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In silico investigation into dendritic cell regulation of CD8Treg mediated killing of Th1 cells in murine experimental autoimmune encephalomyelitis
BMC Bioinformatics volume 14, Article number: S9 (2013)
Experimental autoimmune encephalomyelitis has been used extensively as an animal model of T cell mediated autoimmunity. A down-regulatory pathway through which encephalitogenic CD4Th1 cells are killed by CD8 regulatory T cells (Treg) has recently been proposed. With the CD8Treg cells being primed by dendritic cells, regulation of recovery may be occuring around these antigen presenting cells. CD4Treg cells provide critical help within this process, by licensing dendritic cells to prime CD8Treg cells, however the spatial and temporal aspects of this help in the CTL response is currently unclear.
We have previously developed a simulator of experimental autoimmune encephalomyelitis (ARTIMMUS). We use ARTIMMUS to perform novel in silico experimentation regarding the priming of CD8Treg cells by dendritic cells, and the resulting CD8Treg mediated killing of encephalitogenic CD4Th1 cells. Simulations using dendritic cells that present antigenic peptides in a mutually exclusive manner (either MBP or TCR-derived, but not both) suggest that there is no significant reliance on dendritic cells that can prime both encephalitogenic CD4Th1 and Treg cells. Further, in silico experimentation suggests that dynamics of CD8Treg priming are significantly influenced through their spatial competition with CD4Treg cells and through the timing of Qa-1 expression by dendritic cells.
There is no requirement for the encephalitogenic CD4Th1 cells and cytotoxic CD8Treg cells to be primed by the same dendritic cells. We conjecture that no significant portion of CD4Th1 regulation by Qa-1 restricted CD8Treg cells occurs around individual dendritic cells, and as such, that CD8Treg mediated killing of CD4Th1 cells occurring around dendritic cells is not critical for recovery from the murine autoimmune disease. Furthermore, the timing of the CD4Treg licensing of dendritic cells and the spatial competition between CD4Treg and CD8Treg cells around the dendritic cell is critical for the size of the cytotoxic T lymphocyte response, because dendritic cells have a limited lifespan. If treatments can be found to either speed up the licensing process, or increase the spatial competitiveness of CD8Treg cells, the magnitude of the cytotoxic T lymphocyte response can be increased.
Under normal circumstances, self-tolerance mechanisms ensure the host's immune system does not react against self antigens . When these self-tolerance mechanisms fail, autoimmune responses occur, which may culminate in the development of autoimmune disease(s). Experimental autoimmune encephalomyelitis (EAE) is an animal model of T cell mediated autoimmune diseases in general, and multiple sclerosis (MS) in particular . The animal disease is mediated through a network of cells (see Figure 1); encephalitogenic T helper cells are activated in the peripheral lymph nodes following immunization for EAE, and migrate to the central nervous system (CNS) where they induce activation of microglia, macrophages and dendritic cells (DCs) . The resultant inflammation causes demyelination of neurons, prompting the presentation of myelin basic protein (MBP) to additional encephalitogenic T cell populations in the cervical lymph nodes (CLN) by migratory DCs. The spontaneous recovery that occurs following autoimmune episodes is associated with a major reduction in the T cell infiltrate in the CNS . Recent evidence indicates that encephalitogenic CD4Th1 cells undergo selective T cell mediated regulation; CD4 T regulatory cells (CD4Treg) help DCs in priming CD8 T regulatory cells (CD8Treg) that induce selective apoptotic elimination of CD4Th1 cells [5, 6]. The DCs mediate down-regulation of the autoimmune response through the expression of Qa-1 (a MHC class Ib molecule, first discovered by Cantor et al ), which facilitates the priming of CD8Treg cells, for subsequent killing of encephalitogenic CD4Th1 cells .
