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Interleukin 31 in insect bite hypersensitivity—Alleviating clinical symptoms by active vaccination against itch

BACKGROUND: Insect bite hypersensitivity (IBH) is the most common seasonal pruritic allergic dermatitis of horses occurring upon insect bites. In recent years, a major role for IL‐31 in allergic pruritus of humans, monkeys, dogs, and mice was acknowledged. Here, we investigate the role of IL‐31 in I...

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Autores principales: Olomski, Florian, Fettelschoss, Victoria, Jonsdottir, Sigridur, Birkmann, Katharina, Thoms, Franziska, Marti, Eliane, Bachmann, Martin F., Kündig, Thomas M., Fettelschoss‐Gabriel, Antonia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7217000/
https://www.ncbi.nlm.nih.gov/pubmed/31816097
http://dx.doi.org/10.1111/all.14145
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author Olomski, Florian
Fettelschoss, Victoria
Jonsdottir, Sigridur
Birkmann, Katharina
Thoms, Franziska
Marti, Eliane
Bachmann, Martin F.
Kündig, Thomas M.
Fettelschoss‐Gabriel, Antonia
author_facet Olomski, Florian
Fettelschoss, Victoria
Jonsdottir, Sigridur
Birkmann, Katharina
Thoms, Franziska
Marti, Eliane
Bachmann, Martin F.
Kündig, Thomas M.
Fettelschoss‐Gabriel, Antonia
author_sort Olomski, Florian
collection PubMed
description BACKGROUND: Insect bite hypersensitivity (IBH) is the most common seasonal pruritic allergic dermatitis of horses occurring upon insect bites. In recent years, a major role for IL‐31 in allergic pruritus of humans, monkeys, dogs, and mice was acknowledged. Here, we investigate the role of IL‐31 in IBH of horses and developed a therapeutic vaccine against equine IL‐31 (eIL‐31). METHODS: IL‐31 levels were quantified in allergen‐stimulated peripheral blood mononuclear cells (PBMCs) and skin punch biopsies of IBH lesions and healthy skin from IBH‐affected and healthy horses. The vaccine consisted of eIL‐31 covalently coupled to a virus‐like particle (VLP) derived from cucumber mosaic virus containing a tetanus toxoid universal T‐cell epitope (CuMVTT). Eighteen IBH‐affected horses were recruited and immunized with 300 μg of eIL‐31‐CuMVTT vaccine or placebo and IBH severity score was recorded. RESULTS: IL‐31 was increased in PBMCs and exclusively detectable in skin lesions of IBH‐affected horses. Vaccination against eIL‐31 reduced delta clinical scores when compared to previous untreated IBH season of the same horses and to placebo‐treated horses in the same year. The vaccine was well tolerated without safety concerns throughout the study. CONCLUSION: TH2‐derived IL‐31 is involved in IBH pathology and accordingly the immunotherapeutic vaccination approach targeting IL‐31 alleviated clinical scores in affected horses.
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spelling pubmed-72170002020-05-13 Interleukin 31 in insect bite hypersensitivity—Alleviating clinical symptoms by active vaccination against itch Olomski, Florian Fettelschoss, Victoria Jonsdottir, Sigridur Birkmann, Katharina Thoms, Franziska Marti, Eliane Bachmann, Martin F. Kündig, Thomas M. Fettelschoss‐Gabriel, Antonia Allergy ORIGINAL ARTICLES BACKGROUND: Insect bite hypersensitivity (IBH) is the most common seasonal pruritic allergic dermatitis of horses occurring upon insect bites. In recent years, a major role for IL‐31 in allergic pruritus of humans, monkeys, dogs, and mice was acknowledged. Here, we investigate the role of IL‐31 in IBH of horses and developed a therapeutic vaccine against equine IL‐31 (eIL‐31). METHODS: IL‐31 levels were quantified in allergen‐stimulated peripheral blood mononuclear cells (PBMCs) and skin punch biopsies of IBH lesions and healthy skin from IBH‐affected and healthy horses. The vaccine consisted of eIL‐31 covalently coupled to a virus‐like particle (VLP) derived from cucumber mosaic virus containing a tetanus toxoid universal T‐cell epitope (CuMVTT). Eighteen IBH‐affected horses were recruited and immunized with 300 μg of eIL‐31‐CuMVTT vaccine or placebo and IBH severity score was recorded. RESULTS: IL‐31 was increased in PBMCs and exclusively detectable in skin lesions of IBH‐affected horses. Vaccination against eIL‐31 reduced delta clinical scores when compared to previous untreated IBH season of the same horses and to placebo‐treated horses in the same year. The vaccine was well tolerated without safety concerns throughout the study. CONCLUSION: TH2‐derived IL‐31 is involved in IBH pathology and accordingly the immunotherapeutic vaccination approach targeting IL‐31 alleviated clinical scores in affected horses. John Wiley and Sons Inc. 2020-02-06 2020-04 /pmc/articles/PMC7217000/ /pubmed/31816097 http://dx.doi.org/10.1111/all.14145 Text en © 2019 EAACI and John Wiley and Sons A/S. Published by John Wiley and Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle ORIGINAL ARTICLES
Olomski, Florian
Fettelschoss, Victoria
Jonsdottir, Sigridur
Birkmann, Katharina
Thoms, Franziska
Marti, Eliane
Bachmann, Martin F.
Kündig, Thomas M.
Fettelschoss‐Gabriel, Antonia
Interleukin 31 in insect bite hypersensitivity—Alleviating clinical symptoms by active vaccination against itch
title Interleukin 31 in insect bite hypersensitivity—Alleviating clinical symptoms by active vaccination against itch
title_full Interleukin 31 in insect bite hypersensitivity—Alleviating clinical symptoms by active vaccination against itch
title_fullStr Interleukin 31 in insect bite hypersensitivity—Alleviating clinical symptoms by active vaccination against itch
title_full_unstemmed Interleukin 31 in insect bite hypersensitivity—Alleviating clinical symptoms by active vaccination against itch
title_short Interleukin 31 in insect bite hypersensitivity—Alleviating clinical symptoms by active vaccination against itch
title_sort interleukin 31 in insect bite hypersensitivity—alleviating clinical symptoms by active vaccination against itch
topic ORIGINAL ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7217000/
https://www.ncbi.nlm.nih.gov/pubmed/31816097
http://dx.doi.org/10.1111/all.14145
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