Genetic dissection of eosinophilic esophagitis provides insight into disease pathogenesis and treatment strategies

doi:10.1016/j.jaci.2011.03.046

J Allergy Clin Immunol. Author manuscript; available in PMC 2012 July 1.

Published in final edited form as:

J Allergy Clin Immunol. 2011 July; 128(1): 23–32.

Published online 2011 May 13. doi: 10.1016/j.jaci.2011.03.046

PMCID: PMC3129465

NIHMSID: NIHMS290904

Genetic dissection of eosinophilic esophagitis provides insight into disease pathogenesis and treatment strategies

Joseph D. Sherrill, Ph.D. and Marc E. Rothenberg, M.D., Ph.D.^*

Division of Allergy and Immunology, Cincinnati Children’s Hospital Medical Center, University of Cincinnati, Cincinnati, OH 45229 USA

^* Corresponding Author: Marc E. Rothenberg, MD, PhD, Cincinnati Children’s Hospital Medical Center, Division of Allergy and Immunology, MLC 7028, 3333 Burnet Avenue, Cincinnati, OH 45229, Phone: 513-803-0257, Fax: 513-636-3310, Email: Rothenberg/at/cchmc.org

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Abstract

Eosinophilic esophagitis (EoE) is a chronic inflammatory disorder of the esophagus that is compounded by both genetic predisposition and aberrant responses to environmental antigens, particularly those that are food-derived. Data have indicated a unique transcriptional response in vivo that defines EoE and which is partially attributable to the Th2 cytokine interleukin 13 (IL-13). Moreover, a number of genetic risk variants in pro-inflammatory and epithelial cell genes associate with EoE susceptibility, demonstrating novel heritable mechanisms that contribute to disease risk. Here, we discuss recent advances in our understanding of the intrinsic (genetic) and extrinsic (environmental) components that illustrate the complex nature of EoE.

Keywords: Eosinophilic esophagitis, genetics, candidate gene, genome-wide association, polymorphism

The phenomenon of esophageal eosinophilia can be traced through the published literature as far back as 1962¹. Since these early reports, much progress has been made at the molecular and clinical levels to tease apart the intricacies that distinguish EoE from other inflammatory disorders including gastroesophageal reflux disease (GERD). As the prevalence of these diseases has increased since the late 1990s, the need for improved diagnoses, both from a therapeutic and research standpoint, has arisen. Moreover, the high degree of overlap in presenting symptoms in EoE and GERD have been problematic clinically and have necessitated the establishment of diagnostic criteria to differentiate the two diseases.

In 2007, the First International Gastrointestinal Research Symposium (FIGERS) published initial guidelines for the clinical diagnosis of EoE based on the symptomology and histology of the disease². More recently, updated consensus recommendations from a panel of allergists, pathologists, and gastroenterologists have been stated (see Liacouras, et al. in this issue of J Allergy Clin Immunol). These recommendations emphasize that EoE is a chronic, antigen-driven clinicohistopathological disorder that is etiologically and epidemiologically distinct from GERD. Clinically, EoE is characterized by a spectrum of symptoms indicative of esophageal dysfunction. Pathologically, one or more esophageal mucosal biopsy specimens show eosinophil predominant inflammation in excess of 15 intraepithelial eosinophils per high-powered field (HPF). The disease is isolated to the esophagus and other causes of esophageal eosinophilia should be excluded. The peak age of EoE diagnosis occurs within the first three years of life³, most likely resulting from antigen hypersensitivity as solid foods are introduced, although diagnoses in adults is also common. Disease remission typically occurs with treatment, which may include dietary exclusion and/or topical corticosteroids⁴. The symptomology of EoE, if untreated, follows a progressive trend according to patient age. In pediatric patients, these symptoms begin as difficulty feeding and vomiting and can result in failure to thrive^{5, 6}. In adolescent and adult patients, abdominal pain, dysphagia, and food impaction are the chief presentations of disease^{6, 7}. Endoscopic examination has identified common esophageal abnormalities associated with EoE such as linear furrowing with loss of vascularity, ring-like structures, and the presence of white exudate on the esophageal epithelium^{2, 8}. Histologically, the esophageal epithelium exhibits extensive basal layer hyperplasia with papillae elongation and fibrosis within the lamina propria and accumulation of eosinophils, B lymphocytes⁹, and CD4+ and CD8+T lymphocytes¹⁰, regulatory T cells¹¹, and mast cells^12–14.

