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噬菌体疗法的欧洲监管方面:法定噬菌体制剂

European regulatory aspects of phage therapy: magistral phage preparations.

作者信息

Verbeken Gilbert, Pirnay Jean-Paul

机构信息

Laboratory for Molecular and Cellular Technology, Queen Astrid Military Hospital, Bruynstraat 1, Brussels, 1120, Belgium.

Laboratory for Molecular and Cellular Technology, Queen Astrid Military Hospital, Bruynstraat 1, Brussels, 1120, Belgium.

出版信息

Curr Opin Virol. 2022 Feb;52:24-29. doi: 10.1016/j.coviro.2021.11.005. Epub 2021 Nov 23.

Abstract

Bacteriophages (phages) are bacterial viruses, and have been used for more than a century to combat bacterial infections, particularly in Poland and in the former Soviet Union. The antimicrobial resistance crisis has triggered a renewed interest in the therapeutic use of natural phages. The capacity of phages to specifically target pathogenic strains (sparing commensal bacteria), to adapt to these strains, and to rapidly overcome bacterial resistance, makes them suitable for flexible therapeutic approaches. To maximally exploit these advantages phages offer over conventional 'static' drugs such as traditional small molecule-type antibiotics, it is important that these sustainable phage products are not submitted to the traditional (long and expensive) medicinal product development and licensing pathways. Here we discuss the extrapolation of the Belgian 'magistral preparation' phage therapy framework to the European level, enabling an expeditious re-introduction of personalized phage therapy into Europe.

摘要

噬菌体是细菌病毒,在波兰和前苏联,人们使用噬菌体对抗细菌感染已有一个多世纪。抗菌药物耐药性危机引发了人们对天然噬菌体治疗用途的新兴趣。噬菌体能够特异性靶向致病菌株(不影响共生细菌)、适应这些菌株并迅速克服细菌耐药性,使其适用于灵活的治疗方法。为了最大程度地利用噬菌体相对于传统“静态”药物(如传统小分子型抗生素)所具有的这些优势,重要的是这些可持续的噬菌体产品无需遵循传统的(漫长且昂贵的)药品研发和许可途径。在此,我们讨论将比利时的“调剂制剂”噬菌体治疗框架推广至欧洲层面,以便能迅速将个性化噬菌体治疗重新引入欧洲。

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