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Aluminum salts as an adjuvant for pre-pandemic influenza vaccines: a meta-analysis

Avian-origin H5/H7 influenza has the potential to cause the next influenza pandemic. Availability of effective vaccines is an essential part of pre-pandemic preparedness. However, avian influenza surface antigens are poorly immunogenic to humans, which necessitates the use of adjuvants to augment th...

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Autores principales: Lin, Yu-Ju, Shih, Yun-Jui, Chen, Chang-Hsun, Fang, Chi-Tai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6065440/
https://www.ncbi.nlm.nih.gov/pubmed/30061656
http://dx.doi.org/10.1038/s41598-018-29858-w
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author Lin, Yu-Ju
Shih, Yun-Jui
Chen, Chang-Hsun
Fang, Chi-Tai
author_facet Lin, Yu-Ju
Shih, Yun-Jui
Chen, Chang-Hsun
Fang, Chi-Tai
author_sort Lin, Yu-Ju
collection PubMed
description Avian-origin H5/H7 influenza has the potential to cause the next influenza pandemic. Availability of effective vaccines is an essential part of pre-pandemic preparedness. However, avian influenza surface antigens are poorly immunogenic to humans, which necessitates the use of adjuvants to augment the immunogenicity of pre-pandemic influenza vaccines. Aluminum salts are approved, safe, and affordable adjuvants, but their adjuvanticity for influenza vaccines remains unverified. We conducted the first meta-analysis on this issue. A total of nine randomized controlled trials (2006–2013, 22 comparisons, 2,467 participants in total) compared aluminum-adjuvanted H5N1 vaccines versus non-adjuvanted counterparts. The weighted estimate for the ratio of the seroprotection rate after a single dose of H5N1 vaccine is 0.66 (95% CI: 0.53 to 0.83) by hemagglutination-inhibition assay or 0.56 (95% CI: 0.42 to 0.74) by neutralizing titer assay. The weighted estimate for the risk ratio of pain/tenderness at injection sites is 1.85 (95% CI: 1.56 to 2.19). The quality of evidence is low to very low for seroprotection (due to indirectness and potential reporting bias) and moderate for pain/tenderness (due to potential reporting bias), respectively. The significantly lower seroprotection rate after aluminum-adjuvanted H5N1 vaccines and the significantly higher risk of pain at injection sites indicate that aluminum salts decrease immunogenicity but increase local reactogenicity of pre-pandemic H5N1 vaccines in humans.
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spelling pubmed-60654402018-08-06 Aluminum salts as an adjuvant for pre-pandemic influenza vaccines: a meta-analysis Lin, Yu-Ju Shih, Yun-Jui Chen, Chang-Hsun Fang, Chi-Tai Sci Rep Article Avian-origin H5/H7 influenza has the potential to cause the next influenza pandemic. Availability of effective vaccines is an essential part of pre-pandemic preparedness. However, avian influenza surface antigens are poorly immunogenic to humans, which necessitates the use of adjuvants to augment the immunogenicity of pre-pandemic influenza vaccines. Aluminum salts are approved, safe, and affordable adjuvants, but their adjuvanticity for influenza vaccines remains unverified. We conducted the first meta-analysis on this issue. A total of nine randomized controlled trials (2006–2013, 22 comparisons, 2,467 participants in total) compared aluminum-adjuvanted H5N1 vaccines versus non-adjuvanted counterparts. The weighted estimate for the ratio of the seroprotection rate after a single dose of H5N1 vaccine is 0.66 (95% CI: 0.53 to 0.83) by hemagglutination-inhibition assay or 0.56 (95% CI: 0.42 to 0.74) by neutralizing titer assay. The weighted estimate for the risk ratio of pain/tenderness at injection sites is 1.85 (95% CI: 1.56 to 2.19). The quality of evidence is low to very low for seroprotection (due to indirectness and potential reporting bias) and moderate for pain/tenderness (due to potential reporting bias), respectively. The significantly lower seroprotection rate after aluminum-adjuvanted H5N1 vaccines and the significantly higher risk of pain at injection sites indicate that aluminum salts decrease immunogenicity but increase local reactogenicity of pre-pandemic H5N1 vaccines in humans. Nature Publishing Group UK 2018-07-30 /pmc/articles/PMC6065440/ /pubmed/30061656 http://dx.doi.org/10.1038/s41598-018-29858-w Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lin, Yu-Ju
Shih, Yun-Jui
Chen, Chang-Hsun
Fang, Chi-Tai
Aluminum salts as an adjuvant for pre-pandemic influenza vaccines: a meta-analysis
title Aluminum salts as an adjuvant for pre-pandemic influenza vaccines: a meta-analysis
title_full Aluminum salts as an adjuvant for pre-pandemic influenza vaccines: a meta-analysis
title_fullStr Aluminum salts as an adjuvant for pre-pandemic influenza vaccines: a meta-analysis
title_full_unstemmed Aluminum salts as an adjuvant for pre-pandemic influenza vaccines: a meta-analysis
title_short Aluminum salts as an adjuvant for pre-pandemic influenza vaccines: a meta-analysis
title_sort aluminum salts as an adjuvant for pre-pandemic influenza vaccines: a meta-analysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6065440/
https://www.ncbi.nlm.nih.gov/pubmed/30061656
http://dx.doi.org/10.1038/s41598-018-29858-w
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