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Article ; Online: Comprehensive mapping of immune tolerance yields a regulatory TNF receptor 2 signature in a murine model of successful Fel d 1-specific immunotherapy using high-dose CpG adjuvant.

Leonard, Cathy / Montamat, Guillem / Davril, Caroline / Domingues, Olivia / Hunewald, Oliver / Revets, Dominique / Guerin, Coralie / Blank, Simon / Heckendorn, Justine / Jardon, Gauthier / Hentges, François / Ollert, Markus

Allergy

2021  Volume 76, Issue 7, Page(s) 2153–2165

Abstract: Background: The prevalence of allergy to cat is expanding worldwide. Allergen-specific immunotherapy (AIT) has advantages over symptomatic pharmacotherapy and promises long-lasting disease control in allergic patients. However, there is still a need to ... ...

Abstract Background: The prevalence of allergy to cat is expanding worldwide. Allergen-specific immunotherapy (AIT) has advantages over symptomatic pharmacotherapy and promises long-lasting disease control in allergic patients. However, there is still a need to improve cat AIT regarding efficacy, safety, and adherence to the treatment. Here, we aim to boost immune tolerance to the major cat allergen Fel d 1 by increasing the anti-inflammatory activity of AIT with the established immunomodulatory adjuvant CpG, but at a higher dose than previously used in AIT.
Methods: Together with CpG, we used endotoxin-free Fel d 1 as therapeutic allergen throughout the study in a BALB/c model of allergy to Fel d 1, thus mimicking the conditions of human AIT trials. Multidimensional immune phenotyping including mass cytometry (CyTOF) was applied to analyze AIT-specific immune signatures.
Results: We show that AIT with high-dose CpG in combination with endotoxin-free Fel d 1 reverts all major hallmarks of allergy. High-dimensional CyTOF analysis of the immune cell signatures initiating and sustaining the AIT effect indicates the simultaneous engagement of both, the pDC-Treg and B-cell axis, with the emergence of a systemic GATA3
Conclusion: Our results highlight the potential of CpG adjuvant in a novel formulation to be further exploited for inducing allergen-specific tolerance in patients with cat allergy or other allergic diseases.
MeSH term(s) Allergens ; Animals ; Cats ; Desensitization, Immunologic ; Disease Models, Animal ; Glycoproteins/immunology ; Humans ; Hypersensitivity/therapy ; Immune Tolerance ; Mice ; Receptors, Tumor Necrosis Factor, Type II
Chemical Substances Allergens ; Glycoproteins ; Receptors, Tumor Necrosis Factor, Type II ; Fel d 1 protein, Felis domesticus (G408EE88II)
Language English
Publishing date 2021-01-05
Publishing country Denmark
Document type Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID 391933-x
ISSN 1398-9995 ; 0105-4538
ISSN (online) 1398-9995
ISSN 0105-4538
DOI 10.1111/all.14716
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