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Computational modeling of the immune response in multiple sclerosis using epimod framework
BACKGROUND: Multiple Sclerosis (MS) represents nowadays in Europe the leading cause of non-traumatic disabilities in young adults, with more than 700,000 EU cases. Although huge strides have been made over the years, MS etiology remains partially unknown. Furthermore, the presence of various endogen...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734848/ https://www.ncbi.nlm.nih.gov/pubmed/33308135 http://dx.doi.org/10.1186/s12859-020-03823-9 |
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author | Pernice, Simone Follia, Laura Maglione, Alessandro Pennisi, Marzio Pappalardo, Francesco Novelli, Francesco Clerico, Marinella Beccuti, Marco Cordero, Francesca Rolla, Simona |
author_facet | Pernice, Simone Follia, Laura Maglione, Alessandro Pennisi, Marzio Pappalardo, Francesco Novelli, Francesco Clerico, Marinella Beccuti, Marco Cordero, Francesca Rolla, Simona |
author_sort | Pernice, Simone |
collection | PubMed |
description | BACKGROUND: Multiple Sclerosis (MS) represents nowadays in Europe the leading cause of non-traumatic disabilities in young adults, with more than 700,000 EU cases. Although huge strides have been made over the years, MS etiology remains partially unknown. Furthermore, the presence of various endogenous and exogenous factors can greatly influence the immune response of different individuals, making it difficult to study and understand the disease. This becomes more evident in a personalized-fashion when medical doctors have to choose the best therapy for patient well-being. In this optics, the use of stochastic models, capable of taking into consideration all the fluctuations due to unknown factors and individual variability, is highly advisable. RESULTS: We propose a new model to study the immune response in relapsing remitting MS (RRMS), the most common form of MS that is characterized by alternate episodes of symptom exacerbation (relapses) with periods of disease stability (remission). In this new model, both the peripheral lymph node/blood vessel and the central nervous system are explicitly represented. The model was created and analysed using Epimod, our recently developed general framework for modeling complex biological systems. Then the effectiveness of our model was shown by modeling the complex immunological mechanisms characterizing RRMS during its course and under the DAC administration. CONCLUSIONS: Simulation results have proven the ability of the model to reproduce in silico the immune T cell balance characterizing RRMS course and the DAC effects. Furthermore, they confirmed the importance of a timely intervention on the disease course. |
format | Online Article Text |
id | pubmed-7734848 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77348482020-12-15 Computational modeling of the immune response in multiple sclerosis using epimod framework Pernice, Simone Follia, Laura Maglione, Alessandro Pennisi, Marzio Pappalardo, Francesco Novelli, Francesco Clerico, Marinella Beccuti, Marco Cordero, Francesca Rolla, Simona BMC Bioinformatics Research BACKGROUND: Multiple Sclerosis (MS) represents nowadays in Europe the leading cause of non-traumatic disabilities in young adults, with more than 700,000 EU cases. Although huge strides have been made over the years, MS etiology remains partially unknown. Furthermore, the presence of various endogenous and exogenous factors can greatly influence the immune response of different individuals, making it difficult to study and understand the disease. This becomes more evident in a personalized-fashion when medical doctors have to choose the best therapy for patient well-being. In this optics, the use of stochastic models, capable of taking into consideration all the fluctuations due to unknown factors and individual variability, is highly advisable. RESULTS: We propose a new model to study the immune response in relapsing remitting MS (RRMS), the most common form of MS that is characterized by alternate episodes of symptom exacerbation (relapses) with periods of disease stability (remission). In this new model, both the peripheral lymph node/blood vessel and the central nervous system are explicitly represented. The model was created and analysed using Epimod, our recently developed general framework for modeling complex biological systems. Then the effectiveness of our model was shown by modeling the complex immunological mechanisms characterizing RRMS during its course and under the DAC administration. CONCLUSIONS: Simulation results have proven the ability of the model to reproduce in silico the immune T cell balance characterizing RRMS course and the DAC effects. Furthermore, they confirmed the importance of a timely intervention on the disease course. BioMed Central 2020-12-14 /pmc/articles/PMC7734848/ /pubmed/33308135 http://dx.doi.org/10.1186/s12859-020-03823-9 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Pernice, Simone Follia, Laura Maglione, Alessandro Pennisi, Marzio Pappalardo, Francesco Novelli, Francesco Clerico, Marinella Beccuti, Marco Cordero, Francesca Rolla, Simona Computational modeling of the immune response in multiple sclerosis using epimod framework |
title | Computational modeling of the immune response in multiple sclerosis using epimod framework |
title_full | Computational modeling of the immune response in multiple sclerosis using epimod framework |
title_fullStr | Computational modeling of the immune response in multiple sclerosis using epimod framework |
title_full_unstemmed | Computational modeling of the immune response in multiple sclerosis using epimod framework |
title_short | Computational modeling of the immune response in multiple sclerosis using epimod framework |
title_sort | computational modeling of the immune response in multiple sclerosis using epimod framework |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734848/ https://www.ncbi.nlm.nih.gov/pubmed/33308135 http://dx.doi.org/10.1186/s12859-020-03823-9 |
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