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人胎盘间充质基质细胞衍生的小细胞外囊泡治疗重症 COVID-19:一项双盲随机对照临床试验。

Human placental mesenchymal stromal cell-derived small extracellular vesicles as a treatment for severe COVID-19: A double-blind randomized controlled clinical trial.

机构信息

Infectious Diseases Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran.

Medical Biology Research Centre, Health Technology Institute, Kermanshah University of Medical Sciences, Kermanshah, Iran.

出版信息

J Extracell Vesicles. 2024 Jul;13(7):e12492. doi: 10.1002/jev2.12492.

DOI:10.1002/jev2.12492
PMID:39051747
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11270582/
Abstract

The current study aimed to investigate the effects of human placental mesenchymal stromal cell-derived small extracellular vesicles (hPMSC-sEVs) as a treatment for COVID-19. This double-blind, randomized, controlled clinical trial was conducted on two groups of patients with COVID-19-associated acute respiratory distress syndrome. After randomization, the control group received standard treatment and placebo, and the intervention arm received standard treatment plus hPMSC-sEVs. The number of hospital deaths was considered the primary outcome. After meeting the exclusion and inclusion criteria, 21 and 24 patients were allocated to intervention and control arms, respectively. Besides admission SpO levels, which were significantly lower in the intervention arm (p = 0.008), all the baseline demo-biographic and laboratory variables were similar between the groups. It was shown that hPMSC-sEVs could significantly (p = 0.015) decrease the mortality ratio in the intervention group (4/21 [19.04%]) compared to the controls (13/24 [54.16%]). The mean time to death in the intervention and control groups was 28.06 and 11.10 days, respectively (p < 0.001). This study showed that hPMSC-sEVs are a possible treatment for critically ill patients with COVID-19.

摘要

本研究旨在探讨人胎盘间充质基质细胞衍生的小细胞外囊泡(hPMSC-sEVs)作为 COVID-19 治疗方法的效果。这是一项双盲、随机、对照临床试验,在两组 COVID-19 相关急性呼吸窘迫综合征患者中进行。随机分组后,对照组接受标准治疗和安慰剂,干预组接受标准治疗加 hPMSC-sEVs。住院死亡人数被认为是主要结局。符合排除和纳入标准后,分别有 21 名和 24 名患者被分配到干预组和对照组。除了干预组入院时 SpO 水平明显较低(p = 0.008)外,两组的基线人口统计学和实验室变量均相似。结果表明,与对照组(4/24 [19.04%])相比,hPMSC-sEVs 可显著(p = 0.015)降低干预组的死亡率(21/4 [47.50%])。干预组和对照组的平均死亡时间分别为 28.06 和 11.10 天(p < 0.001)。这项研究表明,hPMSC-sEVs 可能是治疗 COVID-19 危重症患者的一种方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b92/11270582/f084736e63b3/JEV2-13-e12492-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b92/11270582/bd00334843ad/JEV2-13-e12492-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b92/11270582/f084736e63b3/JEV2-13-e12492-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b92/11270582/bd00334843ad/JEV2-13-e12492-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b92/11270582/f084736e63b3/JEV2-13-e12492-g001.jpg

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