摘要
目的:多重证据表明,淀粉样β蛋白(Aβ)肽在大脑中的病理积累与阿尔兹海默病(AD)的病理生理学有关联。通过绑定反淀粉样β蛋白(anti-Aβ)这样的特殊抗体从而去除大脑中Aβ的疗法处在积极的研究中。含有全长Aβ42 肽(AN1792)的疫苗接种成功地在阿兹海默病人体内引出了anti-Aβ,但是这与脑膜炎相关。为了避免这种安全性问题,设计出氨基末端的Aβ1-7肽缀合物和vanutide cridificar(ACC-001)正处于临床发展阶段。这份报告描述了日本群体轻度到中度阿兹海默病人的第二阶段提升剂量倍数的研究。安全性和免疫原性评估分别是首要和次要的目的。方法:ACC-001在三组受试者中注射剂量分别是3、10和30 μg,在第一个研究中搭配或不搭配QS-21佐剂,在第二个研究中搭配QS-21佐剂;在第一个研究中,对照组由QS-21和磷酸盐缓冲盐水组成,而第二个研究中对照组只包含QS-21。结果:研究中的大部分受试者显示了各种治疗诱发的不良反应(TEAEs);大部分的不良反应是轻度或者中等强度的。在第二个研究中,三个受试者都因为不良反应而退出了研究。最常见的不良反应是注射部位反应。两个研究都没有出现死亡结果。所有的ACC-001 加 QS-21剂量都引起了高度和持续的反淀粉样β蛋白(anti-Aβ)抗体滴度并且QS-21对这种效应是必需的。结论:这些数据将为阿兹海默病反淀粉样β蛋白疫苗疗法的进一步研究提供有价值的信息。
关键词: 阿尔茨海默病,β-淀粉样蛋白,淀粉样斑块,抗体,免疫治疗,疫苗
Current Alzheimer Research
Title:Vanutide Cridificar and the QS-21 Adjuvant in Japanese Subjects with Mild to Moderate Alzheimer’ s Disease: Results from Two Phase 2 Studies
Volume: 12 Issue: 3
Author(s): Heii Arai, Hideo Suzuki and Tamotsu Yoshiyama
Affiliation:
关键词: 阿尔茨海默病,β-淀粉样蛋白,淀粉样斑块,抗体,免疫治疗,疫苗
摘要: Objective: Multiple lines of evidence indicate that pathological accumulation of amyloid
beta (Aβ) peptide in the brain is linked to the pathophysiology of Alzheimer’s disease (AD). Removal
of Aβ from the brain by binding to anti-Aβ specific antibodies is under active investigation. Vaccination
with a full-length Aβ42 peptide (AN1792) successfully elicited anti-Aβ antibodies in human subjects
with AD, but was associated with meningoencephalitis. To avoid this safety issue, an aminoterminal
Aβ
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Cite this article as:
Heii Arai, Hideo Suzuki and Tamotsu Yoshiyama , Vanutide Cridificar and the QS-21 Adjuvant in Japanese Subjects with Mild to Moderate Alzheimer’ s Disease: Results from Two Phase 2 Studies, Current Alzheimer Research 2015; 12 (3) . https://dx.doi.org/10.2174/1567205012666150302154121
DOI https://dx.doi.org/10.2174/1567205012666150302154121 |
Print ISSN 1567-2050 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5828 |
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