The exact location of killing of the encephalitogenic CD4Th1 cells, and thus down-regulation of the autoimmune response by CD8Treg cells, is unknown. One possibility is that DCs migrating from the CNS, potentially carrying both MBP (from neurons) and T cell receptor (TCR) derived peptides, are simultaneously priming both CD4Th1 and Treg cell populations , and that regulation of autoimmunity is taking place around the DC. Effector CD4Th1 cells contain framework region 3 (Fr3) and complementarity determining region 1/2 (CDR1/2) peptides within their TCR molecules, and once efferocytosed by a DC, there is a probabilistic chance that the DC will present the Fr3 and CDR1/2 peptides on MHC class II molecules. Tang et al  suggest that the CD8Treg response is cross-primed by DCs that have efferocytosed apoptotic CD4Th1 cells and present TCR-derived peptide to both CD4Treg and CD8Treg cells [8, 10]. Kumar and colleagues [11–13] found that CD4Treg cells may then become activated by binding to the Fr3-MHCII complex of an antigen presenting cell (e.g. DC or microglia). Conversely, CD8Treg cells recognise TCR-derived peptides relating to the CDR1/2 regions, which have been cross-presented on MHC class I molecules.
The spatial and temporal features of EAE lend themselves well to being modelled using an agent-based approach. In this paper we investigate the effect of regulation of CD4Th1 cells by CD8Treg cells through use of a simulation (ARTIMMUS), which we have previously developed to support investigation into EAE . We investigate three hypotheses, the first hypothesis is that a significant portion of CD4Th1 and CD8Treg cell priming occurs simultaneously around the same DCs. The second hypothesis (termed the age of licensing hypothesis) is that the timing of Qa-1 expression by DCs has a significant effect on the size of the CD8Treg effector cell population. The third hypothesis (termed the spatial saturation hypothesis) is that spatial competition between CD4Treg and CD8Treg cells around DCs on which they prime, has a significant effect on the size of the CD8Treg effector cell population. We have performed a number of in silico experiments to further understand the priming dynamics of CD8Treg cells by DCs against these three hypotheses. In order to establish control simulation dynamics, we have reproduced the baseline generated from development of the simulator . Figure 2 illustrates the relevant cell populations within the simulator under control conditions.
Although much is known on the mechanics of antigen-presentation , it is unknown whether the individual DC can simultaneously prime both encephalitogenic CD4Th1 and Treg cell populations. If so, then key regulatory action might be taking place around the DCs that prime these populations. The first experiment therefore examined priming dynamics of CD8Treg cells in relation to the antigenic peptide presentation by DCs to ascertain whether an individual DC can prime both encephalitogenic CD4Th1 and CD8Treg cells in parallel. The second and third experiments investigate the manner that help (as provided by CD4Treg cells) can modulate the regulatory immune response. The time required for CD4Treg to license the DC for Qa-1 expression, and spatial competition between CD4Treg and CD8Treg priming on the same DC, may in fact have a limiting effect on the magnitude of the CD8Treg cytotoxic T lymphocyte (CTL) response. In the control simulation, it takes approximetaly 60 hours for CD4Treg cells to mature into effectors and license DCs for Qa-1 expression. Manipulation of the time at which DCs express Qa-1 may affect the timing of CD8Treg cell priming and activation, with earlier expression of Qa-1, permitting populations of CD8Treg cells more time for proliferative activity within the lifetime of DCs on which they prime. Similarly, manipulation of the spatial competition between CD4Treg and CD8Treg cells for binding space around DCs, may also affect CD8Treg dynamics. Both CD4Treg and CD8Treg cells can prime on the same DCs, and therefore compete for spatial access to DC. Since CD4Treg cells may begin priming immediately upon DC maturation, with CD8Treg cells waiting for the DC to be licensed, CD4Treg cells would be expected to occupy a greater fraction of the total space around the DC. If spatial competition is a limiting factor in CD8Treg population expansion, then an increase in the competitive strength shown by CD8Treg cells, would enhance the resulting CTL response, as a greater number of CD8Treg cells would be primed.
Results and discussion
Effective regulation does not require CD4Th1 and CD8Treg to prime on the same DC
We examined the peptide presentation profiles for DCs in silico using ARTIMMUS, and showed that the vast majority (circa 90%) do not present antigenic peptides, and of those that do, the overwhelming majority (circa 90%; or 9% of total DCs) present either MBP or TCR-derived peptides, but not both. In fact, only 1% of DCs within the simulation present both MBP and TCR-derived peptides.
