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本文引用的文献

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Metabolic Disease Epidemics: Emerging Challenges in Regenerative Medicine.代谢性疾病的流行:再生医学面临的新挑战。
Trends Endocrinol Metab. 2019 Mar;30(3):147-149. doi: 10.1016/j.tem.2019.01.001. Epub 2019 Jan 29.
2
Notes from the Field: Infections After Receipt of Bacterially Contaminated Umbilical Cord Blood-Derived Stem Cell Products for Other Than Hematopoietic or Immunologic Reconstitution - United States, 2018.实地记录:2018年美国接受用于非造血或免疫重建的受细菌污染的脐带血来源干细胞产品后的感染情况
MMWR Morb Mortal Wkly Rep. 2018 Dec 21;67(50):1397-1399. doi: 10.15585/mmwr.mm6750a5.
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Biomaterial-guided delivery of gene vectors for targeted articular cartilage repair.生物材料引导基因载体靶向关节软骨修复。
Nat Rev Rheumatol. 2019 Jan;15(1):18-29. doi: 10.1038/s41584-018-0125-2.
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Prospect of mesenchymal stem cells in therapy of osteoporosis: A review.间充质干细胞在骨质疏松症治疗中的应用前景:综述。
J Cell Physiol. 2019 Jun;234(6):8570-8578. doi: 10.1002/jcp.27833. Epub 2018 Nov 29.
5
Step-Wise Chondrogenesis of Human Induced Pluripotent Stem Cells and Purification Via a Reporter Allele Generated by CRISPR-Cas9 Genome Editing.人诱导多能干细胞的逐步软骨形成和通过 CRISPR-Cas9 基因组编辑产生的报告基因等位基因的纯化。
Stem Cells. 2019 Jan;37(1):65-76. doi: 10.1002/stem.2931. Epub 2018 Oct 31.
6
Clear up this stem-cell mess.清理干细胞领域的这团乱麻。
Nature. 2018 Sep;561(7724):455-457. doi: 10.1038/d41586-018-06756-9.
7
Effectiveness of mesenchymal stem cells for treating patients with knee osteoarthritis: a meta-analysis toward the establishment of effective regenerative rehabilitation.间充质干细胞治疗膝骨关节炎患者的有效性:建立有效再生康复的荟萃分析
NPJ Regen Med. 2018 Sep 17;3:15. doi: 10.1038/s41536-018-0041-8. eCollection 2018.
8
Concise Review: A Comprehensive Analysis of Reported Adverse Events in Patients Receiving Unproven Stem Cell-Based Interventions.简明综述:接受未经证实的干细胞干预治疗的患者报告不良事件的综合分析。
Stem Cells Transl Med. 2018 Sep;7(9):676-685. doi: 10.1002/sctm.17-0282. Epub 2018 Jul 31.
9
Designing cell function: assembly of synthetic gene circuits for cell biology applications.设计细胞功能:用于细胞生物学应用的合成基因回路的组装。
Nat Rev Mol Cell Biol. 2018 Aug;19(8):507-525. doi: 10.1038/s41580-018-0024-z.
10
Limited evidence for adipose-derived stem cell therapy on the treatment of osteoarthritis.脂肪来源干细胞治疗骨关节炎的有限证据。
Knee Surg Sports Traumatol Arthrosc. 2018 Nov;26(11):3499-3507. doi: 10.1007/s00167-018-4955-x. Epub 2018 Apr 30.

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.

DOI:10.1002/jor.24304
PMID:30977548
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6546536/
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.