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脐带间充质干细胞治疗新型冠状病毒肺炎患者的疗效和安全性。

Efficacy and safety of umbilical cord mesenchymal stem cells for the treatment of patients with COVID-19.

机构信息

Department of Cardiology, the Second Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China.

Department of Hematology, the Second Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China.

出版信息

Clinics (Sao Paulo). 2021 May 17;76:e2604. doi: 10.6061/clinics/2021/e2604. eCollection 2021.

DOI:10.6061/clinics/2021/e2604
PMID:34008772
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8101688/
Abstract

OBJECTIVES

The coronavirus disease (COVID-19) outbreak has catastrophically threatened public health worldwide and presented great challenges for clinicians. To date, no specific drugs are available against severe acute respiratory syndrome coronavirus 2. Mesenchymal stem cells (MSCs) appear to be a promising cell therapy owing to their potent modulatory effects on reducing and healing inflammation-induced lung and other tissue injuries. The present pilot study aimed to explore the therapeutic potential and safety of MSCs isolated from healthy cord tissues in the treatment of patients with COVID-19.

METHODS

Twelve patients with COVID-19 treated with MSCs plus conventional therapy and 13 treated with conventional therapy alone (control) were included. The efficacy of MSC infusion was evaluated by changes in oxygenation index, clinical chemistry and hematology tests, immunoglobulin (Ig) levels, and pulmonary computerized tomography (CT) imaging. The safety of MSC infusion was evaluated based on the occurrence of allergic reactions and serious adverse events.

RESULTS

The MSC-treated group demonstrated significantly improved oxygenation index. The area of pulmonary inflammation decreased significantly, and the CT number in the inflammatory area tended to be restored. Decreased IgM levels were also observed after MSC therapy. Laboratory biomarker levels at baseline and after therapy showed no significant changes in either the MSC-treated or control group.

CONCLUSION

Intravenous infusion of MSCs in patients with COVID-19 was effective and well tolerated. Further studies involving a large cohort or randomized controlled trials are warranted.

摘要

目的

冠状病毒病(COVID-19)的爆发对全球公共卫生造成了灾难性的威胁,也给临床医生带来了巨大的挑战。迄今为止,还没有针对严重急性呼吸综合征冠状病毒 2 的特效药物。间充质干细胞(MSCs)因其对减轻和治愈炎症引起的肺和其他组织损伤具有强大的调节作用,似乎是一种很有前途的细胞治疗方法。本初步研究旨在探索从健康脐带组织中分离出的 MSCs 治疗 COVID-19 患者的治疗潜力和安全性。

方法

纳入 12 名接受 MSC 联合常规治疗的 COVID-19 患者和 13 名接受常规治疗的患者(对照组)。通过氧合指数、临床化学和血液学检查、免疫球蛋白(Ig)水平和肺部计算机断层扫描(CT)成像的变化来评估 MSC 输注的疗效。根据过敏反应和严重不良事件的发生情况来评估 MSC 输注的安全性。

结果

MSC 治疗组的氧合指数明显改善。肺部炎症面积明显减少,炎症区域的 CT 数趋于恢复。MSC 治疗后 IgM 水平也有所下降。治疗前后,MSC 治疗组和对照组的实验室生物标志物水平均无明显变化。

结论

静脉输注 MSCs 治疗 COVID-19 患者有效且耐受性良好。需要进一步进行涉及大样本量或随机对照试验的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/888c/8101688/42df31ebf094/cln-76-e2604-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/888c/8101688/42df31ebf094/cln-76-e2604-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/888c/8101688/42df31ebf094/cln-76-e2604-g001.jpg

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