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Allergen-specific B cell responses in oral immunotherapy-induced desensitization, remission, and natural outgrowth in cow's milk allergy.
Satitsuksanoa, Pattraporn; van de Veen, Willem; Tan, Ge; Lopez, Juan-Felipe; Wirz, Oliver; Jansen, Kirstin; Sokolowska, Milena; Mirer, David; Globinska, Anna; Boonpiyathad, Tadech; Schneider, Stephan R; Barletta, Elena; Spits, Hergen; Chang, Iris; Babayev, Huseyn; Tahrali, Ilhan; Deniz, Gunnur; Yücel, Esra Özek; Kiykim, Ayca; Boyd, Scott D; Akdis, Cezmi A; Nadeau, Kari; Akdis, Mübeccel.
Afiliação
  • Satitsuksanoa P; Swiss Institute of Allergy and Asthma Research (SIAF), University of Zürich, Davos, Switzerland.
  • van de Veen W; Swiss Institute of Allergy and Asthma Research (SIAF), University of Zürich, Davos, Switzerland.
  • Tan G; Swiss Institute of Allergy and Asthma Research (SIAF), University of Zürich, Davos, Switzerland.
  • Lopez JF; Functional Genomics Center Zürich, ETH Zürich, Zürich, Switzerland.
  • Wirz O; Swiss Institute of Allergy and Asthma Research (SIAF), University of Zürich, Davos, Switzerland.
  • Jansen K; Swiss Institute of Allergy and Asthma Research (SIAF), University of Zürich, Davos, Switzerland.
  • Sokolowska M; Department of Pathology, Stanford University, Stanford, California, USA.
  • Mirer D; Swiss Institute of Allergy and Asthma Research (SIAF), University of Zürich, Davos, Switzerland.
  • Globinska A; Swiss Institute of Allergy and Asthma Research (SIAF), University of Zürich, Davos, Switzerland.
  • Boonpiyathad T; Christine Kühne-Center for Allergy Research and Education (CK-CARE), Davos, Switzerland.
  • Schneider SR; Swiss Institute of Allergy and Asthma Research (SIAF), University of Zürich, Davos, Switzerland.
  • Barletta E; Swiss Institute of Allergy and Asthma Research (SIAF), University of Zürich, Davos, Switzerland.
  • Spits H; Swiss Institute of Allergy and Asthma Research (SIAF), University of Zürich, Davos, Switzerland.
  • Chang I; Swiss Institute of Allergy and Asthma Research (SIAF), University of Zürich, Davos, Switzerland.
  • Babayev H; Swiss Institute of Allergy and Asthma Research (SIAF), University of Zürich, Davos, Switzerland.
  • Tahrali I; Swiss Institute of Bioinformatics, Laussane, Switzerland.
  • Deniz G; Department of Experimental Immunology, Academic Medical Center of the University of Amsterdam, Amsterdam, the Netherlands.
  • Yücel EÖ; Sean N. Parker Center for Allergy and Asthma Research, Stanford, California, USA.
  • Kiykim A; Swiss Institute of Allergy and Asthma Research (SIAF), University of Zürich, Davos, Switzerland.
  • Boyd SD; Department of Immunology, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul, Turkey.
  • Akdis CA; Department of Immunology, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul, Turkey.
  • Nadeau K; Division of Pediatrics, Department of Pediatric Allergy and Immunology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.
  • Akdis M; Department of Pediatric Allergy and Immunology, Cerrahpasa Medical Faculty, Istanbul University-Cerrahpasa, Istanbul, Turkey.
Allergy ; 2024 Jul 11.
Article em En | MEDLINE | ID: mdl-38989779
ABSTRACT

BACKGROUND:

Antigen-specific memory B cells play a key role in the induction of desensitization and remission to food allergens in oral immunotherapy and in the development of natural tolerance (NT). Here, we characterized milk allergen Bos d 9-specific B cells in oral allergen-specific immunotherapy (OIT) and in children spontaneously outgrowing cow's milk allergy (CMA) due to NT.

METHODS:

Samples from children with CMA who received oral OIT (before, during, and after), children who naturally outgrew CMA (NT), and healthy individuals were received from Stanford biobank. Bos d 9-specific B cells were isolated by flow cytometry and RNA-sequencing was performed. Protein profile of Bos d 9-specific B cells was analyzed by proximity extension assay.

RESULTS:

Increased frequencies of circulating milk allergen Bos d 9-specific B cells were observed after OIT and NT. Milk-desensitized subjects showed the partial acquisition of phenotypic features of remission, suggesting that desensitization is an earlier stage of remission. Within these most significantly expressed genes, IL10RA and TGFB3 were highly expressed in desensitized OIT patients. In both the remission and desensitized groups, B cell activation-, Breg cells-, BCR-signaling-, and differentiation-related genes were upregulated. In NT, pathways associated with innate immunity characteristics, development of marginal zone B cells, and a more established suppressor function of B cells prevail that may play a role in long-term tolerance. The analyses of immunoglobulin heavy chain genes in specific B cells demonstrated that IgG2 in desensitization, IgG1, IgA1, IgA2, IgG4, and IgD in remission, and IgD in NT were predominating. Secreted proteins from allergen-specific B cells revealed higher levels of regulatory cytokines, IL-10, and TGF-ß after OIT and NT.

CONCLUSION:

Allergen-specific B cells are essential elements in regulating food allergy towards remission in OIT-received and naturally resolved individuals.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article