catherine
Lloyd
Auckland Bioengineering Institute, The University of Auckland
Model Status
This CellML model represents the second model in the original paper (this builds on the first 'core' model describing the basic dynamics of the cytotoxic T lymphocyte (CTL) infection by including a description of the CTL response to the virus infection). The model runs in OpenCell to recreate the results in the published paper. The units have been checked and they are consistent. The model also runs in COR but due to the long duration of the simulation is not ideal for use in COR.
Model Structure
ABSTRACT: Upon acute viral infection, a typical cytotoxic T lymphocyte (CTL) response is characterized by a phase of expansion and contraction after which it settles at a relatively stable memory level. Recently, experimental data from mice infected with murine cytomegalovirus (MCMV) showed different and unusual dynamics. After acute infection had resolved, some antigen specific CTL started to expand over time despite the fact that no replicative virus was detectable. This phenomenon has been termed as "CTL memory inflation". In order to examine the dynamics of this system further, we developed a mathematical model analysing the impact of innate and adaptive immune responses. According to this model, a potentially important contributor to CTL inflation is competition between the specific CTL response and an innate natural killer (NK) cell response. Inflation occurs most readily if the NK cell response is more efficient than the CTL at reducing virus load during acute infection, but thereafter maintains a chronic virus load which is sufficient to induce CTL proliferation. The model further suggests that weaker NK cell mediated protection can correlate with more pronounced CTL inflation dynamics over time. We present experimental data from mice infected with MCMV which are consistent with the theoretical predictions. This model provides valuable information and may help to explain the inflation of CMV specific CD8+T cells seen in humans as they age.
The original paper reference is cited below:
Dynamics of killer T cell inflation in viral infections, Dominik Wodarz, Sophie Sierro and Paul Klenerman, 2007, Journal of the Royal Society, Interface, volume 4, issue 14, 533-543. PubMed ID: 17251133
model diagram
Schematic diagram of the different components and variables included in the mathematical model of the dynamics of killer T cell inflation. The core model comprises five components: susceptible host cells (x), free virus particles (v), early-infected cells (y0), late-infected cells (y1), and latently-infected cells (L). When susceptible host cells become infected with virus, the product cells are either productively infected or are latently infected. Productively infected cells can be divided into two subsets; those which express early-gene products and those which express late-gene products. The latter produce new free virus particles and the replication cycle is completed. Latently infected cells are initially silent but can become activated, giving rise to more productively infected cells. Virus-specific CTL (za) divide on antigenic stimulation (ca) and kill virus-infected host cells through lysis (pa).
2007-06-22
Catherine Lloyd
Journal of the Royal Society, Interface
2007-07-17T00:00:00+00:00
Wodarz, Sierro and Klenerman's 2007 mathematical model of the dynamics of killer T cell inflation in viral infections.
basic reproductive ratio of the virus
R0
CMV specific effector CTL
za
Catherine
Lloyd
May
free virus particles
v
viral dynamics
NK cell
CTL
CD8+ T cell
immunology
murine cytomegalovirus
susceptible host cells
x
infected cells expressing late-viral gene products
y1
The University of Auckland
The Bioengineering Institute
543
4
533
Dynamics of killer T cell inflation in viral infections
c.lloyd@auckland.ac.nz
100
latently infected cells
L
Dominik
Wodarz
keyword
Dynamics of killer T cell inflation in viral infections (Core Model + CTL Response)
The University of Auckland, Bioengineering Institute
infected cells expressing early-viral gene products
y0
Paul
Klenerman
Sophie
Sierro
This is a CellML description of Wodarz, Sierro and Klenerman's 2007 mathematical model of the dynamics of killer T cell inflation in viral infections.
17251133
$\frac{d x}{d \mathrm{time}}=\mathrm{lambda}-dx+\mathrm{beta}xv+\mathrm{gamma}xv$
$\frac{d \mathrm{y0}}{d \mathrm{time}}=\mathrm{beta}xv-\mathrm{a0}\mathrm{y0}+\mathrm{eta}\mathrm{y0}+\mathrm{pa}\mathrm{y0}\mathrm{za}+\mathrm{phi}L$
$\frac{d \mathrm{y1}}{d \mathrm{time}}=\mathrm{eta}\mathrm{y0}-\mathrm{a1}\mathrm{y1}+\mathrm{pa}\mathrm{y1}\mathrm{za}$
$\frac{d L}{d \mathrm{time}}=\mathrm{gamma}xv-\mathrm{phi}L+dL$
$\frac{d v}{d \mathrm{time}}=k\mathrm{y1}-uv$
$\frac{d \mathrm{m\_8}}{d \mathrm{time}}=2r\mathrm{m\_7}-r\mathrm{m\_8}$
$\frac{d \mathrm{m\_7}}{d \mathrm{time}}=2r\mathrm{m\_6}-r\mathrm{m\_7}$
$\frac{d \mathrm{m\_6}}{d \mathrm{time}}=2r\mathrm{m\_5}-r\mathrm{m\_6}$
$\frac{d \mathrm{m\_5}}{d \mathrm{time}}=2r\mathrm{m\_4}-r\mathrm{m\_5}$
$\frac{d \mathrm{m\_4}}{d \mathrm{time}}=2r\mathrm{m\_3}-r\mathrm{m\_4}$
$\frac{d \mathrm{m\_3}}{d \mathrm{time}}=2r\mathrm{m\_2}-r\mathrm{m\_3}$
$\frac{d \mathrm{m\_2}}{d \mathrm{time}}=2r\mathrm{m\_1}-r\mathrm{m\_2}$
$\frac{d \mathrm{m\_1}}{d \mathrm{time}}=2r\mathrm{m\_0}-r\mathrm{m\_1}$
$\frac{d \mathrm{m\_0}}{d \mathrm{time}}=-r\mathrm{m\_0}$
$\frac{d \mathrm{za}}{d \mathrm{time}}=\mathrm{alpha}\mathrm{m\_8}+\mathrm{ca}(\mathrm{y0}+\mathrm{y1})\mathrm{za}-\mathrm{ba}\mathrm{za}\mathrm{log\_za}=\lg \mathrm{za}$
$\mathrm{R0}=\frac{\mathrm{lambda}\mathrm{eta}}{d\mathrm{a1}(\mathrm{a0}+\mathrm{eta})}(\mathrm{beta}+\frac{\mathrm{gamma}\mathrm{phi}}{\mathrm{phi}+d})$