[Retinal Cell Therapy Using iPS Cells].

Nippon Ganka Gakkai zasshi Pub Date : 2016-03-01
Masayo Takahashi
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Abstract

Progress in basic research, starting with the work on neural stem cells in the middle 1990's to embryonic stem (ES) cells and induced pluripotent stem (iPS) cells at present, will lead the cell therapy (regenerative medicine) of various organs, including the central nervous system to a big medical field in the future. The author's group transplanted iPS cell-derived retinal pigment epithelial (RPE) cell sheets to the eye of a patient with exudative age-related macular degeneration (AMD) in 2014 as a clinical research. Replacement of the RPE with the patient's own iPS cell-derived young healthy cell sheet will be one new radical treatment of AMD that is caused by cellular senescence of RPE cells. Since it was the first clinical study using iPS cell-derived cells, the primary endpoint was safety judged by the outcome one year after surgery. The safety of the cell sheet has been confirmed by repeated tumorigenisity tests using immunodeficient mice, as well as purity of the cells, karyotype and genetic analysis. It is, however, also necessary to prove the safety by clinical studies. Following this start, a good strategy considering cost and benefit is needed to make regenerative medicine a standard treatment in the future. Scientifically, the best choice is the autologous RPE cell sheet, but autologous cell are expensive and sheet transplantation involves a risky part of surgical procedure. We should consider human leukocyte antigen (HLA) matched allogeneic transplantation using the HLA 6 loci homozyous iPS cell stock that Prof. Yamanaka of Kyoto University is working on. As the required forms of donor cells will be different depending on types and stages of the target diseases, regenerative medicine will be accomplished in a totally different manner from the present small molecule drugs. Proof of concept (POC) of photoreceptor transplantation in mouse is close to being accomplished using iPS cell-derived photoreceptor cells. The shortest possible course for treatment is now being investigated in preclinical research. Among the mixture of rod and cone photoreceptors in the donor cells, the percentage of cone photoreceptors is still low. Donor cells with more. cone photoreceptors will be needed. If that will work well, photoreceptor transplantation will be the first example of neural network reconstruction in the central nervous system. These efforts will reach to variety of retinal cell transplantations in the future.

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[利用iPS细胞治疗视网膜细胞]。
从20世纪90年代中期的神经干细胞开始,到目前的胚胎干细胞(ES)和诱导多能干细胞(iPS),基础研究的进展将引领包括中枢神经系统在内的各种器官的细胞治疗(再生医学)走向未来的大医学领域。作者小组于2014年将iPS细胞来源的视网膜色素上皮(RPE)细胞片移植到一位渗出性年龄相关性黄斑变性(AMD)患者的眼睛中作为临床研究。用患者自身的iPS细胞衍生的年轻健康细胞片替代RPE将是一种新的根治方法,用于治疗由RPE细胞衰老引起的AMD。由于这是第一个使用iPS细胞衍生细胞的临床研究,主要终点是通过手术后一年的结果来判断安全性。该细胞片的安全性已通过免疫缺陷小鼠的反复致瘤性试验以及细胞纯度、核型和遗传分析得到证实。然而,还需要通过临床研究来证明其安全性。在这个开始之后,需要一个考虑成本和收益的好策略,使再生医学成为未来的标准治疗。从科学上讲,最佳选择是自体RPE细胞片,但自体细胞昂贵,且细胞片移植是手术过程中有风险的一部分。我们应该考虑使用京都大学山中教授正在研究的HLA 6位点纯合iPS细胞库进行人类白细胞抗原(HLA)匹配的同种异体移植。由于所需要的供体细胞的形式将根据目标疾病的类型和阶段而不同,再生医学将以与目前的小分子药物完全不同的方式完成。利用iPS细胞衍生的光感受器细胞进行小鼠光感受器移植的概念验证(POC)即将完成。目前正在临床前研究中研究最短的治疗过程。在供体细胞中杆状和锥状光感受器的混合中,锥状光感受器的比例仍然很低。供体细胞有更多。锥状光感受器是必需的。如果效果良好,光感受器移植将成为中枢神经系统中神经网络重建的第一个例子。这些努力将在未来达到各种视网膜细胞移植。
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