In addition to being resistant to acid neutralization therapy, another distinguishing feature of EoE is the high rate of concurrent atopy. Studies have indicated a prominent role for food allergies in EoE with published frequencies ranging from 46–79% within the EoE population^{3, 5, 15, 16}. In comparison to the estimated 22% of peanut allergic individuals who develop tolerance later in life¹⁷, only a very small percentage (< 10%) of EoE patients develop tolerance to food antigens as defined by sustained disease remission¹⁵, demonstrating the chronic nature of EoE. The most effective therapies currently used to manage EoE are food antigen avoidance or swallowed glucocorticoid treatment¹⁸. While these treatments can reduce or eliminate disease symptoms, relapse commonly occurs following re-introduction of allergens or discontinuation of treatment, suggesting food antigen hypersensitivity is a fundamental feature of EoE. A number of empirical and test-based food elimination trials have further implicated food hypersensitivity in the EoE population, however, the high variability and low predictive value of skin-prick tests and serum IgE measurements as demonstrated in these studies suggest that the clinical utility for standardized assessment for food-specific reactivity in EoE patients remains to be determined (see Chehade and Aceves¹⁶ for a thorough review of clinical food trials in EoE). Other atopic diseases such as atopic dermatitis (AD), asthma, and allergic rhinitis are also common in the EoE population⁵. Although these diseases are largely mediated by enhanced sensitivity to aeroallergens, the exacerbated Th2 inflammation and tissue remodeling that occurs within the affected tissues indicate shared mechanisms of disease with EoE.

Epidemiology

With the expansion of EoE cases reported worldwide, multiple studies have aimed to establish a baseline prevalence of EoE and determine whether disease incidence has increased. From 2000–2003, the estimated prevalence of EoE in a pediatric population was approximately 4 in 10,000 with an incidence rate of 0.9–1.3 in 10,000 new cases per year ⁵. A similar prevalence (~2 cases per 10,000) and incidence rate (1.4 per 100,000) during a 16-year period were observed in an adult Swiss cohort¹⁹. A study of 1000 esophageal biopsies from a randomized Swedish cohort showed a disease prevalence of 0.4% as defined using an esophageal eosinophil level of > 20/hpf²⁰. However, in a retrospective study examining esophageal biopsies from 666 pediatric patients diagnosed with esophagitis from 1982–1999, data suggest that while the prevalence of EoE was increasing, the incidence of disease was relatively stable despite the marked increase in esophagogastroduodenoscopies during that time period²¹. Using the current recommended eosinophil threshold for EoE diagnosis (> 15/hpf), 198 of these patients had sufficient eosinophils levels with many having histologic indication of basal layer expansion and lamina propria fibrosis to indicate a retrospective diagnosis of EoE²¹. These findings suggest that enhanced disease recognition, rather than a true increase in disease incidence, underlies the emergence of EoE within the last decade. Notably, dysphagia was significantly associated with retrospective EoE cases, and the ancestry and gender of these cases were similar to those currently reported, with the majority being Caucasians (81%) and male (72%)²¹.

An interesting questionnaire-based study on the geographic distribution of EoE across the U.S. has indicated higher disease prevalence in urbanized areas, with a higher concentration of EoE observed in the northeastern states. Here, the estimated prevalence of EoE in the entire U.S. was 52 per 100,000²². A similar trend of a higher EoE prevalence in urban areas was shown to be independent of race, indicating that environment has an equally important contribution as genetics to EoE risk²³. Certainly the high incidence of asthma among urban populations as demonstrated by multiple groups has garnered significant attention²⁴ and given credence to the general hypothesis that increased exposure to aeroallergens is a predisposing factor. The findings by Spergel et al. and Franciosi et al., which define these EoE “hotzones” within urban settings, implicate a similar impact of socioeconomic factors in EoE susceptibility.

