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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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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. |
format | Online Article Text |
id | pubmed-8709782 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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