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Treatment of severe COVID-19 with human umbilical cord mesenchymal stem cells
BACKGROUND: COVID-19 is a highly infectious respiratory disease. No therapeutics have yet been proven effective for treating severe COVID-19. OBJECTIVES: To determine whether human umbilical cord mesenchymal stem cell infusion may be effective and safe for the treatment of severe COVID-19. METHODS:...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7432540/ https://www.ncbi.nlm.nih.gov/pubmed/32811531 http://dx.doi.org/10.1186/s13287-020-01875-5 |
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author | Shu, Lei Niu, Changming Li, Ruyou Huang, Tingrong Wang, Yan Huang, Mao Ji, Ningfei Zheng, You Chen, Xiaolin Shi, Lei Wu, Mingjing Deng, Kaili Wei, Jing Wang, Xueli Cao, Yang Yan, Jiaxin Feng, Ganzhu |
author_facet | Shu, Lei Niu, Changming Li, Ruyou Huang, Tingrong Wang, Yan Huang, Mao Ji, Ningfei Zheng, You Chen, Xiaolin Shi, Lei Wu, Mingjing Deng, Kaili Wei, Jing Wang, Xueli Cao, Yang Yan, Jiaxin Feng, Ganzhu |
author_sort | Shu, Lei |
collection | PubMed |
description | BACKGROUND: COVID-19 is a highly infectious respiratory disease. No therapeutics have yet been proven effective for treating severe COVID-19. OBJECTIVES: To determine whether human umbilical cord mesenchymal stem cell infusion may be effective and safe for the treatment of severe COVID-19. METHODS: Patients with severe COVID-19 were randomly divided into 2 groups: the standard treatment group and the standard treatment plus hUC-MSC infusion group. The incidence of progression from severe to critical illness, 28-day mortality, clinical symptom improvement, time to clinical symptom improvement, hematologic indicators including C-reactive protein, lymphocyte number, and interleukin 6, and imaging changes were observed and compared between the two groups. MEASUREMENTS AND MAIN RESULTS: The incidence of progression from severe to critical illness and the 28-day mortality rate were 0 in the hUC-MSC treatment group, while 4 patients in the control group deteriorated to critical condition and received invasive ventilation; 3 of them died, and the 28-day mortality rate was 10.34%. In the hUC-MSC treatment group, the time to clinical improvement was shorter than that in the control group. Clinical symptoms of weakness and fatigue, shortness of breath, and low oxygen saturation obviously improved beginning on the third day of stem cell infusion and reached a significant difference on day 7. CRP and IL-6 levels were significantly lower from day 3 of infusion, the time for the lymphocyte count to return to the normal range was significantly faster, and lung inflammation absorption was significantly shorter on CT imaging in the hUC-MSC group than in the control group. CONCLUSIONS: Intravenous transplantation of hUC-MSCs is a safe and effective method that can be considered a salvage and priority treatment option for severe COVID-19. TRIAL REGISTRATION: Chinese Clinical Trial Registration; ChiCTR2000031494; Registered on 2 April 2020; http://www.medresman.org |
format | Online Article Text |
id | pubmed-7432540 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-74325402020-08-18 Treatment of severe COVID-19 with human umbilical cord mesenchymal stem cells Shu, Lei Niu, Changming Li, Ruyou Huang, Tingrong Wang, Yan Huang, Mao Ji, Ningfei Zheng, You Chen, Xiaolin Shi, Lei Wu, Mingjing Deng, Kaili Wei, Jing Wang, Xueli Cao, Yang Yan, Jiaxin Feng, Ganzhu Stem Cell Res Ther Research BACKGROUND: COVID-19 is a highly infectious respiratory disease. No therapeutics have yet been proven effective for treating severe COVID-19. OBJECTIVES: To determine whether human umbilical cord mesenchymal stem cell infusion may be effective and safe for the treatment of severe COVID-19. METHODS: Patients with severe COVID-19 were randomly divided into 2 groups: the standard treatment group and the standard treatment plus hUC-MSC infusion group. The incidence of progression from severe to critical illness, 28-day mortality, clinical symptom improvement, time to clinical symptom improvement, hematologic indicators including C-reactive protein, lymphocyte number, and interleukin 6, and imaging changes were observed and compared between the two groups. MEASUREMENTS AND MAIN RESULTS: The incidence of progression from severe to critical illness and the 28-day mortality rate were 0 in the hUC-MSC treatment group, while 4 patients in the control group deteriorated to critical condition and received invasive ventilation; 3 of them died, and the 28-day mortality rate was 10.34%. In the hUC-MSC treatment group, the time to clinical improvement was shorter than that in the control group. Clinical symptoms of weakness and fatigue, shortness of breath, and low oxygen saturation obviously improved beginning on the third day of stem cell infusion and reached a significant difference on day 7. CRP and IL-6 levels were significantly lower from day 3 of infusion, the time for the lymphocyte count to return to the normal range was significantly faster, and lung inflammation absorption was significantly shorter on CT imaging in the hUC-MSC group than in the control group. CONCLUSIONS: Intravenous transplantation of hUC-MSCs is a safe and effective method that can be considered a salvage and priority treatment option for severe COVID-19. TRIAL REGISTRATION: Chinese Clinical Trial Registration; ChiCTR2000031494; Registered on 2 April 2020; http://www.medresman.org BioMed Central 2020-08-18 /pmc/articles/PMC7432540/ /pubmed/32811531 http://dx.doi.org/10.1186/s13287-020-01875-5 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Shu, Lei Niu, Changming Li, Ruyou Huang, Tingrong Wang, Yan Huang, Mao Ji, Ningfei Zheng, You Chen, Xiaolin Shi, Lei Wu, Mingjing Deng, Kaili Wei, Jing Wang, Xueli Cao, Yang Yan, Jiaxin Feng, Ganzhu Treatment of severe COVID-19 with human umbilical cord mesenchymal stem cells |
title | Treatment of severe COVID-19 with human umbilical cord mesenchymal stem cells |
title_full | Treatment of severe COVID-19 with human umbilical cord mesenchymal stem cells |
title_fullStr | Treatment of severe COVID-19 with human umbilical cord mesenchymal stem cells |
title_full_unstemmed | Treatment of severe COVID-19 with human umbilical cord mesenchymal stem cells |
title_short | Treatment of severe COVID-19 with human umbilical cord mesenchymal stem cells |
title_sort | treatment of severe covid-19 with human umbilical cord mesenchymal stem cells |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7432540/ https://www.ncbi.nlm.nih.gov/pubmed/32811531 http://dx.doi.org/10.1186/s13287-020-01875-5 |
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