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Design and Evaluation of a Hypoallergenic Peptide-Based Vaccine for Salsola Kali Allergy Publisher Pubmed



Tabesh S1, 2 ; Fanuel S3, 4 ; Fazlollahi MR2 ; Yekaninejad MS5 ; Kardar GA2, 3 ; Razavi SA1
Authors
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Authors Affiliations
  1. 1. Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Iran
  2. 2. Immunology Asthma & Allergy Research Institute, Tehran University of Medical Sciences, Iran
  3. 3. Department of Medical Biotechnology, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Iran
  4. 4. Department of Applied Biosciences and Biotechnology, Faculty of Science and Technology, Midlands State University (MSU), Zimbabwe
  5. 5. Department of epidemiology and biostatics, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran

Source: International Immunopharmacology Published:2019


Abstract

Background: The Salsola kali (S. kali) pollen is one of the most important causes of allergic rhinitis in the deserts and semi-desert areas. Immunotherapy with allergen extracts remains the only available treatment addressing the underlying mechanism of allergy. However, given the low efficacy of this method, it is necessary to find more effective and alternative therapeutic interventions using molecular biology and bioinformatics tools. In this study, a hypoallergenic vaccine was designed on the basis of B-cell epitope approach for S. kali immunotherapy. Methods: Using the Immune Epitope Database (IEDB), a 35-mer peptide was selected and chemically conjugated to a keyhole limpet hemocyanin (KLH) molecule. Specific IgG and IgE from immunized BALB/c mice sera against the vaccine (Sal k 1-KLH), S. kali extract and the recombinant protein, rSal k 1, were measured using ELISA. Also, inhibition of IgE by mouse IgG was evaluated using an inhibitory ELISA. Finally, the IgE reactivity and T-cell reactivity of the designed vaccine were evaluated by dot blot assay and MTT assay. Results: Vaccination with the vaccine produced high levels of protective IgG in mice, which inhibited the binding of patients IgE to recombinant proteins. The result showed that the designed vaccine, unlike the recombinant protein and extract, did not induce T-cell lymphocytes response and also exhibited decreased IgE reactivity. Conclusion: The designed vaccine can be considered as a promising candidate for therapeutic allergen-specific immunotherapy. © 2018 Elsevier B.V.