Mesenchymal Stem Cells With Adjuvant Dexamethasone in Patients With Alzheimer's Disease: A Phase IIa Trial.

Dementia and neurocognitive disorders Pub Date : 2025-10-01 Epub Date: 2025-10-24 DOI:10.12779/dnd.2025.24.4.272
Na Kyung Lee, Hyemin Jang, Yejoo Choi, Song Hwangbo, Seunghoon Lee, Jung Il Lee, Young Ju Kim, Juhee Chin, Jong Wook Chang, Sang Won Seo, Hyo Jin Son, Soo Jin Choi, Duk L Na, Hee Jin Kim
{"title":"Mesenchymal Stem Cells With Adjuvant Dexamethasone in Patients With Alzheimer's Disease: A Phase IIa Trial.","authors":"Na Kyung Lee, Hyemin Jang, Yejoo Choi, Song Hwangbo, Seunghoon Lee, Jung Il Lee, Young Ju Kim, Juhee Chin, Jong Wook Chang, Sang Won Seo, Hyo Jin Son, Soo Jin Choi, Duk L Na, Hee Jin Kim","doi":"10.12779/dnd.2025.24.4.272","DOIUrl":null,"url":null,"abstract":"<p><strong>Background and purpose: </strong>This phase IIa trial assessed the safety and efficacy of mesenchymal stem cell (MSC) therapy for Alzheimer's disease (AD). An open-label extension (OLE) further explored the adjunctive role of dexamethasone.</p><p><strong>Methods: </strong>MSCs (n=24) or a saline placebo (n=12) were administered intraventricularly three times at four-week intervals. In the OLE, MSCs and dexamethasone (15 mg, n=5) were administered to patients who received saline in phase IIa. Clinical parameters and cerebrospinal fluid (CSF) markers were evaluated.</p><p><strong>Results: </strong>MSC therapy exhibited no significant clinical benefits, but was associated with reductions in CSF AD biomarkers (amyloid-beta, phosphorylated-tau, and total-tau) compared to placebo. The MSC group experienced more adverse events (fever, headache, nausea, and vomiting), while co-administration of dexamethasone appeared to attenuate immune-related reactions and limit increases in CSF white blood cell and interleukin-6.</p><p><strong>Conclusions: </strong>These findings suggest exploratory biological effects of MSCs on AD biomarkers, with dexamethasone potentially mitigating MSC-induced immune responses.</p><p><strong>Trial registration: </strong>ClinicalTrials.gov Identifier: NCT02054208, NCT03172117, and NCT04954534.</p>","PeriodicalId":72779,"journal":{"name":"Dementia and neurocognitive disorders","volume":"24 4","pages":"272-285"},"PeriodicalIF":0.0000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12599408/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Dementia and neurocognitive disorders","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.12779/dnd.2025.24.4.272","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/10/24 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background and purpose: This phase IIa trial assessed the safety and efficacy of mesenchymal stem cell (MSC) therapy for Alzheimer's disease (AD). An open-label extension (OLE) further explored the adjunctive role of dexamethasone.

Methods: MSCs (n=24) or a saline placebo (n=12) were administered intraventricularly three times at four-week intervals. In the OLE, MSCs and dexamethasone (15 mg, n=5) were administered to patients who received saline in phase IIa. Clinical parameters and cerebrospinal fluid (CSF) markers were evaluated.

Results: MSC therapy exhibited no significant clinical benefits, but was associated with reductions in CSF AD biomarkers (amyloid-beta, phosphorylated-tau, and total-tau) compared to placebo. The MSC group experienced more adverse events (fever, headache, nausea, and vomiting), while co-administration of dexamethasone appeared to attenuate immune-related reactions and limit increases in CSF white blood cell and interleukin-6.

Conclusions: These findings suggest exploratory biological effects of MSCs on AD biomarkers, with dexamethasone potentially mitigating MSC-induced immune responses.

Trial registration: ClinicalTrials.gov Identifier: NCT02054208, NCT03172117, and NCT04954534.

Abstract Image

Abstract Image

Abstract Image

间充质干细胞辅助地塞米松治疗阿尔茨海默病患者:一项IIa期试验
背景和目的:这项IIa期试验评估了间充质干细胞(MSC)治疗阿尔茨海默病(AD)的安全性和有效性。开放标签扩展(OLE)进一步探讨了地塞米松的辅助作用。方法:骨髓间充质干细胞(n=24)或生理盐水安慰剂(n=12)在脑室内注射三次,每隔四周注射一次。在OLE中,IIa期接受生理盐水的患者给予MSCs和地塞米松(15 mg, n=5)。评估临床参数和脑脊液(CSF)标志物。结果:与安慰剂相比,MSC治疗没有表现出显著的临床益处,但与CSF AD生物标志物(淀粉样蛋白- β、磷酸化tau蛋白和总tau蛋白)的减少有关。MSC组出现了更多的不良事件(发烧、头痛、恶心和呕吐),而联合使用地塞米松似乎可以减轻免疫相关反应,并限制脑脊液白细胞和白细胞介素-6的增加。结论:这些发现提示MSCs对AD生物标志物的探索性生物学效应,地塞米松可能减轻MSCs诱导的免疫反应。试验注册:ClinicalTrials.gov标识符:NCT02054208、NCT03172117和NCT04954534。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书