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A Lentiviral Vaccine Expressing Kmp11-Haspb Fusion Protein Increases Immune Response to Leishmania Major in Balb/C Publisher Pubmed



Mortazavidehkordi N1 ; Fallah A2, 3 ; Abdollahi A4 ; Kia V5 ; Khanahmad H6 ; Najafabadi ZG7 ; Hashemi N8 ; Estiri B9 ; Roudbari Z10 ; Najafi A11 ; Farjadfar A1 ; Hejazi SH12
Authors
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Authors Affiliations
  1. 1. Department of Medical Biotechnology, Fasa University of Medical Sciences, Fasa, Iran
  2. 2. Systems and Synthetic Biology Group, Mede Bioeconomy Company, Tehran, Iran
  3. 3. BioViva USA Inc, Bainbridge Island, WA, United States
  4. 4. Department of Medical Microbiology, Fasa University of Medical Sciences, Fars, Iran
  5. 5. Department of Medical Biotechnology and Nanotechnology, Faculty of Medicine, Zanjan University of Medical Sciences, Zanjan, Iran
  6. 6. Department of Genetics, Faculty of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
  7. 7. Department of Parasitology and Mycology, Isfahan University of Medical Sciences, Isfahan, Iran
  8. 8. Vector-borne Diseases Research Center, North Khorasan University of Medical Sciences, Bojnurd, Iran
  9. 9. Iranian Institute of Cell and Gene Therapy, Tehran, Iran
  10. 10. Department of Animal Science, Faculty of Agriculture, University of Jiroft, P.O. Box 364, Jiroft, Iran
  11. 11. Department of Immunology, Pasteur Institute of Iran, Tehran, Iran
  12. 12. Skin Diseases and Leishmaniasis Research Center, Department of Parasitology and Mycology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran

Source: Parasitology Research Published:2018


Abstract

Hydrophilic acylated surface protein B (HASPB) is an immunogenic Leishmania-specific protein that antibodies are produced against it in the sera of Leishmania-infected individuals. Kinetoplastid membrane protein 11 (KMP11) is another Leishmania antigen and considered as the suitable candidate for vaccine development Leishmaniasis. It is a highly conserved surface protein expressed in both promastigotes and amastigotes. In this study, KMP11 and HASPB coding sequences were cloned into a pCDH-cGFP lentiviral vector as a fusion protein to be used as a DNA vaccine against L. major. The KMP11-HASPB fusion protein was successfully expressed as evidenced by RT-PCR and Western blot assays. The effect of the vaccine was determined by evaluating the level of IFN-γ, IL-10, IgG1, and IgG2a performed using ELISA as well as determining the parasite load after challenge with L. major in vaccinated mice. The results revealed that IFN-γ, IL-10, IgG1, and IgG2a significantly increased after vaccination using KMP11-HASPB-expressing lentiviruses in BALB/c mice. It is noteworthy that the level of IFN-γ and IgG2a was higher than that of IL-10 and IgG1, respectively, which indicates the activation Th1 cells, macrophages, and cellular immunity. Moreover, the parasite load in the spleen and lymph node of vaccinated mice after challenge was significantly lower than that of controls. © 2018, Springer-Verlag GmbH Germany, part of Springer Nature.
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