Epigallocatechin-3-Gallate as a Novel Vaccine Adjuvant

Vaccine adjuvants from natural resources have been utilized for enhancing vaccine efficacy against infectious diseases. This study examined the potential use of catechins, polyphenolic materials derived from green tea, as adjuvants for subunit and inactivated vaccines. Previously, catechins have bee...

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Autores principales: Yucheol Cheong, Minjin Kim, Jina Ahn, Hana Oh, Jongkwan Lim, Wonil Chae, Seung Won Yang, Min Seok Kim, Ji Eun Yu, Sanguine Byun, Yo Han Jang, Baik Lin Seong
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Publicado: Frontiers Media S.A. 2021
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Acceso en línea:https://doaj.org/article/4f49ccb7cfa84854a546face6860009a
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spelling oai:doaj.org-article:4f49ccb7cfa84854a546face6860009a2021-11-12T04:46:03ZEpigallocatechin-3-Gallate as a Novel Vaccine Adjuvant1664-322410.3389/fimmu.2021.769088https://doaj.org/article/4f49ccb7cfa84854a546face6860009a2021-11-01T00:00:00Zhttps://www.frontiersin.org/articles/10.3389/fimmu.2021.769088/fullhttps://doaj.org/toc/1664-3224Vaccine adjuvants from natural resources have been utilized for enhancing vaccine efficacy against infectious diseases. This study examined the potential use of catechins, polyphenolic materials derived from green tea, as adjuvants for subunit and inactivated vaccines. Previously, catechins have been documented to have irreversible virucidal function, with the possible applicability in the inactivated viral vaccine platform. In a mouse model, the coadministration of epigallocatechin-3-gallate (EGCG) with influenza hemagglutinin (HA) antigens induced high levels of neutralizing antibodies, comparable to that induced by alum, providing complete protection against the lethal challenge. Adjuvant effects were observed for all types of HA antigens, including recombinant full-length HA and HA1 globular domain, and egg-derived inactivated split influenza vaccines. The combination of alum and EGCG further increased neutralizing (NT) antibody titers with the corresponding hemagglutination inhibition (HI) titers, demonstrating a dose-sparing effect. Remarkably, EGCG induced immunoglobulin isotype switching from IgG1 to IgG2a (approximately >64–700 fold increase), exerting a more balanced TH1/TH2 response compared to alum. The upregulation of IgG2a correlated with significant enhancement of antibody-dependent cellular cytotoxicity (ADCC) function (approximately 14 fold increase), providing a potent effector-mediated protection in addition to NT and HI. As the first report on a novel class of vaccine adjuvants with built-in virucidal activities, the results of this study will help improve the efficacy and safety of vaccines for pandemic preparedness.Yucheol CheongMinjin KimJina AhnHana OhJongkwan LimWonil ChaeSeung Won YangMin Seok KimJi Eun YuSanguine ByunYo Han JangYo Han JangBaik Lin SeongBaik Lin SeongFrontiers Media S.A.articleEGCGadjuvantIgG isotype switchinginfluenzaADCCImmunologic diseases. AllergyRC581-607ENFrontiers in Immunology, Vol 12 (2021)
institution DOAJ
collection DOAJ
language EN
topic EGCG
adjuvant
IgG isotype switching
influenza
ADCC
Immunologic diseases. Allergy
RC581-607
spellingShingle EGCG
adjuvant
IgG isotype switching
influenza
ADCC
Immunologic diseases. Allergy
RC581-607
Yucheol Cheong
Minjin Kim
Jina Ahn
Hana Oh
Jongkwan Lim
Wonil Chae
Seung Won Yang
Min Seok Kim
Ji Eun Yu
Sanguine Byun
Yo Han Jang
Yo Han Jang
Baik Lin Seong
Baik Lin Seong
Epigallocatechin-3-Gallate as a Novel Vaccine Adjuvant
description Vaccine adjuvants from natural resources have been utilized for enhancing vaccine efficacy against infectious diseases. This study examined the potential use of catechins, polyphenolic materials derived from green tea, as adjuvants for subunit and inactivated vaccines. Previously, catechins have been documented to have irreversible virucidal function, with the possible applicability in the inactivated viral vaccine platform. In a mouse model, the coadministration of epigallocatechin-3-gallate (EGCG) with influenza hemagglutinin (HA) antigens induced high levels of neutralizing antibodies, comparable to that induced by alum, providing complete protection against the lethal challenge. Adjuvant effects were observed for all types of HA antigens, including recombinant full-length HA and HA1 globular domain, and egg-derived inactivated split influenza vaccines. The combination of alum and EGCG further increased neutralizing (NT) antibody titers with the corresponding hemagglutination inhibition (HI) titers, demonstrating a dose-sparing effect. Remarkably, EGCG induced immunoglobulin isotype switching from IgG1 to IgG2a (approximately >64–700 fold increase), exerting a more balanced TH1/TH2 response compared to alum. The upregulation of IgG2a correlated with significant enhancement of antibody-dependent cellular cytotoxicity (ADCC) function (approximately 14 fold increase), providing a potent effector-mediated protection in addition to NT and HI. As the first report on a novel class of vaccine adjuvants with built-in virucidal activities, the results of this study will help improve the efficacy and safety of vaccines for pandemic preparedness.
format article
author Yucheol Cheong
Minjin Kim
Jina Ahn
Hana Oh
Jongkwan Lim
Wonil Chae
Seung Won Yang
Min Seok Kim
Ji Eun Yu
Sanguine Byun
Yo Han Jang
Yo Han Jang
Baik Lin Seong
Baik Lin Seong
author_facet Yucheol Cheong
Minjin Kim
Jina Ahn
Hana Oh
Jongkwan Lim
Wonil Chae
Seung Won Yang
Min Seok Kim
Ji Eun Yu
Sanguine Byun
Yo Han Jang
Yo Han Jang
Baik Lin Seong
Baik Lin Seong
author_sort Yucheol Cheong
title Epigallocatechin-3-Gallate as a Novel Vaccine Adjuvant
title_short Epigallocatechin-3-Gallate as a Novel Vaccine Adjuvant
title_full Epigallocatechin-3-Gallate as a Novel Vaccine Adjuvant
title_fullStr Epigallocatechin-3-Gallate as a Novel Vaccine Adjuvant
title_full_unstemmed Epigallocatechin-3-Gallate as a Novel Vaccine Adjuvant
title_sort epigallocatechin-3-gallate as a novel vaccine adjuvant
publisher Frontiers Media S.A.
publishDate 2021
url https://doaj.org/article/4f49ccb7cfa84854a546face6860009a
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