Immunogenicity of a Whole-Cell Pertussis Vaccine with Low Lipopolysaccharide Content in Infants
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 UNIFESP |
Texto Completo: | http://dx.doi.org/10.1128/CVI.00339-08 http://repositorio.unifesp.br/handle/11600/31400 |
Resumo: | The lack of a clear correlation between the levels of antibody to pertussis antigens and protection against disease lends credence to the possibility that cell-mediated immunity provides primary protection against disease. This phase I comparative trial had the aim of comparing the in vitro cellular immune response and anti-pertussis toxin (anti-PT) immunoglobulin G (IgG) titers induced by a cellular pertussis vaccine with low lipopolysaccharide (LPS) content (wP(low) vaccine) with those induced by the conventional whole-cell pertussis (wP) vaccine. A total of 234 infants were vaccinated at 2, 4, and 6 months with the conventional wP vaccine or the wP(low) vaccine. Proliferation of CD3(+) T cells was evaluated by flow cytometry after 6 days of peripheral blood mononuclear cell culture with stimulation with heat-killed Bordetella pertussis or phytohemagglutinin (PHA). CD3(+), CD4(+), CD8(+), and T-cell receptor gamma delta-positive (gamma delta(+)) cells were identified in the gate of blast lymphocytes. Gamma interferon, tumor necrosis factor alpha, interleukin-4 (IL-4), and IL-10 levels in super-natants and serum anti-PT IgG levels were determined using enzyme-linked immunosorbent assay (ELISA). the net percentage of CD3(+) blasts in cultures with B. pertussis in the group vaccinated with wP was higher than that in the group vaccinated with the wP(low) vaccine (medians of 6.2% for the wP vaccine and 3.9% for the wP(low) vaccine; P = 0.029). the frequencies of proliferating CD4(+), CD8(+), and gamma delta(+) cells, cytokine concentrations in supernatants, and the geometric mean titers of anti-PT IgG were similar for the two vaccination groups. There was a significant difference between the T-cell subpopulations for B. pertussis and PHA cultures, with a higher percentage of gamma delta(+) cells in the B. pertussis cultures (P < 0.001). the overall data did suggest that wP vaccination resulted in modestly better specific CD3(+) cell proliferation, and gamma delta(+) cell expansions were similar with the two vaccines. |
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Immunogenicity of a Whole-Cell Pertussis Vaccine with Low Lipopolysaccharide Content in InfantsThe lack of a clear correlation between the levels of antibody to pertussis antigens and protection against disease lends credence to the possibility that cell-mediated immunity provides primary protection against disease. This phase I comparative trial had the aim of comparing the in vitro cellular immune response and anti-pertussis toxin (anti-PT) immunoglobulin G (IgG) titers induced by a cellular pertussis vaccine with low lipopolysaccharide (LPS) content (wP(low) vaccine) with those induced by the conventional whole-cell pertussis (wP) vaccine. A total of 234 infants were vaccinated at 2, 4, and 6 months with the conventional wP vaccine or the wP(low) vaccine. Proliferation of CD3(+) T cells was evaluated by flow cytometry after 6 days of peripheral blood mononuclear cell culture with stimulation with heat-killed Bordetella pertussis or phytohemagglutinin (PHA). CD3(+), CD4(+), CD8(+), and T-cell receptor gamma delta-positive (gamma delta(+)) cells were identified in the gate of blast lymphocytes. Gamma interferon, tumor necrosis factor alpha, interleukin-4 (IL-4), and IL-10 levels in super-natants and serum anti-PT IgG levels were determined using enzyme-linked immunosorbent assay (ELISA). the net percentage of CD3(+) blasts in cultures with B. pertussis in the group vaccinated with wP was higher than that in the group vaccinated with the wP(low) vaccine (medians of 6.2% for the wP vaccine and 3.9% for the wP(low) vaccine; P = 0.029). the frequencies of proliferating CD4(+), CD8(+), and gamma delta(+) cells, cytokine concentrations in supernatants, and the geometric mean titers of anti-PT IgG were similar for the two vaccination groups. There was a significant difference between the T-cell subpopulations for B. pertussis and PHA cultures, with a higher percentage of gamma delta(+) cells in the B. pertussis cultures (P < 0.001). the overall data did suggest that wP vaccination resulted in modestly better specific CD3(+) cell proliferation, and gamma delta(+) cell expansions were similar with the two vaccines.Univ Estadual Campinas, Sch Med, Ctr Investigat Pediat, BR-13083887 São Paulo, BrazilUniv Estadual Campinas, Sch Med, Dept Pediat, BR-13083887 São Paulo, BrazilButantan Inst, BR-05503900 São Paulo, BrazilUniv São Paulo, Fac Ciencias Farmaceut, BR-05508000 São Paulo, BrazilWeb of ScienceFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Financiadora de Estudos e Projetos, BrazilFAPESP: 2005/03539-1Financiadora de Estudos e Projetos, Brazil: 01040957/0Amer Soc MicrobiologyUniversidade Estadual de Campinas (UNICAMP)Universidade Federal de São Paulo (UNIFESP)Butantan InstUniversidade de São Paulo (USP)Zorzeto, Tatiane QueirozHigashi, Hisako GondoNolasco da Silva, Marcos TadeuCarniel, Emilia de FariaDias, Waldely de Oliveira [UNIFESP]Ramalho, Vanessa DominguesMazzola, Tais NitschBatista Souza Lima, Simone CorteMorcillo, Andre MorenoStephano, Marco AntonioReis de Goes Antonio, Maria AngelaZanolli, Maria de LurdesRaw, IsaiasSantos Vilela, Maria Marluce dos2016-01-24T13:52:23Z2016-01-24T13:52:23Z2009-04-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion544-550application/pdfhttp://dx.doi.org/10.1128/CVI.00339-08Clinical and Vaccine Immunology. Washington: Amer Soc Microbiology, v. 16, n. 4, p. 544-550, 2009.10.1128/CVI.00339-08WOS000264938400017.pdf1556-6811http://repositorio.unifesp.br/handle/11600/31400WOS:000264938400017engClinical and Vaccine Immunologyinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-07T19:08:32Zoai:repositorio.unifesp.br/:11600/31400Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-07T19:08:32Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Immunogenicity of a Whole-Cell Pertussis Vaccine with Low Lipopolysaccharide Content in Infants |
title |
Immunogenicity of a Whole-Cell Pertussis Vaccine with Low Lipopolysaccharide Content in Infants |
spellingShingle |
Immunogenicity of a Whole-Cell Pertussis Vaccine with Low Lipopolysaccharide Content in Infants Zorzeto, Tatiane Queiroz |
title_short |
Immunogenicity of a Whole-Cell Pertussis Vaccine with Low Lipopolysaccharide Content in Infants |
title_full |
Immunogenicity of a Whole-Cell Pertussis Vaccine with Low Lipopolysaccharide Content in Infants |
title_fullStr |
Immunogenicity of a Whole-Cell Pertussis Vaccine with Low Lipopolysaccharide Content in Infants |
title_full_unstemmed |
Immunogenicity of a Whole-Cell Pertussis Vaccine with Low Lipopolysaccharide Content in Infants |
title_sort |
Immunogenicity of a Whole-Cell Pertussis Vaccine with Low Lipopolysaccharide Content in Infants |
author |
Zorzeto, Tatiane Queiroz |
author_facet |
Zorzeto, Tatiane Queiroz Higashi, Hisako Gondo Nolasco da Silva, Marcos Tadeu Carniel, Emilia de Faria Dias, Waldely de Oliveira [UNIFESP] Ramalho, Vanessa Domingues Mazzola, Tais Nitsch Batista Souza Lima, Simone Corte Morcillo, Andre Moreno Stephano, Marco Antonio Reis de Goes Antonio, Maria Angela Zanolli, Maria de Lurdes Raw, Isaias Santos Vilela, Maria Marluce dos |
author_role |
author |
author2 |
Higashi, Hisako Gondo Nolasco da Silva, Marcos Tadeu Carniel, Emilia de Faria Dias, Waldely de Oliveira [UNIFESP] Ramalho, Vanessa Domingues Mazzola, Tais Nitsch Batista Souza Lima, Simone Corte Morcillo, Andre Moreno Stephano, Marco Antonio Reis de Goes Antonio, Maria Angela Zanolli, Maria de Lurdes Raw, Isaias Santos Vilela, Maria Marluce dos |
