Department of Physiology and Neuroscience, New York University School of Medicine, 550 First Avenue, New York, NY 10016, United States.
N Biotechnol. 2011 Sep;28(5):511-7. doi: 10.1016/j.nbt.2011.03.020. Epub 2011 Apr 5.
Neurodegenerative diseases such as Alzheimer's disease (AD), Parkinson's disease, Huntington's disease (HD) or amyotrophic lateral sclerosis (ALS) are all characterised histologically by the presence of deposits of misfolded proteins, tau and amyloid-β, α-synuclein, huntingtin or superoxide dismutase, respectively. Currently, these illnesses do not have any disease modifying treatment options. A novel therapeutic strategy that is being pursued is immunomodulation, which is using the body's immune system to target the self-proteins that are deposited. Most of these promising approaches are still in preclinical development while some have progressed to Phase III clinical trials. As new insights are gained, it is hoped that these immunotherapies will be effective tools at slowing the progression of these debilitating diseases.
神经退行性疾病,如阿尔茨海默病(AD)、帕金森病、亨廷顿病(HD)或肌萎缩侧索硬化症(ALS),在组织学上均以错误折叠蛋白、tau 和淀粉样β、α-突触核蛋白、亨廷顿蛋白或超氧化物歧化酶的沉积为特征。目前,这些疾病没有任何能够改变疾病进程的治疗选择。正在探索的一种新的治疗策略是免疫调节,它利用人体的免疫系统来靶向沉积的自身蛋白。这些有前景的方法中的大多数仍处于临床前开发阶段,而有些方法已经进展到 III 期临床试验。随着新的见解的获得,人们希望这些免疫疗法将成为减缓这些使人衰弱的疾病进展的有效工具。