Dietary restriction abrogates antibody production induced by a DNA vaccine encoding the mycobacterial 65 kDa heat shock protein
Autor(a) principal: | |
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Data de Publicação: | 2009 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1186/1479-0556-7-11 http://hdl.handle.net/11449/71090 |
Resumo: | Background: 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. |
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Dietary restriction abrogates antibody production induced by a DNA vaccine encoding the mycobacterial 65 kDa heat shock proteinDNA vaccinegamma interferonheat shock protein 65immunoglobulin G1immunoglobulin G2interleukin 4animal experimentantibody productionatrophybody weightcontrolled studydiet restrictionfemalefood intakegenetic immunizationhematological parametershumoral immunityimmune responselymphocyte countmalnutritionmouseMycobacterium tuberculosisnonhumanspleen cellspleen weightStaphylococcus aureusAnimaliaCorynebacterineaeMusBackground: 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.Department of Microbiology and Immunology Biosciences Institute São Paulo State University (UNESP), Botucatu, São Paulo 18618-000Department of Parasitology Biosciences Institute São Paulo State University (UNESP), Botucatu, São Paulo 18618-000Department of Tropical Diseases Medical School São Paulo State University (UNESP), Botucatu, São Paulo 18618-000Department of Biochemistry and Immunology University of São Paulo (USP), Ribeirão Preto, São Paulo 14049-900Department of Microbiology and Immunology Biosciences Institute São Paulo State University (UNESP), Botucatu, São Paulo 18618-000Department of Parasitology Biosciences Institute São Paulo State University (UNESP), Botucatu, São Paulo 18618-000Department of Tropical Diseases Medical School São Paulo State University (UNESP), Botucatu, São Paulo 18618-000Universidade Estadual Paulista (Unesp)Universidade de São Paulo (USP)Ishikawa, Larissa Lumi Watanabe [UNESP]França, Thaís Graziela Donegá [UNESP]Chiuso-Minicucci, Fernanda [UNESP]Zorzella-Pezavento, Sofia Fernanda Gonçalves [UNESP]Marra, Nelson Mendes [UNESP]Pereira, Paulo Câmara Marques [UNESP]Silva, Célio LopesSartori, Alexandrina [UNESP]2014-05-27T11:23:56Z2014-05-27T11:23:56Z2009-07-16info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://dx.doi.org/10.1186/1479-0556-7-11Genetic Vaccines and Therapy, v. 7.1479-0556http://hdl.handle.net/11449/7109010.1186/1479-0556-7-112-s2.0-684490881312-s2.0-68449088131.pdf497757241612952713653204274182040000-0001-5771-8943Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengGenetic Vaccines and Therapyinfo:eu-repo/semantics/openAccess2024-08-15T15:22:48Zoai:repositorio.unesp.br:11449/71090Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-15T15:22:48Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Dietary restriction abrogates antibody production induced by a DNA vaccine encoding the mycobacterial 65 kDa heat shock protein |
title |
Dietary restriction abrogates antibody production induced by a DNA vaccine encoding the mycobacterial 65 kDa heat shock protein |
spellingShingle |
Dietary restriction abrogates antibody production induced by a DNA vaccine encoding the mycobacterial 65 kDa heat shock protein Ishikawa, Larissa Lumi Watanabe [UNESP] DNA vaccine gamma interferon heat shock protein 65 immunoglobulin G1 immunoglobulin G2 interleukin 4 animal experiment antibody production atrophy body weight controlled study diet restriction female food intake genetic immunization hematological parameters humoral immunity immune response lymphocyte count malnutrition mouse Mycobacterium tuberculosis nonhuman spleen cell spleen weight Staphylococcus aureus Animalia Corynebacterineae Mus |
