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A Model of Dendritic Cell Therapy for Melanoma

Dendritic cells are a promising immunotherapy tool for boosting an individual’s antigen-specific immune response to cancer. We develop a mathematical model using differential and delay-differential equations to describe the interactions between dendritic cells, effector-immune cells, and tumor cells...

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Detalles Bibliográficos
Autores principales: DePillis, Lisette, Gallegos, Angela, Radunskaya, Ami
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3601335/
https://www.ncbi.nlm.nih.gov/pubmed/23516248
http://dx.doi.org/10.3389/fonc.2013.00056
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author DePillis, Lisette
Gallegos, Angela
Radunskaya, Ami
author_facet DePillis, Lisette
Gallegos, Angela
Radunskaya, Ami
author_sort DePillis, Lisette
collection PubMed
description Dendritic cells are a promising immunotherapy tool for boosting an individual’s antigen-specific immune response to cancer. We develop a mathematical model using differential and delay-differential equations to describe the interactions between dendritic cells, effector-immune cells, and tumor cells. We account for the trafficking of immune cells between lymph, blood, and tumor compartments. Our model reflects experimental results both for dendritic cell trafficking and for immune suppression of tumor growth in mice. In addition, in silico experiments suggest more effective immunotherapy treatment protocols can be achieved by modifying dose location and schedule. A sensitivity analysis of the model reveals which patient-specific parameters have the greatest impact on treatment efficacy.
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spelling pubmed-36013352013-03-19 A Model of Dendritic Cell Therapy for Melanoma DePillis, Lisette Gallegos, Angela Radunskaya, Ami Front Oncol Oncology Dendritic cells are a promising immunotherapy tool for boosting an individual’s antigen-specific immune response to cancer. We develop a mathematical model using differential and delay-differential equations to describe the interactions between dendritic cells, effector-immune cells, and tumor cells. We account for the trafficking of immune cells between lymph, blood, and tumor compartments. Our model reflects experimental results both for dendritic cell trafficking and for immune suppression of tumor growth in mice. In addition, in silico experiments suggest more effective immunotherapy treatment protocols can be achieved by modifying dose location and schedule. A sensitivity analysis of the model reveals which patient-specific parameters have the greatest impact on treatment efficacy. Frontiers Media S.A. 2013-03-19 /pmc/articles/PMC3601335/ /pubmed/23516248 http://dx.doi.org/10.3389/fonc.2013.00056 Text en Copyright © 2013 DePillis, Gallegos and Radunskaya. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Oncology
DePillis, Lisette
Gallegos, Angela
Radunskaya, Ami
A Model of Dendritic Cell Therapy for Melanoma
title A Model of Dendritic Cell Therapy for Melanoma
title_full A Model of Dendritic Cell Therapy for Melanoma
title_fullStr A Model of Dendritic Cell Therapy for Melanoma
title_full_unstemmed A Model of Dendritic Cell Therapy for Melanoma
title_short A Model of Dendritic Cell Therapy for Melanoma
title_sort model of dendritic cell therapy for melanoma
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3601335/
https://www.ncbi.nlm.nih.gov/pubmed/23516248
http://dx.doi.org/10.3389/fonc.2013.00056
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