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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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Detalles Bibliográficos
Autor principal: Pennisi, Marzio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
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.
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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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