Genetic Heritability

An underlying genetic predisposition to EoE has been proposed by multiple groups that show a disproportionate prevalence of disease in Caucasians and males, and within families of affected individuals^{15, 23}. For instance, data over a 14-year period demonstrated that 90% of the EoE patients were Caucasian and 75% were male¹⁵. Reports of a familial occurrence of EoE and esophageal dilatation in 6.8% and 9.7% of EoE patients, respectively, suggest the prevalence of EoE and associated esophageal dysfunction is high among related individuals⁵. Furthermore, the increased risk of EoE among siblings is dramatic when compared to other disorders. For instance, the estimated sibling recurrence risk among siblings of EoE patients (λ_s = ~ 80) is markedly higher compared to that of other atopic diseases with familial inheritance patterns such as asthma (λ_s = ~ 2)²⁶. However, despite this strong familial inheritance, comparison of familial to sporadic cases of EoE showed no difference in esophageal pathology (with the exception of linear furrowing) and gene expression profiles²⁵. Nonetheless, genetic predisposition and family history likely have a significant role in EoE susceptibility and thus detailed family histories are paramount when encountering these patients.

Transcriptome Analysis

A major step toward the molecular mapping of EoE was achieved when gene expression profiling of patient esophageal biopsies showed a remarkable transcript signature that distinguishes EoE from normal controls and patients with chronic esophagitis²⁷. Altered expression of approximately 574 genes comprise this EoE “transcriptome”, which exhibits a high level of conservation among patient gender, age, and atopic history and strongly correlates with esophageal eosinophil levels. The most highly induced gene in the esophagus of EoE patients is the eosinophil chemoattractant eotaxin-3 (CCL26), which was overexpressed 53-fold in EoE esophageal biopsies compared to normal esophageal biopsies in this study²⁷. Eotaxin-3 belongs to the eotaxin family (eotaxins 1–3) of CC chemokines and, through its receptor CCR3, activates downstream G protein signaling to drive eosinophil chemotaxis and activation. Of the eotaxins, only CCL26 is upregulated in EoE, and its expression correlates with eosinophil (and mast cell) levels within esophageal biopsies, indicating a specific contribution in the disease²⁷. Notably, levels of CCL26 transcript in a single biopsy are highly sensitive (89%) in distinguishing EoE from control populations²⁸ despite the histological “patchiness” of EoE across multiple biopsy specimens. In fact, histological examination of at least three biopsies is required to achieve similar diagnostic sensitivity^{2, 4}. Immunofluorescence and in situ hybridization studies on esophageal biopsies identify the esophageal epithelium as the main source of eotaxin-3 production²⁷. In vivo models of EoE further illustrate the crucial role of eotaxin-3 in disease as mice deficient in the eotaxin receptor Ccr3 are protected from esophageal eosinophilia following allergen challenge²⁷. Steroid therapy, in particular swallowed glucocorticoids, effectively normalizes as much as 98% of the EoE transcriptome²⁹, including CCL26, indicating the dynamic nature and reversibility of the gene dysregulation.

In addition to eotaxin-3, a number of immune cell-specific genes exhibit differential expression levels in EoE. For instance, immunoglobulin genes and genes involved in antibody class switching are elevated, reflecting the increase in the esophageal B cell population in EoE⁹. Mast cell-specific genes, specifically carboxypeptidase 3A (CPA3), high-affinity IgE receptor (FcεRI), and tryptase-α (TPSAB1), are abundantly represented in the EoE transcriptome, and mast cells are indeed a prominent inflammatory cell in the esophagus of EoE patients when specifically examined using anti-tryptase staining^{12, 27}. Based on mast cell levels, a specific esophageal transcriptome is also identified in EoE patients, which only partially overlaps with the transcriptome defined by eosinophil levels alone¹², indicating that mast cells and eosinophils are likely independently involved, at least in part. Significant increases in mast cell degranulation and mastocytosis within the epithelium, lamina propria, and smooth muscle layer^{12, 13}, which can be ameliorated with steroid therapy¹², further implicate these cells in the local inflammatory milieu within the esophagus.

