基于 mRNA 和合成的治疗蛋白质:经济实惠的非重组选择

Biologics Pub Date : 2023-11-15 DOI:10.3390/biologics3040020
Sarfaraz K. Niazi, Matthias Magoola
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引用次数: 0

摘要

重组技术已经存在了近四分之三个世纪,并彻底改变了蛋白质疗法。然而,重组治疗蛋白的开发成本和生产基础设施却让大多数患者难以承受。蛋白质在体内通过信使核糖核酸(mRNA)翻译产生。通过服用化学核酸产品,可以很容易地复制这一过程,从而重组制造出相同的蛋白质。在无细胞系统中体内外制造这些蛋白质方面取得的进展也为生产治疗性蛋白质提供了一种成本更低的选择。本文比较了这些重组蛋白生产的替代方法,评估了它们各自的优势和局限性。虽然开发商和监管机构在产品审批过程中可能会遇到巨大挑战,包括许多尚未解决的知识产权问题,但这些技术现已得到验证,为大多数患者获得治疗性蛋白质提供了最合理的解决方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
mRNA and Synthesis-Based Therapeutic Proteins: A Non-Recombinant Affordable Option
Recombinant technology has been around for nearly three quarters of a century and has revolutionized protein therapy. However, the cost of developing recombinant therapeutic proteins and the manufacturing infrastructure keeps their cost unaffordable for most patients. Proteins are produced in the body via messenger RNA (mRNA) translation. This process can be readily replicated through administering a chemical nucleic acid product to manufacture the same protein recombinantly. The progress made in creating these proteins ex vivo in a cell-free system also offers a lower-cost option to produce therapeutic proteins. This article compares these alternative methods for recombinant protein production, assessing their respective advantages and limitations. While developers and regulatory agencies may encounter significant challenges in navigating product approval, including many unresolved intellectual property issues, these technologies are now proven and offer the most logical solution to making therapeutic proteins accessible to most patients.
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