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Adjuvant system AS01: from mode of action to effective vaccines

Authors :
François Roman
Wivine Burny
Maria Angeles Ceregido
Béatrice Laupèze
Stéphane T Temmerman
Lucile Warter
Margherita Coccia
Source :
Expert Review of Vaccines, Vol 23, Iss 1, Pp 715-729 (2024)
Publication Year :
2024
Publisher :
Taylor & Francis Group, 2024.

Abstract

Introduction The use of novel adjuvants in human vaccines continues to expand as their contribution to preventing disease in challenging populations and caused by complex pathogens is increasingly understood. AS01 is a family of liposome-based vaccine Adjuvant Systems containing two immunostimulants: 3-O-desacyl-4’-monophosphoryl lipid A and the saponin QS-21. AS01-containing vaccines have been approved and administered to millions of individuals worldwide.Areas covered Here, we report advances in our understanding of the mode of action of AS01 that contributed to the development of efficacious vaccines preventing disease due to malaria, herpes zoster, and respiratory syncytial virus. AS01 induces early innate immune activation that induces T cell-mediated and antibody-mediated responses with optimized functional characteristics and induction of immune memory. AS01-containing vaccines appear relatively impervious to baseline immune status translating into high efficacy across populations. Currently licensed AS01-containing vaccines have shown acceptable safety profiles in clinical trials and post-marketing settings.Expert opinion Initial expectations that adjuvantation with AS01 could support effective vaccine responses and contribute to disease control have been realized. Investigation of the utility of AS01 in vaccines to prevent other challenging diseases, such as tuberculosis, is ongoing, together with efforts to fully define its mechanisms of action in different vaccine settings.

Details

Language :
English
ISSN :
14760584 and 17448395
Volume :
23
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Expert Review of Vaccines
Publication Type :
Academic Journal
Accession number :
edsdoj.81dc6633736e41b888d3b814f3660234
Document Type :
article
Full Text :
https://doi.org/10.1080/14760584.2024.2382725