Bulk T-Cell receptor sequencing confirms clonality in pediatric EoE and identifies a food-specific repertoire

被引:3
|
作者
Janarthanam, Rethavathi [1 ]
Kuang, Fei Li [2 ]
Zalewski, Angelika [3 ]
Amsden, Katie [1 ]
Wang, Ming-Yu [1 ]
Ostilla, Lorena [1 ]
Keeley, Kaitlyn [1 ]
Hirano, Ikuo [3 ]
Kagalwalla, Amir [4 ]
Wershil, Barry K. [1 ]
Gonsalves, Nirmala [3 ]
Wechsler, Joshua B. [1 ,2 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, Ann & Robert H Lurie Childrens Hosp Chicago, Div Gastroenterol Hepatol & Nutr, Chicago, IL 60611 USA
[2] Northwestern Univ, Feinberg Sch Med, Div Allergy Immunol, Chicago, IL USA
[3] Northwestern Univ, Feinberg Sch Med, Dept Med, Div Gastroenterol & Hepatol, Chicago, IL USA
[4] John H Stroger Cook Cty Hosp Chicago, Dept Pediat, Chicago, IL USA
关键词
biomarker; diet elimination; EoE; food trigger; TCR; EOSINOPHILIC ESOPHAGITIS; ELIMINATION DIET; CHILDREN; IMMUNITY;
D O I
10.1111/all.15773
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
BackgroundEosinophilic 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 TCR alpha/beta 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 similar to 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.
引用
收藏
页码:2487 / 2496
页数:10
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