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铝佐剂——“回到未来”

Aluminum Adjuvants-'Back to the Future'.

作者信息

Laera Donatello, HogenEsch Harm, O'Hagan Derek T

机构信息

Technical Research & Development, Drug Product, GSK, 53100 Siena, Italy.

Global Manufacturing Division, Corporate Industrial Analytics, Chiesi Pharmaceuticals, 43122 Parma, Italy.

出版信息

Pharmaceutics. 2023 Jul 4;15(7):1884. doi: 10.3390/pharmaceutics15071884.

Abstract

Aluminum-based adjuvants will continue to be a key component of currently approved and next generation vaccines, including important combination vaccines. The widespread use of aluminum adjuvants is due to their excellent safety profile, which has been established through the use of hundreds of millions of doses in humans over many years. In addition, they are inexpensive, readily available, and are well known and generally accepted by regulatory agencies. Moreover, they offer a very flexible platform, to which many vaccine components can be adsorbed, enabling the preparation of liquid formulations, which typically have a long shelf life under refrigerated conditions. Nevertheless, despite their extensive use, they are perceived as relatively 'weak' vaccine adjuvants. Hence, there have been many attempts to improve their performance, which typically involves co-delivery of immune potentiators, including Toll-like receptor (TLR) agonists. This approach has allowed for the development of improved aluminum adjuvants for inclusion in licensed vaccines against HPV, HBV, and COVID-19, with others likely to follow. This review summarizes the various aluminum salts that are used in vaccines and highlights how they are prepared. We focus on the analytical challenges that remain to allowing the creation of well-characterized formulations, particularly those involving multiple antigens. In addition, we highlight how aluminum is being used to create the next generation of improved adjuvants through the adsorption and delivery of various TLR agonists.

摘要

铝基佐剂将继续成为当前获批疫苗和下一代疫苗(包括重要的联合疫苗)的关键组成部分。铝佐剂的广泛使用归因于其出色的安全性,多年来在数亿剂人类疫苗的使用中已得到证实。此外,它们价格低廉、易于获取,并且为监管机构所熟知和普遍接受。而且,它们提供了一个非常灵活的平台,许多疫苗成分都可以吸附在其上,从而能够制备液体制剂,这类制剂在冷藏条件下通常具有较长的保质期。然而,尽管它们被广泛使用,但仍被视为相对“弱效”的疫苗佐剂。因此,人们进行了许多尝试来提高它们的性能,这通常涉及共同递送免疫增强剂,包括 Toll 样受体(TLR)激动剂。这种方法已促成了改良铝佐剂的开发,可用于已获许可的针对人乳头瘤病毒(HPV)、乙肝病毒(HBV)和新冠病毒(COVID - 19)的疫苗,其他疫苗可能也会相继采用。本综述总结了疫苗中使用的各种铝盐,并着重介绍了它们的制备方法。我们关注在制备特性明确的制剂(尤其是涉及多种抗原的制剂)方面仍存在哪些分析挑战。此外,我们还强调了铝如何通过吸附和递送各种 TLR 激动剂来打造下一代改良佐剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c7d/10383759/ea57d1145de7/pharmaceutics-15-01884-g001.jpg

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