亟需对基于外泌体的干预措施制定简明扼要的规定。

IF 5.9 2区医学 Q1 CELL & TISSUE ENGINEERING Stem Cell Reports Pub Date : 2024-11-12 Epub Date: 2024-10-24 DOI:10.1016/j.stemcr.2024.09.008

Misao Fujita, Taichi Hatta, Tsunakuni Ikka, Tatsuo Onishi

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引用次数: 0

摘要

特纳及其同事最近提出，对于干细胞、外泌体和其他再生医学产品法律法规不明确的国家，应制定并实施更全面的监管结构。我们完全同意这一观点，并认为不这样做可能会导致令人不安的困境，如日本的案例，患者面临严重并发症甚至死亡的风险。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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The urgent need for clear and concise regulations on exosome-based interventions.

Turner and colleagues recently argued that countries with unclear laws and regulations regarding stem cells, exosomes, and other regenerative medicine products should develop and enforce more comprehensive regulatory structures. We fully agree with this opinion and discuss that failure to do so may lead to troubling predicaments, such as the Japanese cases, where patients are at risk of serious complications or even death.

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来源期刊

Stem Cell Reports CELL & TISSUE ENGINEERING-CELL BIOLOGY

CiteScore

10.50

自引率

1.70%

发文量

200

审稿时长

28 weeks

期刊介绍： Stem Cell Reports publishes high-quality, peer-reviewed research presenting conceptual or practical advances across the breadth of stem cell research and its applications to medicine. Our particular focus on shorter, single-point articles, timely publication, strong editorial decision-making and scientific input by leaders in the field and a "scoop protection" mechanism are reasons to submit your best papers.