Allogeneic mesenchymal stromal cell therapy on primary graft dysfunction after lung transplantation

Abbas Ali Qayyum MD, MSc, PhD , Thomas Kromann Lund MD, PhD , Pia Bredahl Jensen MD , Kristine Jensen MD , Mandana Haack-Sørensen MSc, PhD , Annette Ekblond MSc, PhD , Morten Juhl Nørgaard MSc, PhD , Hasse Møller-Sørensen MD, PhD , Anders Bruun Mathiasen MD, PhD , Christian Holdflod Møller MD, PhD , Sara Bird Rørvig MD , Anna Kalhauge MD , Helle Bruunsgaard MD, PhD, DMSc , Thomas Litman MSc , Ellen Mønsted Johansen MSc , Lisbeth Drozd Højgaard MSc, PhD , Jens Kastrup MD, DMSc , Michael Perch MD
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引用次数: 0

Abstract

Background

Primary graft dysfunction (PGD) is common in lung transplantation affecting 15–30% of recipients. It represents a multifactorial injury to the transplanted lung within the first 72 hours after transplantation.
We aimed to investigate clinical safety and efficacy of allogeneic adipose tissue-derived stromal cells (ASCs), as an add-on therapy in patients undergoing double lung transplantation.

Methods

Single center, double-blinded, investigator-initiated randomized phase I/II study with intravenous infusion of either ASCs or placebo within two hours after lung transplantation. A total of 31 patients were included and randomized 1:1:1 to either 200 million or 100 million ASCs, or placebo infusion.
The primary endpoint was difference in PGD grade 72 hours after transplantation between groups.

Results

No significant differences in PGD were seen between the 3 groups 72 hours after lung transplantation (P=0.426). Combined ASC groups compared to placebo group did not show any difference in PGD 72 hours after transplantation (P=0.252). A reduced progression in PGD from day 1 to day 3 and day 2 to day 3 was observed between the ASC treated patients and patients in the placebo group (P=0.034 and P=0.034, respectively). There were no significant differences in number of serious adverse events or in secondary endpoints such as kidney function, lung function, or quality-of-life between groups.

Conclusions

Intravenous infusion of allogeneic ASCs in patients immediately after double lung transplantation was safe. The therapy did not show statistic difference in PGD between groups 72 hours after lung transplantation.

Clinical trial registration information

EudraCT number 2019–004848-30 and NCT04714801.
同种异体间充质间质细胞治疗肺移植术后原发性移植物功能障碍
原发性移植物功能障碍(PGD)在肺移植中很常见,影响了15-30%的受体。它代表移植后72小时内移植肺的多因素损伤。我们的目的是研究异体脂肪组织源性基质细胞(ASCs)作为双肺移植患者的附加治疗的临床安全性和有效性。方法单中心、双盲、研究者发起的随机I/II期研究,在肺移植后2小时内静脉输注ASCs或安慰剂。共纳入31例患者,按1:1:1的比例随机分为2亿个或1亿个ASCs,或安慰剂输注。主要终点是两组移植后72小时PGD分级的差异。结果3组肺移植术后72 h PGD比较差异无统计学意义(P=0.426)。联合ASC组与安慰剂组相比,移植后72小时PGD无显著差异(P=0.252)。ASC治疗组和安慰剂组患者的PGD进展从第1天到第3天和第2天到第3天均有所减少(P分别=0.034和P=0.034)。两组之间严重不良事件的数量或次要终点(如肾功能、肺功能或生活质量)没有显著差异。结论双肺移植术后立即静脉输注异体造血干细胞是安全的。肺移植后72小时组间PGD无统计学差异。临床试验注册信息:eudraft号2019-004848-30和NCT04714801。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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