進行性多発性硬化症における免疫療法
Tradite Neziraj1, Ludwig Kappos2, Anne-Katrin Pröbstel3
1Department of Neurology, University Hospital Basel and University of Basel, Basel, Switzerland; Departments of Biomedicine and of Clinical Research, University Hospital Basel and University of Basel, Basel, Switzerland; Research Center for Clinical Neuroimmunology and Neuroscience Basel (RC2NB), University Hospital Basel and University of Basel, Basel, Switzerland.
Abstract:
Multiple sclerosis (MS) is an autoimmune disease of the central nervous system, with both genetic and environmental risk factors. While traditionally, a relapsing and progressive disease course has been distinguished, it has increasingly become evident that elements of progression are the dominant factor for accumulating MS-related neurologic disability across all clinical courses and can be detected throughout the full disease trajectory in patients with MS. Therefore, defining the dominant pathophysiologic processes driving progression has become indispensable. Pathologic hallmarks of progressive MS include a compartmentalized inflammation within the central nervous system as well as associated neurodegenerative processes, finally leading to neuroaxonal and synaptic loss. Growing understanding of the pathophysiology has led to the development of an increasing number of targeted immunomodulatory treatment approaches for progressive MS. With the development of novel clinical trial designs and the evolution of clinical and paraclinical measures allowing accurate and rapid assessment of progression, new opportunities for personalized treatment regimens are likely to emerge.
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