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医院环境下良好生产规范下细胞治疗生产的挑战和优势。

Challenges and advantages of cell therapy manufacturing under Good Manufacturing Practices within the hospital setting.

机构信息

Department of Oncology, Center of Experimental Therapeutics, Centre Hospitalier Universitaire Vaudois, 1011 Lausanne, Switzerland.

Department of Oncology, Center of Experimental Therapeutics, Centre Hospitalier Universitaire Vaudois, 1011 Lausanne, Switzerland; Department of Oncology, Ludwig Institute for Cancer Research, University of Lausanne, 1011 Lausanne, Switzerland.

出版信息

Curr Opin Biotechnol. 2020 Oct;65:233-241. doi: 10.1016/j.copbio.2020.05.005. Epub 2020 Jul 11.

Abstract

Academic medicine serves to advance the scientific field and provide the highest quality of clinical care. This applies to cancer where there is a continuous unmet need for innovation. In the last decade, we have observed a significant development of commercial cell and gene-therapy products with a rapid growth of the industry. Hospital-based Good Manufacturing Practice (GMP) facilities which support primarily investigator-initiated clinical trials, are increasingly involved in interactions with industry. Although the missions of academic and commercial GMP facilities are different, both are bound by industry standards and often engage in technology transfer with industry partners. The successful set-up of an academic GMP facility requires striking a unique balance between commercial and academic priorities. Here we review the role of academic facilities in the development of cellular therapies with a focus on cancer immunotherapy and we highlight some of the most challenging operational aspects and point to potential solutions.

摘要

学术医学致力于推进科学领域的发展,并提供最高质量的临床护理。这适用于癌症领域,癌症领域需要不断创新以满足未满足的需求。在过去的十年中,我们观察到商业细胞和基因治疗产品的显著发展,该行业迅速增长。以支持主要由研究人员发起的临床试验为主要任务的医院级良好生产规范 (GMP) 设施越来越多地参与与行业的互动。尽管学术和商业 GMP 设施的使命不同,但两者都受到行业标准的约束,并且经常与行业合作伙伴进行技术转让。成功建立学术 GMP 设施需要在商业和学术重点之间取得独特的平衡。在这里,我们回顾了学术设施在细胞疗法开发中的作用,重点是癌症免疫疗法,并强调了一些最具挑战性的运营方面,并指出了潜在的解决方案。

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