title_short |
Dietary restriction abrogates antibody production induced by a DNA vaccine encoding the mycobacterial 65 kDa heat shock protein |
title_full |
Dietary restriction abrogates antibody production induced by a DNA vaccine encoding the mycobacterial 65 kDa heat shock protein |
title_fullStr |
Dietary restriction abrogates antibody production induced by a DNA vaccine encoding the mycobacterial 65 kDa heat shock protein |
title_full_unstemmed |
Dietary restriction abrogates antibody production induced by a DNA vaccine encoding the mycobacterial 65 kDa heat shock protein |
title_sort |
Dietary restriction abrogates antibody production induced by a DNA vaccine encoding the mycobacterial 65 kDa heat shock protein |
author |
Ishikawa, Larissa Lumi Watanabe [UNESP] |
author_facet |
Ishikawa, Larissa Lumi Watanabe [UNESP] França, Thaís Graziela Donegá [UNESP] Chiuso-Minicucci, Fernanda [UNESP] Zorzella-Pezavento, Sofia Fernanda Gonçalves [UNESP] Marra, Nelson Mendes [UNESP] Pereira, Paulo Câmara Marques [UNESP] Silva, Célio Lopes Sartori, Alexandrina [UNESP] |
author_role |
author |
author2 |
França, Thaís Graziela Donegá [UNESP] Chiuso-Minicucci, Fernanda [UNESP] Zorzella-Pezavento, Sofia Fernanda Gonçalves [UNESP] Marra, Nelson Mendes [UNESP] Pereira, Paulo Câmara Marques [UNESP] Silva, Célio Lopes Sartori, Alexandrina [UNESP] |
author2_role |
author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) Universidade de São Paulo (USP) |
dc.contributor.author.fl_str_mv |
Ishikawa, Larissa Lumi Watanabe [UNESP] França, Thaís Graziela Donegá [UNESP] Chiuso-Minicucci, Fernanda [UNESP] Zorzella-Pezavento, Sofia Fernanda Gonçalves [UNESP] Marra, Nelson Mendes [UNESP] Pereira, Paulo Câmara Marques [UNESP] Silva, Célio Lopes Sartori, Alexandrina [UNESP] |
dc.subject.por.fl_str_mv |
DNA vaccine gamma interferon heat shock protein 65 immunoglobulin G1 immunoglobulin G2 interleukin 4 animal experiment antibody production atrophy body weight controlled study diet restriction female food intake genetic immunization hematological parameters humoral immunity immune response lymphocyte count malnutrition mouse Mycobacterium tuberculosis nonhuman spleen cell spleen weight Staphylococcus aureus Animalia Corynebacterineae Mus |
topic |
DNA vaccine gamma interferon heat shock protein 65 immunoglobulin G1 immunoglobulin G2 interleukin 4 animal experiment antibody production atrophy body weight controlled study diet restriction female food intake genetic immunization hematological parameters humoral immunity immune response lymphocyte count malnutrition mouse Mycobacterium tuberculosis nonhuman spleen cell spleen weight Staphylococcus aureus Animalia Corynebacterineae Mus |
description |
Background: 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. |
publishDate |
2009 |
dc.date.none.fl_str_mv |
2009-07-16 2014-05-27T11:23:56Z 2014-05-27T11:23:56Z |
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://dx.doi.org/10.1186/1479-0556-7-11 Genetic Vaccines and Therapy, v. 7. 1479-0556 http://hdl.handle.net/11449/71090 10.1186/1479-0556-7-11 2-s2.0-68449088131 2-s2.0-68449088131.pdf 4977572416129527 1365320427418204 0000-0001-5771-8943 |
url |
http://dx.doi.org/10.1186/1479-0556-7-11 http://hdl.handle.net/11449/71090 |
identifier_str_mv |
Genetic Vaccines and Therapy, v. 7. 1479-0556 10.1186/1479-0556-7-11 2-s2.0-68449088131 2-s2.0-68449088131.pdf 4977572416129527 1365320427418204 0000-0001-5771-8943 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Genetic Vaccines and Therapy |
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.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
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1808128144231628800 |