Dietary restriction abrogates antibody production induced by a DNA vaccine encoding the mycobacterial 65 kDa heat shock protein

Detalhes bibliográficos
Autor(a) principal: Ishikawa, Larissa Lumi Watanabe [UNESP]
Data de Publicação: 2009
Outros Autores: 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]
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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spelling 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/openAccess2023-11-13T06:16:35Zoai:repositorio.unesp.br:11449/71090Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-11-13T06:16:35Repositório 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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