Mesenchymal stem cells derived from perinatal tissues for treatment of critically ill COVID-19-induced ARDS patients: a case series

Seyed Mohammad Reza Hashemian(Masih Daneshvari Hospital), Rasoul Aliannejad(Shariati Hospital), Morteza Zarrabi(Royan Institute), Masoud Soleimani(Tarbiat Modares University), Massoud Vosough(Royan Institute), Seyedeh-Esmat Hosseini(Royan Institute), Hamed Hossieni(Tehran University of Medical Sciences), Saeed Heidari Keshel(Shahid Beheshti University of Medical Sciences), Zeinab Naderpour(Shariati Hospital), Ensiyeh Hajizadeh‐Saffar(Royan Institute), Elham Shajareh(Shariati Hospital), Hamidreza Jamaati(Masih Daneshvari Hospital), Mina Soufizomorrod(Tarbiat Modares University), Naghmeh Khavandgar(Shariati Hospital), Hediyeh Alemi(Shariati Hospital), Aliasghar Karimi(Fasa University of Medical Sciences), Neda Pak(Children's Medical Center), Negin Hossieni Rouzbahani(Aja University of Medical Sciences), Masoumeh Nouri(Royan Institute), Majid Sorouri(Tehran University of Medical Sciences), Ladan Kashani(Tehran University of Medical Sciences), Hoda Madani(Royan Institute), Nasser Aghdami(Royan Institute), Mohammad Vasei(University of Tehran), Hossein Baharvand(University of Science and Culture)
Stem Cell Research & Therapy
January 29, 2021
Cited by 206Open Access
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Abstract

BACKGROUND: Acute respiratory distress syndrome (ARDS) is a fatal complication of coronavirus disease 2019 (COVID-19). There are a few reports of allogeneic human mesenchymal stem cells (MSCs) as a potential treatment for ARDS. In this phase 1 clinical trial, we present the safety, feasibility, and tolerability of the multiple infusions of high dose MSCs, which originated from the placenta and umbilical cord, in critically ill COVID-19-induced ARDS patients. METHODS: human umbilical cord MSCs (UC-MSCs; 6 cases) or placental MSCs (PL-MSCs; 5 cases). FINDINGS: There were eight men and three women who were 42 to 66 years of age. Of these, six (55%) patients had comorbidities of diabetes, hypertension, chronic lymphocytic leukemia (CLL), and cardiomyopathy (CMP). There were no serious adverse events reported 24-48 h after the cell infusions. We observed reduced dyspnea and increased SpO2 within 48-96 h after the first infusion in seven patients. Of these seven patients, five were discharged from the ICU within 2-7 days (average: 4 days), one patient who had signs of acute renal and hepatic failure was discharged from the ICU on day 18, and the last patient suddenly developed cardiac arrest on day 7 of the cell infusion. Significant reductions in serum levels of tumor necrosis factor-alpha (TNF-α; P < 0.01), IL-8 (P < 0.05), and C-reactive protein (CRP) (P < 0.01) were seen in all six survivors. IL-6 levels decreased in five (P = 0.06) patients and interferon gamma (IFN-γ) levels decreased in four (P = 0.14) patients. Four patients who had signs of multi-organ failure or sepsis died in 5-19 days (average: 10 days) after the first MSC infusion. A low percentage of lymphocytes (< 10%) and leukocytosis were associated with poor outcome (P = 0.02). All six survivors were well with no complaints of dyspnea on day 60 post-infusion. Radiological parameters of the lung computed tomography (CT) scans showed remarkable signs of recovery. INTERPRETATION: We suggest that multiple infusions of high dose allogeneic prenatal MSCs are safe and can rapidly improve respiratory distress and reduce inflammatory biomarkers in some critically ill COVID-19-induced ARDS cases. Patients that develop sepsis or multi-organ failure may not be good candidates for stem cell therapy. Large randomized multicenter clinical trials are needed to discern the exact therapeutic potentials of MSC in COVID-19-induced ARDS.


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