When imposing mutually exclusive presentation on DCs (Figure 3), where a DC cannot simultaneously present both MBP- and TCR-derived peptides, we find a small reduction (A-Test score = 0.427) in the number of DCs presenting TCR-derived peptides, and a small increase in the number of DCs presenting MBP-derived peptides (A-Test score = 0.635). This leads to an approximate 10% reduction in the priming of CD8Treg cells within the system, which leads to an approximate 5% reduction overall in the total number of CD4Th1 cells which are killed by the CD8Treg population. Next we examined the effect of mutually exclusive presentation on priming DCs within the cervical lymph node (CLN) where DCs prime both populations of T cells (CD4Th1 and CD4Treg). We find a small, but not scientifically significant, reduction in the CD4Th1 killing facilitated by CD8Treg cells with respect to control simulations (A-Test score for total CD4Th1 apoptosis = 0.415, and CD4Th1 apoptosis within the CLN = 0.44). This indicates that enforcing mutually exclusive antigenic presentation has no scientifically significant effect on the regulating capacity, and as such, we conjecture that killing does not take place around the DC.
Timing of Qa-1 expression by dendritic cells modulates the regulatory response
The control simulation uses two-way signalling between DCs and CD4Treg cells. CD4Treg cells are activated through a MHCII-Fr3 complex (signal 1), and once they become effector cells, if a CD40-CD40L bind is also formed (signal 2), the CD4Treg licenses the DC to express Qa-1 (we have termed this help within the abstracted model represented by the simulator). Expression of Qa-1 leads to the activation of CD8Treg cells (through cross-priming by a Qa-1-CDR1/2 complex), and subsequent apoptosis of CD4Th1 cells. This raises the question of how variations in the timing of CD40-CD40L interactions may modulate the CD8Treg CTL response.
The limiting nature of time required for DC licensing on the CD8Treg response was investigated through delaying the time upon which a DC can express Qa-1, and thus gain the ability to prime CD8Treg cells (Figure 4, see methods section for the derivation of this figure). In this context, timing of Qa-1 expression, means the expression of optimal levels of Qa-1/TCR-peptide complexes (along with costimulatory molecules) on the surface of DCs enabling the priming of the CD8Treg. This Qa-1 expression delay has been defined within the simulation as the median time taken for a DC to become licensed by a CD4Treg under control conditions (60 hours). We removed the CD4Treg population from our experimental simulations to allow manipulation of the time delay before Qa-1 is constitutively expressed, and upregulate Qa-1 expression on DCs after a pre-specified period of time following their maturation. We demonstrate a medium-level increase to the peak population of CD8Treg cells (relative to the control dynamics) following the shorter delay in Qa-1 expression (A-Test score = 0.704). Conversely, simulations employing an increased delay to Qa-1 expression (82 hours) demonstrate a large, and scientifically significant, decrease in the peak population of CD8Treg cells with respect to control dynamics (A-Test score = 0.163). As would be expected, this demonstrates a large, and scientifically significant decrease between the two delay periods (A-Test score = 0.090). This indicates that the timing of Qa-1 expression by DCs has a significant affect on modulating the regulatory CD8Treg CTL response.
Spatial competition between CD4Treg and CD8Treg cells around the dendritic cell modulates the regulatory response
Along with the temporal dynamics, the nature of help from CD4Treg cells within this system also imposes a spatial effect on CD8Treg priming. Simulations employing modified CD8Treg spatial occupancy rules, which allow CD8Treg cells to occupy space regardless of the CD4Treg that may already reside there (see Figure 5), demonstrate that the peak population of CD8Treg cells has undergone a large, scientifically significant, increase relative to the control simulation (A-Test score = 0.999). This indicates that spatial competition between CD4Treg and CD8Treg cells has a significant effect on modulating the regulatory CD8Treg CTL response.
