Otsuka Ryo, Wada Haruka, Murata Tomoki, Seino Ken-Ichiro
Institute for Genetic Medicine, Hokkaido University, Kita-15, Nishi-7, Sapporo, Hokkaido 060-0815 Japan.
Inflamm Regen. 2020 Jul 1;40:12. doi: 10.1186/s41232-020-00125-8. eCollection 2020.
The development of pluripotent stem cell (PSC)-based technologies provides us a new therapeutic approach that generates grafts for transplantation. In order to minimize the risk of immune reaction, the banking of induced pluripotent stem cells (iPSCs) from donors with homozygous human leukocyte antigen (HLA) haplotype is planned in Japan. Even though pre-stocked and safety validated HLA-homozygous iPSCs are selected, immunological rejection may potentially occur because the causes of rejection are not always due to HLA mismatches. A couple of studies concerning such immunological issues have reported that genetic ablation of HLA molecules from PSC combined with gene transduction of several immunoregulatory molecules may be effective in avoiding immunological rejection. Also, our research group has recently proposed a concept that attempts to regulate recipient immune system by PSC-derived immunoregulatory cells, which results in prolonged survival of the same PSC-derived allografts. PSC-based technologies enable us to choose a new therapeutic option; however, considering its safety from an immunological point of view should be of great importance for safe clinical translation of this technology.
基于多能干细胞(PSC)技术的发展为我们提供了一种新的治疗方法,即生成用于移植的移植物。为了将免疫反应风险降至最低,日本计划储存来自具有纯合人类白细胞抗原(HLA)单倍型供体的诱导多能干细胞(iPSC)。即使选择了预先储存且经过安全性验证的HLA纯合iPSC,免疫排斥仍可能发生,因为排斥的原因并不总是由于HLA不匹配。一些关于此类免疫学问题的研究报告称,从PSC中基因去除HLA分子并结合几种免疫调节分子的基因转导可能有效避免免疫排斥。此外,我们的研究小组最近提出了一个概念,即试图通过PSC衍生的免疫调节细胞调节受体免疫系统,这会导致相同PSC衍生的同种异体移植物的存活期延长。基于PSC的技术使我们能够选择一种新的治疗方案;然而,从免疫学角度考虑其安全性对于该技术的安全临床转化至关重要。