Computational modeling of the immune response in multiple sclerosis using epimod framework

BackgroundMultiple 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 endogenou...

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Veröffentlicht in:BMC bioinformatics 2020-12, Vol.21 (Suppl 17), p.550-550, Article 550
Hauptverfasser: Pernice, Simone, Follia, Laura, Maglione, Alessandro, Pennisi, Marzio, Pappalardo, Francesco, Novelli, Francesco, Clerico, Marinella, Beccuti, Marco, Cordero, Francesca, Rolla, Simona
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Sprache:eng
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Zusammenfassung:BackgroundMultiple 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.ResultsWe 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.ConclusionsSimulation 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.
ISSN:1471-2105
1471-2105
DOI:10.1186/s12859-020-03823-9