Department of Experimental Pharmacology and Toxicology (E.Q., M.R., D.K., S.R., B.G., B.U., M.S., T.K., M.L., J.S., A.S., T.S., C.v.B., Y.N., I.M., T.C., A.H., T.E., F.W.), University Medical Center, Hamburg-Eppendorf, Germany.
German Centre for Cardiovascular Research (DZHK), partner site Hamburg/Kiel/Lübeck (E.Q., M.R., L.C., D.K., B.U., M.S., M.D.L., T.K., M.L., J.S., A.S., T.S., M. Köhne, C.v.B., S.P., I.M., T.C., H.R., A.H., T.E., F.W.).
Circulation. 2021 May 18;143(20):1991-2006. doi: 10.1161/CIRCULATIONAHA.120.047904. Epub 2021 Mar 2.
Human engineered heart tissue (EHT) transplantation represents a potential regenerative strategy for patients with heart failure and has been successful in preclinical models. Clinical application requires upscaling, adaptation to good manufacturing practices, and determination of the effective dose.
Cardiomyocytes were differentiated from 3 different human induced pluripotent stem cell lines including one reprogrammed under good manufacturing practice conditions. Protocols for human induced pluripotent stem cell expansion, cardiomyocyte differentiation, and EHT generation were adapted to substances available in good manufacturing practice quality. EHT geometry was modified to generate patches suitable for transplantation in a small-animal model and perspectively humans. Repair efficacy was evaluated at 3 doses in a cryo-injury guinea pig model. Human-scale patches were epicardially transplanted onto healthy hearts in pigs to assess technical feasibility.
We created mesh-structured tissue patches for transplantation in guinea pigs (1.5×2.5 cm, 9-15×10 cardiomyocytes) and pigs (5×7 cm, 450×10 cardiomyocytes). EHT patches coherently beat in culture and developed high force (mean 4.6 mN). Cardiomyocytes matured, aligned along the force lines, and demonstrated advanced sarcomeric structure and action potential characteristics closely resembling human ventricular tissue. EHT patches containing ≈4.5, 8.5, 12×10, or no cells were transplanted 7 days after cryo-injury (n=18-19 per group). EHT transplantation resulted in a dose-dependent remuscularization (graft size: 0%-12% of the scar). Only high-dose patches improved left ventricular function (+8% absolute, +24% relative increase). The grafts showed time-dependent cardiomyocyte proliferation. Although standard EHT patches did not withstand transplantation in pigs, the human-scale patch enabled successful patch transplantation.
EHT patch transplantation resulted in a partial remuscularization of the injured heart and improved left ventricular function in a dose-dependent manner in a guinea pig injury model. Human-scale patches were successfully transplanted in pigs in a proof-of-principle study.
人类工程心脏组织(EHT)移植代表了心力衰竭患者的一种潜在再生策略,并且已经在临床前模型中取得成功。临床应用需要扩大规模、适应良好的生产规范,并确定有效剂量。
从 3 种不同的人类诱导多能干细胞系中分化出心肌细胞,其中一种是在良好生产规范条件下重新编程的。人类诱导多能干细胞扩增、心肌细胞分化和 EHT 生成的方案适用于良好生产规范质量的可用物质。修改 EHT 几何形状以生成适合在小动物模型和前瞻性人类中移植的补丁。在冷冻损伤豚鼠模型中,在 3 个剂量下评估修复效果。将人类规模的补丁心外膜移植到猪的健康心脏上,以评估技术可行性。
我们为豚鼠(1.5×2.5cm,9-15×10 个心肌细胞)和猪(5×7cm,450×10 个心肌细胞)创建了用于移植的网格式组织补丁。EHT 补丁在培养中一致跳动,并产生高力(平均 4.6mN)。心肌细胞成熟,沿力线排列,并表现出高级肌节结构和动作电位特征,与人类心室组织非常相似。在冷冻损伤后 7 天(每组 18-19 只)移植含有约 4.5、8.5、12×10 或无细胞的 EHT 补丁(n=18-19 只/组)。EHT 移植导致剂量依赖性再肌化(移植物大小:0%-12%的疤痕)。只有高剂量补丁可改善左心室功能(绝对值增加 8%,相对值增加 24%)。移植后,移植物表现出时间依赖性的心肌细胞增殖。尽管标准的 EHT 补丁不能在猪中耐受移植,但人类规模的补丁能够成功移植。
EHT 补丁移植导致受伤心脏的部分再肌化,并在豚鼠损伤模型中以剂量依赖性方式改善左心室功能。在原理验证研究中,成功地在猪中移植了人类规模的补丁。