急性呼吸窘迫综合征
医学
肿瘤坏死因子α
2019年冠状病毒病(COVID-19)
脐带
肿瘤坏死因子受体
间充质干细胞
受体
干细胞
内科学
2019-20冠状病毒爆发
免疫学
男科
肺
病毒学
生物
细胞生物学
病理
爆发
传染病(医学专业)
疾病
作者
Dimitrios Kouroupis,Giacomo Lanzoni,Elina Linetsky,Shari Messinger Cayetano,Sarah Wishnek Metalonis,Clarissa Leñero,Logan D. Stone,Pedro Luiz Menin Ruiz,Diego Correa,C. Ricordi
出处
期刊:PubMed
日期:2021-06-01
卷期号:25 (12): 4435-4438
被引量:24
标识
DOI:10.26355/eurrev_202106_26156
摘要
We aimed at explaining the mechanism of therapeutic effect of Umbilical Cord Mesenchymal Stem Cells (UC-MSC) in subjects with COVID-19 Acute Respiratory Distress Syndrome (ARDS). Patients with COVID-19 ARDS present with a hyperinflammatory response characterized by high levels of circulating pro-inflammatory mediators, including tumor necrosis factor α and β (TNFα and TNFβ). Inflammatory functions of these TNFs can be inhibited by soluble TNF Receptor 2 (sTNFR2). In patients with COVID-19 ARDS, UC-MSC appear to impart a robust anti-inflammatory effect, and treatment is associated with remarkable clinical improvements. We investigated the levels of TNFα, TNFβ and sTNFR2 in blood plasma samples collected from subjects with COVID-19 ARDS enrolled in our trial of UC-MSC treatment.We analyzed plasma samples from subjects with COVID-19 ARDS (n=24) enrolled in a Phase 1/2a randomized controlled trial of UC-MSC treatment. Plasma samples were obtained at Day 0 (baseline, before UC-MSC or control infusion), and Day 6 post infusion. Plasma concentrations of sTNFR2, TNFα, and TNFβ were evaluated using a quantitative multiplex protein array.Our data indicate that at Day 6 after infusion, UC-MSC recipients develop significantly increased levels of plasma sTNFR2 and significantly decreased levels of TNFα and TNFβ, compared to controls.These observations suggest that sTNFR2 plays a mechanistic role in mediating UC-MSC effect on TNFα and TNFβ plasma levels, determining a decrease in inflammation in COVID-19 ARDS.
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