Kim Kyoung Mi, Albaira Koudai I, Kang Jayoung, Cho Yong Gon, Kwon Soon Sung, Lee Jaecheol, Ko Dae-Hyun, Kim Sinyoung, Lee Seung Yeob
Department of Laboratory Medicine, Jeonbuk National University Medical School and Hospital, Jeonju, Korea.
Research Institute of Clinical Medicine of Jeonbuk National University, Biomedical Research Institute of Jeonbuk National University Hospital, Jeonju, Korea.
Blood Res. 2025 May 27;60(1):32. doi: 10.1007/s44313-025-00071-9.
Cell-based artificial platelet production has made remarkable progress over the past three decades, driven by the need for safe and stable platelet sources in the face of donor limitations and transfusion-related risks. This review provides a chronological overview of the evolution of in vitro platelet production from various cell sources (CD34+ hematopoietic stem cells, embryonic stem cells, induced pluripotent stem cells (iPSCs), and others) and highlights key advances in the field. We outline developments from the foundational experiments of the 1990s, through the introduction of iPSCs in the mid-2000s, to the adoption of three-dimensional culture and bioreactor technologies in the late 2010s and the emergence of clinical trials in the 2020s. In addition, we discuss future perspectives, including the role of advanced gene editing and scalable biomanufacturing technologies in accelerating clinical translation. This comprehensive review underscores the promise of artificial platelet production technologies for clinical applications and discusses the remaining challenges, such as scalability, cost-effectiveness, and regulatory hurdles. The recent completion of the first human clinical trials using iPSC-derived platelets marks a significant milestone, pointing to a future in which patient-specific or human leukocyte antigen-universal platelets may be transformed into transfusion medicine and regenerative therapies.
在过去三十年中,基于细胞的人工血小板生产取得了显著进展,这是由于面对供体限制和输血相关风险,需要安全稳定的血小板来源所推动的。本综述按时间顺序概述了从各种细胞来源(CD34+造血干细胞、胚胎干细胞、诱导多能干细胞(iPSC)等)进行体外血小板生产的演变,并突出了该领域的关键进展。我们概述了从20世纪90年代的基础实验,到21世纪中期iPSC的引入,再到2010年代后期三维培养和生物反应器技术的采用以及2020年代临床试验的出现等发展情况。此外,我们还讨论了未来展望,包括先进基因编辑和可扩展生物制造技术在加速临床转化中的作用。这篇全面的综述强调了人工血小板生产技术在临床应用中的前景,并讨论了剩余的挑战,如可扩展性、成本效益和监管障碍。最近使用iPSC衍生血小板完成的首例人体临床试验标志着一个重要的里程碑,预示着一个未来,即患者特异性或人类白细胞抗原通用的血小板可能会转变为输血医学和再生疗法。