Please use this identifier to cite or link to this item: https://www.arca.fiocruz.br/handle/icict/7934
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dc.contributor.authorSouza, Juliana Vitoriano
dc.contributor.authorFujiwara, Ricardo Toshio
dc.contributor.authorMelo, Maria Norma
dc.contributor.authorMoreira, Nádia das Dores
dc.contributor.authorCarneiro, Cláudia Martins
dc.contributor.authorSiqueira, Fernando Augusto Mathias
dc.contributor.authorVieira, Paula Melo de Abreu
dc.contributor.authorGiunchetti, Rodolfo Cordeiro
dc.contributor.authorMoura, Sandra Aparecida Lima de
dc.contributor.authorCarvalho, Andréa Teixeira de
dc.contributor.authorCarneiro, Cláudia Martins
dc.contributor.authorReis, Alexandre Barbosa
dc.date.accessioned2014-07-11T18:03:34Z
dc.date.available2014-07-11T18:03:34Z
dc.date.issued2012
dc.identifier.citationVITORIANO SOUZA, Juliana et al. Cell recruitment and cytokines in skin mice sensitized with the vaccine adjuvants: saponin, incomplete freund’s adjuvant, and monophosphoryl lipid A. Plos one. 2012, vol.7, pp. e40745
dc.identifier.issn1932-6203
dc.identifier.urihttps://www.arca.fiocruz.br/handle/icict/7934
dc.language.isoeng
dc.publisherPublic Library of Science
dc.rightsopen access
dc.titleCell recruitment and cytokines in skin mice sensitized with the vaccine adjuvants: saponin, incomplete freund s adjuvant, and monophosphoryl Lipid A
dc.typeArticle
dc.identifier.doi10.1371/journal.pone.0040745
dc.description.abstractenVaccine adjuvants are substances associated with antigens that are fundamental to the formation of an intense, durable, and fast immune response. In this context, the use of vaccine adjuvants to generate an effective cellular immune response is crucial for the design and development of vaccines against visceral leishmaniasis. The objective of this study was to evaluate innate inflammatory response induced by the vaccine adjuvants saponin (SAP), incomplete Freund’s adjuvant (IFA), and monophosphoryl lipid A (MPL). After a single dose of adjuvant was injected into the skin of mice, we analyzed inflammatory reaction, selective cell migration, and cytokine production at the injection site, and inflammatory cell influx in the peripheral blood. We found that all vaccine adjuvants were able to promote cell recruitment to the site without tissue damage. In addition, they induced selective migration of neutrophils, macrophages, and lymphocytes. The influx of neutrophils was notable at 12 h in all groups, but at other time points it was most evident after inoculation with SAP. With regard to cytokines, the SAP led to production of interleukin (IL)-2, IL-6, and IL-4. IFA promoted production of tumor necrosis factor (TNF)-α, interferon (IFN)-γ, IL-6, IL-17, IL-4, and IL-10. We also observed that MPL induced high production of IL-2, TNF-α, and IFN-γ, in addition to IL-6, IL-17, and IL-10. In peripheral blood, values of certain cell populations in the local response changed after stimulation. Our data demonstrate that the three vaccine adjuvants stimulate the early events of innate immune response at the injection site, suggesting their ability to increase the immunogenicity of co-administered antigens. Moreover, this work provides relevant information about elements of innate and acquired immune response induced by vaccine adjuvants administered alone.
dc.creator.affilliationUniversidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Parasitologia. Belo Horizonte, MG, Brasil/Universidade Federal de Ouro Preto. Núcleo de Pesquisas em Ciências Biológicas. Laboratório de Imunopatologia. Ouro Preto, MG, Brazil
dc.creator.affilliationUniversidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Parasitologia. Belo Horizonte, MG, Brasil
dc.creator.affilliationUniversidade Federal de Minas Gerais. Instituto de Ciências Biológicas. Departamento de Parasitologia. Belo Horizonte, MG, Brasil
dc.creator.affilliationUniversidade Federal de Ouro Preto. Núcleo de Pesquisas em Ciências Biológicas. Laboratório de Imunopatologia. Ouro Preto, MG, Brazil
dc.creator.affilliationUniversidade Federal de Ouro Preto. Núcleo de Pesquisas em Ciências Biológicas. Laboratório de Imunopatologia. Ouro Preto, MG, Brazil
dc.creator.affilliationUniversidade Federal de Ouro Preto. Núcleo de Pesquisas em Ciências Biológicas. Laboratório de Imunopatologia. Ouro Preto, MG, Brazil
dc.creator.affilliationUniversidade Federal de Ouro Preto. Núcleo de Pesquisas em Ciências Biológicas. Laboratório de Imunopatologia. Ouro Preto, MG, Brazil
dc.creator.affilliationUniversidade Federal de Ouro Preto. Núcleo de Pesquisas em Ciências Biológicas. Laboratório de Imunopatologia. Ouro Preto, MG, Brazil
dc.creator.affilliationUniversidade Federal de Ouro Preto. Núcleo de Pesquisas em Ciências Biológicas. Laboratório de Imunopatologia. Ouro Preto, MG, Brazil
dc.creator.affilliationFundação Oswaldo Cruz. Centro de Pesquisas René Rachou. Laboratório de Biomarcadores de Diagnóstico e Monitoração. Belo Horizonte, MG, Brazil
dc.creator.affilliationUniversidade Federal de Ouro Preto. Escola de Farmácia. Departamento de Análises Clínicas. Ouro Preto, MG, Brazil
dc.creator.affilliationUniversidade Federal de Ouro Preto. Escola de Farmácia. Departamento de Análises Clínicas. Ouro Preto, MG, Brazil/Universidade Federal de Ouro Preto. Núcleo de Pesquisas em Ciências Biológicas. Laboratório de Imunopatologia. Ouro Preto, Minas Gerais, Brazil
dc.subject.enAntigens
dc.subject.enCytokines
dc.subject.enImmune response
dc.subject.enInflammation
dc.subject.enInoculation
dc.subject.enLymphocytes
dc.subject.enNeutrophils
Appears in Collections:MG - IRR - Artigos de Periódicos

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