将病原生物菌株作为活体生物治疗产品供人类使用的可行性

IF 23.7 Q1 MICROBIOLOGY
iMeta Pub Date : 2024-05-26 DOI:10.1002/imt2.202
Pengfei Jin, Xiong Lin, Wenfeng Xu, Kangning Li, Xiaoxiao Zhao, Sirui Guo, Zinan Zhao, Lujie Jiang, Feng Liao, Longgang Chang, Min Wang, Yanmin Liu, Shaolei Huang, Zhangran Chen, Fusui Ji
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引用次数: 0

摘要

病原生物菌株的评估应在菌株水平上进行,包括功能基因的鉴定,同时考虑生态位和药物相互作用的影响。活体生物治疗产品(LBPs),尤其是病原生物菌株的安全性、有效性和质量管理具有一定的特殊性。有前景的开发方法包括重组枸杞多糖和活性代谢物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The feasibility of using pathobiome strains as live biotherapeutic products for human use

The feasibility of using pathobiome strains as live biotherapeutic products for human use

The evaluation of pathobiome strains should be conducted at the strain level, involving the identification of the functional genes, while considering the impact of ecological niche and drug interactions. The safety, efficacy, and quality management of live biotherapeutic products (LBPs), especially pathobiome strains, have certain peculiarities. Promising development methods include the recombinant LBP and active metabolites.

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