Adipose-derived mesenchymal stromal cells for the treatment of patients with severe SARS-CoV-2 pneumonia requiring mechanical ventilation. A proof of concept study

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Título: Adipose-derived mesenchymal stromal cells for the treatment of patients with severe SARS-CoV-2 pneumonia requiring mechanical ventilation. A proof of concept study
Autor/es: 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 Ortells, José Miguel | Zapata, Agustín G. | Moraleda, José M. | Soria, Bernat | Fernández-Avilés, Francisco | García-Olmo, Damián | Prósper, Felipe
Grupo/s de investigación o GITE: Grupo de Inmunología, Biología Celular y del Desarrollo
Centro, Departamento o Servicio: Universidad de Alicante. Departamento de Biotecnología
Palabras clave: COVID-19 | SARS-CoV-2 | Pneumonia | Mechanical ventilation | Mesenchymal stromal cells | Cellular therapy | Case series
Área/s de conocimiento: Inmunología
Fecha de publicación: ago-2020
Editor: Elsevier
Cita bibliográfica: EClinicalMedicine. 2020, 25: 100454. https://doi.org/10.1016/j.eclinm.2020.100454
Resumen: 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.
Patrocinador/es: We would like to acknowledge the Instituto de Salud Carlos III (ISCIII) through the project “RD16/0011: Red de Terapia Celular”, from the sub-program RETICS, integrated in the “Plan Estatal de I+D+I 2013-2016” and co-financed by the European Regional Development Fund “A way to make Europe”, groups RD16/0011/0001, -/0002, -/005, -/0013, -/0015, -/0029), the Centro en Red de Medicina Regenerativa y Terapia Celular de Castilla y León, Spain and AvanCell-CM (Red de Investigación de Terapia Celular de la Comunidad de Madrid, Spain), for supporting some personnel and networking activities.
URI: http://hdl.handle.net/10045/108919
ISSN: 2589-5370
DOI: 10.1016/j.eclinm.2020.100454
Idioma: eng
Tipo: info:eu-repo/semantics/article
Derechos: © 2020 The Authors. Published by Elsevier Ltd. This is an open access article under the CC BY-NC-ND license. (http://creativecommons.org/licenses/by-nc-nd/4.0/)
Revisión científica: si
Versión del editor: https://doi.org/10.1016/j.eclinm.2020.100454
Aparece en las colecciones:INV - Grupo de Inmunología - Artículos de Revistas

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