Potential of mannan or dextrin nanogels as vaccine carrier/adjuvant systems
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/1822/43871 |
Resumo: | Polymeric nanogels have been sophisticatedly designed promising a new generation of vaccine delivery/adjuvant systems capable of boosting immune response, a strategic priority in vaccine design. Here, nanogels made of mannan or dextrin were evaluated for their potential as carriers/adjuvants in vaccine formulations. Since lymph nodes are preferential target organs for vaccine delivery systems, nanogels were biotin-labeled, injected in the footpad of rats, and their presence in draining lymph nodes was assessed by immunofluorescence. Nanogels were detected in the popliteal and inguinal lymph nodes by 24h upon subcutaneous administration, indicating entrapment in lymphatic organs. Moreover, the model antigen ovalbumin was physically encapsulated within nanogels and physicochemically characterized concerning size, zeta potential, ovalbumin loading, and entrapment efficiency. The immunogenicity of these formulations was assessed in mice intradermally immunized with ovalbuminmannan or ovalbumindextrin by determining ovalbumin-specific antibody serum titers. Intradermal vaccination using ovalbuminmannan elicited a humoral immune response in which ovalbumin-specific IgG1 levels were significantly higher than those obtained with ovalbumin alone, indicating a TH2-type response. In contrast, dextrin nanogel did not show adjuvant potential. Altogether, these results indicate that mannan nanogel is a material that should be explored as a future antigen delivery system. |
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Potential of mannan or dextrin nanogels as vaccine carrier/adjuvant systemsMannanDextrinNanogelsLymph nodeOvalbuminVaccinationScience & TechnologyPolymeric nanogels have been sophisticatedly designed promising a new generation of vaccine delivery/adjuvant systems capable of boosting immune response, a strategic priority in vaccine design. Here, nanogels made of mannan or dextrin were evaluated for their potential as carriers/adjuvants in vaccine formulations. Since lymph nodes are preferential target organs for vaccine delivery systems, nanogels were biotin-labeled, injected in the footpad of rats, and their presence in draining lymph nodes was assessed by immunofluorescence. Nanogels were detected in the popliteal and inguinal lymph nodes by 24h upon subcutaneous administration, indicating entrapment in lymphatic organs. Moreover, the model antigen ovalbumin was physically encapsulated within nanogels and physicochemically characterized concerning size, zeta potential, ovalbumin loading, and entrapment efficiency. The immunogenicity of these formulations was assessed in mice intradermally immunized with ovalbuminmannan or ovalbumindextrin by determining ovalbumin-specific antibody serum titers. Intradermal vaccination using ovalbuminmannan elicited a humoral immune response in which ovalbumin-specific IgG1 levels were significantly higher than those obtained with ovalbumin alone, indicating a TH2-type response. In contrast, dextrin nanogel did not show adjuvant potential. Altogether, these results indicate that mannan nanogel is a material that should be explored as a future antigen delivery system.The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This work is supported by the Fundação para a Ciência e a Tecnologia (FCT) Portugal, post-doc grant SFRH/BPD/70524/2010 and the International Iberian Nanotechnology Laboratory (INL), PhD grant. The authors thank the Portuguese Foundation for Science and Technology (FCT) under the scope of the strategic funding of UID/BIO/04469/2013 unit and COMPETE 2020 (POCI-01-0145-FEDER-006684). The authors also acknowledge the Project RECI/BBB-EBI/0179/2012 (FCOMP-01-0124-FEDER-027462).SAGE PublicationsUniversidade do MinhoGonçalves, CatarinaFerreira, S.Correia, Alexandra L.Lopes, CéliaFleming, Carolina E.Rocha, EduardoVilanova, ManuelGama, F. M.2016-092016-09-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/43871engGonçalves, Catarina; Ferreira, S.; Correia, Alexandra L.; Lopes, Célia; Fleming, Carolina E.; Rocha, Eduardo; Vilanova, Manuel; Gama, F. M., Potential of mannan or dextrin nanogels as vaccine carrier/adjuvant systems. Journal of Bioactive and Compatible Polymers, 31(5), 453-466, 20160883-91151530-803010.1177/0883911516631354http://www.sagepub.com/journals/Journal201575info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-21T12:12:50Zoai:repositorium.sdum.uminho.pt:1822/43871Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:04:50.961510Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Potential of mannan or dextrin nanogels as vaccine carrier/adjuvant systems |
