Study of angiogenic cell therapy for progressive pulmonary arterial hypertension: intervention with repeat dosing of eNOS-enhanced EPCs: the SAPPHIRE trial.

IF 6.4 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Duncan J Stewart, Sanjay Mehta, George Chandy, Naushad Hirani, John Granton, Nathan Hambly, John Swiston, Kim Danovitch, Elham Sabri, Antonio Giulivi, David W Courtman, Dean A Fergusson
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引用次数: 0

Abstract

Pulmonary arterial hypertension (PAH) is characterized by widespread pruning of the distal pulmonary arterial bed, leading to increased pulmonary vascular resistance, right heart failure, and death. PAH patients receiving background therapy were randomized to receive a course of 4 monthly infusions of placebo or angiogenic endothelial progenitor cells (EPCs) transfected with endothelial NO synthase (eNOS) over the first 6-month period for a cumulative dose of 80 M cells. Due to the COVID-19 pandemic, the trial was stopped after 12 of the planned 45 patients were enrolled (five placebo, seven eNOS-EPCs). While the small sample size precluded appropriately powered analyses, a possible difference was seen in 6MWD between the eNOS-EPC and placebo groups over 6 months, with a greater proportion of patients in the cell therapy group achieving a minimal clinically important increase in 6MWD of 33-m (71.4% vs 40%, respectively). Treatment of PAH patients with a course of 4 monthly infusions of eNOS-EPCs was well tolerated and may have resulted in clinical benefit.

血管生成细胞治疗进行性肺动脉高压的研究:重复给药enos增强EPCs的干预:蓝宝石试验。
肺动脉高压(PAH)的特点是肺动脉远端床广泛修剪,导致肺血管阻力增加,右心衰和死亡。接受背景治疗的PAH患者在前6个月内随机接受4个月输注安慰剂或转染内皮NO合成酶(eNOS)的血管生成内皮祖细胞(EPCs),累计剂量为80M细胞。由于COVID-19大流行,在计划的45例患者中有12例入组(5例安慰剂,7例eNOS-EPCs)后,试验停止。虽然小样本量排除了适当的功率分析,但在6个月内,eNOS-EPC组和安慰剂组之间的6MWD可能存在差异,细胞治疗组中更大比例的患者实现了33米的最小临床重要增加(分别为71.4%和40%)。对PAH患者进行为期4个月的eNOS-EPCs输注治疗耐受性良好,并可能产生临床获益。
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来源期刊
CiteScore
10.10
自引率
6.70%
发文量
1667
审稿时长
69 days
期刊介绍: The Journal of Heart and Lung Transplantation, the official publication of the International Society for Heart and Lung Transplantation, brings readers essential scholarly and timely information in the field of cardio-pulmonary transplantation, mechanical and biological support of the failing heart, advanced lung disease (including pulmonary vascular disease) and cell replacement therapy. Importantly, the journal also serves as a medium of communication of pre-clinical sciences in all these rapidly expanding areas.
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