Phase 1 clinical trial for intravenous administration of mesenchymal stem cells derived from umbilical cord and placenta in patients with moderate COVID-19 virus pneumonia: results of stage 1 of the study.

IF 1.5 Q4 CELL BIOLOGY
A. Sharma, Rohit N. Kulkarni, H. Sane, N. Awad, A. Bopardikar, Anagha R. Joshi, Sujata Baweja, Mohan A Joshi, C. Vishwanathan, N. Gokulchandran, P. Badhe, Mazhar I. Khan, A. Paranjape, P. Kulkarni, Arjun K Methal
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引用次数: 5

Abstract

OBJECTIVE Mesenchymal stem cells can serve as a therapeutic option for COVID-19. Their immunomodulatory and anti-inflammatory properties can regulate the exaggerated inflammatory response and promote recovery of lung damage. METHOD Phase-1, single-centre open-label, prospective clinical trial was conducted to evaluate the safety and efficacy of intravenous administration of mesenchymal stem cells derived from umbilical cord and placenta in moderate COVID-19. The study was done in 2 stages with total 20 patients. Herein, the results of stage 1 including first 10 patients receiving 100 million cells on day 1 and 4 with a follow up of 6 months have been discussed. RESULTS No adverse events were recorded immediately after the administration of MSCs or on follow up. There was no deterioration observed in clinical, laboratory and radiological parameters. All symptoms of the study group resolved within 10 days. Levels of inflammatory biomarkers such as NLR, CRP, IL6, ferritin and D-dimer improved in all patients after intervention along with improved oxygenation demonstrated by improvement in the SpO2/FiO2 ratio and PaO2/FiO2 ratio. None of the patients progressed to severe stage. 9 out of 10 patients were discharged within 9 days of their admission. Improvements were noted in chest x-ray and chest CT scan scores at day 7 in most patients. No post-covid fibrosis was observed on chest CT 28 days after intervention and Chest X ray after 6 months of the intervention. CONCLUSION Administration of 100 million mesenchymal stem cells in combination with standard treatment was found to be safe and resulted in prevention of the cytokine storm, halting of the disease progression and acceleration of recovery in moderate COVID-19. This clinical trial has been registered with the Clinical Trial Registry- India (CTRI) as CTRI/2020/08/027043. http://www.ctri.nic.in/Clinicaltrials/pmaindet2.php?trialid=43175.
在中度新冠肺炎病毒性肺炎患者中静脉注射脐带和胎盘来源的间充质干细胞的1期临床试验:研究的1期结果。
目的间充质干细胞可作为新冠肺炎的治疗选择。它们的免疫调节和抗炎特性可以调节夸大的炎症反应,促进肺损伤的恢复。方法进行1期、单中心开放标记、前瞻性临床试验,评估静脉注射脐带和胎盘间充质干细胞治疗中度新冠肺炎的安全性和有效性。该研究分两个阶段进行,共有20名患者。在此,已经讨论了第1阶段的结果,包括在第1天和第4天接受1亿个细胞并随访6个月的前10名患者。结果MSCs给药后或随访时均未记录不良事件。临床、实验室和放射学参数均未出现恶化。研究组的所有症状均在10天内得到缓解。干预后,所有患者的炎症生物标志物(如NLR、CRP、IL6、铁蛋白和D-二聚体)水平都有所改善,氧合也有所改善,表现为SpO2/FiO2比率和PaO2/FiO2比率的改善。没有一个病人发展到严重阶段。10名患者中有9名在入院后9天内出院。大多数患者在第7天的胸部x光和胸部CT扫描评分均有改善。在干预后28天的胸部CT和干预后6个月的胸部X光检查中未观察到冠状病毒后纤维化。结论1亿间充质干细胞联合标准治疗是安全的,可预防细胞因子风暴,阻止疾病进展,加速中度新冠肺炎患者的康复。该临床试验已在印度临床试验注册中心(CTRI)注册为CTRI/2020/08/027043。http://www.ctri.nic.in/Clinicaltrials/pmaindet2.php?trialid=43175.
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