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设计的干细胞:基因组工程与下一代基于细胞的治疗方法。

Designer Stem Cells: Genome Engineering and the Next Generation of Cell-Based Therapies.

机构信息

Department of Orthopaedic Surgery, Washington University, St. Louis, Missouri.

Shriners Hospitals for Children-St. Louis, St. Louis, Missouri.

出版信息

J Orthop Res. 2019 Jun;37(6):1287-1293. doi: 10.1002/jor.24304. Epub 2019 May 2.

Abstract

Stem cells provide tremendous promise for the development of new therapeutic approaches for musculoskeletal conditions. In addition to their multipotency, certain types of stem cells exhibit immunomodulatory effects that can mitigate inflammation and enhance tissue repair. However, the translation of stem cell therapies to clinical practice has proven difficult due to challenges in intradonor and interdonor variability, engraftment, variability in recipient microenvironment and patient indications, and limited therapeutic biological activity. In this regard, the success of stem cell-based therapies may benefit from cellular engineering approaches to enhance factors such as purification, homing and cell survival, trophic effects, or immunomodulatory signaling. By combining recent advances in gene editing, synthetic biology, and tissue engineering, the potential exists to create new classes of "designer" cells that have prescribed cell-surface molecules and receptors as well as synthetic gene circuits that provide for autoregulated drug delivery or enhanced tissue repair. Published by Wiley Periodicals, Inc. J Orthop Res 37:1287-1293, 2019.

摘要

干细胞为开发肌肉骨骼疾病的新治疗方法提供了巨大的希望。除了它们的多能性外,某些类型的干细胞还具有免疫调节作用,可以减轻炎症并增强组织修复。然而,由于供体内部和供体之间的变异性、植入、受者微环境和患者适应证的变异性以及治疗生物学活性有限等挑战,将干细胞疗法转化为临床实践证明是困难的。在这方面,细胞工程方法的成功可能会受益于增强因子的纯化、归巢和细胞存活、营养作用或免疫调节信号等因素。通过结合基因编辑、合成生物学和组织工程的最新进展,有可能创造出新型的“设计”细胞,这些细胞具有预定的细胞表面分子和受体,以及提供自动调节药物输送或增强组织修复的合成基因电路。由 Wiley Periodicals, Inc. 出版。J Orthop Res 37:1287-1293, 2019.

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