author2_role |
author author author author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual de Campinas (UNICAMP) Universidade Federal de São Paulo (UNIFESP) Butantan Inst Universidade de São Paulo (USP) |
dc.contributor.author.fl_str_mv |
Zorzeto, Tatiane Queiroz Higashi, Hisako Gondo Nolasco da Silva, Marcos Tadeu Carniel, Emilia de Faria Dias, Waldely de Oliveira [UNIFESP] Ramalho, Vanessa Domingues Mazzola, Tais Nitsch Batista Souza Lima, Simone Corte Morcillo, Andre Moreno Stephano, Marco Antonio Reis de Goes Antonio, Maria Angela Zanolli, Maria de Lurdes Raw, Isaias Santos Vilela, Maria Marluce dos |
description |
The lack of a clear correlation between the levels of antibody to pertussis antigens and protection against disease lends credence to the possibility that cell-mediated immunity provides primary protection against disease. This phase I comparative trial had the aim of comparing the in vitro cellular immune response and anti-pertussis toxin (anti-PT) immunoglobulin G (IgG) titers induced by a cellular pertussis vaccine with low lipopolysaccharide (LPS) content (wP(low) vaccine) with those induced by the conventional whole-cell pertussis (wP) vaccine. A total of 234 infants were vaccinated at 2, 4, and 6 months with the conventional wP vaccine or the wP(low) vaccine. Proliferation of CD3(+) T cells was evaluated by flow cytometry after 6 days of peripheral blood mononuclear cell culture with stimulation with heat-killed Bordetella pertussis or phytohemagglutinin (PHA). CD3(+), CD4(+), CD8(+), and T-cell receptor gamma delta-positive (gamma delta(+)) cells were identified in the gate of blast lymphocytes. Gamma interferon, tumor necrosis factor alpha, interleukin-4 (IL-4), and IL-10 levels in super-natants and serum anti-PT IgG levels were determined using enzyme-linked immunosorbent assay (ELISA). the net percentage of CD3(+) blasts in cultures with B. pertussis in the group vaccinated with wP was higher than that in the group vaccinated with the wP(low) vaccine (medians of 6.2% for the wP vaccine and 3.9% for the wP(low) vaccine; P = 0.029). the frequencies of proliferating CD4(+), CD8(+), and gamma delta(+) cells, cytokine concentrations in supernatants, and the geometric mean titers of anti-PT IgG were similar for the two vaccination groups. There was a significant difference between the T-cell subpopulations for B. pertussis and PHA cultures, with a higher percentage of gamma delta(+) cells in the B. pertussis cultures (P < 0.001). the overall data did suggest that wP vaccination resulted in modestly better specific CD3(+) cell proliferation, and gamma delta(+) cell expansions were similar with the two vaccines. |
publishDate |
2009 |
dc.date.none.fl_str_mv |
2009-04-01 2016-01-24T13:52:23Z 2016-01-24T13:52:23Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1128/CVI.00339-08 Clinical and Vaccine Immunology. Washington: Amer Soc Microbiology, v. 16, n. 4, p. 544-550, 2009. 10.1128/CVI.00339-08 WOS000264938400017.pdf 1556-6811 http://repositorio.unifesp.br/handle/11600/31400 WOS:000264938400017 |
url |
http://dx.doi.org/10.1128/CVI.00339-08 http://repositorio.unifesp.br/handle/11600/31400 |
identifier_str_mv |
Clinical and Vaccine Immunology. Washington: Amer Soc Microbiology, v. 16, n. 4, p. 544-550, 2009. 10.1128/CVI.00339-08 WOS000264938400017.pdf 1556-6811 WOS:000264938400017 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Clinical and Vaccine Immunology |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
544-550 application/pdf |
dc.publisher.none.fl_str_mv |
Amer Soc Microbiology |
publisher.none.fl_str_mv |
Amer Soc Microbiology |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
_version_ |
1814268368877780992 |