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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:...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
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
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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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