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符合 GMP 标准的 iPS 细胞系在一组新的细胞替代和癌症免疫治疗分化工作流程中表现出广泛的可塑性。

GMP-compliant iPS cell lines show widespread plasticity in a new set of differentiation workflows for cell replacement and cancer immunotherapy.

机构信息

Catalent Düsseldorf GmbH, 40764 Langenfeld, Germany.

Center for Regenerative Therapies Dresden (CRTD) and Center for Molecular and Cellular Bioengineering, Dresden University of Technology, 01307 Dresden, Germany.

出版信息

Stem Cells Transl Med. 2024 Sep 10;13(9):898-911. doi: 10.1093/stcltm/szae047.

Abstract

Cell therapeutic applications based on induced pluripotent stem cells (iPSCs) appear highly promising and challenging at the same time. Good manufacturing practice (GMP) regulations impose necessary yet demanding requirements for quality and consistency when manufacturing iPSCs and their differentiated progeny. Given the scarcity of accessible GMP iPSC lines, we have established a corresponding production workflow to generate the first set of compliant cell banks. Hence, these lines met a comprehensive set of release specifications and, for instance, displayed a low overall mutation load reflecting their neonatal origin, cord blood. Based on these iPSC lines, we have furthermore developed a set of GMP-compatible workflows enabling improved gene targeting at strongly enhanced efficiencies and directed differentiation into critical cell types: A new protocol for the generation of retinal pigment epithelium (RPE) features a high degree of simplicity and efficiency. Mesenchymal stromal cells (MSCs) derived from iPSCs displayed outstanding expansion capacity. A fully optimized cardiomyocyte differentiation protocol was characterized by a particularly high batch-to-batch consistency at purities above 95%. Finally, we introduce a universal immune cell induction platform that converts iPSCs into multipotent precursor cells. These hematopoietic precursors could selectively be stimulated to become macrophages, T cells, or natural killer (NK) cells. A switch in culture conditions upon NK-cell differentiation induced a several thousand-fold expansion, which opens up perspectives for upscaling this key cell type in a feeder cell-independent approach. Taken together, these cell lines and improved manipulation platforms will have broad utility in cell therapy as well as in basic research.

摘要

基于诱导多能干细胞 (iPSC) 的细胞治疗应用具有很高的应用前景和挑战性。良好的生产规范 (GMP) 规定在制造 iPSC 及其分化后代时对质量和一致性提出了必要且苛刻的要求。鉴于可用的 GMP iPSC 系数量稀少,我们已经建立了相应的生产工作流程,以生成第一批符合规范的细胞库。因此,这些细胞系符合一套全面的放行规格,例如,具有较低的整体突变负荷,反映了它们源自新生儿、脐血的起源。基于这些 iPSC 系,我们进一步开发了一套 GMP 兼容的工作流程,能够以更高的效率进行基因靶向,并定向分化为关键细胞类型:一种新的视网膜色素上皮 (RPE) 生成方案具有高度的简单性和高效性。源自 iPSC 的间充质基质细胞 (MSC) 显示出出色的扩增能力。完全优化的心肌细胞分化方案的特点是在纯度高于 95%时具有特别高的批次间一致性。最后,我们引入了一种通用的免疫细胞诱导平台,可将 iPSC 转化为多能前体细胞。这些造血前体细胞可以选择性地被刺激成为巨噬细胞、T 细胞或自然杀伤 (NK) 细胞。在 NK 细胞分化时改变培养条件会诱导数千倍的扩增,这为在无饲养细胞的方法中扩大这种关键细胞类型开辟了前景。总之,这些细胞系和改进的操作平台将在细胞治疗以及基础研究中具有广泛的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18f5/11386223/2dd0e45984f7/szae047_fig7.jpg

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