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Immunotherapy in Alzheimer's disease: Do we have all the pieces of the puzzle?

机译:阿尔茨海默氏病的免疫疗法:我们是否能解决所有难题?

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Results of Phase III studies involving a large number of Alzheimer's disease (AD) patients treated by passive immunotherapy with humanized anti-amyloid β monoclonal antibodies have recently been released. These approaches failed to show a significant clinical benefit in patients with mild to moderate AD. The most considered explanation is that the patients have been treated too late. Whereas targeting patients at asymptomatic stages of the disease is a critical step in the goal of improving the efficacy of such antibody-based strategies, several other important factors should be considered in the development and clinical evaluation of anti-amyloid β immunotherapies, including the as yet poorly understood relationship of AD with the immune system and the importance of cerebral amyloid angiopathy. Better understanding the role of immune responses in AD and their impact on immunotherapy appears essential in the design of alternative or combinatorial immunotherapy approaches in AD, which may imply effectors other than antibodies and even additional antigenic targets.
机译:最近发布了涉及大量阿尔茨海默氏病(AD)患者的III期研究结果,这些患者已通过被动免疫疗法与人源化抗淀粉样蛋白β单克隆抗体进行了治疗。这些方法未能在轻度至中度AD患者中显示出显着的临床益处。最周到的解释是,患者接受治疗的时间太晚了。尽管以患者的无症状阶段为目标是提高此类基于抗体的策略的疗效的关键步骤,但在抗淀粉样β免疫疗法的开发和临床评估中应考虑其他几个重要因素,包括但对AD与免疫系统的关系以及脑淀粉样血管病的重要性了解甚少。更好地了解免疫应答在AD中的作用及其对免疫疗法的影响,在设计AD替代或组合免疫疗法方法中显得至关重要,这可能意味着除抗体甚至其他抗原靶标以外的效应子。

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