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利用胎盘源蜕膜基质细胞攻克 COVID-19 诱导的 ARDS 中的细胞因子风暴。

Conquering the cytokine storm in COVID-19-induced ARDS using placenta-derived decidua stromal cells.

机构信息

Translational Cell Therapy Research (TCR), Department of Clinical Science, Intervention and Technology, CLINTEC, Karolinska Institutet, Huddinge, Sweden.

Hematopoietic Stem Cell Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

出版信息

J Cell Mol Med. 2021 Nov;25(22):10554-10564. doi: 10.1111/jcmm.16986. Epub 2021 Oct 10.


DOI:10.1111/jcmm.16986
PMID:34632708
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8581334/
Abstract

Acute respiratory distress syndrome (ARDS) is the most common cause of death in COVID-19 patients. The cytokine storm is the main driver of the severity and magnitude of ARDS. Placenta-derived decidua stromal cells (DSCs) have a stronger immunosuppressive effect than other sources of mesenchymal stromal cells. Safety and efficacy study included 10 patients with a median age of 50 (range 14-68) years with COVID-19-induced ARDS. DSCs were administered 1-2 times at a dose of 1 × 10 /kg. End points were safety and efficacy by survival, oxygenation and effects on levels of cytokines. Oxygenation levels increased from a median of 80.5% (range 69-88) to 95% (range 78-99) (p = 0.012), and pulmonary infiltrates disappeared in all patients. Levels of IL-6 decreased from a median of 69.3 (range 35.0-253.4) to 11 (range 4.0-38.3) pg/ml (p = 0.018), and CRP decreased from 69 (range 5-169) to 6 (range 2-31) mg/ml (p = 0.028). Two patients died, one of a myocardial infarction and the other of multiple organ failure, diagnosed before the DSC therapy. The other patients recovered and left the intensive care unit (ICU) within a median of 6 (range 3-12) days. DSC therapy is safe and capable of improving oxygenation, decreasing inflammatory cytokine level and clearing pulmonary infiltrates in patients with COVID-19.

摘要

急性呼吸窘迫综合征(ARDS)是 COVID-19 患者死亡的最常见原因。细胞因子风暴是导致 ARDS 严重程度和程度的主要驱动因素。胎盘来源的蜕膜基质细胞(DSC)比其他间充质基质细胞来源具有更强的免疫抑制作用。安全性和疗效研究包括 10 名中位年龄为 50 岁(范围 14-68 岁)的 COVID-19 诱导的 ARDS 患者。DSC 以 1×10 6 /kg 的剂量给药 1-2 次。终点是通过生存、氧合和对细胞因子水平的影响来评估安全性和疗效。氧合水平从中位数 80.5%(范围 69-88%)增加到 95%(范围 78-99%)(p=0.012),所有患者的肺部浸润均消失。IL-6 水平从中位数 69.3(范围 35.0-253.4)降至 11(范围 4.0-38.3)pg/ml(p=0.018),CRP 从 69(范围 5-169)降至 6(范围 2-31)mg/ml(p=0.028)。两名患者死亡,其中一名死于心肌梗死,另一名死于多器官衰竭,这两名患者在 DSC 治疗前被诊断出。其余患者恢复并在中位数 6(范围 3-12)天内离开重症监护病房(ICU)。DSC 治疗安全,能够改善 COVID-19 患者的氧合、降低炎症细胞因子水平和清除肺部浸润。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39f3/8581334/e312aaa7dcda/JCMM-25-10554-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39f3/8581334/3512cc6bc3e0/JCMM-25-10554-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39f3/8581334/4ae36644ae73/JCMM-25-10554-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39f3/8581334/b6ff5907842d/JCMM-25-10554-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39f3/8581334/e312aaa7dcda/JCMM-25-10554-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39f3/8581334/3512cc6bc3e0/JCMM-25-10554-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39f3/8581334/4ae36644ae73/JCMM-25-10554-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39f3/8581334/b6ff5907842d/JCMM-25-10554-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39f3/8581334/e312aaa7dcda/JCMM-25-10554-g003.jpg

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Conquering the cytokine storm in COVID-19-induced ARDS using placenta-derived decidua stromal cells.

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[7]
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引用本文的文献

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[2]
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[3]
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[4]
Comprehensive Review of COVID-19: Epidemiology, Pathogenesis, Advancement in Diagnostic and Detection Techniques, and Post-Pandemic Treatment Strategies.

Int J Mol Sci. 2024-7-26

[5]
Challenges of mesenchymal stem cells in the clinical treatment of COVID-19.

Cell Tissue Res. 2024-6

[6]
Placenta-Derived Decidua Stromal Cells: A New Frontier in the Therapy of Acute Graft-Versus-Host Disease.

Stem Cells. 2024-4-15

[7]
Immune-Cell-Based Therapy for COVID-19: Current Status.

Viruses. 2023-10-25

[8]
Novel therapies for graft versus host disease with a focus on cell therapies.

Front Immunol. 2023

[9]
Mesenchymal Stem Cells in the Treatment of COVID-19.

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[10]
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本文引用的文献

[1]
Corticosteroids in COVID-19 and non-COVID-19 ARDS: a systematic review and meta-analysis.

Intensive Care Med. 2021-5

[2]
Umbilical cord mesenchymal stem cells for COVID-19 acute respiratory distress syndrome: A double-blind, phase 1/2a, randomized controlled trial.

Stem Cells Transl Med. 2021-5

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Repurposed Antiviral Drugs for Covid-19 - Interim WHO Solidarity Trial Results.

N Engl J Med. 2021-2-11

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World J Stem Cells. 2020-10-26

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N Engl J Med. 2020-10-21

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Cytokine elevation in severe and critical COVID-19: a rapid systematic review, meta-analysis, and comparison with other inflammatory syndromes.

Lancet Respir Med. 2020-10-16

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Human umbilical cord-derived mesenchymal stem cell therapy in patients with COVID-19: a phase 1 clinical trial.

Signal Transduct Target Ther. 2020-8-27

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Mortality in COVID-19 patients with acute respiratory distress syndrome and corticosteroids use: a systematic review and meta-analysis.

Expert Rev Respir Med. 2020-9-29

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MSC Therapies for COVID-19: Importance of Patient Coagulopathy, Thromboprophylaxis, Cell Product Quality and Mode of Delivery for Treatment Safety and Efficacy.

Front Immunol. 2020-5-19

[10]
Cytokine storm and leukocyte changes in mild versus severe SARS-CoV-2 infection: Review of 3939 COVID-19 patients in China and emerging pathogenesis and therapy concepts.

J Leukoc Biol. 2020-6-13

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