The adjuvanticity of Chiococca alba saponins increases with the length and hydrophilicity of their sugar chains
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1016/j.vaccine.2012.03.006 http://repositorio.unifesp.br/handle/11600/34887 |
Resumo: | The saponins of Chiococca alba are triterpene bidesmosides that contain glycidic moieties attached to the C-3 and C-28 carbon of their aglycone. We describe that their adjuvant potential increases in direct relationship to the length and hydrophilicity of the C-28 attached sugar chain which contains: arabinose-rhamnose in the CA2, arabinose-rhamnose-xylose in the CA3X; arabinose-rhamnose-apiose in the CA3 and arabinose-rhamnose-apiose-apiose in the CA4 saponin. the hydrophile/lipophile balance calculated for CA2 was 12.7, for CA3 and CA3X was 15.8 and for CA4 19.9. All saponins were formulated with the FML antigen for mice prophylaxis against visceral leishmaniasis. the immune response was studied using an ELISA-antibody assay and monitoring of the intradermal response (IDR) to Leishmania antigens, the cytokine expression in supernatants and the intracellular staining of in vitro cultured splenocytes. After challenge, significant increases of IgG and IgG2a antibodies were noted only in the CA4 vaccinated mice that showed extended IDR, higher IFN-gamma production by CD8+ and TNF-alpha production by CD4+ T cells, higher TNF-alpha secretion and the highest reduction of the parasite load (78%). the increases in IDR, CD4-TNF-alpha,CD8-IFN-gamma and CD8-TNF-alpha by the CA4 vaccine were strong correlates of protection and were significantly correlated to the decrease of parasite load (p=-0.007). Protection generated by the CA4 vaccine was mainly mediated by a CD4+ T cell and a TNF-alpha driven response with a lower contribution of CD8+ T cells, as confirmed by an in vivo depletion with monoclonal antibodies and by vaccination assays in TNF-alpha-receptor knock-out mice. Our results confirm that the superiority of the CA4 saponin is related to the higher hydrophilicity of its longer carbohydrate chain. C. alba saponins were non-toxic and only the xylose-containing saponin CA3X was hemolytic (HD50 = 87 mu g/ml). the increase in sugar units of the saponins is positively correlated to the increase of IDR and to the decrease of parasite load. (C) 2012 Elsevier B.V. All rights reserved. |
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The adjuvanticity of Chiococca alba saponins increases with the length and hydrophilicity of their sugar chainsSaponinsAdjuvantsQS21 saponinChiococca albaVisceral leishmaniasisFML antigenThe saponins of Chiococca alba are triterpene bidesmosides that contain glycidic moieties attached to the C-3 and C-28 carbon of their aglycone. We describe that their adjuvant potential increases in direct relationship to the length and hydrophilicity of the C-28 attached sugar chain which contains: arabinose-rhamnose in the CA2, arabinose-rhamnose-xylose in the CA3X; arabinose-rhamnose-apiose in the CA3 and arabinose-rhamnose-apiose-apiose in the CA4 saponin. the hydrophile/lipophile balance calculated for CA2 was 12.7, for CA3 and CA3X was 15.8 and for CA4 19.9. All saponins were formulated with the FML antigen for mice prophylaxis against visceral leishmaniasis. the immune response was studied using an ELISA-antibody assay and monitoring of the intradermal response (IDR) to Leishmania antigens, the cytokine expression in supernatants and the intracellular staining of in vitro cultured splenocytes. After challenge, significant increases of IgG and IgG2a antibodies were noted only in the CA4 vaccinated mice that showed extended IDR, higher IFN-gamma production by CD8+ and TNF-alpha production by CD4+ T cells, higher TNF-alpha secretion and the highest reduction of the parasite load (78%). the increases in IDR, CD4-TNF-alpha,CD8-IFN-gamma and CD8-TNF-alpha by the CA4 vaccine were strong correlates of