Investigation of immune-related diseases using patient-derived induced pluripotent stem cells.

Hirofumi Shoda, Bunki Natsumoto, Keishi Fujio
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Abstract

The precise pathogenesis of immune-related diseases remains unclear, and new effective therapeutic choices are required for the induction of remission or cure in these diseases. Basic research utilizing immune-related disease patient-derived induced pluripotent stem (iPS) cells is expected to be a promising platform for elucidating the pathogenesis of the diseases and for drug discovery. Since autoinflammatory diseases are usually monogenic, genetic mutations affect the cell function and patient-derived iPS cells tend to exhibit disease-specific phenotypes. In particular, iPS cell-derived monocytic cells and macrophages can be used for functional experiments, such as inflammatory cytokine production, and are often employed in research on patients with autoinflammatory diseases.On the other hand, the utilization of disease-specific iPS cells is less successful for research on autoimmune diseases. One reason for this is that autoimmune diseases are usually polygenic, which makes it challenging to determine which factors cause the phenotypes of patient-derived iPS cells are caused by. Another reason is that protocols for differentiating some lymphocytes associated with autoimmunity, such as CD4+T cells or B cells, from iPS cells have not been well established. Nevertheless, several groups have reported studies utilizing autoimmune disease patient-derived iPS cells, including patients with rheumatoid arthritis, systemic lupus erythematosus (SLE), and systemic sclerosis. Particularly, non-hematopoietic cells, such as fibroblasts and cardiomyocytes, differentiated from autoimmune patient-derived iPS cells have shown promising results for further research into the pathogenesis. Recently, our groups established a method for differentiating dendritic cells that produce interferon-alpha, which can be applied as an SLE pathological model. In summary, patient-derived iPS cells can provide a promising platform for pathological research and new drug discovery in the field of immune-related diseases.

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利用患者来源的诱导多能干细胞研究免疫相关疾病。
免疫相关疾病的确切发病机制尚不清楚,需要新的有效治疗选择来诱导这些疾病的缓解或治愈。利用免疫相关疾病患者来源的诱导多能干细胞(iPS)进行的基础研究有望成为阐明疾病发病机制和药物发现的一个有前途的平台。由于自身炎症性疾病通常是单基因的,基因突变会影响细胞功能,患者来源的iPS细胞往往表现出疾病特异性表型。特别是,iPS细胞衍生的单核细胞和巨噬细胞可用于功能实验,如炎性细胞因子的产生,并经常用于对自身炎症性疾病患者的研究。另一方面,利用疾病特异性iPS细胞研究自身免疫性疾病的成功率较低。其中一个原因是自身免疫性疾病通常是多基因的,这使得确定导致患者来源的iPS细胞表型的因素具有挑战性。另一个原因在于,将一些与自身免疫相关的淋巴细胞(如CD4+T细胞或B细胞)与iPS细胞区分开来的方案尚未建立。然而,一些研究小组已经报道了利用自身免疫性疾病患者来源的iPS细胞的研究,包括类风湿性关节炎、系统性红斑狼疮(SLE)和系统性硬化症患者。特别是,从自身免疫性患者来源的iPS细胞分化而来的非造血细胞,如成纤维细胞和心肌细胞,已显示出对发病机制的进一步研究的有希望的结果。最近,我们的小组建立了一种分化产生干扰素α的树突细胞的方法,该方法可作为SLE的病理模型。总之,患者来源的iPS细胞可以为免疫相关疾病领域的病理研究和新药发现提供一个有前景的平台。
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