Inflammation and Huntington's disease - a neglected therapeutic target?

被引:4
|
作者
Field, Sophie E. [1 ]
Curle, Annabel J. [1 ]
Barker, Roger A. [1 ,2 ]
机构
[1] Univ Cambridge, John van Geest Ctr Brain Repair, Dept Clin Neurosci, Cambridge, England
[2] Univ Cambridge, MRC WT Cambridge Stem Cell Inst, Cambridge, England
关键词
Huntington's disease; immune system; clinical trials; microglia; complement system; peripheral immune system; cytokines; astrocytes; PET imaging; microbiome; BLOOD-BRAIN-BARRIER; CENTRAL-NERVOUS-SYSTEM; YAC128 MOUSE MODEL; MUTANT HUNTINGTIN; MICROGLIAL ACTIVATION; CEREBROSPINAL-FLUID; MINOCYCLINE; CELLS; EXPRESSION; AUTOIMMUNE;
D O I
10.1080/13543784.2024.2348738
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
IntroductionHuntington's Disease (HD) is a genetic neurodegenerative disease for which there is currently no disease-modifying treatment. One of several underlying mechanisms proposed to be involved in HD pathogenesis is inflammation; there is now accumulating evidence that the immune system may play an integral role in disease pathology and progression. As such, modulation of the immune system could be a potential therapeutic target for HD.Areas coveredTo date, the number of trials targeting immune aspects of HD has been limited. However, targeting it, may have great advantages over other therapeutic areas, given that many drugs already exist that have actions in this system coupled to the fact that inflammation can be measured both peripherally and, to some extent, centrally using CSF and PET imaging. In this review, we look at evidence that the immune system and the newly emerging area of the microbiome are altered in HD patients, and then present and discuss clinical trials that have targeted different parts of the immune system.Expert opinionWe then conclude by discussing how this field might develop going forward, focusing on the role of imaging and other biomarkers to monitor central immune activation and response to novel treatments in HD.
引用
收藏
页码:451 / 467
页数:17
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