We have sought to investigate, through simulation, whether CD4Th1 and CD8Treg cells need to be primed on the same DC, and whether temporal and spatial mechanisms may regulate the CD8Treg CTL response within EAE. As Beeston et al  have firmly established that CD8Treg cells induce the killing of encephalitogenic CD4Th1 cells, our first hypothesis was that a significant degree of priming of these two cell populations occurs simultaneously around the same DCs. Observation of DC peptide presentation profiles has established that only 10% of DCs that are able to prime T cells simultaneously prime both CD4Th1 and CD8Treg populations. Furthermore, given our criteria for scientifically significant results, A-Test scores indicate that no significant difference in the ability of CD8Treg cells to regulate the CD4Th1 population arises from this manipulation. We therefore conclude that the killing of CD4Th1 cells as induced by CD8Treg cells does not critically rely on these T cell populations being primed on the same DCs, and conjecture that it is probable that killing of CD4Th1 cells does not take place around the DC, as such we reject the first hypothesis.
The second hypothesis concerned the timing of help provided by CD4Treg cells, through the time at which Qa-1 was expressed by DCs. We have found that delaying Qa-1 expression by DCs has a significant effect on the CD8Treg effector cell population. We therefore conclude that the timing of Qa-1 expression by DCs modulates the regulatory response, and as such accept the second age of licensing hypothesis, that the time delay in licensing is significant in modulating the regulatory CD8Treg CTL response. The third hypothesis concerned the binding space available around DCs, because although CD4Treg cells license DCs to provide critical help for the recovery from autoimmune response, their physical presence may limit the size of this CD8Treg CTL response. By relaxing spatial competition for CD8Treg, allowing them to occupy space and gain access to DCs regardless of CD4Treg presence, we found a significant effect on the CD8Treg effector cell population. We therefore conclude that spatial competition between CD4Treg and CD8Treg cells around the DC modulates the regulatory response, and as such accept the third spatial saturation hypothesis.
Results from the experiments regarding temporal dynamics and spatial dynamics suggest that both factors could serve to control the CTL response through altering the size of the CD8Treg cell population. Through this work, it is evident that although CD4Treg cells are required as part of the regulatory response via their capacity to provide help, they also exert a restraining influence on the population size of CD8Treg cells by virtue of their modulation of CD8Treg-DC interactions through spatial competition. Although these results are grounded specifically in the EAE system, we believe the spatial and temporal constraints that CD4Th help (provided by CD4Treg to CD8Treg in our simulation) imposes are applicable to CTL responses in general, and have significance in the design of treatments based on manipulating the CTL response. For example, by providing artificial help to DCs (through anti-CD40 antibodies) that prime cytotoxic T cells, the CD4Th cell-imposed delay in licensing can be removed, invoking an earlier CTL response of larger magnitude. If the CD4Th population were to be abrogated and suitable artificial cytokine and signalling surrogates administered, the spatial restrictions that help imposes, could be alleviated to effect a larger CTL response.
Taken together the analysis from these experiments show that CD4Th1 cells and Treg cells do not need to be primed by the same DC in order for down-regulation of the autoimmune response to occur. They have also shown that regulation of CTL responses (through CD8Treg cells within our simulation) appears to be limited by the nature of help provided by CD4Treg cells, and the spatial competition that results around priming dendritic cells. Although simulation results cannot, as yet, be confirmed using in vitro or in vivo testing, our work has shown that temporal dynamics of Qa-1 expression and spatial competition around DCs is very important for the modulation of the CTL regulatory response.
The simulator (ARTIMMUS) was previously developed  in Java and the MASON modelling and simulation framework . Within simulation runs, immunization is through MBP, a myelin derivative, and adjuvant. CD4Th cells are initially naive and start without a polarisation; once polarised they make a probabilistic decision to become either type1 or type2. This is affected by the cytokine profiles present locally at the time of priming. The adjuvant produces a type1 polarisation in DCs that perceive them. Type 1 DCs secrete type1 cytokine, which faciltate the majority of CD4Th cells to adopt a type1 polarisation upon their activation, with a small residual number adopting a type2 polarisation. For the purposes of statistical analysis, 1000 individual simulations for each experiment were run on a server cluster. Matlab was used to analyze cell populations and population level behavior.
