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DNA immunization of Mycobacterium tuberculosis resuscitation-promoting factor B elicits polyfunctional CD8+ T cell responses
Clinical and Experimental Vaccine Research ; : 235-243, 2014.
Article in English | WPRIM | ID: wpr-108899
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.
Subject(s)

Full text: Available Index: WPRIM (Western Pacific) Main subject: Peptides / Phenotype / Plasmids / Tuberculosis / DNA / T-Lymphocytes / Complement Factor B / Cytokines / Immunization / Interferon-gamma Type of study: Prognostic study Limits: Animals Language: English Journal: Clinical and Experimental Vaccine Research Year: 2014 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Peptides / Phenotype / Plasmids / Tuberculosis / DNA / T-Lymphocytes / Complement Factor B / Cytokines / Immunization / Interferon-gamma Type of study: Prognostic study Limits: Animals Language: English Journal: Clinical and Experimental Vaccine Research Year: 2014 Type: Article