Cargando…

Peripheral blood basophils are the main source for early interleukin-4 secretion upon in vitro stimulation with Culicoides allergen in allergic horses

Interleukin-4 (IL-4) is a key cytokine secreted by type 2 T helper (Th2) cells that orchestrates immune responses during allergic reactions. Human and mouse studies additionally suggest that basophils have a unique role in the regulation of allergic diseases by providing initial IL-4 to drive T cell...

Descripción completa

Detalles Bibliográficos
Autores principales: Raza, Fahad, Babasyan, Susanna, Larson, Elisabeth M., Freer, Heather S., Schnabel, Christiane L., Wagner, Bettina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153460/
https://www.ncbi.nlm.nih.gov/pubmed/34038479
http://dx.doi.org/10.1371/journal.pone.0252243
_version_ 1783698803480592384
author Raza, Fahad
Babasyan, Susanna
Larson, Elisabeth M.
Freer, Heather S.
Schnabel, Christiane L.
Wagner, Bettina
author_facet Raza, Fahad
Babasyan, Susanna
Larson, Elisabeth M.
Freer, Heather S.
Schnabel, Christiane L.
Wagner, Bettina
author_sort Raza, Fahad
collection PubMed
description Interleukin-4 (IL-4) is a key cytokine secreted by type 2 T helper (Th2) cells that orchestrates immune responses during allergic reactions. Human and mouse studies additionally suggest that basophils have a unique role in the regulation of allergic diseases by providing initial IL-4 to drive T cell development towards the Th2 phenotype. Equine Culicoides hypersensitivity (CH) is a seasonal immunoglobulin E (IgE)-mediated allergic dermatitis in horses in response to salivary allergens from Culicoides (Cul) midges. Here, we analyzed IL-4 production in peripheral blood mononuclear cells (PBMC) of CH affected (n = 8) and healthy horses (n = 8) living together in an environment with natural Cul exposure. During Cul exposure when allergic horses had clinical allergy, IL-4 secretion from PBMC after stimulation with Cul extract was similar between healthy and CH affected horses. In contrast, allergic horses had higher IL-4 secretion from PBMC than healthy horses during months without allergen exposure. In addition, allergic horses had increased percentages of IL-4(+) cells after Cul stimulation compared to healthy horses, while both groups had similar percentages of IL-4(+) cells following IgE crosslinking. The IL-4(+) cells were subsequently characterized using different cell surface markers as basophils, while very few allergen-specific CD4(+) cells were detected in PBMC after Cul extract stimulation. Similarly, IgE crosslinking by anti-IgE triggered basophils to produce IL-4 in all horses. PMA/ionomycin consistently induced high percentages of IL-4(+) Th2 cells in both groups confirming that T cells of all horses studied were capable of IL-4 production. In conclusion, peripheral blood basophils produced high amounts of IL-4 in allergic horses after stimulation with Cul allergens, and allergic horses also maintained higher basophil percentages throughout the year than healthy horses. These new findings suggest that peripheral blood basophils may play a yet underestimated role in innate IL-4 production upon allergen activation in horses with CH. Basophil-derived IL-4 might be a crucial early signal for immune induction, modulating of immune responses towards Th2 immunity and IgE production.
format Online
Article
Text
id pubmed-8153460
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-81534602021-06-09 Peripheral blood basophils are the main source for early interleukin-4 secretion upon in vitro stimulation with Culicoides allergen in allergic horses Raza, Fahad Babasyan, Susanna Larson, Elisabeth M. Freer, Heather S. Schnabel, Christiane L. Wagner, Bettina PLoS One Research Article Interleukin-4 (IL-4) is a key cytokine secreted by type 2 T helper (Th2) cells that orchestrates immune responses during allergic reactions. Human and mouse studies additionally suggest that basophils have a unique role in the regulation of allergic diseases by providing initial IL-4 to drive T cell development towards the Th2 phenotype. Equine Culicoides hypersensitivity (CH) is a seasonal immunoglobulin E (IgE)-mediated allergic dermatitis in horses in response to salivary allergens