The ARTIMMUS simulator generates large volumes of data for each simulation run. Non-parametric effect magnitude tests [18, 19], termed A-Tests, are used to measure scientific significance (effect size) of the difference between cell populations from simulation experiments with respect to control cell populations. The A-Test provides a score in the range [0.0, 1.0] that represents the probability that a randomly selected sample from population one is larger than a randomly selected sample from population two. Vargha and Delaney  provide thresholds to indicate the magnitude of difference between two populations. They indicate scores >0.71 and <0.29 to represent large differences, and we assume these boundaries to indicate scientific significance. For completeness, they also indicate: 0.64< score <0.71 and 0.29< score <0.36 to represent medium differences, and 0.50< score <0.56 and 0.44< score <0.50 to represent small differences. We have chosen to use a non-parametric test in order to avoid the assumption that the underlying populations of simulator results tend towards normality. We use an effect magnitude test to determine scientific significance in place of statistical significance because with computer simulations, a sufficiently large enough number of simulation runs can always be performed, which will reveal a statistical significance, unless the variable of interest truly has no effect. We use the A-Test in preference to simply measuring the difference in median values since the differences in medians does not take the spread of the data into account (for a more detailed justification please refer to Read et al ). The A-Test was used to assess the significance of experimental results with the control data.
Mutually exclusive peptide presentation by dendritic cells
The significance of antigenic peptide presentation by DCs on the dynamics of CD8Treg priming was assessed. To investigate peptide presentation dynamics, we have manipulated ARTIMMUS such that presentation of antigenic peptide by DCs is mutually exclusive; DCs are no longer able to present both MBP- and TCR-derived peptides. This manipulation to ARTIMMUS allows DCs to efferocytose cells as normal, however only the peptide type (MBP- or TCR-derived) associated with the cell that was first engulfed and processed into functional peptides, can become presented on major histocompatibility complexes (MHCs) of the DC. This negates the ability of a single DC to prime both CD4Th1 and CD4Treg cells, allowing us to observe the effects on the system. To ensure individual DCs were only counted once, counts were taken of DCs that had entered apoptosis by the end of the simulation.
Temporal dynamics of CD8Treg priming by dendritic cells
The significance of the effect of the time at which Qa-1 is expressed by DCs was assessed. Licensing of DCs to express Qa-1 within the control simulation code is via CD4Treg cells. In order to manipulate the time at which Qa-1 is expressed, we abrogated CD4Treg cells from the simulation, and to ensure continued priming of CD8Treg cells we incorporated functionality for expression of Qa-1 by DCs, following specific time delays. In this context, timing of Qa-1 expression, means the expression of optimal levels of Qa-1/TCR-peptide complexes (along with costimulatory molecules) on the surface of DCs enabling the priming of the CD8Treg.
A control experiment was performed to record the distribution of ages of DCs at their time of licensing. The overall median age of licensing was calculated as 74 hours. An investigation of variation in DC age at time of licensing showed that the overall age distribution could be divided into two distinct sub-populations. The median ages at the time of DC licensing for these two sub-populations were calculated as 60 hours and 82 hours . These medians were used to parametrize enforced delays in the Qa-1 expression by DCs. The division between the two sub-populations related to DCs created before or after day 20. This is the point in the simulation (see Figure 2 Control Dynamics) where the number of CD4Treg cells and CD4Th1 cells are equal, with the CD4Treg cell population rapidly increasing and the CD4Th1 cell population rapidly decreasing.
Spatial dynamics of CD8Treg priming by dendritic cells
In a preliminary experiment we recorded the number and nature of all T-cell neighbours of apoptotic DCs. From this data we were able to ascertain a median number of CD8Treg cells that were neighbours around a DC in a control experiment in which the CD4Treg population had been abrogated. We then used this number as an upper limit for the number of CD8Treg cells that could occupy a simulation grid space irrespective of how many CD4Treg cells were currently resident in that space. Using these modified CD8Treg occupancy rules, we ran further baseline simulations to examine the effect of reduced CD8Treg/CD4Treg spatial competition on CD8Treg cell population size.
van Parijs L, Abbas A: Homeostasis and Self-Tolerance in the Immune System: Turning Lymphocytes off. Science. 1998, 280: 243-248. 10.1126/science.280.5361.243.
