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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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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