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Adjuvanted influenza vaccines
File | Description | Size | Format | |
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Adjuvanted influenza vaccines.pdf | 948.32 kB | Accepted version | View/Open |
Title: | Adjuvanted influenza vaccines |
Authors: | Tregoning, JS Russell, RF Kinnear, E |
Item Type: | Journal Article |
Abstract: | In spite of current influenza vaccines being immunogenic, evolution of the influenza virus can reduce efficacy and so influenza remains a major threat to public health. One approach to improve influenza vaccines is to include adjuvants; substances that boost the immune response. Adjuvants are particularly beneficial for influenza vaccines administered during a pandemic when a rapid response is required or for use in patients with impaired immune responses, such as infants and the elderly. This review outlines the current use of adjuvants in human influenza vaccines, including what they are, why they are used and what is known of their mechanism of action. To date, six adjuvants have been used in licensed human vaccines: Alum, MF59, AS03, AF03, virosomes and heat labile enterotoxin (LT). In general these adjuvants are safe and well tolerated, but there have been some rare adverse events when adjuvanted vaccines are used at a population level that may discourage the inclusion of adjuvants in influenza vaccines, for example the association of LT with Bell's Palsy. Improved understanding about the mechanisms of the immune response to vaccination and infection has led to advances in adjuvant technology and we describe the experimental adjuvants that have been tested in clinical trials for influenza but have not yet progressed to licensure. Adjuvants alone are not sufficient to improve influenza vaccine efficacy because they do not address the underlying problem of mismatches between circulating virus and the vaccine. However, they may contribute to improved efficacy of next-generation influenza vaccines and will most likely play a role in the development of effective universal influenza vaccines, though what that role will be remains to be seen. |
Issue Date: | 25-Jan-2018 |
Date of Acceptance: | 1-Dec-2017 |
URI: | http://hdl.handle.net/10044/1/55674 |
DOI: | https://dx.doi.org/10.1080/21645515.2017.1415684 |
ISSN: | 2164-5515 |
Publisher: | Taylor & Francis |
Start Page: | 550 |
End Page: | 564 |
Journal / Book Title: | Human Vaccines and Immunotherapeutics |
Volume: | 14 |
Issue: | 3 |
Copyright Statement: | © 2018 Taylor & Francis. This is an Accepted Manuscript of an article published by Taylor & Francis in Human Vaccines and Immunotherapeutics on 25 Jan 2018, available online: https://www.tandfonline.com/doi/full/10.1080/21645515.2017.1415684 |
Sponsor/Funder: | Commission of the European Communities Commission of the European Communities |
Funder's Grant Number: | 280873 ADITEC-BIOTECH |
Keywords: | Science & Technology Life Sciences & Biomedicine Biotechnology & Applied Microbiology Immunology Alum antibody AS03 MF59 formulation IN-WATER EMULSION RANDOMIZED CLINICAL-TRIAL ALUMINUM-CONTAINING ADJUVANTS RESPIRATORY SYNCYTIAL VIRUS RTS,S/AS01 MALARIA VACCINE HUMORAL IMMUNE-RESPONSES TOLL-LIKE RECEPTORS B-CELL RESPONSES SEASONAL INFLUENZA DENDRITIC CELLS |
Publication Status: | Published |
Conference Place: | United States |
Open Access location: | http://www.tandfonline.com/doi/abs/10.1080/21645515.2017.1415684?journalCode=khvi20 |
Online Publication Date: | 2017-12-12 |
Appears in Collections: | Department of Medicine (up to 2019) |