Cargando…
The Encapsulation of Hemagglutinin in Protein Bodies Achieves a Stronger Immune Response in Mice than the Soluble Antigen
Zein is a water-insoluble polymer from maize seeds that has been widely used to produce carrier particles for the delivery of therapeutic molecules. We encapsulated a recombinant model vaccine antigen in newly formed zein bodies in planta by generating a fusion construct comprising the ectodomain of...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754457/ https://www.ncbi.nlm.nih.gov/pubmed/26909090 http://dx.doi.org/10.3389/fpls.2016.00142 |
_version_ | 1782416022926524416 |
---|---|
author | Hofbauer, Anna Melnik, Stanislav Tschofen, Marc Arcalis, Elsa Phan, Hoang T. Gresch, Ulrike Lampel, Johannes Conrad, Udo Stoger, Eva |
author_facet | Hofbauer, Anna Melnik, Stanislav Tschofen, Marc Arcalis, Elsa Phan, Hoang T. Gresch, Ulrike Lampel, Johannes Conrad, Udo Stoger, Eva |
author_sort | Hofbauer, Anna |
collection | PubMed |
description | Zein is a water-insoluble polymer from maize seeds that has been widely used to produce carrier particles for the delivery of therapeutic molecules. We encapsulated a recombinant model vaccine antigen in newly formed zein bodies in planta by generating a fusion construct comprising the ectodomain of hemagglutinin subtype 5 and the N-terminal part of γ-zein. The chimeric protein was transiently produced in tobacco leaves, and H5-containing protein bodies (PBs) were used to immunize mice. An immune response was achieved in all mice treated with H5-zein, even at low doses. The fusion to zein markedly enhanced the IgG response compared the soluble H5 control, and the effect was similar to a commercial adjuvant. The co-administration of adjuvants with the H5-zein bodies did not enhance the immune response any further, suggesting that the zein portion itself mediates an adjuvant effect. While the zein portion used to induce protein body formation was only weakly immunogenic, our results indicate that zein-induced PBs are promising production and delivery vehicles for subunit vaccines. |
format | Online Article Text |
id | pubmed-4754457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-47544572016-02-23 The Encapsulation of Hemagglutinin in Protein Bodies Achieves a Stronger Immune Response in Mice than the Soluble Antigen Hofbauer, Anna Melnik, Stanislav Tschofen, Marc Arcalis, Elsa Phan, Hoang T. Gresch, Ulrike Lampel, Johannes Conrad, Udo Stoger, Eva Front Plant Sci Plant Science Zein is a water-insoluble polymer from maize seeds that has been widely used to produce carrier particles for the delivery of therapeutic molecules. We encapsulated a recombinant model vaccine antigen in newly formed zein bodies in planta by generating a fusion construct comprising the ectodomain of hemagglutinin subtype 5 and the N-terminal part of γ-zein. The chimeric protein was transiently produced in tobacco leaves, and H5-containing protein bodies (PBs) were used to immunize mice. An immune response was achieved in all mice treated with H5-zein, even at low doses. The fusion to zein markedly enhanced the IgG response compared the soluble H5 control, and the effect was similar to a commercial adjuvant. The co-administration of adjuvants with the H5-zein bodies did not enhance the immune response any further, suggesting that the zein portion itself mediates an adjuvant effect. While the zein portion used to induce protein body formation was only weakly immunogenic, our results indicate that zein-induced PBs are promising production and delivery vehicles for subunit vaccines. Frontiers Media S.A. 2016-02-16 /pmc/articles/PMC4754457/ /pubmed/26909090 http://dx.doi.org/10.3389/fpls.2016.00142 Text en Copyright © 2016 Hofbauer, Melnik, Tschofen, Arcalis, Phan, Gresch, Lampel, Conrad and Stoger. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Hofbauer, Anna Melnik, Stanislav Tschofen, Marc Arcalis, Elsa Phan, Hoang T. Gresch, Ulrike Lampel, Johannes Conrad, Udo Stoger, Eva The Encapsulation of Hemagglutinin in Protein Bodies Achieves a Stronger Immune Response in Mice than the Soluble Antigen |
title | The Encapsulation of Hemagglutinin in Protein Bodies Achieves a Stronger Immune Response in Mice than the Soluble Antigen |
title_full | The Encapsulation of Hemagglutinin in Protein Bodies Achieves a Stronger Immune Response in Mice than the Soluble Antigen |
title_fullStr | The Encapsulation of Hemagglutinin in Protein Bodies Achieves a Stronger Immune Response in Mice than the Soluble Antigen |
title_full_unstemmed | The Encapsulation of Hemagglutinin in Protein Bodies Achieves a Stronger Immune Response in Mice than the Soluble Antigen |
title_short | The Encapsulation of Hemagglutinin in Protein Bodies Achieves a Stronger Immune Response in Mice than the Soluble Antigen |
title_sort | encapsulation of hemagglutinin in protein bodies achieves a stronger immune response in mice than the soluble antigen |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754457/ https://www.ncbi.nlm.nih.gov/pubmed/26909090 http://dx.doi.org/10.3389/fpls.2016.00142 |
work_keys_str_mv | AT hofbaueranna theencapsulationofhemagglutinininproteinbodiesachievesastrongerimmuneresponseinmicethanthesolubleantigen AT melnikstanislav theencapsulationofhemagglutinininproteinbodiesachievesastrongerimmuneresponseinmicethanthesolubleantigen AT tschofenmarc theencapsulationofhemagglutinininproteinbodiesachievesastrongerimmuneresponseinmicethanthesolubleantigen AT arcaliselsa theencapsulationofhemagglutinininproteinbodiesachievesastrongerimmuneresponseinmicethanthesolubleantigen AT phanhoangt theencapsulationofhemagglutinininproteinbodiesachievesastrongerimmuneresponseinmicethanthesolubleantigen AT greschulrike theencapsulationofhemagglutinininproteinbodiesachievesastrongerimmuneresponseinmicethanthesolubleantigen AT lampeljohannes theencapsulationofhemagglutinininproteinbodiesachievesastrongerimmuneresponseinmicethanthesolubleantigen AT conradudo theencapsulationofhemagglutinininproteinbodiesachievesastrongerimmuneresponseinmicethanthesolubleantigen AT stogereva theencapsulationofhemagglutinininproteinbodiesachievesastrongerimmuneresponseinmicethanthesolubleantigen AT hofbaueranna encapsulationofhemagglutinininproteinbodiesachievesastrongerimmuneresponseinmicethanthesolubleantigen AT melnikstanislav encapsulationofhemagglutinininproteinbodiesachievesastrongerimmuneresponseinmicethanthesolubleantigen AT tschofenmarc encapsulationofhemagglutinininproteinbodiesachievesastrongerimmuneresponseinmicethanthesolubleantigen AT arcaliselsa encapsulationofhemagglutinininproteinbodiesachievesastrongerimmuneresponseinmicethanthesolubleantigen AT phanhoangt encapsulationofhemagglutinininproteinbodiesachievesastrongerimmuneresponseinmicethanthesolubleantigen AT greschulrike encapsulationofhemagglutinininproteinbodiesachievesastrongerimmuneresponseinmicethanthesolubleantigen AT lampeljohannes encapsulationofhemagglutinininproteinbodiesachievesastrongerimmuneresponseinmicethanthesolubleantigen AT conradudo encapsulationofhemagglutinininproteinbodiesachievesastrongerimmuneresponseinmicethanthesolubleantigen AT stogereva encapsulationofhemagglutinininproteinbodiesachievesastrongerimmuneresponseinmicethanthesolubleantigen |