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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.


DOI:10.3390/pharmaceutics15071884
PMID:37514070
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10383759/
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
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c7d/10383759/1f896c9e468f/pharmaceutics-15-01884-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c7d/10383759/ea57d1145de7/pharmaceutics-15-01884-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c7d/10383759/f299cd4905b3/pharmaceutics-15-01884-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c7d/10383759/1f896c9e468f/pharmaceutics-15-01884-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c7d/10383759/ea57d1145de7/pharmaceutics-15-01884-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c7d/10383759/f299cd4905b3/pharmaceutics-15-01884-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2c7d/10383759/1f896c9e468f/pharmaceutics-15-01884-g003.jpg

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[1]
Aluminum Adjuvants-'Back to the Future'.

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[7]
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[8]
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本文引用的文献

[1]
Maturation of Aluminium Adsorbed Antigens Contributes to the Creation of Homogeneous Vaccine Formulations.

Vaccines (Basel). 2023-1-11

[2]
Systems analysis of human responses to an aluminium hydroxide-adsorbed TLR7 agonist (AS37) adjuvanted vaccine reveals a dose-dependent and specific activation of the interferon-mediated antiviral response.

Vaccine. 2023-1-16

[3]
Breadth of SARS-CoV-2 neutralization and protection induced by a nanoparticle vaccine.

Nat Commun. 2022-10-23

[4]
Development of a TLR7/8 agonist adjuvant formulation to overcome early life hyporesponsiveness to DTaP vaccination.

Sci Rep. 2022-10-18

[5]
Mass Spectrometry-Based Quantification of the Antigens in Aluminum Hydroxide-Adjuvanted Diphtheria-Tetanus-Acellular-Pertussis Combination Vaccines.

Vaccines (Basel). 2022-7-5

[6]
Physico-chemical properties of aluminum adjuvants in vaccines: Implications for toxicological evaluation.

Vaccine. 2022-8-5

[7]
Risk factors for granulomas in children following immunization with aluminium-adsorbed vaccines: A Danish population-based cohort study.

Contact Dermatitis. 2022-11

[8]
CpG-Containing Oligodeoxynucleotides and Freund Adjuvant in Combination with Alum Augment the Production of Monoclonal Antibodies Against Recombinant HBsAg.

Avicenna J Med Biotechnol. 2022

[9]
Adjuvanting a subunit SARS-CoV-2 vaccine with clinically relevant adjuvants induces durable protection in mice.

NPJ Vaccines. 2022-5-23

[10]
Receptor-binding domain recombinant protein on alum-CpG induces broad protection against SARS-CoV-2 variants of concern.

Vaccine. 2022-6-9

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