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A Mathematical Model of Immune-System-Melanoma Competition
We present a mathematical model developed to reproduce the immune response entitled with the combined administration of activated OT1 cytotoxic T lymphocytes (CTLs) and Anti-CD137 monoclonal antibodies. The treatment is directed against melanoma in B16 OVA mouse models exposed to a specific immunoth...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3371685/ https://www.ncbi.nlm.nih.gov/pubmed/22701144 http://dx.doi.org/10.1155/2012/850754 |
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author | Pennisi, Marzio |
author_facet | Pennisi, Marzio |
author_sort | Pennisi, Marzio |
collection | PubMed |
description | We present a mathematical model developed to reproduce the immune response entitled with the combined administration of activated OT1 cytotoxic T lymphocytes (CTLs) and Anti-CD137 monoclonal antibodies. The treatment is directed against melanoma in B16 OVA mouse models exposed to a specific immunotherapy strategy. We model two compartments: the injection point compartment where the treatment is administered and the skin compartment where melanoma tumor cells proliferate. To model the migration of OT1 CTLs and antibodies from the injection to the skin compartment, we use delay differential equations (DDEs). The outcomes of the mathematical model are in good agreement with the in vivo results. Moreover, sensitivity analysis of the mathematical model underlines the key role of OT1 CTLs and suggests that a possible reduction of the number of injected antibodies should not affect substantially the treatment efficacy. |
format | Online Article Text |
id | pubmed-3371685 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-33716852012-06-13 A Mathematical Model of Immune-System-Melanoma Competition Pennisi, Marzio Comput Math Methods Med Research Article We present a mathematical model developed to reproduce the immune response entitled with the combined administration of activated OT1 cytotoxic T lymphocytes (CTLs) and Anti-CD137 monoclonal antibodies. The treatment is directed against melanoma in B16 OVA mouse models exposed to a specific immunotherapy strategy. We model two compartments: the injection point compartment where the treatment is administered and the skin compartment where melanoma tumor cells proliferate. To model the migration of OT1 CTLs and antibodies from the injection to the skin compartment, we use delay differential equations (DDEs). The outcomes of the mathematical model are in good agreement with the in vivo results. Moreover, sensitivity analysis of the mathematical model underlines the key role of OT1 CTLs and suggests that a possible reduction of the number of injected antibodies should not affect substantially the treatment efficacy. Hindawi Publishing Corporation 2012 2012-06-03 /pmc/articles/PMC3371685/ /pubmed/22701144 http://dx.doi.org/10.1155/2012/850754 Text en Copyright © 2012 Marzio Pennisi. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Pennisi, Marzio A Mathematical Model of Immune-System-Melanoma Competition |
title | A Mathematical Model of Immune-System-Melanoma Competition |
title_full | A Mathematical Model of Immune-System-Melanoma Competition |
title_fullStr | A Mathematical Model of Immune-System-Melanoma Competition |
title_full_unstemmed | A Mathematical Model of Immune-System-Melanoma Competition |
title_short | A Mathematical Model of Immune-System-Melanoma Competition |
title_sort | mathematical model of immune-system-melanoma competition |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3371685/ https://www.ncbi.nlm.nih.gov/pubmed/22701144 http://dx.doi.org/10.1155/2012/850754 |
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