title |
Potential of mannan or dextrin nanogels as vaccine carrier/adjuvant systems |
spellingShingle |
Potential of mannan or dextrin nanogels as vaccine carrier/adjuvant systems Gonçalves, Catarina Mannan Dextrin Nanogels Lymph node Ovalbumin Vaccination Science & Technology |
title_short |
Potential of mannan or dextrin nanogels as vaccine carrier/adjuvant systems |
title_full |
Potential of mannan or dextrin nanogels as vaccine carrier/adjuvant systems |
title_fullStr |
Potential of mannan or dextrin nanogels as vaccine carrier/adjuvant systems |
title_full_unstemmed |
Potential of mannan or dextrin nanogels as vaccine carrier/adjuvant systems |
title_sort |
Potential of mannan or dextrin nanogels as vaccine carrier/adjuvant systems |
author |
Gonçalves, Catarina |
author_facet |
Gonçalves, Catarina Ferreira, S. Correia, Alexandra L. Lopes, Célia Fleming, Carolina E. Rocha, Eduardo Vilanova, Manuel Gama, F. M. |
author_role |
author |
author2 |
Ferreira, S. Correia, Alexandra L. Lopes, Célia Fleming, Carolina E. Rocha, Eduardo Vilanova, Manuel Gama, F. M. |
author2_role |
author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade do Minho |
dc.contributor.author.fl_str_mv |
Gonçalves, Catarina Ferreira, S. Correia, Alexandra L. Lopes, Célia Fleming, Carolina E. Rocha, Eduardo Vilanova, Manuel Gama, F. M. |
dc.subject.por.fl_str_mv |
Mannan Dextrin Nanogels Lymph node Ovalbumin Vaccination Science & Technology |
topic |
Mannan Dextrin Nanogels Lymph node Ovalbumin Vaccination Science & Technology |
description |
Polymeric nanogels have been sophisticatedly designed promising a new generation of vaccine delivery/adjuvant systems capable of boosting immune response, a strategic priority in vaccine design. Here, nanogels made of mannan or dextrin were evaluated for their potential as carriers/adjuvants in vaccine formulations. Since lymph nodes are preferential target organs for vaccine delivery systems, nanogels were biotin-labeled, injected in the footpad of rats, and their presence in draining lymph nodes was assessed by immunofluorescence. Nanogels were detected in the popliteal and inguinal lymph nodes by 24h upon subcutaneous administration, indicating entrapment in lymphatic organs. Moreover, the model antigen ovalbumin was physically encapsulated within nanogels and physicochemically characterized concerning size, zeta potential, ovalbumin loading, and entrapment efficiency. The immunogenicity of these formulations was assessed in mice intradermally immunized with ovalbuminmannan or ovalbumindextrin by determining ovalbumin-specific antibody serum titers. Intradermal vaccination using ovalbuminmannan elicited a humoral immune response in which ovalbumin-specific IgG1 levels were significantly higher than those obtained with ovalbumin alone, indicating a TH2-type response. In contrast, dextrin nanogel did not show adjuvant potential. Altogether, these results indicate that mannan nanogel is a material that should be explored as a future antigen delivery system. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016-09 2016-09-01T00:00:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/1822/43871 |
url |
http://hdl.handle.net/1822/43871 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Gonçalves, Catarina; Ferreira, S.; Correia, Alexandra L.; Lopes, Célia; Fleming, Carolina E.; Rocha, Eduardo; Vilanova, Manuel; Gama, F. M., Potential of mannan or dextrin nanogels as vaccine carrier/adjuvant systems. Journal of Bioactive and Compatible Polymers, 31(5), 453-466, 2016 0883-9115 1530-8030 10.1177/0883911516631354 http://www.sagepub.com/journals/Journal201575 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
SAGE Publications |
publisher.none.fl_str_mv |
SAGE Publications |
dc.source.none.fl_str_mv |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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