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再生医学中快速微生物检测方法的标准制定工作和现状。

Standards efforts and landscape for rapid microbial testing methodologies in regenerative medicine.

机构信息

Biosystems and Biomaterials Division, National Institute of Standards and Technology, Gaithersburg, Maryland, USA.

University Health Network, Toronto, Canada; University of Toronto, Toronto, Canada.

出版信息

Cytotherapy. 2021 May;23(5):390-398. doi: 10.1016/j.jcyt.2020.07.006. Epub 2021 Mar 26.

Abstract

The Standards Coordinating Body for Gene, Cell, and Regenerative Medicines and Cell-Based Drug Discovery (SCB) supports the development and commercialization of regenerative medicine products by identifying and addressing industry-wide challenges through standards. Through extensive stakeholder engagement, the implementation of rapid microbial testing methods (RMTMs) was identified as a high-priority need that must be addressed to facilitate more timely release of products. Since 2017, SCB has coordinated efforts to develop standards for this area through surveys, weekly meetings, workshops, leadership in working groups and participation in standards development organizations. This article describes the results of these efforts and discusses the current landscape of RMTMs for regenerative medicine products. Based on discussions with stakeholders across the field, an overview of traditional culture-based methods and limitations, alternative microbial testing technologies and current challenges, fit-for-purpose rapid microbial testing and case studies, risk-based strategies for selection of novel rapid microbial test methods and ongoing standards efforts for rapid microbial testing are captured here. To this end, SCB is facilitating several initiatives to address challenges associated with rapid microbial testing for regenerative medicine products. Two documentary standards are under development: an International Organization for Standardization standard to provide the framework for a risk-based approach to selecting fit-for-purpose assays primarily intended for cell and gene therapy products and an ASTM standard guide focused on sampling methods for microbial testing methods in tissue-engineered medical products. Working with the National Institute of Standards and Technology, SCB expects to facilitate the process of developing publicly available microbial materials for inter-laboratory testing. These studies will help collect the data necessary to facilitate validation of novel rapid methods. Finally, SCB has been working to increase awareness of, dialog about and participation in efforts to develop standards in the regenerative medicine field.

摘要

基因、细胞和再生医学及基于细胞的药物发现标准协调机构(SCB)通过识别和解决全行业的挑战来支持再生医学产品的开发和商业化。通过广泛的利益相关者参与,确定并必须解决快速微生物检测方法(RMTMs)的实施问题,以促进产品更及时地放行。自 2017 年以来,SCB 通过调查、每周会议、研讨会、工作组领导和参与标准制定组织,协调了该领域的标准制定工作。本文描述了这些努力的结果,并讨论了再生医学产品的 RMTMs 现状。基于与该领域各个利益相关者的讨论,本文概述了传统基于培养的方法及其局限性、替代微生物检测技术和当前挑战、适合目的的快速微生物检测以及案例研究、新型快速微生物检测方法选择的基于风险的策略,以及正在进行的快速微生物检测标准工作。为此,SCB 正在促进几项举措,以解决与再生医学产品快速微生物检测相关的挑战。正在制定两项文献标准:一项国际标准化组织标准,为选择适合目的的检测方法提供基于风险的方法框架,主要针对细胞和基因治疗产品;以及一项 ASTM 标准指南,重点介绍组织工程医疗产品中微生物检测方法的抽样方法。与美国国家标准与技术研究院合作,SCB 有望促进开发用于实验室间测试的公共微生物材料的流程。这些研究将有助于收集必要的数据,以促进新型快速方法的验证。最后,SCB 一直致力于提高对再生医学领域标准制定工作的认识、开展相关对话并参与其中。

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