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DNA immunization of Mycobacterium tuberculosis resuscitation-promoting factor B elicits polyfunctional CD8+ T cell responses
Article en En | WPRIM | ID: wpr-108899
Biblioteca responsable: WPRO
ABSTRACT
PURPOSE: T cell-mediated immune responses, and particularly activation of polyfunctional T cells that simultaneously produce multiple cytokines, are necessary for the control of Mycobacterium tuberculosis. In the present study, we examined if DNA immunization of Mycobacterium tuberculosis resuscitation-promoting factor B (RpfB) elicits polyfunctional T cell responses in mice. MATERIALS AND METHODS: C57BL/6 mice were immunized intramuscularly three times, at 3-week intervals, with RpfB-expressing plasmid DNA. For comparison, protein immunization was performed with recombinant RpfB in control mice. After immunization, RpfB-specific T cell responses were assessed by interferon-gamma (IFN-gamma) enzyme-linked immunosorbent spot assay and intracellular cytokine staining (ICS), and T cell polyfunctionality was assessed from the ICS data. RESULTS: RpfB DNA immunization induced not only humoral immune responses, but also CD8+ and CD4+ T cell responses. Immunodominant T-cell epitopes were identified within RpfB by assays with overlapping peptides. RpfB DNA immunization elicited a polyfunctional CD8+ T cell response that was dominated by a functional phenotype of IFN-gamma+/TNF-alpha+/IL-2-/CD107a+. CONCLUSION: RpfB DNA immunization elicits polyfunctional CD8+ T cell responses, suggesting that RpfB DNA immunization might induce protective immunity against tuberculosis.
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Texto completo: 1 Índice: WPRIM Asunto principal: Péptidos / Fenotipo / Plásmidos / Tuberculosis / ADN / Linfocitos T / Factor B del Complemento / Citocinas / Inmunización / Interferón gamma Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Clinical and Experimental Vaccine Research Año: 2014 Tipo del documento: Article
Texto completo: 1 Índice: WPRIM Asunto principal: Péptidos / Fenotipo / Plásmidos / Tuberculosis / ADN / Linfocitos T / Factor B del Complemento / Citocinas / Inmunización / Interferón gamma Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: Clinical and Experimental Vaccine Research Año: 2014 Tipo del documento: Article