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Human mesenchymal stem cells treatment for severe COVID-19: 1-year follow-up results of a randomized, double-blind, placebo-controlled trial

BACKGROUND: The long-term consequences of human umbilical cord-derived mesenchymal stem cell (UC-MSC) treatment for COVID-19 patients are yet to be reported. This study assessed the 1-year outcomes in patients with severe COVID-19, who were recruited in our previous UC-MSC clinical trial. METHODS: I...

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Autores principales: Shi, Lei, Yuan, Xin, Yao, Weiqi, Wang, Siyu, Zhang, Chao, Zhang, Bo, Song, Jinwen, Huang, Lei, Xu, Zhe, Fu, Jun-Liang, Li, Yuanyuan, Xu, Ruonan, Li, Tian-Tian, Dong, Jinghui, Cai, Jianming, Li, Genshi, Xie, Yunbo, Shi, Ming, Li, Yonggang, Zhang, Yu, Xie, Wei-Fen, Wang, Fu-Sheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8709782/
https://www.ncbi.nlm.nih.gov/pubmed/34963099
http://dx.doi.org/10.1016/j.ebiom.2021.103789
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author Shi, Lei
Yuan, Xin
Yao, Weiqi
Wang, Siyu
Zhang, Chao
Zhang, Bo
Song, Jinwen
Huang, Lei
Xu, Zhe
Fu, Jun-Liang
Li, Yuanyuan
Xu, Ruonan
Li, Tian-Tian
Dong, Jinghui
Cai, Jianming
Li, Genshi
Xie, Yunbo
Shi, Ming
Li, Yonggang
Zhang, Yu
Xie, Wei-Fen
Wang, Fu-Sheng
author_facet Shi, Lei
Yuan, Xin
Yao, Weiqi
Wang, Siyu
Zhang, Chao
Zhang, Bo
Song, Jinwen
Huang, Lei
Xu, Zhe
Fu, Jun-Liang
Li, Yuanyuan
Xu, Ruonan
Li, Tian-Tian
Dong, Jinghui
Cai, Jianming
Li, Genshi
Xie, Yunbo
Shi, Ming
Li, Yonggang
Zhang, Yu
Xie, Wei-Fen
Wang, Fu-Sheng
author_sort Shi, Lei
collection PubMed
description BACKGROUND: The long-term consequences of human umbilical cord-derived mesenchymal stem cell (UC-MSC) treatment for COVID-19 patients are yet to be reported. This study assessed the 1-year outcomes in patients with severe COVID-19, who were recruited in our previous UC-MSC clinical trial. METHODS: In this prospective, longitudinal, cohort study, 100 patients enrolled in our phase 2 trial were prospectively followed up at 3-month intervals for 1 year to evaluate the long-term safety and effectiveness of UC-MSC treatment. The primary endpoint was an altered proportion of whole-lung lesion volumes measured by high-resolution CT. Other imaging outcomes, 6 min walking distance (6-MWD), lung function, plasma biomarkers, and adverse events were also recorded and analyzed. This trial was registered with ClinicalTrials.gov (NCT04288102). FINDINGS: MSC administration improved in whole-lung lesion volume compared with the placebo with a difference of −10.8% (95% CI: −20.7%, −1.5%, p = 0.030) on day 10. MSC also reduced the proportion of solid component lesion volume compared with the placebo at each follow-up point. More interestingly, 17.9% (10/56) of patients in the MSC group had normal CT images at month 12, but none in the placebo group (p = 0.013). The incidence of symptoms was lower in the MSC group than in the placebo group at each follow-up time. Neutralizing antibodies were all positive, with a similar median inhibition rate (61.6% vs. 67.6%) in both groups at month 12. No difference in adverse events at the 1-year follow-up and tumor markers at month 12 were observed between the two groups. INTERPRETATION: UC-MSC administration achieves a long-term benefit in the recovery of lung lesions and symptoms in COVID-19 patients. FUNDING: The National Key R&D Program of China, the Innovation Groups of the National Natural Science Foundation of China, and the National Science and Technology Major Project.