Huitinga I, van Rooijen N, de Groot C, Uitdehaag B, Dijkstra C: Suppression of Experimental Allergic Encephalomyelitis in Lewis Rats after Elimination of Macrophages. Journal of Experimental Medicine. 1990, 172: 1025-1033. 10.1084/jem.172.4.1025.
Pender M: Experimental autoimmune encephalomyelitis. Autoimmune Neurological Disease. Edited by: Pender M, McCombe P. 1995, Cambridge: Cambridge University Press, 26-88.
McCombe P, de Jersey J, Pender M: Inflammatory Cells, Microglia and MHC Class II Antigen-Positive Cells in the Spatial Cord of Lewis Rats with Acute and Chronic Relapsing Experimental Autoimmune Encephalomyelitis. Journal of Neuroimmunology. 1994, 51: 163-167.
Tang X, Smith T, Kumar V: Specific control of immunity by regulatory CD8 T cells. Cellular and Molecular Immunology. 2005, 2: 11-19.
Cantor H, Hugenberger J, McVay-Boudreau L, Eardley D, KEmp J, Shen F, Gershon R: Immunoregulatory Circuits among T Cell Sets: Identification of a Subpopulation of T-Helper Cells that Induces Feedback Inhibition. Journal of Experimental Medicine. 1978, 148: 871-877. 10.1084/jem.148.4.871.
Panoutsakopoulou V, Huster K, McCarty N, Feinberg E, Wang R, Wucherpfennig K, Cantor H: Suppression of Autoimmune Disease after Vaccination with Autoreactive T Cells that Express Qa-1 Peptide Complexes. Journal of Clinical Investigation. 2004, 113: 1218-1224.
Kumar V, Sercarz E: Distinct Levels of Regulation in Organ-Specific Autoimmune Diseases. Life Sciences. 1999, 65 (15): 1523-1530. 10.1016/S0024-3205(99)00198-8.
Tang X, Maricic I, Purohit N, Bakamjian B, Reed-Loisel LM, Beeston T, Jensen P, Kumar V: Regulation of Immunity by a Novel Population of Qa-1-Restricted CD8 αα+TCRαβ+ T Cells. Journal of Immunology. 2006, 177: 7645-7655.
Smith T, Kumar V: Immune Suppression by a Novel Population of CD8 αα+TCR αβ+ Regulatory T Cells. Regulatory T Cells and Clinical Applications. Edited by: Jiang S. 2008, Springer, 489-500.
Kumar V, Sercarz E: The Involvement of T Cell Receptor Peptide-Specific Regulatory CD4+ T Cells in Recovery from Antigen-induced Autoimmune Disease. Journal of Experimental Medicine. 1993, 178: 909-916. 10.1084/jem.178.3.909.
Kumar V, Tabibiazar R, Geysen H, Sercarz E: Immunodominant Framework Region 3 Peptide from TCR Vβ 8.2 Chain Controls Murine Experimental Autoimmune Encephalomyelitis. Journal of Immunology. 1995, 154: 1941-1950.
Kumar V, Stellrecht K, Sercarz E: Inactivation of T Cell Receptor Peptide-Specific CD4 Regulatory T Cells Induces Chronic Experimental Autoimmune Encephalomyelitis (EAE). Journal of Experimental Medicine. 1996, 184: 1609-1617. 10.1084/jem.184.5.1609.
Read M: Statistical and modelling techniques to investigate immunology through agent-based simulation. PhD thesis. 2011, University of York, Computer Science Department, [http://etheseswhiterose.ac.uk/2174]
Guermonprez P, Valladeau J, Zitvogel L, Thery C, Amigorena S: Antigen Presentation and T Cell Stimulation by Dendritic Cells. Annual Review of Immunology. 2002, 20: 621-667. 10.1146/annurev.immunol.20.100301.064828.