A significant portion of the gene transcriptional changes associated with EoE occurs within the esophageal epithelium. These structural, non-immune cells can influence multiple aspects of disease phenotype, including inflammatory cell recruitment, tissue remodeling and hyperproliferation. The human esophageal epithelium is composed of non-keratinized, stratified squamous epithelia with a proliferating basal layer of one to three cells in depth and a differentiating suprabasal layer migrating towards the esophageal lumen³⁰. Many of the histopathological features of the esophagus that are associated with EoE indicate gross defects in cell adherence as indicated by dilated intercellular spaces, expansion of the basal cell layer, and extracellular matrix deposition within the lamina propria. Studies have highlighted IL-13 as a critical signaling molecule capable of altering global gene expression of the esophageal epithelium. Ex vivo microarray analysis showed that treatment of biopsy-derived primary esophageal epithelial cells with IL-13, which is upregulated at the mRNA level in EoE, can largely recapitulate the EoE transcriptome²⁹. This study also confirmed epithelial cells as the primary source of CCL26 in EoE, which was upregulated by an astounding 279-fold following IL-13 stimulation ex vivo²⁹. Notably, esophageal epithelial cells derived from EoE and control individuals respond similarly to IL-13 as assessed by CCL26 production³¹.

Animal models have provided demonstrative data highlighting the robust pro-inflammatory action of IL-13 in an in vivo setting. Lung-specific overexpression of ll13 in mice induces an asthma-like phenotype in the absence of antigen challenge that is characterized by marked inflammatory cell infiltration into the lungs and enhanced airway mucus production³². However, this model also promotes inflammation within the esophagus, such as esophageal eosinophilia and tissue remodeling including fibrosis, angiogenesis, and epithelial hyperplasia³³. The esophageal remodeling in this model occurs independent of eosinophilia and is inhibited by the type 2 IL-13 receptor (IL13Rα2)³³. In summary, these findings implicate the esophageal epithelium as the pathogenic target of IL-13 signaling in EoE as demonstrated by the induction of pronounced histologic and molecular changes that occur in the presence of this potent Th2 cytokine.

The epidermal differentiation complex (EDC) on human chromosome 1q21 is a cluster of genes that regulates terminal differentiation and formation of the cornified envelope of the epithelium³⁴. Despite the lack of a cornified layer in the esophagus, the EDC locus contains the highest density of dysregulated genes in the EoE transcriptome compared with all other loci in the genome³¹. Loss-of-function mutations in several EDC genes, including filaggrin (FLG), have been reported for various cutaneous disorders^35–39. FLG, involucrin (IVL), and several small proline-rich repeat (SPRR) family members (2C, 2D, and 3) are expressed in esophageal epithelial cells but are downregulated in response to IL-13 ex vivo³¹, implicating a homeostatic role for the EDC in the esophageal epithelium.. Loss of FLG expression and subsequent defects in epidermal barrier function have been demonstrated in AD^{40, 41}, which frequently co-occurs with EoE. However, no significant difference in FLG expression is observed between atopic and non-atopic EoE patients³¹, suggesting an alternative function for filaggrin in regulating the epithelial structure within the human esophagus.

It is important to note that 2% of the EoE transcriptome is not reversible following disease remission induced by swallowed glucocorticoids²⁹. Interestingly, these transcripts include genes that are involved in regulating homeostatic and pathogenic responses in the epithelium, such as cadherin-like 26 (CDH26), uroplakin 1B (UPK1B), periostin (POSTN), and desmoglein-1 (DSG1)²⁹. DSG1 is a transmembrane desmosomal cadherin component of desmosomes and facilitates the calcium-dependent homotypic interactions between adjacent cells that impart both structure and mechanical strength to the epithelia. Expression of DSG1 is decreased in both glucocorticoid-treated and untreated EoE patients (77% and 87%, respectively) compared to normal controls. DSG1 is of particular importance as it is the target of multiple inherited and acquired cutaneous disorders. Pemphigus foliaceus and pemphigus vulgaris are autoimmune diseases in which autoantibodies targeting DSG1 decrease cellular adhesion, resulting in epidermal blistering⁴². Notably, epithelial microabcesses exhibiting pronounced eosinophilic inflammation that can be associated with pemphigoid disorders have also been demonstrated within the esophagus, such as in pemphigus vegetans⁴³. Furthermore, multiple heterozygous mutations in the extracellular domain coding region of DSG1 have been linked with striate palmoplantar keratoderma (SPPK), a disease characterized by epidermal thickening on the palms and soles⁴⁴. Collectively, these findings substantiate the significance of alterations in DSG1 in a spectrum of human diseases; it is tempting to speculate that tissue-specific decreases in DSG1 may be pathogenic and partially responsible for the tissue-specific inflammation in EoE.

