Author/Authors :
Keikha, Reza Cellular and Molecular Biology Research Center - Shahid Beheshti University of Medical Sciences, Tehran, Iran , bandehpor, mojgan Department of Biotechnology - School of Medicine - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Jeibouei, Shabnam Department of Biotechnology - School of Medicine - Shahid Beheshti University of Medical Sciences, Tehran, Iran
Abstract :
Background: About 12 million people are affected by les leishmaniosis worldwide. It is an important public health problem due to
the difficulty in its control and causing epidemic outbreaks. An effective anti-leishmanial vaccine remains elusive. Isolated dominant
epitopes arranged as polytope DNA vaccine represent a promising approach.
Methods: Balb/c mice were vaccinated subcutaneously with pCDNA3.1/LAKJB93 DNA and challenged with Leishmania major promastigotes;
then, the level of interferon (INF)-
and interleukin (IL)-4 were measured by the enzyme-linked immunosorbent assay
(ELISA) technique. Production of immunoglobulin (Ig)-G1 and IgG2a antigen specific antibodies were measured against LAKJB93.
Results: The enhanced production of antigen-specific INF-
and IgG2a in serum showed the stimulation of T helper type 1 (Th1)
response. This protectiveimmune response was induced by the expression of pcDNA3.1/ LAKJB93 plasmid against leishmaniosis and
therefore, pcDNA3.1/ LAKJB93 can be considered an appropriate vaccine for leishmaniosis.
Conclusions: Immunization with DNA vaccine may offer an effective route to prevent leishmaniosis.
Keywords :
Leishmaniosis , Epitopes , DNA Vaccine , LACK Antigen , GP63