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Estudio de casos y controles2019Solo mecanismosSin ajuste declarado por estilo de vida

An integrated framework using high-dimensional mass cytometry and fluorescent flow cytometry identifies discrete B cell subsets in patients with red meat allergy

Cox KM, Commins SP, Capaldo BJ, Workman LJ, Platts-Mills TAE, Amir ED, Lannigan JA, Schuyler AJ, Erickson LD

Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 14 citas

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Cómo se estudió

Diseño
Estudio de casos y controles (indexado por PubMed)
Estudiado en
Personas
Resultado principal
Solo mecanismos
Consumo medido con
No se indica

Quién lo pagó

Financiación
Financiación independiente
Universidad u hospital
University of Virginia
Gobierno
National Institutes of Health
Gobierno
National Institute of Allergy and Infectious Diseases
Gobierno
NIAID NIH HHS
Subvenciones
National Institute of Allergy and Infectious Diseases (R56 AI113095); National Institute of Allergy and Infectious Diseases (R37 AI020565); National Institute of Allergy and Infectious Diseases (R21 AI124490); National Institute of Allergy and Infectious Diseases (R01AI-020565); National Institute of Allergy and Infectious Diseases (R01 AI135049); National Institutes of Health (R21 AI124490); National Institutes of Health (R01-AI20565)

Según 4 financiadores declarados.

Publicación

Publicado
2018-12-02 · Clin Exp Allergy · vol. 49 · número 5 · págs. 615–625
Editorial
Wiley
Citado
18 citas · más que el 73% de estudios similares · 1.0× el promedio de su campo
Referencias
54 trabajos
Acceso
Acceso abierto (copia en repositorio)
Áreas de investigación
Food Allergy and Anaphylaxis Research · T-cell and B-cell Immunology · Celiac Disease Research and Management
Palabras clave
Flow cytometry, ELISPOT, Immunoglobulin D, Immunoglobulin E, Immunology, Peripheral blood mononuclear cell, Food allergy, Cytometry, Allergy, B cell, Mass cytometry, Biology, Antibody, T cell, Phenotype, In vitro, Immune system, Genetics, Gene
MeSH
b-lymphocyte subsets, leukocytes, mononuclear, humans, food hypersensitivity, immunoglobulin e, lymphocyte count, flow cytometry, cluster analysis, case-control studies, immunophenotyping, adult, aged, middle aged, disease management, female, male, young adult, biomarkers, red meat

9 autores

  • Kelly M. Cox🇺🇸Carter Center; University of Virginia
  • Scott P. Commins🇺🇸University of North Carolina at Chapel Hill
  • Brian J. Capaldo🇺🇸University of Virginia
  • Lisa J. Workman🇺🇸University of Virginia
  • Thomas A.E. Platts‐Mills🇺🇸Carter Center; University of Virginia
  • El-ad David Amir
  • Josephine A. Lannigan🇺🇸University of Virginia
  • Alexander J. Schuyler🇺🇸University of Virginia
  • Loren D. Erickson🇺🇸 · autor de correspondenciaCarter Center; University of Virginia

Resumen

El texto original del estudio, en el idioma en que se publicó.

Background

B cells play a critical role in the development and maintenance of food allergy by producing allergen-specific IgE. Despite the importance of B cells in IgE-mediated food allergy, the identity of sIgE-producing human B cells and how IgE is regulated are poorly understood.

Objective

To identify the immunophenotypes of circulating B cells associated with the production of galactose-alpha-1,3-galactose-specific IgE production in patients with red meat allergy.

Methods

B cells in PBMC samples obtained from 19 adults with physician-diagnosed red meat allergy and 20 non-meat allergic healthy controls were assessed by mass cytometry along with a bioinformatics analysis pipeline to identify discrete B cell phenotypes that associated with serum sIgE. Fluorescent flow cytometry was then applied to sort purify discrete B cell subsets, and B cells were functionally evaluated on an individual cell level for the production of sIgE by ELISPOT.

Results

Discrete B cell phenotypes abundant in meat allergic subjects compared to non-meat allergic controls were found in peripheral blood that do not share typical characteristics of classical isotype-switched memory B cells that express high levels of CD27. These B cell subsets shared higher IgD and lower IgM expression levels coupled with CXCR4, CCR6 and CD25 expression. In vitro polyclonal stimulation of purified B cell subsets from meat allergic subjects demonstrated that these subsets were enriched for cells induced to secrete sIgE.

Conclusions and clinical relevance

Circulating B cells display increased abundance of discrete B cell subsets in meat allergic subjects. This observation, coupled with the capacity of individual B cell subsets to produce sIgE following activation, implicates these novel B cell phenotypes in promoting IgE in meat allergy.

Resumen vía Europe PMC. Los derechos de autor siguen siendo de los autores o la editorial.

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