Frontiers in Cardiovascular Medicine (Aug 2022)

First-in-human pilot trial of combined intracoronary and intravenous mesenchymal stem cell therapy in acute myocardial infarction

  • Lien-Cheng Hsiao,
  • Lien-Cheng Hsiao,
  • Yen-Nien Lin,
  • Yen-Nien Lin,
  • Woei-Cherng Shyu,
  • Woei-Cherng Shyu,
  • Ming Ho,
  • Chiung-Ray Lu,
  • Shih-Sheng Chang,
  • Shih-Sheng Chang,
  • Yu-Chen Wang,
  • Jan-Yow Chen,
  • Jan-Yow Chen,
  • Shang-Yeh Lu,
  • Mei-Yao Wu,
  • Mei-Yao Wu,
  • Keng-Yuan Li,
  • Yu-Kai Lin,
  • Wen-Yih I. Tseng,
  • Mao-Yuan Su,
  • Chin-Ting Hsu,
  • Cheng-Kang Tsai,
  • Lu-Ting Chiu,
  • Chien-Lin Chen,
  • Cheng-Li Lin,
  • Cheng-Li Lin,
  • Kai-Chieh Hu,
  • Kai-Chieh Hu,
  • Der-Yang Cho,
  • Der-Yang Cho,
  • Chang-Hai Tsai,
  • Kuan-Cheng Chang,
  • Kuan-Cheng Chang,
  • Long-Bin Jeng,
  • Long-Bin Jeng

DOI
https://doi.org/10.3389/fcvm.2022.961920
Journal volume & issue
Vol. 9

Abstract

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BackgroundAcute ST-elevation myocardial infarction (STEMI) elicits a robust cardiomyocyte death and inflammatory responses despite timely revascularization.ObjectivesThis phase 1, open-label, single-arm, first-in-human study aimed to assess the safety and efficacy of combined intracoronary (IC) and intravenous (IV) transplantation of umbilical cord-derived mesenchymal stem cells (UMSC01) for heart repair in STEMI patients with impaired left ventricular ejection fraction (LVEF 30-49%) following successful reperfusion by percutaneous coronary intervention.MethodsConsenting patients received the first dose of UMSC01 through IC injection 4-5 days after STEMI followed by the second dose of UMSC01 via IV infusion 2 days later. The primary endpoint was occurrence of any treatment-related adverse events and the secondary endpoint was changes of serum biomarkers and heart function by cardiac magnetic resonance imaging during a 12-month follow-up period.ResultsEight patients gave informed consents, of whom six completed the study. None of the subjects experienced treatment-related serious adverse events or major adverse cardiovascular events during IC or IV infusion of UMSC01 and during the follow-up period. The NT-proBNP level decreased (1362 ± 1801 vs. 109 ± 115 pg/mL, p = 0.0313), the LVEF increased (52.67 ± 12.75% vs. 62.47 ± 17.35%, p = 0.0246), and the wall motion score decreased (26.33 ± 5.57 vs. 22.33 ± 5.85, p = 0.0180) at the 12-month follow-up compared to the baseline values. The serial changes of LVEF were 0.67 ± 3.98, 8.09 ± 6.18, 9.04 ± 10.91, and 9.80 ± 7.56 at 1, 3, 6, and 12 months, respectively as compared to the baseline.ConclusionThis pilot study shows that combined IC and IV transplantation of UMSC01 in STEMI patients with impaired LVEF appears to be safe, feasible, and potentially beneficial in improving heart function. Further phase 2 studies are required to explore the effectiveness of dual-route transplantation of UMSC01 in STEMI patients.

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