痴呆
药物发现
机制(生物学)
认知功能衰退
医学
药品
免疫疗法
疾病
淀粉样蛋白(真菌学)
模式
阿尔茨海默病
治疗方式
药理学
神经科学
生物信息学
免疫学
生物
内科学
免疫系统
病理
哲学
认识论
社会科学
社会学
作者
Jimin Kim,Hanna Jeon,Hye Yun Kim,Young Soo Kim
出处
期刊:ChemBioChem
[Wiley]
日期:2023-08-09
卷期号:24 (19)
被引量:2
标识
DOI:10.1002/cbic.202300328
摘要
Alzheimer's disease (AD) is the most prevalent cause of dementia and has become a health concern worldwide urging for an effective therapeutic. The amyloid hypothesis, currently the most pursued basis of AD drug discovery, points the cause of AD to abnormal production and ineffective removal of pathogenic aggregated amyloid-β (Aβ). AD therapeutic research has been focused on targeting different species of Aβ in the amyloidogenic process to control Aβ content and recover cognitive decline. Among the different processes targeted, the clearance mechanism has been found to be the most effective, supported by the recent clinical approval of an Aβ-targeting immunotherapeutic drug which significantly slowed cognitive decline. Although the current AD drug discovery field is extensively researching immunotherapeutic drugs, there are numerous properties of immunotherapy in need of improvements that could be overcome by an equally performing chemical drug. Here, we review chemical and immunotherapy drug candidates, based on their mechanism of modulating the amyloid cascade, selected from the AlzForum database. Through this review, we aim to summarize and evaluate the prospect of Aβ-targeting chemical drugs.
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