Department of Obstetrics and Gynecology, Keck School of Medicine, University of Southern California, Los Angeles, CA.
Department of Surgery, Keck School of Medicine, University of Southern California, Los Angeles, CA.
Transplantation. 2019 Jul;103(7):e182-e187. doi: 10.1097/TP.0000000000002735.
Advances in prenatal screening and early diagnosis of genetic disease will potentially allow for preemptive treatment of anticipated postnatal disease by in utero cell transplantation (IUCT). This strategy carries potential benefits over postnatal treatment, which might allow for improved engraftment and function of the transplanted cells. Congenital metabolic disorders may be an ideal target for this type of therapy, as in most cases, they require replacement of a single deficient hepatic enzyme, and multiple small-animal models exist for preclinical testing.
The Gunn rat, a Crigler-Najjar syndrome model animal lacking UDP-glucuronosyltransferase (UGT1A1), was used as recipient. Human amniotic epithelial cells (hAECs), which possess hepatic differentiation potential, were transplanted into the midgestation fetal Gunn rat liver via ultrasound-guided IUCT. The impact of IUCT on live birth and postnatal survival was evaluated. Human cell engraftment was immunohistochemically analyzed on postnatal day 21.
Ultrasound-guided IUCT was conducted in rat fetuses on embryonic day 16. Following IUCT, the antihuman mitochondria-positive cells were detected in the liver of recipient rats at postnatal day 21.
Here, we have introduced ultrasound-guided IUCT of hAEC using a small-animal model of a congenital metabolic disorder without immunosuppression. The immunological advantage of IUCT was demonstrated with xenogeneic IUCT. This procedure is suitable to conduct preclinical studies for exploring the feasibility and efficacy of ultrasound-guided transuterine cell injection using rodent disease models.
产前筛查和遗传疾病早期诊断的进步,可能使通过宫内细胞移植(IUCT)对预期的产后疾病进行预防性治疗成为可能。与产后治疗相比,这种策略具有潜在的优势,因为产后治疗可能会改善移植细胞的植入和功能。先天性代谢紊乱可能是这种治疗类型的理想目标,因为在大多数情况下,它们只需要替换单个缺乏的肝酶,并且存在多个用于临床前测试的小动物模型。
Gunn 大鼠是一种缺乏 UDP-葡糖醛酸基转移酶(UGT1A1)的 Crigler-Najjar 综合征模型动物,被用作受体。具有肝分化潜能的人羊膜上皮细胞(hAEC)通过超声引导的 IUCT 移植到中孕期 Gunn 大鼠的胎肝中。通过超声引导的 IUCT 对活产和产后生存的影响进行了评估。在产后第 21 天,通过免疫组织化学分析了人细胞的植入情况。
在胚胎第 16 天对大鼠胎儿进行了超声引导的 IUCT。在 IUCT 之后,在接受大鼠的肝脏中在产后第 21 天检测到抗人线粒体阳性细胞。
在这里,我们在没有免疫抑制的先天性代谢紊乱的小动物模型中引入了使用 hAEC 的超声引导的 IUCT。通过异种 IUCT 证明了 IUCT 的免疫优势。该程序适用于使用啮齿动物疾病模型进行超声引导的跨胎盘细胞注射的临床前研究,以探索其可行性和疗效。