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spelling pubmed-87097822021-12-28 Human mesenchymal stem cells treatment for severe COVID-19: 1-year follow-up results of a randomized, double-blind, placebo-controlled trial Shi, Lei Yuan, Xin Yao, Weiqi Wang, Siyu Zhang, Chao Zhang, Bo Song, Jinwen Huang, Lei Xu, Zhe Fu, Jun-Liang Li, Yuanyuan Xu, Ruonan Li, Tian-Tian Dong, Jinghui Cai, Jianming Li, Genshi Xie, Yunbo Shi, Ming Li, Yonggang Zhang, Yu Xie, Wei-Fen Wang, Fu-Sheng EBioMedicine Article BACKGROUND: The long-term consequences of human umbilical cord-derived mesenchymal stem cell (UC-MSC) treatment for COVID-19 patients are yet to be reported. This study assessed the 1-year outcomes in patients with severe COVID-19, who were recruited in our previous UC-MSC clinical trial. METHODS: In this prospective, longitudinal, cohort study, 100 patients enrolled in our phase 2 trial were prospectively followed up at 3-month intervals for 1 year to evaluate the long-term safety and effectiveness of UC-MSC treatment. The primary endpoint was an altered proportion of whole-lung lesion volumes measured by high-resolution CT. Other imaging outcomes, 6 min walking distance (6-MWD), lung function, plasma biomarkers, and adverse events were also recorded and analyzed. This trial was registered with ClinicalTrials.gov (NCT04288102). FINDINGS: MSC administration improved in whole-lung lesion volume compared with the placebo with a difference of −10.8% (95% CI: −20.7%, −1.5%, p = 0.030) on day 10. MSC also reduced the proportion of solid component lesion volume compared with the placebo at each follow-up point. More interestingly, 17.9% (10/56) of patients in the MSC group had normal CT images at month 12, but none in the placebo group (p = 0.013). The incidence of symptoms was lower in the MSC group than in the placebo group at each follow-up time. Neutralizing antibodies were all positive, with a similar median inhibition rate (61.6% vs. 67.6%) in both groups at month 12. No difference in adverse events at the 1-year follow-up and tumor markers at month 12 were observed between the two groups. INTERPRETATION: UC-MSC administration achieves a long-term benefit in the recovery of lung lesions and symptoms in COVID-19 patients. FUNDING: The National Key R&D Program of China, the Innovation Groups of the National Natural Science Foundation of China, and the National Science and Technology Major Project. Elsevier 2021-12-25 /pmc/articles/PMC8709782/ /pubmed/34963099 http://dx.doi.org/10.1016/j.ebiom.2021.103789 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Shi, Lei
Yuan, Xin
Yao, Weiqi
Wang, Siyu
Zhang, Chao
Zhang, Bo
Song, Jinwen
Huang, Lei
Xu, Zhe
Fu, Jun-Liang
Li, Yuanyuan
Xu, Ruonan
Li, Tian-Tian
Dong, Jinghui
Cai, Jianming
Li, Genshi
Xie, Yunbo
Shi, Ming
Li, Yonggang
Zhang, Yu
Xie, Wei-Fen
Wang, Fu-Sheng
Human mesenchymal stem cells treatment for severe COVID-19: 1-year follow-up results of a randomized, double-blind, placebo-controlled trial
title Human mesenchymal stem cells treatment for severe COVID-19: 1-year follow-up results of a randomized, double-blind, placebo-controlled trial
title_full Human mesenchymal stem cells treatment for severe COVID-19: 1-year follow-up results of a randomized, double-blind, placebo-controlled trial
title_fullStr Human mesenchymal stem cells treatment for severe COVID-19: 1-year follow-up results of a randomized, double-blind, placebo-controlled trial
title_full_unstemmed Human mesenchymal stem cells treatment for severe COVID-19: 1-year follow-up results of a randomized, double-blind, placebo-controlled trial
title_short Human mesenchymal stem cells treatment for severe COVID-19: 1-year follow-up results of a randomized, double-blind, placebo-controlled trial
title_sort human mesenchymal stem cells treatment for severe covid-19: 1-year follow-up results of a randomized, double-blind, placebo-controlled trial
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8709782/
https://www.ncbi.nlm.nih.gov/pubmed/34963099
http://dx.doi.org/10.1016/j.ebiom.2021.103789
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