Beeston T, Smith T, Maricic I, Tang X, Kumar V: Involvement of IFN-γ and Perforin, but not Fas/FasL Interactions in Regulatory T cell-mediated Suppression of Experimental Autoimmune Encephalomyelitis. Journal of Neuroimmunology. 2010, 229: 91-97. 10.1016/j.jneuroim.2010.07.007.
Luke S, Cioffi-Revilla C, Panait L, Sullivan K, Balan G: MASON: A Multiagent Simulation Environment. Simulation. 2005, 81: 517-527. 10.1177/0037549705058073.
Mann H, Whitney D: On a Test of Whether One of Two Random Variables is Stochastically Larger than the Other. The Annals of Mathematical Statistics. 1947, 18: 50-60. 10.1214/aoms/1177730491.
Vargha A, Delaney H: A Critique and Improvement of the CL Common Language Effect Size Statistics of McGraw and Wong. Journal of Educational and Behavioral Statistics. 2000, 25: 101-132.
Read M, Andrews P, Timmis J, Kumar V: Techniques for grounding agent-based simulations in the real domain: a case study in experimental autoimmune encephalomyelitis. Mathematical and Computer Modelling of Dynamical Systems. 2012, 18: 67-86. 10.1080/13873954.2011.601419.
Greaves R: Computational Modelling of Treg Networks in Experimental Autoimmune Encephalomyelitis. Master's thesis. 2011, University of York, Computer Science Department, [http://etheseswhiterose.ac.uk/1980/]
Williams RA, Read M, Timmis J, Andrews PS, Kumar V: In Silico Investigation into CD8Treg Mediated Recovery in Murine Experimental Autoimmune Encephalomyelitis. International Conference on Artificial Immune Systems (ICARIS), Volume 6825 of. Edited by: Lio P, Nicosia G, Stibor T. 2011, Lecture Notes in Computer Science, 51-54.
Kumar V, Sercarz E: An integrative model of regulation centered on recognition of TCR peptide/MHC complexes. Immunological Reviews. 2001, 182: 113-121. 10.1034/j.1600-065X.2001.1820109.x.
This paper represents a major extension of an abstract  that was presented at the 10th International Conference on Artificial Immune Systems (ICARIS 2011), held in Cambridge, July 2011. Paul S Andrews was supported by EPSRC grant number EP/E053505/1 and now EPSRC grant number EP/I005943/1. Mark Read and Jon Timmis are supported by the EC funded CoCoRo Project, GA 270382 [http://cocoro.uni-graz.at/drupal/]. Richard A Williams, Jon Timmis and Mark Read also acknowledge financial support from EP/E053505/1 and the Non-Standard Computation Group, University of York. Jon Timmis would also like to acknowledge support from the Royal Society. VK is supported by grants from the National Institutes of Health, USA and from the Multiple Sclerosis National Research Institute.
This article has been published as part of BMC Bioinformatics Volume 14 Supplement 6, 2013: Selected articles from the 10th International Conference on Artificial Immune Systems (ICARIS). The full contents of the supplement are available online at http://www.biomedcentral.com/bmcbioinformatics/supplements/14/S6.
The authors declare that they have no competing interests.
Williams undertook the mutually exclusive peptide presentation experimentation and was lead author on the development of the manuscript, Greaves performed the temporal dynamics and spatial dynamics experimentation and assisted in the manuscript production. Andrews, Read, Kumar and Timmis were involved in the design of the experiments and manuscript production. Kumar provided immunological interpretation of the results.
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Williams, R.A., Greaves, R., Read, M. et al. In silico investigation into dendritic cell regulation of CD8Treg mediated killing of Th1 cells in murine experimental autoimmune encephalomyelitis. BMC Bioinformatics 14, S9 (2013). https://doi.org/10.1186/1471-2105-14-S6-S9
- Dendritic Cell
- Experimental Autoimmune Encephalomyelitis
- Myelin Basic Protein
- Control Simulation
- Spatial Competition