Periostin (POSTN) is another key molecule that demonstrates steroid resistance in EoE. Periostin, which functions as a cell adhesion molecule that regulates extracellular matrix deposition^{45, 46}, is dramatically upregulated in EoE by approximately 52-fold and while glucocorticoid therapy can reduce a significant portion this overexpression, POSTN remains elevated in glucocorticoid-treated patients (~2-fold)⁴⁷. Periostin is expressed in the basal epithelium and papillae⁴⁷ of the esophagus, suggesting a contributing role for the increased lamina propria fibrosis. Indeed, TGF-β, a pro-fibrotic stimulus that is expressed by eosinophils and mast cells in EoE patient biopsies^{13, 48}, can induce a dramatic upregulation of POSTN expression in primary esophageal fibroblasts, supporting this potential mechanism for tissue fibrosis observed in EoE^{47, 49}. Moreover, periostin can enhance eosinophil adhesion in vitro and Postn-deficient mice are protected from allergen-induced eosinophilia in the lung and esophagus⁴⁷. Interestingly, periostin upregulation in bronchial epithelial cells enhances TGF-β-induced collagen synthesis⁵⁰. As periostin also enhances cross-linking of collagen fibrils through upregulating the cleavage of mature, active lysyl oxidase⁵¹, these cumulative data suggest a positive feedback loop in which periostin has a central role in promoting the fibrotic responses in multiple inflammatory conditions.

In summary, esophageal transcript profiling has defined an EoE specific-transcript signature that is composed of dysregulated gene networks involved in Th2 inflammation and epithelial cell responses. These studies demonstrate that IL-13 is a central mediator and link between the immunological and histological changes that are germane to EoE, largely through its effects on the esophageal epithelium. Given the well-documented role of IL-13 in other atopic diseases such as asthma and AD, it is reasonable to speculate that IL-13 production in response to inhaled or absorbed antigens can also predispose individuals to other Th2 comorbidities such as EoE.

Genetic Variants and Disease Susceptibility

The number of studies investigating genetic variants associated with EoE are few compared to other more common and more widely-recognized atopic diseases such as AD and asthma. Regardless, there have been significant strides in uncovering EoE risk variants in a relatively short period of time^{14, 27, 52, 53} due in part to the technological advances in genotyping single-nucleotide polymorphisms (SNPs) in large case-control cohorts. In all, there have been four candidate gene studies, which tested for polymorphisms in genes with a published (or suspected) functional role in EoE, and one genome-wide association study (GWAS), used to identify EoE risk variants across the entire genome in an unbiased fashion (Table 1).

Table 1

Genetic risk variants in EE

Candidate Gene Studies

Blanchard et al. identified the first EoE risk variant in a likely candidate, CCL26. The CCL26 single-nucleotide polymorphism (rs2302009) was shown to be highly associated with disease risk (P = 0.001) with an odds ratio = 4.55 in a case-control cohort²⁷. Transmission disequilibrium testing, which measures the transmission of a disease allele from unaffected, heterozygous parents to an affected offspring, confirmed the association of rs2302009 with EoE was not due to ancestral differences in the case-control analysis²⁷. Additional studies have also linked this SNP to increased serum IgE levels and asthma susceptibility⁵⁴. However, the observed association between rs2302009 and EoE was independent of atopic status, indicating a direct link with EoE susceptibility. Although rs2302009 is located within the 3′ untranslated region of the CCL26 transcript and could potentially affect mRNA stability, a functional effect of this SNP in either asthma or EoE has yet to be described.

TGF-β, an eosinophil and mast cell-derived mediator of fibrotic tissue responses, has been implicated in the same pathogenic process in EoE⁴⁸. Moreover, TGF-β1 has recently been shown to stimulate esophageal smooth muscle contractility and potentially contribute to esophageal dysmotility in EoE¹³. A SNP within the TGFB1 promoter (C-509T) that associated with asthma susceptibility^{55, 56} was shown to create a binding site for the transcription factor YY1 that subsequently enhanced promoter activity⁵⁶. In a small cohort of 20 EoE patients, homozygotes for the minor T allele of C-509T exhibited increased TGF-β1-positive lamina propria cells¹⁴. Conversely, the major C allele of C-509T was a positive prognostic indicator for therapeutic responses in EoE¹⁴. Determining the association of this and other TGFB1 SNPs in a larger disease cohort will be vital to assess the full genetic contribution of TGFB1 in EoE.

