dc.creatorIborra, Salvador
dc.creatorParody, Nuria
dc.creatorAbánades, Daniel Ruiz
dc.creatorBonay, Pedro
dc.creatorPrates, Deboraci Brito
dc.creatorNovais, Fernanda Oliveira
dc.creatorBarral Netto, Manoel
dc.creatorAlonso, Carlos
dc.creatorSoto, Manuel
dc.date2014-03-13T19:19:59Z
dc.date2014-03-13T19:19:59Z
dc.date2008
dc.date.accessioned2023-09-26T23:23:46Z
dc.date.available2023-09-26T23:23:46Z
dc.identifierIBORRA, S. et al. Vaccination with the Leishmania major ribosomal proteins plus CpG oligodeoxynucleotides induces protection against experimental cutaneous leishmaniasis in mice. Microbes and Infection, v. 10, n. 10/11, p. 1133-1141, 2008.
dc.identifier1286-4579
dc.identifierhttps://www.arca.fiocruz.br/handle/icict/7408
dc.identifier10.1016/j.micinf.2008.06.002
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/8890116
dc.descriptionIn the present work we analyze the antigenicity of Leishmania major ribosomal proteins (LRP) in infected BALB/c mice.We show that BALB/c mice vaccinated with LRP in the presence of CpG oligodeoxynucleotides (CpG-ODN) were protected against the development of dermal pathology and showed a reduction in the parasite load after challenge with L. major. This protection was associated with the induction of an IL-12 dependent specific-IFN-g response mediated mainly by CD4þ T cell, albeit a minor contribution of CD8þ T cells cannot be ruled out. Induction of Th1 responses against LRP also resulted in a reversion of the Th2 responses associated with susceptibility. A marked reduction of IgG1 antibody titer against parasite antigens besides an impaired IL-4 and IL-10 cytokine production by parasite specific T cells was observed. In addition, we show that the administration of the LRP plus CpG-ODN preparation also conferred protection in the naturally resistant C57BL/6 mice. In this strain protection was associated with a LRP specific IFN-g production in lymph nodes draining the challenge site. We believe that these evolutionary conserved proteins, combined with adjuvants that favor Th1 responses, may be relevant components of a pan-Leishmania vaccine. 2008 Elsevier Masson SAS. All rights reserved
dc.formatapplication/pdf
dc.languageeng
dc.publisherElsevier Masson SAS
dc.rightsopen access
dc.subjectLeishmania
dc.subjectBALB/C mice
dc.subjectC57BL/6 mice
dc.subjectTh1/Th2 immune responses;
dc.subjectRibosomal proteins
dc.subjectVaccines
dc.subjectLeishmania major/imunologia
dc.subjectVacinas contra Leishmaniose
dc.subjectLeishmaniose Cutânea/prevenção & controle
dc.subjectOligodesoxirribonucleotídeos/imunologia
dc.subjectProteínas Ribossômicas/imunologia
dc.subjectAnimais
dc.subjectFeminino
dc.subjectImunoglobulina G/metabolismo
dc.subjectInterferon gama/metabolismo
dc.subjectInterleucina-10/metabolismo
dc.subjectInterleucina-4/metabolismo
dc.subjectLeishmaniose Cutânea/imunologia
dc.subjectCamundongos
dc.subjectCamundongos Endogâmicos BALB C
dc.subjectCamundongos Endogâmicos C57BL
dc.subjectOligodesoxirribonucleotídeos/genética
dc.subjectOligodesoxirribonucleotídeos/metabolismo
dc.subjectProteínas de Protozoários/genética
dc.subjectProteínas de Protozoários/imunologia
dc.subjectProteínas de Protozoários/metabolismo
dc.subjectProteínas Ribossômicas/genética
dc.subjectProteínas Ribossômicas/metabolismo
dc.titleVaccination with the Leishmania major ribosomal proteins plus CpG oligodeoxynucleotides induces protection against experimental cutaneous leishmaniasis in mice
dc.typeArticle


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