Division of Hematology, Department of Medicine, Keio University School of Medicine, Tokyo, Japan.
Laboratory for Stem Cell Therapy, Faculty of Medicine, Tsukuba University, Tsukuba, Japan.
Cancer Sci. 2024 Mar;115(3):698-705. doi: 10.1111/cas.16066. Epub 2024 Jan 14.
Hematopoietic stem cells (HSCs) are a rare population of cells found in the bone marrow that play a critical role in lifelong hematopoiesis and the reconstitution of the hematopoietic system after hematopoietic stem cell transplantation. Hematopoietic stem cell transplantation remains the only curative treatment for patients with refractory hematologic disorders, and umbilical cord blood (CB) serves as an alternative stem cell source due to its several advantageous characteristics, including human leukocyte antigen flexibility and reduced donor burden. However, CB also has the disadvantage of containing a small number of cells, resulting in limited donor selection and a longer time for engraftment. Therefore, the development of techniques to expand HSCs ex vivo, particularly umbilical CB, is a goal in hematology. While various combinations of cytokines were once the mainstream approach, these protocols had limited expansion rates and did not lead to clinical application. However, in recent years, the development of a technique in which small molecules are added to cytokines has enabled the stable, long-term ex vivo expansion of human HSCs. Clinical trials of expanded umbilical CB using these techniques have been undertaken and have confirmed their efficacy and safety. In addition, we have successfully developed a recombinant-cytokine-free and albumin-free culture system for the long-term expansion of human HSCs. This approach could offer the potential for more selective expansion of human HSCs compared to previous protocols. This review discusses ex vivo culture protocols for expanding human HSCs and presents the results of clinical trials using these techniques, along with future perspectives.
造血干细胞(HSCs)是骨髓中一种罕见的细胞群体,在终身造血和造血干细胞移植后造血系统的重建中起着关键作用。造血干细胞移植仍然是治疗难治性血液疾病患者的唯一治愈方法,由于其几个有利的特征,包括人类白细胞抗原的灵活性和减少供体负担,脐带血(CB)可用作替代干细胞来源。然而,CB 也有细胞数量少的缺点,导致供体选择有限,植入时间延长。因此,开发体外扩增 HSCs 的技术,特别是脐带 CB,是血液学的一个目标。虽然各种细胞因子的组合曾经是主流方法,但这些方案的扩增率有限,无法应用于临床。然而,近年来,在细胞因子中添加小分子的技术的发展使得人类 HSCs 的稳定、长期体外扩增成为可能。使用这些技术进行的扩展脐带 CB 的临床试验已经进行,并证实了它们的疗效和安全性。此外,我们已经成功开发了一种无重组细胞因子和无白蛋白的培养系统,用于人类 HSCs 的长期扩增。与以前的方案相比,这种方法可能提供更有选择性地扩增人类 HSCs 的潜力。本文综述了体外扩增人类 HSCs 的培养方案,并介绍了使用这些技术进行的临床试验结果以及未来展望。