A Universal Plug-and-Display Vaccine Carrier Based on HBsAg VLP to Maximize Effective Antibody Response

Development of effective malaria vaccines requires delivery platforms to enhance the immunogenicity and efficacy of the target antigens. This is particularly challenging for transmission-blocking malaria vaccines (TBVs), and specifically for those based on the Pfs25 antigen, that need to elicit very...

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Main Authors: Arianna Marini, Yu Zhou, Yuanyuan Li, Iona J. Taylor, Darren B. Leneghan, Jing Jin, Marija Zaric, David Mekhaiel, Carole A. Long, Kazutoyo Miura, Sumi Biswas
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-12-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fimmu.2019.02931/full
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spelling doaj-b455bad731d24a199302dd720d7e9e802020-11-25T00:39:06ZengFrontiers Media S.A.Frontiers in Immunology1664-32242019-12-011010.3389/fimmu.2019.02931500416A Universal Plug-and-Display Vaccine Carrier Based on HBsAg VLP to Maximize Effective Antibody ResponseArianna Marini0Yu Zhou1Yuanyuan Li2Iona J. Taylor3Darren B. Leneghan4Jing Jin5Marija Zaric6David Mekhaiel7Carole A. Long8Kazutoyo Miura9Sumi Biswas10Nuffield Department of Medicine, The Jenner Institute, University of Oxford, Oxford, United KingdomNuffield Department of Medicine, The Jenner Institute, University of Oxford, Oxford, United KingdomNuffield Department of Medicine, The Jenner Institute, University of Oxford, Oxford, United KingdomNuffield Department of Medicine, The Jenner Institute, University of Oxford, Oxford, United KingdomNuffield Department of Medicine, The Jenner Institute, University of Oxford, Oxford, United KingdomNuffield Department of Medicine, The Jenner Institute, University of Oxford, Oxford, United KingdomNuffield Department of Medicine, The Jenner Institute, University of Oxford, Oxford, United KingdomNuffield Department of Medicine, The Jenner Institute, University of Oxford, Oxford, United KingdomLaboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Disease, National Institutes of Health, Rockville, MD, United StatesLaboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Disease, National Institutes of Health, Rockville, MD, United StatesNuffield Department of Medicine, The Jenner Institute, University of Oxford, Oxford, United KingdomDevelopment of effective malaria vaccines requires delivery platforms to enhance the immunogenicity and efficacy of the target antigens. This is particularly challenging for transmission-blocking malaria vaccines (TBVs), and specifically for those based on the Pfs25 antigen, that need to elicit very high antibody titers to stop the parasite development in the mosquito host and its transmission. Presenting antigens to the immune system on virus-like particles (VLPs) is an efficient way to improve the quantity and quality of the immune response generated. Here we introduce for the first time a new VLP vaccine platform, based on the well-established hepatitis B surface antigen (HBsAg) fused to the SpyCatcher protein, so that the antigen of interest, linked to the SpyTag peptide, can be easily displayed on it (Plug-and-Display technology). As little as 10% of the SpyCatcher::HBsAg VLPs decorated with Pfs25::SpyTag (molar ratio) induces a higher antibody response and transmission-reducing activity in mice compared to the soluble protein, with 50 and 90% of the VLP coupled to the antigen further enhancing the response. Importantly, using this carrier that is a vaccine antigen itself could be beneficial, as we show that anti-HBsAg IgG antibodies are induced without interfering with the Pfs25-specific immune response generated. Furthermore, pre-existing anti-HBsAg immunity does not affect the antigen-specific response to Pfs25::SpyTag-SpyCatcher::HBsAg, suggesting that these VLPs can have a broad use as a vaccine platform.https://www.frontiersin.org/article/10.3389/fimmu.2019.02931/fullmalariaPfs25transmission-blockingSpyTagSpyCatcherSMFA
collection DOAJ
language English
format Article
sources DOAJ
author Arianna Marini
Yu Zhou
Yuanyuan Li
Iona J. Taylor
Darren B. Leneghan
Jing Jin
Marija Zaric
David Mekhaiel
Carole A. Long
Kazutoyo Miura
Sumi Biswas
spellingShingle Arianna Marini
Yu Zhou
Yuanyuan Li
Iona J. Taylor
Darren B. Leneghan
Jing Jin
Marija Zaric
David Mekhaiel
Carole A. Long
Kazutoyo Miura
Sumi Biswas
A Universal Plug-and-Display Vaccine Carrier Based on HBsAg VLP to Maximize Effective Antibody Response
Frontiers in Immunology
malaria
Pfs25
transmission-blocking
SpyTag
SpyCatcher
SMFA
author_facet Arianna Marini
Yu Zhou
Yuanyuan Li
Iona J. Taylor
Darren B. Leneghan
Jing Jin
Marija Zaric
David Mekhaiel
Carole A. Long
Kazutoyo Miura
Sumi Biswas
author_sort Arianna Marini
title A Universal Plug-and-Display Vaccine Carrier Based on HBsAg VLP to Maximize Effective Antibody Response
title_short A Universal Plug-and-Display Vaccine Carrier Based on HBsAg VLP to Maximize Effective Antibody Response
title_full A Universal Plug-and-Display Vaccine Carrier Based on HBsAg VLP to Maximize Effective Antibody Response
title_fullStr A Universal Plug-and-Display Vaccine Carrier Based on HBsAg VLP to Maximize Effective Antibody Response
title_full_unstemmed A Universal Plug-and-Display Vaccine Carrier Based on HBsAg VLP to Maximize Effective Antibody Response
title_sort universal plug-and-display vaccine carrier based on hbsag vlp to maximize effective antibody response
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2019-12-01
description Development of effective malaria vaccines requires delivery platforms to enhance the immunogenicity and efficacy of the target antigens. This is particularly challenging for transmission-blocking malaria vaccines (TBVs), and specifically for those based on the Pfs25 antigen, that need to elicit very high antibody titers to stop the parasite development in the mosquito host and its transmission. Presenting antigens to the immune system on virus-like particles (VLPs) is an efficient way to improve the quantity and quality of the immune response generated. Here we introduce for the first time a new VLP vaccine platform, based on the well-established hepatitis B surface antigen (HBsAg) fused to the SpyCatcher protein, so that the antigen of interest, linked to the SpyTag peptide, can be easily displayed on it (Plug-and-Display technology). As little as 10% of the SpyCatcher::HBsAg VLPs decorated with Pfs25::SpyTag (molar ratio) induces a higher antibody response and transmission-reducing activity in mice compared to the soluble protein, with 50 and 90% of the VLP coupled to the antigen further enhancing the response. Importantly, using this carrier that is a vaccine antigen itself could be beneficial, as we show that anti-HBsAg IgG antibodies are induced without interfering with the Pfs25-specific immune response generated. Furthermore, pre-existing anti-HBsAg immunity does not affect the antigen-specific response to Pfs25::SpyTag-SpyCatcher::HBsAg, suggesting that these VLPs can have a broad use as a vaccine platform.
topic malaria
Pfs25
transmission-blocking
SpyTag
SpyCatcher
SMFA
url https://www.frontiersin.org/article/10.3389/fimmu.2019.02931/full
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