Immunological mechanisms involved in the human response to a dog dander allergoid.


Journal

Molecular immunology
ISSN: 1872-9142
Titre abrégé: Mol Immunol
Pays: England
ID NLM: 7905289

Informations de publication

Date de publication:
05 2022
Historique:
received: 30 09 2021
revised: 16 02 2022
accepted: 26 02 2022
pubmed: 21 3 2022
medline: 15 4 2022
entrez: 20 3 2022
Statut: ppublish

Résumé

Dog allergens are a common cause of allergic sensitisation and trigger respiratory symptoms worldwide. However, clinical evidence regarding dog immunotherapy is limited. Therefore, the aim of this study was to analyse the immunomodulatory properties of a new allergoid from dog dander, thereby deepening the understanding of the molecular mechanisms involved in the reestablishment of the tolerogenic response. Three independent batches of dog dander native and allergoid allergen extracts were manufactured and characterised. Allergenic profiles were analysed by the identification of all dog allergens and quantification of the major allergens Can f 1 and Can f 5. The allergenicity profile of the allergoid was studied using biological potency and basophil activation tests. In vitro immunomodulatory parameters was evaluated as the capacity of the allergoid to induce IgG antibodies that block IgE binding to the allergen and cytokine promotion (IFN-γ, IL-4, IL-6, IL-10, IL-13, and TNF-α) in PBMCs from allergic donors. The presence of all dog allergens, including Can f 1 and Can f 5, was confirmed in both types of extracts. The new allergoid showed a low IgE binding capacity, which significantly affected the activation of effector cells, such as basophils. The IgG antibodies induced by the allergoid in rabbits blocked human IgE binding epitopes on the dog native extract and induced Th1 and Treg responses by increasing IFN-γ and IL-10 levels in PBMCs from allergic donors. This new dog dander allergoid containing Can f 1 and Can f 5 showed a low capacity to bind IgE and to activate basophils in dog allergic patients. Furthermore, it showed potent activation of Th1 mediators and induction of tolerance through Treg activation. This allergoid could offer a safer profile than the native extract and could be an effective immunotherapy treatment for dog allergic patients.

Sections du résumé

BACKGROUND
Dog allergens are a common cause of allergic sensitisation and trigger respiratory symptoms worldwide. However, clinical evidence regarding dog immunotherapy is limited. Therefore, the aim of this study was to analyse the immunomodulatory properties of a new allergoid from dog dander, thereby deepening the understanding of the molecular mechanisms involved in the reestablishment of the tolerogenic response.
METHODS
Three independent batches of dog dander native and allergoid allergen extracts were manufactured and characterised. Allergenic profiles were analysed by the identification of all dog allergens and quantification of the major allergens Can f 1 and Can f 5. The allergenicity profile of the allergoid was studied using biological potency and basophil activation tests. In vitro immunomodulatory parameters was evaluated as the capacity of the allergoid to induce IgG antibodies that block IgE binding to the allergen and cytokine promotion (IFN-γ, IL-4, IL-6, IL-10, IL-13, and TNF-α) in PBMCs from allergic donors.
RESULTS
The presence of all dog allergens, including Can f 1 and Can f 5, was confirmed in both types of extracts. The new allergoid showed a low IgE binding capacity, which significantly affected the activation of effector cells, such as basophils. The IgG antibodies induced by the allergoid in rabbits blocked human IgE binding epitopes on the dog native extract and induced Th1 and Treg responses by increasing IFN-γ and IL-10 levels in PBMCs from allergic donors.
CONCLUSION
This new dog dander allergoid containing Can f 1 and Can f 5 showed a low capacity to bind IgE and to activate basophils in dog allergic patients. Furthermore, it showed potent activation of Th1 mediators and induction of tolerance through Treg activation. This allergoid could offer a safer profile than the native extract and could be an effective immunotherapy treatment for dog allergic patients.

Identifiants

pubmed: 35306358
pii: S0161-5890(22)00049-9
doi: 10.1016/j.molimm.2022.02.020
pii:
doi:

Substances chimiques

Allergens 0
Allergoids 0
Immunoglobulin G 0
Plant Extracts 0
Interleukin-10 130068-27-8
Immunoglobulin E 37341-29-0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

88-96

Informations de copyright

Copyright © 2022 Elsevier Ltd. All rights reserved.

Auteurs

D Calzada (D)

R&D Allergy & Immunology Unit, LETI Pharma, Madrid, Spain.

T Aranda (T)

R&D Allergy & Immunology Unit, LETI Pharma, Madrid, Spain.

G M Gallego (G)

R&D Allergy & Immunology Unit, LETI Pharma, Madrid, Spain.

M R Escutia (MR)

R&D Allergy & Immunology Unit, LETI Pharma, Madrid, Spain.

D Balsa (D)

R&D Allergy & Immunology Unit, LETI Pharma, Madrid, Spain.

J Álvarez (J)

R&D Allergy & Immunology Unit, LETI Pharma, Madrid, Spain.

C Mayorga (C)

Allergy Research Group, Instituto de Investigación Biomédica de Málaga-IBIMA, Málaga, Spain; Allergy Clinical Unit, Hospital Regional Universitario de Málaga, Málaga, Spain.

M Salas (M)

Allergy Research Group, Instituto de Investigación Biomédica de Málaga-IBIMA, Málaga, Spain.

M A Odena (MA)

Proteomic Platform Core Facility, Parc Científic de Barcelona, Barcelona, Spain.

E Oliveira (E)

Proteomic Platform Core Facility, Parc Científic de Barcelona, Barcelona, Spain.

M Pascal (M)

Immunology Department, CDB, Hospital Clínic de Barcelona, Barcelona, Spain; Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Spain; Spanish Network for Allergy - RETIC de Asma, Reacciones adversas y Alérgicas (ARADYAL), Madrid, Spain.

J Carnés (J)

R&D Allergy & Immunology Unit, LETI Pharma, Madrid, Spain. Electronic address: jcarnes@leti.com.

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Classifications MeSH