Stem Cell-based Therapeutic and Diagnostic Approaches in Alzheimer'sDisease

作者
Sadaf Abdi,Nima Javanmehr,Maryam Ghasemi-Kasman,Hanie Yavarpour Bali,Marzieh Pirzadeh
出处
期刊:Current Neuropharmacology [Bentham Science Publishers]
卷期号:20 (6): 1093-1115 被引量:21
标识
DOI:10.2174/1570159x20666211231090659
摘要

Background: Alzheimer’s disease (AD) is a neurodegenerative impairment mainly recognized by memory loss and cognitive deficits. However, the current therapies against AD are mostly limited to palliative medications, prompting researchers to investigate more efficient therapeutic approaches for AD, such as stem cell therapy. Recent evidence has proposed that extensive neuronal and synaptic loss and altered adult neurogenesis, which is perceived pivotal in terms of plasticity and network maintenance, occurs early in the course of AD, which exacerbates neuronal vulnerability to AD. Thus, regeneration and replenishing the depleted neuronal networks by strengthening the endogenous repair mechanisms or exogenous stem cells and their cargoes is a rational therapeutic approach. Currently, several stem cell-based therapies as well as stem cell products like exosomes, have shown promising results in the early diagnosis of AD. Objective: This review begins with a comparison between AD and normal aging pathophysiology and a discussion on open questions in the field. Next, summarizing the current stem cell-based therapeutic and diagnostic approaches, we declare the advantages and disadvantages of each method. Also, we comprehensively evaluate the human clinical trials of stem cell therapies for AD. Methodology: Peer-reviewed reports were extracted through Embase, PubMed, and Google Scholar until 2021. Results: With several ongoing clinical trials, stem cells and their derivatives (e.g., exosomes) are an emerging and encouraging field in diagnosing and treating neurodegenerative diseases. Although stem cell therapies have been successful in animal models, numerous clinical trials in AD patients have yielded unpromising results, which we will further discuss.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
CDI和LIB完成签到,获得积分10
1秒前
zeroayanami0完成签到,获得积分10
1秒前
lilei完成签到,获得积分10
3秒前
小小吴发布了新的文献求助10
3秒前
Lily完成签到 ,获得积分10
4秒前
yy关闭了yy的文献求助
4秒前
打打的应助被科研通管家采纳,获得10
5秒前
草根喵完成签到,获得积分10
6秒前
Owen的应助被科研通管家采纳,获得10
6秒前
6秒前
6秒前
大胆绿柳完成签到,获得积分10
6秒前
我是老大的应助被科研通管家采纳,获得10
6秒前
星辰大海的应助被科研通管家采纳,获得10
6秒前
FashionBoy的应助被科研通管家采纳,获得10
6秒前
6秒前
蒙蒙的神完成签到,获得积分10
7秒前
Deathmask完成签到,获得积分10
7秒前
钱笑完成签到,获得积分10
8秒前
杨乐完成签到,获得积分10
8秒前
zhuao完成签到,获得积分10
9秒前
yys完成签到 ,获得积分10
9秒前
10秒前
快乐小夏发布了新的文献求助10
10秒前
周一一完成签到,获得积分10
10秒前
杨思悦完成签到 ,获得积分10
11秒前
cccjjjhhh完成签到,获得积分10
13秒前
温眼张完成签到,获得积分10
13秒前
满意的醉蝶完成签到,获得积分10
13秒前
CCwu完成签到,获得积分10
14秒前
ZYW完成签到,获得积分10
14秒前
15秒前
xingyong发布了新的文献求助10
16秒前
哈哈完成签到,获得积分10
16秒前
Lojong完成签到,获得积分10
17秒前
浩浩凿石岩完成签到,获得积分10
17秒前
17秒前
MuMu完成签到,获得积分10
18秒前
科研通AI6.2的应助被月亮采纳,获得10
18秒前
18秒前
高分求助中
(应助此贴封号)通过应助OA文献获取积分 10000
Rosenblum, Global Change Biology 800
Computational Chemical Reaction Engineering: Modeling, Simulation, and Design with MATLAB 600
Organizational Behavior 510
Management and the Arts 510
Deformation and Fracture of the Lumbar Vertebral End Plate 500
CLSI C56QG Examples of Hemolyzed, Icteric, and Lipemic/Turbid Samples Quick Guide 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 计算机科学 工程类 纳米技术 内科学 物理 有机化学 化学工程 生物化学 复合材料 光电子学 细胞生物学 心理学 量子力学 催化作用 物理化学 电极
热门帖子
关注 科研通微信公众号,转发送积分 7802624
求助须知:如何正确求助?哪些是违规求助? 9336592
关于积分的说明 20480977
捐赠科研通 7394196
什么是DOI,文献DOI怎么找? 3326929
关于科研通互助平台的介绍 2474009
邀请新用户注册赠送积分活动 2344938