Polymorphisms in epithelial-specific genes have also been associated with EoE susceptibility. First, a loss-of-function SNP in FLG (2282del4) that was previously linked with AD susceptibility³⁸ also associates with EoE risk; similar to the CCL26 SNP, this association is specific to EoE as atopy was found not to be a confounding factor³¹. A second and larger candidate gene study examined 736 SNPs in 52 genes known to be involved in epithelial cell structure or inflammatory responses. Here, an EoE cohort of 170 patients was genotyped using a custom SNP chip and compared to similarly genotyped controls with various atopic histories⁵³. Importantly, SNPs in thymic stromal lymphopoietin (TSLP), a cytokine recently described as a “master regulator” of Th2 responses⁵⁷, were shown to associate with EoE independent of patient atopic status. TSLP is derived primarily from epithelial cells in response to cytokines⁵⁸, noxious substances⁵⁹ and mechanical stress⁶⁰ and exerts its effects on nearly every cell type involved in Th2 inflammation including eosinophils⁶¹ and mast cells⁶². For instance, TSLP activates dendritic cells to adopt a Th2 priming phenotype through the secretion of the chemokines TARC, MDC, and eotaxin-2 and OX40L expression, which activates Th2 cytokine production by naïve CD4+ T cells^63–65. Thus, it is remarkable that TSLP critically regulates the exact processes involved in allergen sensitization that underscore the EoE phenotype. This study also identified an association between male EoE patients and a non-synonymous SNP in the TSLP receptor (CRLF2)⁵³, which, given the male predilection for EoE, presents an intriguing scenario as CRLF2 is encoded on pseudoautosomal region 1 of the X and Y chromosomes⁶⁶.

EoE GWAS

A broader, unbiased GWAS approach was undertaken to identify SNPs associated with EoE susceptibility. Here, two relatively large cohorts of EoE cases and normal controls were genotyped for 550,000 SNPs across the genome⁵². While only one locus on chromosome 5q22 was genome-wide significant following multiple testing correction, this region contains the genes encoding for TSLP and WD repeat domain 36 (WDR36). Esophageal expression of TSLP but not WDR36 is increased in EoE, and the protective minor allele for the most significantly EoE-associated SNP on 5q22 (rs3806932), which lies upstream of the TSLP locus, correlates with decreased TSLP expression in the esophagus. Notably, rs3806932 is in linkage disequilibrium (LD) with rs3806933^{52, 67}, suggesting that these two SNPs are inherited together more often than would be expected by chance. Data recently implicated rs3806933 in altering the binding of the transcription factor activator protein-1 to the TSLP promoter with a modest increase in promoter activity⁶⁷. The other genome-wide significant SNP on 5q22 is upstream of the WDR36 gene, located approximately 14 kb away from TSLP, and lies within the same linkage block as rs3806932⁵². WDR36 is critically involved in ribosomal RNA processing⁶⁸ and is co-regulated with IL2 in activated T lymphocytes⁶⁹. Moreover, SNPs in the region of WDR36 have been associated with peripheral blood eosinophilia⁷⁰ as well as glaucoma susceptibility⁷¹. Thus, while TSLP appears to be the likely disease candidate on the 5q22 locus, the role of WDR36 warrants further investigation.

GWASs on other more-common gastrointestinal inflammatory diseases such as Crohn’s disease⁷², ulcerative colitis⁷³, and celiac disease^74–76 have successfully identified numerous disease risk variants aided in part by the well-developed patient cohorts being historically investigated for these diseases. For example, meta-analyses across large, independent case-control cohorts (often in excess of 10,000 combined patients) along with further refinement of the human genome polymorphism map have yielded sufficient sample sizes to detect significant disease associations with common variants that have relatively low effect sizes. The low sample size of the current EoE GWAS (251 EoE cases in total) not only emphasizes the magnitude of the 5q22 SNP associations but also suggests that there are likely additional EoE risk variants to be uncovered as further EoE cohorts are subjected to genome-wide genotyping and similar meta-analyses are performed (in essence, boosting the statistical power). A hint at what SNPs or gene loci may hold potential significance in these future studies can be gained by investigation into those that failed to reach the statistical threshold for significance from the previous GWAS⁵². For instance, SNPs in STAT6, the major signaling molecule downstream of IL-13 signaling, and in the aforementioned DSG1, which is largely resistant to steroid-dependent regulation in EoE, are highly associated with EoE but under the genome-wide significance threshold⁵². Given the robust immune component of EoE and the overexpression of HLA-DR in the esophagus of EoE patients⁷⁷ it is quite surprising there was a lack of an association between EoE and polymorphisms in the HLA locus previously linked to other gastrointestinal diseases such as celiac disease^{75, 78}.