from Culicoides (Cul) midges. Here, we analyzed IL-4 production in peripheral blood mononuclear cells (PBMC) of CH affected (n = 8) and healthy horses (n = 8) living together in an environment with natural Cul exposure. During Cul exposure when allergic horses had clinical allergy, IL-4 secretion from PBMC after stimulation with Cul extract was similar between healthy and CH affected horses. In contrast, allergic horses had higher IL-4 secretion from PBMC than healthy horses during months without allergen exposure. In addition, allergic horses had increased percentages of IL-4(+) cells after Cul stimulation compared to healthy horses, while both groups had similar percentages of IL-4(+) cells following IgE crosslinking. The IL-4(+) cells were subsequently characterized using different cell surface markers as basophils, while very few allergen-specific CD4(+) cells were detected in PBMC after Cul extract stimulation. Similarly, IgE crosslinking by anti-IgE triggered basophils to produce IL-4 in all horses. PMA/ionomycin consistently induced high percentages of IL-4(+) Th2 cells in both groups confirming that T cells of all horses studied were capable of IL-4 production. In conclusion, peripheral blood basophils produced high amounts of IL-4 in allergic horses after stimulation with Cul allergens, and allergic horses also maintained higher basophil percentages throughout the year than healthy horses. These new findings suggest that peripheral blood basophils may play a yet underestimated role in innate IL-4 production upon allergen activation in horses with CH. Basophil-derived IL-4 might be a crucial early signal for immune induction, modulating of immune responses towards Th2 immunity and IgE production. Public Library of Science 2021-05-26 /pmc/articles/PMC8153460/ /pubmed/34038479 http://dx.doi.org/10.1371/journal.pone.0252243 Text en © 2021 Raza et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Raza, Fahad
Babasyan, Susanna
Larson, Elisabeth M.
Freer, Heather S.
Schnabel, Christiane L.
Wagner, Bettina
Peripheral blood basophils are the main source for early interleukin-4 secretion upon in vitro stimulation with Culicoides allergen in allergic horses
title Peripheral blood basophils are the main source for early interleukin-4 secretion upon in vitro stimulation with Culicoides allergen in allergic horses
title_full Peripheral blood basophils are the main source for early interleukin-4 secretion upon in vitro stimulation with Culicoides allergen in allergic horses
title_fullStr Peripheral blood basophils are the main source for early interleukin-4 secretion upon in vitro stimulation with Culicoides allergen in allergic horses
title_full_unstemmed Peripheral blood basophils are the main source for early interleukin-4 secretion upon in vitro stimulation with Culicoides allergen in allergic horses
title_short Peripheral blood basophils are the main source for early interleukin-4 secretion upon in vitro stimulation with Culicoides allergen in allergic horses
title_sort peripheral blood basophils are the main source for early interleukin-4 secretion upon in vitro stimulation with culicoides allergen in allergic horses
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153460/
https://www.ncbi.nlm.nih.gov/pubmed/34038479
http://dx.doi.org/10.1371/journal.pone.0252243
work_keys_str_mv AT razafahad peripheralbloodbasophilsarethemainsourceforearlyinterleukin4secretionuponinvitrostimulationwithculicoidesallergeninallergichorses
AT babasyansusanna peripheralbloodbasophilsarethemainsourceforearlyinterleukin4secretionuponinvitrostimulationwithculicoidesallergeninallergichorses
AT larsonelisabethm peripheralbloodbasophilsarethemainsourceforearlyinterleukin4secretionuponinvitrostimulationwithculicoidesallergeninallergichorses
AT freerheathers peripheralbloodbasophilsarethemainsourceforearlyinterleukin4secretionuponinvitrostimulationwithculicoidesallergeninallergichorses
AT schnabelchristianel peripheralbloodbasophilsarethemainsourceforearlyinterleukin4secretionuponinvitrostimulationwithculicoidesallergeninallergichorses
AT wagnerbettina peripheralbloodbasophilsarethemainsourceforearlyinterleukin4secretionuponinvitrostimulationwithculicoidesallergeninallergichorses