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
American journal of stem cells Pub Date : 2022-06-15 eCollection Date: 2022-01-01
Alok Sharma, Rohit Kulkarni, Hemangi Sane, Nilkanth Awad, Abhijit Bopardikar, Anagha Joshi, Sujata Baweja, Mohan Joshi, Chandra Vishwanathan, Nandini Gokulchandran, Prerna Badhe, Mazhar Khan, Amruta Paranjape, Pooja Kulkarni, Arjun K Methal
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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.

Abstract Image

Abstract Image

静脉注射来自脐带和胎盘的间充质干细胞治疗中度COVID-19病毒肺炎患者的1期临床试验:研究1期结果
目的:间充质干细胞可作为COVID-19的治疗选择。其免疫调节和抗炎作用可调节过度的炎症反应,促进肺损伤的恢复。方法:通过1期单中心、开放标签、前瞻性临床试验,评价静脉给药脐带胎盘间充质干细胞治疗中度COVID-19的安全性和有效性。该研究分两个阶段进行,共有20名患者。本文讨论了第一阶段的结果,包括前10名患者在第1天和第4天接受1亿个细胞治疗,随访6个月。结果:在给药后立即或随访中没有记录不良事件。临床、实验室和放射学参数均未见恶化。研究组的所有症状均在10天内消失。干预后,所有患者的NLR、CRP、il - 6、铁蛋白和d -二聚体等炎症生物标志物水平均有所改善,SpO2/FiO2比率和PaO2/FiO2比率均有所改善。没有患者进展到严重阶段。10例患者中9例在入院后9天内出院。大多数患者在第7天的胸部x线和胸部CT扫描评分均有改善。干预后28天胸部CT和干预后6个月胸部X线均未见术后纤维化。结论:1亿个间充质干细胞联合标准治疗是安全的,可预防中度COVID-19患者的细胞因子风暴,阻止疾病进展,加速康复。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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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