TY - JOUR
T1 - Umbilical cord mesenchymal stromal cells as critical COVID-19 adjuvant therapy
T2 - A randomized controlled trial
AU - Dilogo, Ismail Hadisoebroto
AU - Aditianingsih, Dita
AU - Sugiarto, Adhrie
AU - Burhan, Erlina
AU - Damayanti, Triya
AU - Sitompul, Pompini Agustina
AU - Mariana, Nina
AU - Antarianto, Radiana D.
AU - Liem, Isabella Kurnia
AU - Kispa, Tera
AU - Mujadid, Fajar
AU - Novialdi, Novialdi
AU - Luviah, Evah
AU - Kurniawati, Tri
AU - Lubis, Andri M.T.
AU - Rahmatika, Dina
N1 - Funding Information:
We thank Telly Kamelia, Mefina Aulia Mufidah, Adantio Rashid Santoso, Bernadus Riyan Hartanto, M. Rizal Hermawan, and Hansen Angkasa for their comments and insightful suggestions and careful reading of the manuscript, as well as Dr. Lies Dina Liastuti (Director of Cipto Mangunkusumo Hospital) and Prof. Ari Fahrial Syam (Dean of FMUI) for total continuous support for this project. This research was funded using priority funds for national research from the Ministry of Research and Technology/National Research and Innovation Agency Republic of Indonesia.
Funding Information:
D.A. declared institutional funding from Ministry of Research, Technology and Higher Education, Indonesia. The other authors declared no potential conflicts of interest.
Publisher Copyright:
© 2021 The Authors. STEM CELLS TRANSLATIONAL MEDICINE published by Wiley Periodicals LLC on behalf of AlphaMed Press.
PY - 2021/9
Y1 - 2021/9
N2 - One of the main causes of acute respiratory distress syndrome in coronavirus disease 2019 (COVID-19) is cytokine storm, although the exact cause is still unknown. Umbilical cord mesenchymal stromal cells (UC-MSCs) influence proinflammatory T-helper 2 (Th2) cells to shift to an anti-inflammatory agent. To investigate efficacy of UC-MSC administration as adjuvant therapy in critically ill patients with COVID-19, we conducted a double-blind, multicentered, randomized controlled trial at four COVID-19 referral hospitals in Jakarta, Indonesia. This study included 40 randomly allocated critically ill patients with COVID-19; 20 patients received an intravenous infusion of 1 × 106/kg body weight UC-MSCs in 100 ml saline (0.9%) solution (SS) and 20 patients received 100 ml 0.9% SS as the control group. All patients received standard therapy. The primary outcome was measured by survival rate and/or length of ventilator usage. The secondary outcome was measured by clinical and laboratory improvement, with serious adverse events. Our study showed the survival rate in the UC-MSCs group was 2.5 times higher than that in the control group (P =.047), which is 10 patients and 4 patients in the UC-MSCs and control groups, respectively. In patients with comorbidities, UC-MSC administration increased the survival rate by 4.5 times compared with controls. The length of stay in the intensive care unit and ventilator usage were not statistically significant, and no adverse events were reported. The application of infusion UC-MSCs significantly decreased interleukin 6 in the recovered patients (P =.023). Therefore, application of intravenous UC-MSCs as adjuvant treatment for critically ill patients with COVID-19 increases the survival rate by modulating the immune system toward an anti-inflammatory state.
AB - One of the main causes of acute respiratory distress syndrome in coronavirus disease 2019 (COVID-19) is cytokine storm, although the exact cause is still unknown. Umbilical cord mesenchymal stromal cells (UC-MSCs) influence proinflammatory T-helper 2 (Th2) cells to shift to an anti-inflammatory agent. To investigate efficacy of UC-MSC administration as adjuvant therapy in critically ill patients with COVID-19, we conducted a double-blind, multicentered, randomized controlled trial at four COVID-19 referral hospitals in Jakarta, Indonesia. This study included 40 randomly allocated critically ill patients with COVID-19; 20 patients received an intravenous infusion of 1 × 106/kg body weight UC-MSCs in 100 ml saline (0.9%) solution (SS) and 20 patients received 100 ml 0.9% SS as the control group. All patients received standard therapy. The primary outcome was measured by survival rate and/or length of ventilator usage. The secondary outcome was measured by clinical and laboratory improvement, with serious adverse events. Our study showed the survival rate in the UC-MSCs group was 2.5 times higher than that in the control group (P =.047), which is 10 patients and 4 patients in the UC-MSCs and control groups, respectively. In patients with comorbidities, UC-MSC administration increased the survival rate by 4.5 times compared with controls. The length of stay in the intensive care unit and ventilator usage were not statistically significant, and no adverse events were reported. The application of infusion UC-MSCs significantly decreased interleukin 6 in the recovered patients (P =.023). Therefore, application of intravenous UC-MSCs as adjuvant treatment for critically ill patients with COVID-19 increases the survival rate by modulating the immune system toward an anti-inflammatory state.
KW - adjuvants
KW - cord stem cell transplantation
KW - COVID-19
KW - cytokine release syndrome
KW - immunology
KW - mesenchymal stromal cells
UR - http://www.scopus.com/inward/record.url?scp=85107732762&partnerID=8YFLogxK
U2 - 10.1002/sctm.21-0046
DO - 10.1002/sctm.21-0046
M3 - Article
AN - SCOPUS:85107732762
SN - 2157-6564
VL - 10
SP - 1279
EP - 1287
JO - Stem cells translational medicine
JF - Stem cells translational medicine
IS - 9
ER -