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Toxoplasma gondii: Evaluation of an intranasal vaccine using recombinant proteins against brain cyst formation in BALB/c mice

dc.contributor.authorIgarashi, M.
dc.contributor.authorKano, F.
dc.contributor.authorTamekuni, K.
dc.contributor.authorMachado, R. Z. [UNESP]
dc.contributor.authorNavarro, I. T.
dc.contributor.authorVidotto, O.
dc.contributor.authorVidotto, M. C.
dc.contributor.authorGarcia, J. L.
dc.contributor.institutionUniversidade Estadual de Londrina (UEL)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:16:02Z
dc.date.available2014-05-20T13:16:02Z
dc.date.issued2008-03-01
dc.description.abstractThe purpose of this work was to evaluate protective activity against brain cyst formation in BALB/c mice intranasally vaccinated with recombinant proteins from Toxoplasma gondii. The recombinant proteins rROP2, rGRA5 and rGRA7 were used in vaccine preparation. Thirty-three female mice were divided into three groups, these animals received two doses by intranasal route at days 0 and 21 as follows; group 1 (G1, n = 11) received 12.5 mu g of each recombinant protein plus 0.5 mu g of cholera toxin, group 2 (G2, n = 11) received phosphate buffer saline (PBS) plus 0.5 mu g of cholera toxin, and group 3 (G3, n = 11) received PBS only. At challenge day (day 33) three animals from each group were euthanatized for IgA measure from intestine. Mice were infected orally with 50 cysts from the VEG strain at day 33. At challenge day the G1 animals had high immunoglobulin A levels, however, they only showed IgG antibody titers against rROP2 and rGRAT Animals from G1 also exhibited strong resistance to cyst formation compared with the control group (G3, P < 0.05). However, we did not observe differences in protection against brain cyst formation between G1 and G2 (P > 0.1). These results indicate that intranasal immunization in BALB/c mice with recombinant proteins rROP2, rGRA5 and rGRA7 associated with cholera toxin induced partial protection, when compared with G3, against tissue cyst formation after oral infection with tissue cysts from T gondii. (c) 2007 Elsevier B.V. All rights reserved.en
dc.description.affiliationUniversidade Estadual de Londrina (UEL), Dept Vet Prevent Med, Protozool Lab, BR-86050970 Londrina, PR, Brazil
dc.description.affiliationUNESP, Dept Patol, Immunoparasitol Lab, Jaboticabal, SP, Brazil
dc.description.affiliationUnespUNESP, Dept Patol, Immunoparasitol Lab, Jaboticabal, SP, Brazil
dc.format.extent386-392
dc.identifierhttp://dx.doi.org/10.1016/j.exppara.2007.10.002
dc.identifier.citationExperimental Parasitology. San Diego: Academic Press Inc. Elsevier B.V., v. 118, n. 3, p. 386-392, 2008.
dc.identifier.doi10.1016/j.exppara.2007.10.002
dc.identifier.issn0014-4894
dc.identifier.lattes3254990612451836
dc.identifier.urihttp://hdl.handle.net/11449/3012
dc.identifier.wosWOS:000253875400013
dc.language.isoeng
dc.publisherAcademic Press Inc. Elsevier B.V.
dc.relation.ispartofExperimental Parasitology
dc.relation.ispartofjcr1.821
dc.relation.ispartofsjr0,635
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectToxoplasma gondiien
dc.subjectmouseen
dc.subjectrecombinant proteinsen
dc.subjectrhoptryen
dc.subjectdense granuleen
dc.subjectVaccineen
dc.titleToxoplasma gondii: Evaluation of an intranasal vaccine using recombinant proteins against brain cyst formation in BALB/c miceen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderAcademic Press Inc. Elsevier B.V.
dspace.entity.typePublication
unesp.author.lattes3254990612451836
unesp.author.orcid0000-0001-6493-8645[7]
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Agrárias e Veterinárias, Jaboticabalpt
unesp.departmentPatologia Veterinária - FCAVpt

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