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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/71090
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dc.contributor.authorIshikawa, Larissa Lumi Watanabe-
dc.contributor.authorFrança, Thaís Graziela Donegá-
dc.contributor.authorChiuso-Minicucci, Fernanda-
dc.contributor.authorZorzella-Pezavento, Sofia Fernanda Gonçalves-
dc.contributor.authorMarra, Nelson Mendes-
dc.contributor.authorPereira, Paulo Câmara Marques-
dc.contributor.authorSilva, Célio Lopes-
dc.contributor.authorSartori, Alexandrina-
dc.date.accessioned2014-05-27T11:23:56Z-
dc.date.accessioned2016-10-25T18:27:10Z-
dc.date.available2014-05-27T11:23:56Z-
dc.date.available2016-10-25T18:27:10Z-
dc.date.issued2009-07-16-
dc.identifierhttp://dx.doi.org/10.1186/1479-0556-7-11-
dc.identifier.citationGenetic Vaccines and Therapy, v. 7.-
dc.identifier.issn1479-0556-
dc.identifier.urihttp://hdl.handle.net/11449/71090-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/71090-
dc.description.abstractBackground: Protein-calorie malnutrition (PCM) is the most common type of malnutrition. PCM leads to immunodeficiency and consequent increased susceptibility to infectious agents. In addition, responses to prophylactic vaccines depend on nutritional status. This study aims to evaluate the ability of undernourished mice to mount an immune response to a genetic vaccine (pVAXhsp65) against tuberculosis, containing the gene coding for the heat shock protein 65 from mycobacteria. Methods: Young adult female BALB/c mice were fed ad libitum or with 80% of the amount of food consumed by a normal diet group. We initially characterized a mice model of dietary restriction by determining body and spleen weights, hematological parameters and histopathological changes in lymphoid organs. The ability of splenic cells to produce IFN-gamma and IL-4 upon in vitro stimulation with LPS or S. aureus and the serum titer of specific IgG1 and IgG2a anti-hsp65 antibodies after intramuscular immunization with pVAXhsp65 was then tested. Results: Dietary restriction significantly decreased body and spleen weights and also the total lymphocyte count in blood. This restriction also determined a striking atrophy in lymphoid organs as spleen, thymus and lymphoid tissue associated with the small intestine. Specific antibodies were not detected in mice submitted to dietary restriction whereas the well nourished animals produced significant levels of both, IgG1 and IgG2a anti-hsp65. Conclusion: 20% restriction in food intake deeply compromised humoral immunity induced by a genetic vaccine, alerting, therefore, for the relevance of the nutritional condition in vaccination programs based on these kinds of constructs. © 2009 Ishikawa et al; licensee BioMed Central Ltd.en
dc.language.isoeng-
dc.sourceScopus-
dc.subjectDNA vaccine-
dc.subjectgamma interferon-
dc.subjectheat shock protein 65-
dc.subjectimmunoglobulin G1-
dc.subjectimmunoglobulin G2-
dc.subjectinterleukin 4-
dc.subjectanimal experiment-
dc.subjectantibody production-
dc.subjectatrophy-
dc.subjectbody weight-
dc.subjectcontrolled study-
dc.subjectdiet restriction-
dc.subjectfemale-
dc.subjectfood intake-
dc.subjectgenetic immunization-
dc.subjecthematological parameters-
dc.subjecthumoral immunity-
dc.subjectimmune response-
dc.subjectlymphocyte count-
dc.subjectmalnutrition-
dc.subjectmouse-
dc.subjectMycobacterium tuberculosis-
dc.subjectnonhuman-
dc.subjectspleen cell-
dc.subjectspleen weight-
dc.subjectStaphylococcus aureus-
dc.subjectAnimalia-
dc.subjectCorynebacterineae-
dc.subjectMus-
dc.titleDietary restriction abrogates antibody production induced by a DNA vaccine encoding the mycobacterial 65 kDa heat shock proteinen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.description.affiliationDepartment of Microbiology and Immunology Biosciences Institute São Paulo State University (UNESP), Botucatu, São Paulo 18618-000-
dc.description.affiliationDepartment of Parasitology Biosciences Institute São Paulo State University (UNESP), Botucatu, São Paulo 18618-000-
dc.description.affiliationDepartment of Tropical Diseases Medical School São Paulo State University (UNESP), Botucatu, São Paulo 18618-000-
dc.description.affiliationDepartment of Biochemistry and Immunology University of São Paulo (USP), Ribeirão Preto, São Paulo 14049-900-
dc.description.affiliationUnespDepartment of Microbiology and Immunology Biosciences Institute São Paulo State University (UNESP), Botucatu, São Paulo 18618-000-
dc.description.affiliationUnespDepartment of Parasitology Biosciences Institute São Paulo State University (UNESP), Botucatu, São Paulo 18618-000-
dc.description.affiliationUnespDepartment of Tropical Diseases Medical School São Paulo State University (UNESP), Botucatu, São Paulo 18618-000-
dc.identifier.doi10.1186/1479-0556-7-11-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-68449088131.pdf-
dc.relation.ispartofGenetic Vaccines and Therapy-
dc.identifier.scopus2-s2.0-68449088131-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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