protection and were significantly correlated to the decrease of parasite load (p=-0.007). Protection generated by the CA4 vaccine was mainly mediated by a CD4+ T cell and a TNF-alpha driven response with a lower contribution of CD8+ T cells, as confirmed by an in vivo depletion with monoclonal antibodies and by vaccination assays in TNF-alpha-receptor knock-out mice. Our results confirm that the superiority of the CA4 saponin is related to the higher hydrophilicity of its longer carbohydrate chain. C. alba saponins were non-toxic and only the xylose-containing saponin CA3X was hemolytic (HD50 = 87 mu g/ml). the increase in sugar units of the saponins is positively correlated to the increase of IDR and to the decrease of parasite load. (C) 2012 Elsevier B.V. All rights reserved.Univ Fed Rio de Janeiro, Inst Microbiol Paulo Goes, CCS, Ilha Fundao,Dept Microbiol Geral, BR-21941902 Rio de Janeiro, BrazilUniv Fed Rio de Janeiro, Nucleo Pesquisas Prod Nat, BR-21941902 Rio de Janeiro, BrazilUFRJ, Hosp Univ Clementino Fraga Filho, Fac Med, BR-21941913 Rio de Janeiro, BrazilUniversidade Federal de São Paulo UNIFESP, Ctr Interdisciplinar Terapia Genica, BR-04044010 São Paulo, BrazilUniversidade Federal de São Paulo UNIFESP, Ctr Interdisciplinar Terapia Genica, BR-04044010 São Paulo, BrazilWeb of ScienceConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro (FAPERJ)CNPq: 500992/2008-8FAPERJ: E-26/110305/2007FAPERJ: E-26/110132/2007FAPERJ: E-26/100416/2007FAPERJ: E-22/102733/2008Elsevier B.V.Universidade Federal do Rio de Janeiro (UFRJ)Universidade Federal de São Paulo (UNIFESP)Nico, DirleiBorges, Ricardo MoreiraBrandao, Layza MendesFeijo, Daniel FerreiraGomes, Daniele CrespoPalatnik, MarcosRodrigues, Mauricio Martins [UNIFESP]Ribeiro da Silva, Antonio JorgePalatnik-de-Sousa, Clarisa Beatriz2016-01-24T14:27:14Z2016-01-24T14:27:14Z2012-05-02info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion3169-3179application/pdfhttp://dx.doi.org/10.1016/j.vaccine.2012.03.006Vaccine. Oxford: Elsevier B.V., v. 30, n. 21, p. 3169-3179, 2012.10.1016/j.vaccine.2012.03.006WOS000303302900005.pdf0264-410Xhttp://repositorio.unifesp.br/handle/11600/34887WOS:000303302900005engVaccineinfo:eu-repo/semantics/openAccesshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policyreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-08T12:11:23Zoai:repositorio.unifesp.br/:11600/34887Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-08T12:11:23Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
The adjuvanticity of Chiococca alba saponins increases with the length and hydrophilicity of their sugar chains |
title |
The adjuvanticity of Chiococca alba saponins increases with the length and hydrophilicity of their sugar chains |
spellingShingle |
The adjuvanticity of Chiococca alba saponins increases with the length and hydrophilicity of their sugar chains Nico, Dirlei Saponins Adjuvants QS21 saponin Chiococca alba Visceral leishmaniasis FML antigen |
title_short |
The adjuvanticity of Chiococca alba saponins increases with the length and hydrophilicity of their sugar chains |
title_full |
The adjuvanticity of Chiococca alba saponins increases with the length and hydrophilicity of their sugar chains |
title_fullStr |
The adjuvanticity of Chiococca alba saponins increases with the length and hydrophilicity of their sugar chains |
title_full_unstemmed |
The adjuvanticity of Chiococca alba saponins increases with the length and hydrophilicity of their sugar chains |
title_sort |
The adjuvanticity of Chiococca alba saponins increases with the length and hydrophilicity of their sugar chains |
author |
Nico, Dirlei |
author_facet |
Nico, Dirlei Borges, Ricardo Moreira Brandao, Layza Mendes Feijo, Daniel Ferreira Gomes, Daniele Crespo Palatnik, Marcos Rodrigues, Mauricio Martins [UNIFESP] Ribeiro da Silva, Antonio Jorge Palatnik-de-Sousa, Clarisa Beatriz |
author_role |
author |
author2 |
