TY - JOUR
T1 - A minimal unified model of disease trajectories captures hallmarks of multiple sclerosis
AU - Kannan, Venkateshan
AU - Kiani, Narsis A.
AU - Piehl, Fredrik
AU - Tegner, Jesper
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: We thank Drs. Maja Jagodic, Ingrid Kockum, Tomas Olsson, David Gomez-Cabrero, and Gilad Silberberg for critical discussions and comments. This work was supported by the following grants to J.T; Hjrnfonden, ALF, STATegra (FP7), Torsten Sderberg Foundation, Stockholm County Council, Swedish excellence center for e-science and Swedish Research Council (3R program MH and project grant NT). N.K was supported by a fellowship from VINNOVA. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
PY - 2017/3/29
Y1 - 2017/3/29
N2 - Multiple Sclerosis (MS) is an autoimmune disease targeting the central nervous system (CNS) causing demyelination and neurodegeneration leading to accumulation of neurological disability. Here we present a minimal, computational model involving the immune system and CNS that generates the principal subtypes of the disease observed in patients. The model captures several key features of MS, especially those that distinguish the chronic progressive phase from that of the relapse-remitting. In addition, a rare subtype of the disease, progressive relapsing MS naturally emerges from the model. The model posits the existence of two key thresholds, one in the immune system and the other in the CNS, that separate dynamically distinct behavior of the model. Exploring the two-dimensional space of these thresholds, we obtain multiple phases of disease evolution and these shows greater variation than the clinical classification of MS, thus capturing the heterogeneity that is manifested in patients.
AB - Multiple Sclerosis (MS) is an autoimmune disease targeting the central nervous system (CNS) causing demyelination and neurodegeneration leading to accumulation of neurological disability. Here we present a minimal, computational model involving the immune system and CNS that generates the principal subtypes of the disease observed in patients. The model captures several key features of MS, especially those that distinguish the chronic progressive phase from that of the relapse-remitting. In addition, a rare subtype of the disease, progressive relapsing MS naturally emerges from the model. The model posits the existence of two key thresholds, one in the immune system and the other in the CNS, that separate dynamically distinct behavior of the model. Exploring the two-dimensional space of these thresholds, we obtain multiple phases of disease evolution and these shows greater variation than the clinical classification of MS, thus capturing the heterogeneity that is manifested in patients.
UR - http://hdl.handle.net/10754/623066
UR - http://www.sciencedirect.com/science/article/pii/S0025556416302358
UR - http://www.scopus.com/inward/record.url?scp=85017550154&partnerID=8YFLogxK
U2 - 10.1016/j.mbs.2017.03.006
DO - 10.1016/j.mbs.2017.03.006
M3 - Article
C2 - 28365299
SN - 0025-5564
VL - 289
SP - 1
EP - 8
JO - Mathematical Biosciences
JF - Mathematical Biosciences
ER -