Variants of thymic stromal lymphopoietin and its receptor associate with eosinophilic esophagitis

J Allergy Clin Immunol. 2010 Jul;126(1):160-5.e3. doi: 10.1016/j.jaci.2010.04.037.


Background: The genetic cause of eosinophilic esophagitis (EE) has been largely unexplored until a recent genome-wide association study identified a disease susceptibility locus on 5q22, a region that harbors the thymic stromal lymphopoietin (TSLP) gene. However, it is unclear whether the observed genetic associations with EE are disease-specific or confounded by the high rate of allergy in patients with EE. In addition, the genetic contributions of other allergy-associated genes to EE risk have not been explored.

Objective: We aimed to delineate single nucleotide polymorphisms (SNPs) that associated with EE apart from allergy.

Methods: We used a custom array containing 738 SNPs in 53 genes implicated in allergic responses, immune responses, or both to genotype 220 allergic or 246 nonallergic control subjects and a discovery cohort of 170 patients with EE. We replicated a statistically significant SNP association in an independent case-control cohort and examined the induction of the candidate gene in primary esophageal epithelial cells.

Results: A single SNP residing in the TSLP gene reached Bonferroni linkage disequilibrium-adjusted significance but only when patients with EE were compared with allergic control subjects (rs10062929; P = 4.11 x 10(-5); odds ratio, 0.35). A nonsynonymous polymorphism in the thymic stromal lymphopoietin receptor (TSLPR) gene on Xp22.3 and Yp11.3 was significantly associated with disease only in male patients with EE. Primary esophageal epithelial cells expressed TSLP mRNA after Toll-like receptor 3 stimulation.

Conclusion: These data collectively identify TSLP as a candidate gene critically involved in EE susceptibility beyond its role in promoting T(H)2 responses.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adolescent
  • Child
  • Child, Preschool
  • Cytokines / genetics*
  • Cytokines / physiology
  • Eosinophilia / etiology
  • Eosinophilia / genetics*
  • Esophagitis / etiology
  • Esophagitis / genetics*
  • Female
  • Humans
  • Infant
  • Male
  • Polymorphism, Single Nucleotide*
  • Receptors, Cytokine / genetics
  • Thymic Stromal Lymphopoietin


  • CRLF2 protein, human
  • Cytokines
  • Receptors, Cytokine
  • Thymic Stromal Lymphopoietin