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Immunogenicity of a Dna Vaccine Encoding Ag85a-Tb10.4 Antigens From Mycobacterium Tuberculosis Pubmed



Meshkat Z1 ; Teimourpour A2 ; Rashidian S1 ; Arzanlou M3 ; Teimourpour R3
Authors
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Authors Affiliations
  1. 1. Antimicrobial Resistance Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
  2. 2. Department of Epidemiology and Biostatistics, Tehran University of Medical Science, Tehran, Iran
  3. 3. Department of Microbiology, School of Medicine, Ardabil University of Medical Sciences, Ardabil, Iran

Source: Iranian Journal of Immunology Published:2016


Abstract

Background: Tuberculosis is a life threatening disease that is partially prevented by BCG vaccine. Development of more effective vaccines is an urgent priority in TB control. Ag85a and Tb10.4 are the members of culture filter protein (CFP) of M. tuberculosis that have high immunogenicity. Objective: To analyze the immunogenicity of Ag85a-Tb10.4 DNA vaccine by enzyme-linked immunosorbent assay (ELISA). Methods: In this study a previously described plasmid DNA vaccine encoding Ag85a-Tb10.4 was used to examine its capability in the stimulation of immune responses in an animal model. Female BALB/c mice were vaccinated with 100 µg of purified recombinant vector intramuscularly 3 times at two-week intervals and the levels of five cytokines including IFN-γ, IL-12, IL-4, IL-10 and TGF-β were measured. Results: The levels of IFN-γ and IL-12 for the mice following immunization with Ag85A-Tb10.4 was significantly greater than that of the BCG and control group (p<0.05). However there was no significant difference in the levels of IL-4, IL-10 and TGF-β between groups. Conclusion: IFN-γ and IL-12 Th1 cytokines increased significantly in mice vaccinated with Ag85a-TB10.4 DNA vaccine in comparison to the control and BCG groups. Our results may serve as groundwork for further research into the prevention and treatment of tuberculosis. © 2016, Shiraz University of Medical Sciences. All rights reserved.