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Adipose-derived mesenchymal stromal cells for the treatment of patients with severe SARS-CoV-2 pneumonia requiring mechanical ventilation. A proof of concept study.
Sánchez-Guijo, Fermín; García-Arranz, Mariano; López-Parra, Miriam; Monedero, Pablo; Mata-Martínez, Carmen; Santos, Arnoldo; Sagredo, Víctor; Álvarez-Avello, José-Manuel; Guerrero, José Eugenio; Pérez-Calvo, César; Sánchez-Hernández, Miguel-Vicente; Del-Pozo, José Luis; Andreu, Enrique J; Fernández-Santos, María-Eugenia; Soria-Juan, Barbara; Hernández-Blasco, Luis M; Andreu, Etelvina; Sempere, José M; Zapata, Agustín G; Moraleda, José M; Soria, Bernat; Fernández-Avilés, Francisco; García-Olmo, Damián; Prósper, Felipe.
  • Sánchez-Guijo F; Cell Therapy Area, Hematology Department, IBSAL-Hospital Universitario de Salamanca, Universidad de Salamanca, Salamanca, Spain.
  • García-Arranz M; RETIC TerCel, ISCIII, Madrid, Spain.
  • López-Parra M; Grupo Español de Trasplante y Terapia Celular (GETH), Spain.
  • Monedero P; RETIC TerCel, ISCIII, Madrid, Spain.
  • Mata-Martínez C; New Therapies Unit, Health Research Institute Fundación Jiménez Díaz, Madrid, Spain.
  • Santos A; Surgery Department. School of Medicine, Universidad Autónoma de Madrid, Madrid, Spain.
  • Sagredo V; Cell Therapy Area, Hematology Department, IBSAL-Hospital Universitario de Salamanca, Universidad de Salamanca, Salamanca, Spain.
  • Álvarez-Avello JM; RETIC TerCel, ISCIII, Madrid, Spain.
  • Guerrero JE; Grupo Español de Trasplante y Terapia Celular (GETH), Spain.
  • Pérez-Calvo C; Department of Anesthesia and Intensive Care, Clínica Universidad de Navarra, Pamplona, Spain.
  • Sánchez-Hernández MV; Instituto de Investigación Sanitaria (IiSGM), Hospital General Universitario Gregorio Marañón, Madrid, Spain.
  • Del-Pozo JL; Intensive Care Unit, Hospital Universitario Fundación Jiménez Díaz, Madrid, Spain.
  • Andreu EJ; CIBER de Enfermedades Respiratorias CIBERES, Madrid, Spain.
  • Fernández-Santos ME; Intensive Care Unit, IBSAL- Hospital Universitario de Salamanca, University of Salamanca, Salamanca, Spain.
  • Soria-Juan B; Department of Anesthesia and Intensive Care, Clínica Universidad de Navarra, Pamplona, Spain.
  • Hernández-Blasco LM; Instituto de Investigación Sanitaria (IiSGM), Hospital General Universitario Gregorio Marañón, Madrid, Spain.
  • Andreu E; Intensive Care Unit, Hospital Universitario Fundación Jiménez Díaz, Madrid, Spain.
  • Sempere JM; Department of Anesthesia, IBSAL- Hospital Universitario de Salamanca, University of Salamanca, Salamanca, Spain.
  • Zapata AG; Infectious Diseases Division, Microbiology Department, Clínica Universidad de Navarra, Spain.
  • Moraleda JM; RETIC TerCel, ISCIII, Madrid, Spain.
  • Soria B; Cell Therapy Area and Hematology Department, Clínica Universidad de Navarra, Pamplona, Spain.
  • Fernández-Avilés F; RETIC TerCel, ISCIII, Madrid, Spain.
  • García-Olmo D; Instituto de Investigación Sanitaria (IiSGM), Hospital General Universitario Gregorio Marañón, Madrid, Spain.
  • Prósper F; CIBER Cardiovascular (CIBERCV), Instituto de Salud Carlos III, Madrid, Spain.
EClinicalMedicine ; 25: 100454, 2020 Aug.
Article in English | MEDLINE | ID: covidwho-638357
ABSTRACT

BACKGROUND:

Identification of effective treatments in severe cases of COVID-19 requiring mechanical ventilation represents an unmet medical need. Our aim was to determine whether the administration of adipose-tissue derived mesenchymal stromal cells (AT-MSC) is safe and potentially useful in these patients.

METHODS:

Thirteen COVID-19 adult patients under invasive mechanical ventilation who had received previous antiviral and/or anti-inflammatory treatments (including steroids, lopinavir/ritonavir, hydroxychloroquine and/or tocilizumab, among others) were treated with allogeneic AT-MSC. Ten patients received two doses, with the second dose administered a median of 3 days (interquartile range-IQR- 1 day) after the first one. Two patients received a single dose and another patient received 3 doses. Median number of cells per dose was 0.98 × 106 (IQR 0.50 × 106) AT-MSC/kg of recipient's body weight. Potential adverse effects related to cell infusion and clinical outcome were assessed. Additional parameters analyzed included changes in imaging, analytical and inflammatory parameters.

FINDINGS:

First dose of AT-MSC was administered at a median of 7 days (IQR 12 days) after mechanical ventilation. No adverse events were related to cell therapy. With a median follow-up of 16 days (IQR 9 days) after the first dose, clinical improvement was observed in nine patients (70%). Seven patients were extubated and discharged from ICU while four patients remained intubated (two with an improvement in their ventilatory and radiological parameters and two in stable condition). Two patients died (one due to massive gastrointestinal bleeding unrelated to MSC therapy). Treatment with AT-MSC was followed by a decrease in inflammatory parameters (reduction in C-reactive protein, IL-6, ferritin, LDH and d-dimer) as well as an increase in lymphocytes, particularly in those patients with clinical improvement.

INTERPRETATION:

Treatment with intravenous administration of AT-MSC in 13 severe COVID-19 pneumonia under mechanical ventilation in a small case series did not induce significant adverse events and was followed by clinical and biological improvement in most subjects.

FUNDING:

None.
Keywords

Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Prognostic study Topics: Vaccines Language: English Journal: EClinicalMedicine Year: 2020 Document Type: Article Affiliation country: J.eclinm.2020.100454

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Full text: Available Collection: International databases Database: MEDLINE Type of study: Cohort study / Prognostic study Topics: Vaccines Language: English Journal: EClinicalMedicine Year: 2020 Document Type: Article Affiliation country: J.eclinm.2020.100454