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A Biased Competition Theory of Cytotoxic T Lymphocyte Interaction with Tumor Nodules
The dynamics of the interaction between Cytotoxic T Lymphocytes (CTL) and tumor cells has been addressed in depth, in particular using numerical simulations. However, stochastic mathematical models that take into account the competitive interaction between CTL and tumors undergoing immunoediting, a...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4376944/ https://www.ncbi.nlm.nih.gov/pubmed/25815811 http://dx.doi.org/10.1371/journal.pone.0120053 |
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author | Christophe, Claire Müller, Sabina Rodrigues, Magda Petit, Anne-Elisabeth Cattiaux, Patrick Dupré, Loïc Gadat, Sébastien Valitutti, Salvatore |
author_facet | Christophe, Claire Müller, Sabina Rodrigues, Magda Petit, Anne-Elisabeth Cattiaux, Patrick Dupré, Loïc Gadat, Sébastien Valitutti, Salvatore |
author_sort | Christophe, Claire |
collection | PubMed |
description | The dynamics of the interaction between Cytotoxic T Lymphocytes (CTL) and tumor cells has been addressed in depth, in particular using numerical simulations. However, stochastic mathematical models that take into account the competitive interaction between CTL and tumors undergoing immunoediting, a process of tumor cell escape from immunesurveillance, are presently missing. Here, we introduce a stochastic dynamical particle interaction model based on experimentally measured parameters that allows to describe CTL function during immunoediting. The model describes the competitive interaction between CTL and melanoma cell nodules and allows temporal and two-dimensional spatial progression. The model is designed to provide probabilistic estimates of tumor eradication through numerical simulations in which tunable parameters influencing CTL efficacy against a tumor nodule undergoing immunoediting are tested. Our model shows that the rate of CTL/tumor nodule productive collisions during the initial time of interaction determines the success of CTL in tumor eradication. It allows efficient cytotoxic function before the tumor cells acquire a substantial resistance to CTL attack, due to mutations stochastically occurring during cell division. Interestingly, a bias in CTL motility inducing a progressive attraction towards a few scout CTL, which have detected the nodule enhances early productive collisions and tumor eradication. Taken together, our results are compatible with a biased competition theory of CTL function in which CTL efficacy against a tumor nodule undergoing immunoediting is strongly dependent on guidance of CTL trajectories by scout siblings. They highlight unprecedented aspects of immune cell behavior that might inspire new CTL-based therapeutic strategies against tumors. |
format | Online Article Text |
id | pubmed-4376944 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-43769442015-04-04 A Biased Competition Theory of Cytotoxic T Lymphocyte Interaction with Tumor Nodules Christophe, Claire Müller, Sabina Rodrigues, Magda Petit, Anne-Elisabeth Cattiaux, Patrick Dupré, Loïc Gadat, Sébastien Valitutti, Salvatore PLoS One Research Article The dynamics of the interaction between Cytotoxic T Lymphocytes (CTL) and tumor cells has been addressed in depth, in particular using numerical simulations. However, stochastic mathematical models that take into account the competitive interaction between CTL and tumors undergoing immunoediting, a process of tumor cell escape from immunesurveillance, are presently missing. Here, we introduce a stochastic dynamical particle interaction model based on experimentally measured parameters that allows to describe CTL function during immunoediting. The model describes the competitive interaction between CTL and melanoma cell nodules and allows temporal and two-dimensional spatial progression. The model is designed to provide probabilistic estimates of tumor eradication through numerical simulations in which tunable parameters influencing CTL efficacy against a tumor nodule undergoing immunoediting are tested. Our model shows that the rate of CTL/tumor nodule productive collisions during the initial time of interaction determines the success of CTL in tumor eradication. It allows efficient cytotoxic function before the tumor cells acquire a substantial resistance to CTL attack, due to mutations stochastically occurring during cell division. Interestingly, a bias in CTL motility inducing a progressive attraction towards a few scout CTL, which have detected the nodule enhances early productive collisions and tumor eradication. Taken together, our results are compatible with a biased competition theory of CTL function in which CTL efficacy against a tumor nodule undergoing immunoediting is strongly dependent on guidance of CTL trajectories by scout siblings. They highlight unprecedented aspects of immune cell behavior that might inspire new CTL-based therapeutic strategies against tumors. Public Library of Science 2015-03-27 /pmc/articles/PMC4376944/ /pubmed/25815811 http://dx.doi.org/10.1371/journal.pone.0120053 Text en © 2015 Christophe et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Christophe, Claire Müller, Sabina Rodrigues, Magda Petit, Anne-Elisabeth Cattiaux, Patrick Dupré, Loïc Gadat, Sébastien Valitutti, Salvatore A Biased Competition Theory of Cytotoxic T Lymphocyte Interaction with Tumor Nodules |
title | A Biased Competition Theory of Cytotoxic T Lymphocyte Interaction with Tumor Nodules |
title_full | A Biased Competition Theory of Cytotoxic T Lymphocyte Interaction with Tumor Nodules |
title_fullStr | A Biased Competition Theory of Cytotoxic T Lymphocyte Interaction with Tumor Nodules |
title_full_unstemmed | A Biased Competition Theory of Cytotoxic T Lymphocyte Interaction with Tumor Nodules |
title_short | A Biased Competition Theory of Cytotoxic T Lymphocyte Interaction with Tumor Nodules |
title_sort | biased competition theory of cytotoxic t lymphocyte interaction with tumor nodules |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4376944/ https://www.ncbi.nlm.nih.gov/pubmed/25815811 http://dx.doi.org/10.1371/journal.pone.0120053 |
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