Clinical safety and efficacy of allogenic human adipose mesenchymal stromal cells-derived exosomes in patients with mild to moderate Alzheimer’s disease: a phase I/II clinical trial

医学 间充质干细胞 临床试验 不利影响 内科学 鼻腔给药 疾病 肿瘤科 药理学 病理
作者
Xinyi Xie,Qingxiang Song,Chengxiang Dai,Shishuang Cui,Ran Tang,Suke Li,Jing Chang,Ping Li,Jin‐Tao Wang,Jianping Li,Chao Gao,Hongzhuan Chen,Shengdi Chen,Ru‐Jing Ren,Xiaoling Gao,Gang Wang
出处
期刊:General psychiatry [BMJ]
卷期号:36 (5): e101143-e101143 被引量:32
标识
DOI:10.1136/gpsych-2023-101143
摘要

There have been no effective treatments for slowing or reversing Alzheimer's disease (AD) until now. Growing preclinical evidence, including this study, suggests that mesenchymal stem cells-secreted exosomes (MSCs-Exos) have the potential to cure AD.The first three-arm, drug-intervention, phase I/II clinical trial was conducted to explore the safety and efficacy of allogenic human adipose MSCs-Exos (ahaMSCs-Exos) in patients with mild to moderate AD.The eligible subjects were assigned to one of three dosage groups, intranasally administrated with ahaMSCs-Exos two times per week for 12 weeks, and underwent follow-up visits at weeks 16, 24, 36 and 48.No adverse events were reported. In the medium-dose arm, Alzheimer's Disease Assessment Scale-Cognitive section (ADAS-cog) scores decreased by 2.33 (1.19) and the basic version of Montreal Cognitive Assessment scores increased by 2.38 (0.58) at week 12 compared with baseline levels, indicating improved cognitive function. Moreover, the ADAS-cog scores in the medium-dose arm decreased continuously by 3.98 points until week 36. There were no significant differences in altered amyloid or tau deposition among the three arms, but hippocampal volume shrank less in the medium-dose arm to some extent.Intranasal administration of ahaMSCs-Exos was safe and well tolerated, and a dose of at least 4×108 particles could be selected for further clinical trials.NCT04388982.
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