Design and evaluation of a hypoallergenic peptide-based vaccine for Salsola kali allergy

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...

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Main Authors: Tabesh, Saeideh, Fanuel, Songwe, Fazlollahi, Mohammad Reza, Yekaninejad, Mir Saeed, Kardar, Gholam Ali, Razavi, Seyed Alireza
Format: Article
Language:English
Published: Elsevier 2022
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Online Access:https://doi.org/10.1016/j.intimp.2018.10.037
http://hdl.handle.net/11408/5179
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author Tabesh, Saeideh
Fanuel, Songwe
Fazlollahi, Mohammad Reza
Yekaninejad, Mir Saeed
Kardar, Gholam Ali
Razavi, Seyed Alireza
author_facet Tabesh, Saeideh
Fanuel, Songwe
Fazlollahi, Mohammad Reza
Yekaninejad, Mir Saeed
Kardar, Gholam Ali
Razavi, Seyed Alireza
author_sort Tabesh, Saeideh
collection DSpace
description 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.
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spelling ir-11408-51792022-09-30T10:06:04Z Design and evaluation of a hypoallergenic peptide-based vaccine for Salsola kali allergy Tabesh, Saeideh Fanuel, Songwe Fazlollahi, Mohammad Reza Yekaninejad, Mir Saeed Kardar, Gholam Ali Razavi, Seyed Alireza Allergen Allergen-specific immunotherapy B-epitope Russian thistle Sal k 1 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. 2022-09-30T10:06:04Z 2022-09-30T10:06:04Z 2018-11-13 Article 1567-5769 1878-1705 https://doi.org/10.1016/j.intimp.2018.10.037 http://hdl.handle.net/11408/5179 en International Immunopharmacology;Vol. 66, Pages 62-68 open Elsevier
spellingShingle Allergen
Allergen-specific immunotherapy
B-epitope
Russian thistle
Sal k 1
Tabesh, Saeideh
Fanuel, Songwe
Fazlollahi, Mohammad Reza
Yekaninejad, Mir Saeed
Kardar, Gholam Ali
Razavi, Seyed Alireza
Design and evaluation of a hypoallergenic peptide-based vaccine for Salsola kali allergy
title Design and evaluation of a hypoallergenic peptide-based vaccine for Salsola kali allergy
title_full Design and evaluation of a hypoallergenic peptide-based vaccine for Salsola kali allergy
title_fullStr Design and evaluation of a hypoallergenic peptide-based vaccine for Salsola kali allergy
title_full_unstemmed Design and evaluation of a hypoallergenic peptide-based vaccine for Salsola kali allergy
title_short Design and evaluation of a hypoallergenic peptide-based vaccine for Salsola kali allergy
title_sort design and evaluation of a hypoallergenic peptide-based vaccine for salsola kali allergy
topic Allergen
Allergen-specific immunotherapy
B-epitope
Russian thistle
Sal k 1
url https://doi.org/10.1016/j.intimp.2018.10.037
http://hdl.handle.net/11408/5179
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