Colpo Gabriela Delevati, Stimming Erin Furr, Rocha Natalia Pessoa, Teixeira Antonio Lucio
Neuropsychiatry Program, Department of Psychiatry and Behavioral Sciences, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX, USA.
Department of Neurology, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX, USA.
Neural Regen Res. 2017 Sep;12(9):1422-1425. doi: 10.4103/1673-5374.215245.
Huntington's disease (HD) is an autosomal-dominant neurodegenerative disease characterized by the selective loss of neurons in the striatum and cortex, leading to progressive motor dysfunction, cognitive decline and behavioral symptoms. HD is caused by a trinucleotide (CAG) repeat expansion in the gene encoding for huntingtin. Several studies have suggested that inflammation is an important feature of HD and it is already observed in the early stages of the disease. Recently, new molecules presenting anti-inflammatory and/or immunomodulatory have been investigated for HD. The objective of this review is to discuss the data obtained so far on the immune-based therapeutic strategies for HD.
亨廷顿舞蹈症(HD)是一种常染色体显性神经退行性疾病,其特征是纹状体和皮质中的神经元选择性丧失,导致进行性运动功能障碍、认知衰退和行为症状。HD由编码亨廷顿蛋白的基因中的三核苷酸(CAG)重复扩增引起。多项研究表明,炎症是HD的一个重要特征,并且在疾病早期就已观察到。最近,具有抗炎和/或免疫调节作用的新分子已被用于HD的研究。本综述的目的是讨论目前在基于免疫的HD治疗策略方面所获得的数据。