Background & Objective:
Dendritic cell (DC) is as a key cell in activation of immune response against
microbes and disease. Therefore, the effect of recombinant exotoxin A of
Pseudomonas aeruginosa on the maturity and the activation of DCs was evaluated
in this study.
Materials & Methods:
Recombinant exotoxin A was produced from Pseudomonas aeruginosa DNA. MTT assay
was used to evaluate the cytotoxicity of this protein on DCs. The expression of
co-stimulatory molecules CD40, CD86, and MHCΠ was evaluated by flow cytometry.
Moreover, the effect of this antigen (Ag) on T-cell proliferation was evaluated
using Mixed Lymphocyte Reaction (MLR) assay and the secretion of IL-4 and IFN-
γ. Secretion of IL-12 by DCs was measured with Enzyme-Linked
Immunosorbent Assay (ELISA)
method. The data were collected and analyzed with one way ANOVA test.
Results:
Recombinant exotoxin A had no effect on DCs viability. In addition, expression
of CD40, CD86, and MHCΠ did not change significantly compared to the negative
control cells. Moreover, T-cells proliferation was decreased significantly at
the concentration of 0.1µg/ml of this Ag. The secretion of IL-12 was increased
by DCs, in contrast the secretion of IL-4 and IFN-γ in MLR supernatant did not
decrease significantly.
Conclusion:
Exotoxin A decreases the proliferation of T-cells and also leads to a change in
the pattern of cytokine secretion of immune cells.
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