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Teratocarcinomas Arising from Allogeneic Induced Pluripotent Stem Cell-Derived Cardiac Tissue Constructs Provoked Host Immune Rejection in Mice

机译:由同种异体诱导的多能干细胞衍生心脏组织构建体引起的畸形癌引起小鼠宿主免疫排斥反应

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Transplantation of induced pluripotent stem cell-derived cardiac tissue constructs is a promising regenerative treatment for cardiac failure: however, its tumourigenic potential is concerning. We hypothesised that the tumourigenic potential may be eliminated by the host immune response after allogeneic cell transplantation. Scaffold-free iPSC-derived cardaic tissue sheets of C57BL/6 mouse origin were transplanted into the cardiac surface of syngeneic C57BL/6 mice and allogeneic BALB/c mice with or without tacrolimus injection. Syngeneic mice and tacrolimus-injected immunosuppressed allogeneic mice formed teratocarcinomas with identical phenotypes, characteristic, and time courses, as assessed by imaging tools including 18F-fluorodeoxyglucose-positron emission tomography. In contrast, temporarily immunosuppressed allogeneic mice, following cessation of tacrolimus injection displayed diminished progression of the teratocarcinoma, accompanied by an accumulation of CD4/CD8-positive T cells, and finally achieved complete elimination of the teratocarcinoma. Our results indicated that malignant teratocarcinomas arising from induced pluripotent stem cell-derived cardiac tissue constructs provoked T cell-related host immune rejection to arrest tumour growth in murine allogeneic transplantation models.
机译:诱导多能干细胞衍生心脏组织构建体的移植是心力衰竭的有希望的再生治疗:然而,其巨大的巨大潜力是关于。我们假设在同种异体细胞移植后的宿主免疫应答可能会消除肿瘤潜力。将C57BL / 6鼠标源性的无支腿IPSC衍生的Cardaic组织片移植到同源C57BL / 6小鼠和同种异体BALB / C小鼠的心脏表面中,或没有Tacrolimus注射。作为通过成像工具的成像工具(包括 18)F-氟脱氧葡糖 - 正电子发射断层扫描的成像工具评估,具有相同的表术,特征和时间课程,形成具有相同表型,特征和时间课程的Teratocarcinomas。相比之下,暂时免疫抑制的同种异体小鼠,在梗死的躯干注射停止后显示出畸胎癌的进展减少,伴随着CD4 / CD8阳性T细胞的积累,最后实现了畸胎癌的完全消除。我们的研究结果表明,由诱导多能干细胞衍生的心脏组织产生的恶性畸形瘤引起的T细胞相关宿主免疫排斥反应,以阻止鼠同种异体移植模型中的肿瘤生长。

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