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A Novel Allergen-Specific Immune Signature-Directed Approach to Dietary Elimination in Eosinophilic Esophagitis

OBJECTIVES: Dietary elimination for treatment of eosinophilic esophagitis (EoE) is limited by lack of accuracy in current allergy tests. We aimed to develop an immunologic approach to identify dietary triggers and prospectively test allergen-specific immune signature-guided dietary elimination thera...

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Autores principales: Dellon, Evan S., Guo, Rishu, McGee, Sarah J., Hamilton, Deanna K., Nicolai, Emily, Covington, Jacquelyn, Moist, Susan E., Arrington, Ashley, Wright, Benjamin L., Burks, A. Wesley, Vickery, Brian P., Kulis, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6970559/
https://www.ncbi.nlm.nih.gov/pubmed/31789931
http://dx.doi.org/10.14309/ctg.0000000000000099
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author Dellon, Evan S.
Guo, Rishu
McGee, Sarah J.
Hamilton, Deanna K.
Nicolai, Emily
Covington, Jacquelyn
Moist, Susan E.
Arrington, Ashley
Wright, Benjamin L.
Burks, A. Wesley
Vickery, Brian P.
Kulis, Michael
author_facet Dellon, Evan S.
Guo, Rishu
McGee, Sarah J.
Hamilton, Deanna K.
Nicolai, Emily
Covington, Jacquelyn
Moist, Susan E.
Arrington, Ashley
Wright, Benjamin L.
Burks, A. Wesley
Vickery, Brian P.
Kulis, Michael
author_sort Dellon, Evan S.
collection PubMed
description OBJECTIVES: Dietary elimination for treatment of eosinophilic esophagitis (EoE) is limited by lack of accuracy in current allergy tests. We aimed to develop an immunologic approach to identify dietary triggers and prospectively test allergen-specific immune signature-guided dietary elimination therapy. METHODS: In the first phase, we developed and assessed 2 methods for determining selected food triggers using samples from 24 adults with EoE: a CD4+ T-cell proliferation assay in peripheral blood and food-specific tissue IgG4 levels in esophageal biopsies. In the second phase, we clinically tested elimination diets created from these methods in a prospective cohort treated for 6 weeks (NCT02722148). Outcomes included peak eosinophil counts (eos/hpf), endoscopic findings (measured by the EoE Endoscopic Reference Score), and symptoms (measured by the EoE Symptom Activity Index). RESULTS: Parameters were optimized with a positive test on either assay, yielding agreements of 60%, 75%, 53%, 58%, and 53% between predicted and known triggers of peanut, egg, soy, wheat, and milk, respectively. In clinical testing, the mean number of foods eliminated based on the assays was 3.4, and 19 of 22 subjects were compliant with treatment. After treatment, median peak eosinophil counts decreased from 75 to 35 (P = 0.007); there were 4 histologic responders (21%). The EoE Endoscopic Reference Score and EoE Symptom Activity Index score also decreased after treatment (4.6 vs 3.0; P = 0.002; and 32.5 vs 25.0; P = 0.06, respectively). DISCUSSION: We successfully developed a new testing approach using CD4(+) T-cell proliferation and esophageal food-specific IgG4 levels, with promising accuracy rates. In clinical testing, this led to improvement in eosinophil counts, endoscopic severity, and symptoms of dysphagia, but a smaller than expected number of patients achieved histologic remission.
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spelling pubmed-69705592020-02-10 A Novel Allergen-Specific Immune Signature-Directed Approach to Dietary Elimination in Eosinophilic Esophagitis Dellon, Evan S. Guo, Rishu McGee, Sarah J. Hamilton, Deanna K. Nicolai, Emily Covington, Jacquelyn Moist, Susan E. Arrington, Ashley Wright, Benjamin L. Burks, A. Wesley Vickery, Brian P. Kulis, Michael Clin Transl Gastroenterol Article OBJECTIVES: Dietary elimination for treatment of eosinophilic esophagitis (EoE) is limited by lack of accuracy in current allergy tests. We aimed to develop an immunologic approach to identify dietary triggers and prospectively test allergen-specific immune signature-guided dietary elimination therapy. METHODS: In the first phase, we developed and assessed 2 methods for determining selected food triggers using samples from 24 adults with EoE: a CD4+ T-cell proliferation assay in peripheral blood and food-specific tissue IgG4 levels in esophageal biopsies. In the second phase, we clinically tested elimination diets created from these methods in a prospective cohort treated for 6 weeks (NCT02722148). Outcomes included peak eosinophil counts (eos/hpf), endoscopic findings (measured by the EoE Endoscopic Reference Score), and symptoms (measured by the EoE Symptom Activity Index). RESULTS: Parameters were optimized with a positive test on either assay, yielding agreements of 60%, 75%, 53%, 58%, and 53% between predicted and known triggers of peanut, egg, soy, wheat, and milk, respectively. In clinical testing, the mean number of foods eliminated based on the assays was 3.4, and 19 of 22 subjects were compliant with treatment. After treatment, median peak eosinophil counts decreased from 75 to 35 (P = 0.007); there were 4 histologic responders (21%). The EoE Endoscopic Reference Score and EoE Symptom Activity Index score also decreased after treatment (4.6 vs 3.0; P = 0.002; and 32.5 vs 25.0; P = 0.06, respectively). DISCUSSION: We successfully developed a new testing approach using CD4(+) T-cell proliferation and esophageal food-specific IgG4 levels, with promising accuracy rates. In clinical testing, this led to improvement in eosinophil counts, endoscopic severity, and symptoms of dysphagia, but a smaller than expected number of patients achieved histologic remission. Wolters Kluwer 2019-11-25 /pmc/articles/PMC6970559/ /pubmed/31789931 http://dx.doi.org/10.14309/ctg.0000000000000099 Text en © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of The American College of Gastroenterology This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Article
Dellon, Evan S.
Guo, Rishu
McGee, Sarah J.
Hamilton, Deanna K.
Nicolai, Emily
Covington, Jacquelyn
Moist, Susan E.
Arrington, Ashley
Wright, Benjamin L.
Burks, A. Wesley
Vickery, Brian P.
Kulis, Michael
A Novel Allergen-Specific Immune Signature-Directed Approach to Dietary Elimination in Eosinophilic Esophagitis
title A Novel Allergen-Specific Immune Signature-Directed Approach to Dietary Elimination in Eosinophilic Esophagitis
title_full A Novel Allergen-Specific Immune Signature-Directed Approach to Dietary Elimination in Eosinophilic Esophagitis
title_fullStr A Novel Allergen-Specific Immune Signature-Directed Approach to Dietary Elimination in Eosinophilic Esophagitis
title_full_unstemmed A Novel Allergen-Specific Immune Signature-Directed Approach to Dietary Elimination in Eosinophilic Esophagitis
title_short A Novel Allergen-Specific Immune Signature-Directed Approach to Dietary Elimination in Eosinophilic Esophagitis
title_sort novel allergen-specific immune signature-directed approach to dietary elimination in eosinophilic esophagitis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6970559/
https://www.ncbi.nlm.nih.gov/pubmed/31789931
http://dx.doi.org/10.14309/ctg.0000000000000099
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