Parkinson disease and the immune system - associations, mechanisms and therapeutics

被引:324
作者
Tan, Eng-King [1 ,2 ,3 ]
Chao, Yin-Xia [1 ,2 ,3 ]
West, Andrew [4 ]
Chan, Ling-Ling [3 ,5 ]
Poewe, Werner [6 ]
Jankovic, Joseph [7 ,8 ]
机构
[1] Singapore Gen Hosp, Dept Neurol, Singapore, Singapore
[2] Natl Neurosci Inst, Singapore, Singapore
[3] Duke NUS Med Sch, Singapore, Singapore
[4] Duke Univ, Dept Pharmacol & Canc Biol, Duke Ctr Neurodegenerat & Neurotherapeut, Durham, NC USA
[5] Singapore Gen Hosp, Dept Radiol, Singapore, Singapore
[6] Med Univ Innsbruck, Dept Neurol, Innsbruck, Austria
[7] Baylor Coll Med, Dept Neurol, Parkinsons Dis Ctr, Houston, TX 77030 USA
[8] Baylor Coll Med, Dept Neurol, Movement Disorders Clin, Houston, TX 77030 USA
基金
英国医学研究理事会;
关键词
NLRP3 INFLAMMASOME ACTIVATION; EXTRACELLULAR ALPHA-SYNUCLEIN; GENOME-WIDE ASSOCIATION; CENTRAL-NERVOUS-SYSTEM; GUT-BRAIN AXIS; CEREBROSPINAL-FLUID; TNF-ALPHA; MICROGLIAL ACTIVATION; DOPAMINERGIC-NEURONS; MOUSE MODEL;
D O I
10.1038/s41582-020-0344-4
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Multiple lines of evidence indicate that immune system dysfunction has a role in Parkinson disease (PD); this evidence includes clinical and genetic associations between autoimmune disease and PD, impaired cellular and humoral immune responses in PD, imaging evidence of inflammatory cell activation and evidence of immune dysregulation in experimental models of PD. However, the mechanisms that link the immune system with PD remain unclear, and the temporal relationships of innate and adaptive immune responses with neurodegeneration are unknown. Despite these challenges, our current knowledge provides opportunities to develop immune-targeted therapeutic strategies for testing in PD, and clinical studies of some approaches are under way. In this Review, we provide an overview of the clinical observations, preclinical experiments and clinical studies that provide evidence for involvement of the immune system in PD and that help to define the nature of this association. We consider autoimmune mechanisms, central and peripheral inflammatory mechanisms and immunogenetic factors. We also discuss the use of this knowledge to develop immune-based therapeutic approaches, including immunotherapy that targets alpha-synuclein and the targeting of immune mediators such as inflammasomes. We also consider future research and clinical trials necessary to maximize the potential of targeting the immune system. In this Review, Tan et al. provide an overview of the clinical and preclinical evidence that immune system dysfunction is involved in Parkinson disease, and discuss how increasing knowledge of the underlying mechanisms is driving development of immune-based therapeutic approaches.
引用
收藏
页码:303 / 318
页数:16
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