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间充质基质细胞疗法治疗 2019 年冠状病毒病引起的急性呼吸窘迫综合征。

Mesenchymal stromal cell therapy for acute respiratory distress syndrome due to coronavirus disease 2019.

机构信息

Division of Pulmonary and Critical Care Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.

Division of Hematology and Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, New York, USA; Department of Pathology, Molecular and Cell-Based Medicine, Icahn School of Medicine at Mount Sinai, New York, New York, USA.

出版信息

Cytotherapy. 2022 Aug;24(8):835-840. doi: 10.1016/j.jcyt.2022.03.006. Epub 2022 Apr 11.

Abstract

BACKGROUND AIMS

The acute respiratory distress syndrome (ARDS) resulting from coronavirus disease 2019 (COVID-19) is associated with a massive release of inflammatory cytokines and high mortality. Mesenchymal stromal cells (MSCs) have anti-inflammatory properties and have shown activity in treating acute lung injury. Here the authors report a case series of 11 patients with COVID-19-associated ARDS (CARDS) requiring mechanical ventilation who were treated with remestemcel-L, an allogeneic MSC product, under individual patient emergency investigational new drug applications.

METHODS

Patients were eligible if they were mechanically ventilated for less than 72 h prior to the first infusion. Patients with pre-existing lung disease requiring supplemental oxygen or severe liver or kidney injury were excluded. Each patient received two infusions of remestemcel-L at a dose of 2 million cells/kg per infusion given 48-120 h apart.

RESULTS

Remestemcel-L infusions were well tolerated in all 11 patients. At the end of the 28-day follow-up period, 10 (91%, 95% confidence interval [CI], 59-100%) patients were extubated, nine (82%, 95% CI, 48-97%) patients remained liberated from mechanical ventilation and were discharged from the intensive care unit and two (18%, 95 CI%, 2-52%) patients died. The median time to extubation was 10 days. Eight (73%, 95% CI, 34-100%) patients were discharged from the hospital. C-reactive protein levels significantly declined within 5 days of MSC infusion.

CONCLUSIONS

The authors demonstrate in this case series that remestemcel-L infusions to treat moderate to severe CARDS were safe and well tolerated and resulted in improved clinical outcomes.

摘要

背景目的

由 2019 年冠状病毒病(COVID-19)引起的急性呼吸窘迫综合征(ARDS)与大量炎症细胞因子的释放和高死亡率有关。间充质基质细胞(MSCs)具有抗炎特性,并已显示在治疗急性肺损伤方面具有活性。在这里,作者报告了 11 例 COVID-19 相关 ARDS(CARDS)患者的病例系列,这些患者需要机械通气,并根据个别患者的紧急调查性新药申请,使用异体 MSC 产品 remestemcel-L 进行治疗。

方法

如果患者在第一次输注前机械通气时间少于 72 小时,则符合入组条件。排除需要补充氧气或严重肝或肾功能损伤的预先存在肺部疾病的患者。每位患者接受两次输注 remestemcel-L,剂量为每千克 200 万个细胞/次,两次输注之间间隔 48-120 小时。

结果

11 例患者均能很好地耐受 remestemcel-L 输注。在 28 天的随访期结束时,10 例(91%,95%置信区间[CI],59-100%)患者拔管,9 例(82%,95% CI,48-97%)患者仍无需机械通气,并从重症监护病房出院,2 例(18%,95% CI%,2-52%)患者死亡。拔管的中位时间为 10 天。8 例(73%,95% CI,34-100%)患者出院。MSC 输注后 5 天内 C 反应蛋白水平显著下降。

结论

在本病例系列中,作者证明 remestemcel-L 输注治疗中重度 CARDS 是安全且耐受良好的,并导致临床结局改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2478/8995321/1e395b6aecc8/gr1_lrg.jpg

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