Borges, Ricardo Moreira Brandao, Layza Mendes Feijo, Daniel Ferreira Gomes, Daniele Crespo Palatnik, Marcos Rodrigues, Mauricio Martins [UNIFESP] Ribeiro da Silva, Antonio Jorge Palatnik-de-Sousa, Clarisa Beatriz |
author2_role |
author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal do Rio de Janeiro (UFRJ) Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Nico, Dirlei Borges, Ricardo Moreira Brandao, Layza Mendes Feijo, Daniel Ferreira Gomes, Daniele Crespo Palatnik, Marcos Rodrigues, Mauricio Martins [UNIFESP] Ribeiro da Silva, Antonio Jorge Palatnik-de-Sousa, Clarisa Beatriz |
dc.subject.por.fl_str_mv |
Saponins Adjuvants QS21 saponin Chiococca alba Visceral leishmaniasis FML antigen |
topic |
Saponins Adjuvants QS21 saponin Chiococca alba Visceral leishmaniasis FML antigen |
description |
The saponins of Chiococca alba are triterpene bidesmosides that contain glycidic moieties attached to the C-3 and C-28 carbon of their aglycone. We describe that their adjuvant potential increases in direct relationship to the length and hydrophilicity of the C-28 attached sugar chain which contains: arabinose-rhamnose in the CA2, arabinose-rhamnose-xylose in the CA3X; arabinose-rhamnose-apiose in the CA3 and arabinose-rhamnose-apiose-apiose in the CA4 saponin. the hydrophile/lipophile balance calculated for CA2 was 12.7, for CA3 and CA3X was 15.8 and for CA4 19.9. All saponins were formulated with the FML antigen for mice prophylaxis against visceral leishmaniasis. the immune response was studied using an ELISA-antibody assay and monitoring of the intradermal response (IDR) to Leishmania antigens, the cytokine expression in supernatants and the intracellular staining of in vitro cultured splenocytes. After challenge, significant increases of IgG and IgG2a antibodies were noted only in the CA4 vaccinated mice that showed extended IDR, higher IFN-gamma production by CD8+ and TNF-alpha production by CD4+ T cells, higher TNF-alpha secretion and the highest reduction of the parasite load (78%). the increases in IDR, CD4-TNF-alpha,CD8-IFN-gamma and CD8-TNF-alpha by the CA4 vaccine were strong correlates of protection and were significantly correlated to the decrease of parasite load (p=-0.007). Protection generated by the CA4 vaccine was mainly mediated by a CD4+ T cell and a TNF-alpha driven response with a lower contribution of CD8+ T cells, as confirmed by an in vivo depletion with monoclonal antibodies and by vaccination assays in TNF-alpha-receptor knock-out mice. Our results confirm that the superiority of the CA4 saponin is related to the higher hydrophilicity of its longer carbohydrate chain. C. alba saponins were non-toxic and only the xylose-containing saponin CA3X was hemolytic (HD50 = 87 mu g/ml). the increase in sugar units of the saponins is positively correlated to the increase of IDR and to the decrease of parasite load. (C) 2012 Elsevier B.V. All rights reserved. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-05-02 2016-01-24T14:27:14Z 2016-01-24T14:27:14Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1016/j.vaccine.2012.03.006 Vaccine. Oxford: Elsevier B.V., v. 30, n. 21, p. 3169-3179, 2012. 10.1016/j.vaccine.2012.03.006 WOS000303302900005.pdf 0264-410X http://repositorio.unifesp.br/handle/11600/34887 WOS:000303302900005 |
url |
http://dx.doi.org/10.1016/j.vaccine.2012.03.006 http://repositorio.unifesp.br/handle/11600/34887 |
identifier_str_mv |
Vaccine. Oxford: Elsevier B.V., v. 30, n. 21, p. 3169-3179, 2012. 10.1016/j.vaccine.2012.03.006 WOS000303302900005.pdf 0264-410X WOS:000303302900005 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Vaccine |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy |
dc.format.none.fl_str_mv |
3169-3179 application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier B.V. |
publisher.none.fl_str_mv |
Elsevier B.V. |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
_version_ |
1814268374403776512 |