基于 RNA 的疫苗生产:基础设施、法规和全球影响

Concilium Pub Date : 2024-04-13 DOI:10.53660/clm-3202-24g02
Larissa Fonseca, Valdir Junior, Hayna Malta-Santos, Cristiano Ferreira, Marcelo Moret, Luis Mascarenhas, Leone Andrade, Cintia Minafra, Bruna Aparecida Souza Machado
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摘要

基于 RNA 的疫苗已成为抗击传染病(包括最近的 COVID-19 大流行)的有力工具。然而,要成功生产 RNA 疫苗,需要设计合理的 RNA 合成、纯化和配制设备。这篇综述文章探讨了专业 RNA 疫苗生产的设施要求、监管问题和全球影响。文章强调了良好生产规范 (GMP)、设备和技术在生产过程中的重要性,对世界各地的合作、投资和 RNA 工厂的建立进行了深入分析。最后,文件探讨了中低收入国家面临的挑战,以及大学、企业和政府合作的 "三足鼎立 "生产模式的作用。总之,本文件阐明了基于 RNA 的疫苗生产的最相关方面,强调了质量、安全性和可扩展性的必要性,以满足全球健康需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RNA-Based vaccine manufacturing: infrastructure, regulations, and global implications
RNA-based vaccines have emerged as a powerful tool in the fight against infectious diseases, including the recent COVID-19 pandemic. However, their successful production requires properly designed facilities for RNA synthesis, purification, and formulation. This review article explores the facility requirements, regulatory aspects, and global implications of specialized RNA vaccine production. It highlights the importance of Good Manufacturing Practice (GMP), equipment and technology in the production process, providing a critical analysis of collaborations, investments, and the establishment of RNA plants around the world. Finally, it addresses the challenges faced by low- and middle-income countries and the role of the "tripod" production model involving collaboration between university, industry, and government. Overall, this document clarifies the most relevant aspects of RNA-based vaccine manufacturing, emphasizing the need for quality, safety, and scalability to meet global health demands.
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