Immunomodulatory and Anti-fibrotic Effects Following the Infusion of Umbilical Cord Mesenchymal Stromal Cells in a Critically Ill Patient With COVID-19 Presenting Lung Fibrosis: A Case Report

被引:3
|
作者
da Silva, Katia Nunes [1 ,2 ,3 ]
Guedes Pinheiro, Priscila Carvalho [1 ]
Nunes Gobatto, Andre Luiz [1 ]
Passos, Rogerio da Hora [4 ]
Paredes, Bruno Diaz [1 ,2 ]
de Arago Franca, Luciana Souza [1 ,2 ]
Vasques Nonaka, Carolina Kymie [2 ,4 ]
Barreto-Duarte, Beatriz [3 ,5 ,6 ,7 ]
Araujo-Pereira, Mariana [3 ,7 ,8 ]
Tiburcio, Rafael [3 ]
Cruz, Fernanda Ferreira [9 ,10 ,11 ,12 ]
Soares Martins, Gabriele Louise [1 ,3 ]
Andrade, Bruno B. [3 ,5 ,6 ,7 ,8 ]
de Castro-Faria-Neto, Hugo Caire [10 ,11 ,13 ]
Macedo Rocco, Patricia Rieken [9 ,10 ,11 ,12 ]
de Freitas Souza, Bruno Solano [1 ,2 ,3 ]
机构
[1] Sao Rafael Hosp, Ctr Biotechnol & Cell Therapy, Salvador, BA, Brazil
[2] DOr Inst Res & Educ IDOR, Salvador, BA, Brazil
[3] Oswaldo Cruz Fdn FIOCRUZ, Goncalo Moniz Inst, Salvador, BA, Brazil
[4] Sao Rafael Hosp, Crit Care Unit, Salvador, BA, Brazil
[5] Univ Salvador UNIFACS, Laureate Int Univ, Curso Med, Salvador, BA, Brazil
[6] Univ Fed Rio de Janeiro, Programa Posgrad Clin Med, Rio De Janeiro, Brazil
[7] Multinatl Org Network Sponsoring Translat & Epide, Salvador, BA, Brazil
[8] Univ Fed Bahia, Fac Med, Salvador, BA, Brazil
[9] Univ Fed Rio de Janeiro, Carlos Chagas Filho Inst Biophys, Lab Pulm Invest, Rio De Janeiro, Brazil
[10] COVID 19 Virus Network Brazilian Council Sci & Te, Brasilia, DF, Brazil
[11] COVID 19 Virus Network Fdn Carlos Chagas Filho Re, Rio De Janeiro, Brazil
[12] Natl Inst Sci & Technol Regenerat Med, Rio De Janeiro, Brazil
[13] Oswaldo Cruz Fdn FIOCRUZ, Inst Oswaldo Cruz, Lab Immunopharmacol, Rio De Janeiro, Brazil
关键词
COVID-19; ARDS; mesenchymal stromal cells (MSCs); cell therapy; immunomodulation; fibrosis; STEM-CELLS; MONOCYTES;
D O I
10.3389/fmed.2021.767291
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The patients with coronavirus disease 2019 (COVID-19) associated with severe acute respiratory distress syndrome (ARDS) may require prolonged mechanical ventilation which often results in lung fibrosis, thus worsening the prognosis and increasing fatality rates. A mesenchymal stromal cell (MSC) therapy may decrease lung inflammation and accelerate recovery in COVID-19. In this context, some studies have reported the effects of MSC therapy for patients not requiring invasive ventilation or during the first hours of tracheal intubation. However, this is the first case report presenting the reduction of not only lung inflammation but also lung fibrosis in a critically ill long-term mechanically ventilated patient with COVID-19. Case Presentation: This is a case report of a 30-year-old male patient with COVID-19 under invasive mechanical ventilation for 14 days in the intensive care unit (ICU), who presented progressive clinical deterioration associated with lung fibrosis. The symptoms onset was 35 days before MSC therapy. The patient was treated with allogenic human umbilical-cord derived MSCs [5 x 10(7) (2 doses 2 days interval)]. No serious adverse events were observed during and after MSC administration. After MSC therapy, PaO2/FiO(2) ratio increased, the need for vasoactive drugs reduced, chest CT scan imaging, which initially showed signs of bilateral and peripheral ground-glass, as well as consolidation and fibrosis, improved, and the systemic mediators associated with inflammation decreased. Modulation of the different cell populations in peripheral blood was also observed, such as a reduction in inflammatory monocytes and an increase in the frequency of patrolling monocytes, CD4+ lymphocytes, and type 2 classical dendritic cells (cDC2). The patient was discharged 13 days after the cell therapy. Conclusions: Mesenchymal stromal cell therapy may be a promising option in critically ill patients with COVID-19 presenting both severe lung inflammation and fibrosis. Further clinical trials could better assess the efficacy of MSC therapy in critically ill patients with COVID-19 with lung fibrosis associated with long-term mechanical ventilation.
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