Bulk T‐cell receptor sequencing confirms clonality in pediatric eosinophilic esophagitis and identifies a food‐specific repertoire

Author:

Janarthanam Rethavathi1ORCID,Kuang Fei Li2ORCID,Zalewski Angelika3ORCID,Amsden Katie1,Wang Ming‐Yu1,Ostilla Lorena1,Keeley Kaitlyn1,Hirano Ikuo3ORCID,Kagalwalla Amir4ORCID,Wershil Barry K.1,Gonsalves Nirmala3ORCID,Wechsler Joshua B.12ORCID

Affiliation:

1. Division of Gastroenterology, Hepatology & Nutrition, Ann & Robert H. Lurie Children's Hospital of Chicago Northwestern University Feinberg school of Medicine Chicago Illinois USA

2. Division of Allergy‐Immunology Northwestern University Feinberg School of Medicine Chicago Illinois USA

3. Division of Gastroenterology and Hepatology, Department of Medicine Northwestern University Feinberg School of Medicine Chicago Illinois USA

4. Department of Pediatrics John H. Stroger Cook County Hospital of Chicago Chicago Illinois USA

Abstract

AbstractBackgroundEosinophilic esophagitis (EoE) involves a chronic immune‐mediated response to dietary antigens. Recent work identifies T‐cell clonality in children with EoE, however, it is unknown whether this is true in adults or whether there is a restricted food‐specific T‐cell repertoire. We sought to confirm T‐cell receptor (TCR) clonality in EoE and assess for differences with specific food triggers.MethodsBulk TCR sequencing was performed on mRNA isolated from esophageal biopsies obtained from adults and children with EoE (n = 15) who had food triggers confirmed by endoscopic evaluation. Non‐EoE adult and pediatric controls (n = 10) were included. Differences in TCR clonality by disease and treatment status were assessed. Shared and similar V‐J‐CDR3s were assessed based on specific food triggers.ResultsActive EoE biopsies from children but not adults displayed decreased unique TCRα/β clonotypes and increased relative abundance of TCRs comprising >1% of the total compared to non‐EoE controls and paired inactive EoE samples. Among patients in which baseline, post diet elimination, and food trigger reintroduction samples (n = 6) were obtained, we observed ~1% of TCRs were shared only between pre‐diet elimination and trigger reintroduction. Patients with a shared EoE trigger (milk) had a greater degree of shared and similar TCRs compared to patients with differing triggers (seafood, wheat, egg, soy).ConclusionWe confirmed relative clonality in children but not adults with active EoE and identified potential food‐specific TCRs, particularly for milk‐triggered EoE. Further studies are needed to better identify the broad TCR repertoire relevant to food triggers.

Funder

Campaign Urging Research for Eosinophilic Disease

Publisher

Wiley

Subject

Immunology,Immunology and Allergy

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