Theodor Kocher Institute, University of Bern, Bern, Switzerland.
Servei de Neurologia-Neuroimmunologia, Centre d'Esclerosi Múltiple de Catalunya (Cemcat), Institut de Recerca Vall d'Hebron (VHIR), Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain.
Eur J Immunol. 2022 Jun;52(6):869-881. doi: 10.1002/eji.202149757. Epub 2022 May 6.
MS is the most common autoimmune demyelinating disease of the CNS. For the past decades, several immunomodulatory disease-modifying treatments with multiple presumed mechanisms of action have been developed, but MS remains an incurable disease. Whereas high efficacy, at least in early disease, corroborates underlying immunopathophysiology, there is profound heterogeneity in clinical presentation as well as immunophenotypes that may also vary over time. In addition, functional plasticity in the immune system as well as in the inflamed CNS further contributes to disease heterogeneity. In this review, we will highlight immune-pathophysiological and associated clinical heterogeneity that may have an implication for more precise immunomodulatory therapeutic strategies in MS.
多发性硬化症(MS)是中枢神经系统(CNS)最常见的自身免疫性脱髓鞘疾病。在过去的几十年中,已经开发出了几种具有多种作用机制的免疫调节疾病修饰治疗方法,但 MS 仍然是一种不可治愈的疾病。虽然高疗效(至少在早期疾病中)证实了潜在的免疫发病机制,但临床表现以及免疫表型存在明显的异质性,而且这种异质性可能会随时间而变化。此外,免疫系统和炎症性 CNS 的功能可塑性也进一步导致了疾病的异质性。在这篇综述中,我们将重点介绍免疫病理生理学和相关的临床异质性,这可能对 MS 的更精确的免疫调节治疗策略具有重要意义。