TSLP, thymic stromal lymphopoietin, 85480

N. diseases: 220; N. variants: 9
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
0.500 Biomarker disease BEFREE Finally, several promising therapeutic agents (e.g., sialic acid-binding immunoglobulin-like lectin 8 antibodies, the transforming growth factor-β1 signal blocker losartan, CC chemokine receptor type 3 antagonists, thymic stromal lymphopoietin antibodies, antibodies targeting the α4β7 integrin, anti-interleukin-9 antibodies, and anti-interleukin-15 antibodies) that target specific molecules or cells implicated in the pathogenesis of EoE are proposed. 31352605 2019
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
0.500 Biomarker disease BEFREE Identified genetic variants in FLG, DSG1, CAPN14, SPINK5, and SPINK7 link EoE to epithelial barrier dysfunction, whereas variants in CCL26, POSTN, and TSLP associate EoE with T helper type 2-mediated immunity. 31132551 2019
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
0.500 GeneticVariation disease BEFREE We discuss areas of the genome associated with both EoE and other allergic diseases, including the well-studied variants encoding thymic stromal lymphopoietin and calpain 14, among other "atopic" regions. 30903437 2019
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
0.500 GeneticVariation disease BEFREE We tested for gene-environment interaction between EoE-predisposing polymorphisms (within TSLP, LOC283710/KLF13, CAPN14, CCL26, and TGFB) and implicated early-life factors (antibiotic use in infancy, cesarean delivery, breast-feeding, neonatal intensive care unit [NICU] admission, and absence of pets in the home). 29029802 2018
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
0.500 GeneticVariation disease BEFREE In particular, the main EoE disease susceptibility loci at 2p23 and 5p22 encode for gene products that are produced by the esophageal epithelium: the intracellular protease calpain 14 and thymic stromal lymphopoietin, respectively. 29980278 2018
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
0.500 GeneticVariation disease BEFREE Likewise, <i>TLR3+/TSLP+</i> individuals showed the most decreased susceptibility of developing EoE (OR = 0.16, <i>p</i> = 0.0001). 29774148 2018
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
0.500 Biomarker disease BEFREE A retrospective analysis was performed of all children with EoE who had TSLP genotyping at The Children's Hospital of Philadelphia from 2008-2014. 29511165 2018
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
0.500 Biomarker disease BEFREE Thymic stromal lymphopoietin (TSLP), which has been studied in various allergic diseases such as asthma, atopic dermatitis (AD) and eosinophilic esophagitis (EoE), has been less considered to be involved in IBDs. 27697608 2017
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
0.500 Biomarker disease BEFREE Specific disease-risk loci that are shared between EoE and other allergic diseases (TSLP, LRRC32) or unique to EoE (CAPN14), as well as Mendellian Disorders associated with EoE, will be reviewed in the context of the insight that they provide into the molecular pathoetiology of EoE. 28224995 2017
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
0.500 Biomarker disease BEFREE Treatment with TSLP reconstituted hallmark features of EoE in TRAIL(-/-) mice and recombinant TRAIL induced esophageal TSLP expression in vivo in the absence of allergen. 25981737 2015
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
0.500 GeneticVariation disease BEFREE For TSLP-WDR36 region, rs3806932 (G allele protective against eosinophilic esophagitis) and rs2416257 (A allele associated with lower eosinophil counts and protective against asthma) were correlated with decreased expression of TSLP in BAL (P = 7.9 × 10(-11) and 5.4 × 10(-4) , respectively) and BEC, but not WDR36. 26119467 2015
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
0.500 GeneticVariation disease BEFREE Genetic studies have shown that EoE is associated with single nucleotide polymorphism on genes, which are released by the epithelium and important in atopic inflammation such as thymic stromal lymphopoietin located (TSLP) close to the Th2 cytokine cluster [interleukin (IL)-4, IL-5, IL-13] on chromosome 5q22, Calpain 14, EMSY, and Eotaxin3. 26258919 2015
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
0.500 GeneticVariation disease BEFREE TSLP genetic variants and its dysregulated expression have been linked to atopic diseases such as atopic dermatitis, asthma, allergic rhinitis and eosinophilic esophagitis. 25340427 2014
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
0.500 GeneticVariation disease GWASCAT Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease. 25017104 2014
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
0.500 GeneticVariation disease BEFREE We had previously reported association of the TSLP/WDR36 locus with EoE. 25407941 2014
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
0.500 Biomarker disease BEFREE These data implicate the 5q22 locus in the pathogenesis of EoE and identify TSLP as the most likely candidate gene in the region. 20208534 2010
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
0.500 Biomarker disease CTD_human Common variants at 5q22 associate with pediatric eosinophilic esophagitis. 20208534 2010
CUI: C0341106
Disease: Eosinophilic esophagitis
Eosinophilic esophagitis
0.500 GeneticVariation disease BEFREE 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. 20620568 2010