Conclusions and Future Directions

In just over ten years since the recognition of EoE as a distinct inflammatory disorder, the rapid progress towards characterizing the disease on multiple fronts has underscored its complexity. We now have insight into the natural history of the EoE, its strong association with specific ethnicities and genders, the genetic and environmental factors involved, and the molecular pathogenesis of the disease (Fig. 1). Moreover, the burst of data illustrating EoE risk variants in CCL26, TGFB1, TSLP and CRLF2, and FLG provide insight into the upstream mechanisms that regulate the expression of genes that are operational (and likely synergistic) in multiple aspects of EoE pathogenesis (Fig. 2). For instance, perturbations in the TSLP signaling pathway as a result of variants either increasing TSLP levels or altering receptor function can amplify innate inflammatory responses to food antigens. Moreover, prolonged CCL26 expression may further enhance eosinophil recruitment and TGF-β1 secretion to exacerbate tissue remodeling. Variants affecting FLG expression may disrupt normal esophageal barrier function and result in increased antigen exposure and affect overall tissue integrity. Despite these advances, much work remains in terms of identifying true casual variants and determining their mechanistic function in these pathways. A major initiative currently underway is to expand upon the current genome-wide-associated polymorphisms by increasing the number of genotyped EoE patients; this will undoubtedly greatly expand the number of genetic loci linked with EoE risk. Moreover, deep sequencing efforts and extensive fine-mapping of the established EoE susceptibility loci such as TSLP could identify rare and/or casual variants that affect gene transcription.

Figure 1

The molecular pathogenesis of EoE

Figure 2

Genetic risk variants in EoE

An additional area to be explored in EoE heritability will be the role of epigenetics, which can be defined as the study of heritable changes in gene expression that are not associated with DNA sequence variations which can include non-coding RNAs, histone modifications (acetylation and methylation), and DNA methylation⁸¹. Importantly, as these genomic alterations can be influenced by external stimuli such as diet and drugs, epigenetics can provide insight into the complex interactions between environmental exposures and disease-associated genes. The profiling of global epigenetic changes in large disease cohorts has already yielded promising results for cancer, cardiovascular disease, obesity⁸¹, and asthma⁸². As EoE is also influenced by environmental antigen exposure, the uncovering of an EoE epigenome through microRNA arrays, DNA methylation profiling, and chromatin immunoprecipitation-sequencing (ChIP-seq) technologies will provide a critical link to the global gene transcriptional changes already known to occur in EoE. Recent data have already indicated that IL-13 can elicit acetylation changes to histone H3 at the CCL26 promoter in esophageal epithelial cells, implicating epigenetic modifications represent a novel mechanism of gene regulation in EoE⁸³.

The pivotal role of the esophageal epithelium in EoE and the transcriptional changes that occur within different stratified layers of the epithelium provide potential opportunities for non-invasive biomarkers for EoE. Laser-capture microscopy allows for the isolation of specific cell types from minute sections of tissues that can subsequently be subjected to microarray or mass spectrometry analysis. Such techniques have already be used to define the transcriptomes⁷⁹ and proteomes⁸⁰ of the various esophageal layers in Barrett’s esophagus. Identification of an EoE-specific transcript profile specific to the suprabasal epithelium may yield diagnostic targets from the skin or oral mucosa samples.

In conclusion, it is remarkable how the genetic dissection of EoE susceptibility has uncovered key pathways that are now being considered for treatment strategies. For example, our findings identify new targets for antibody neutralization strategies (such as anti-IL-13) and specific cell types for directed therapy such as mast cells and epithelial cells, which also supports the clinical value of topical steroid therapy. Therefore, over the next ten years, further unraveling of the genetics and environmental factors that compound EoE holds great promise for the future development of novel and highly effective therapies.

Acknowledgments

This work was supported in part by NIH U19 AI070235, R01 DK076893, R37 AI1045898, the PHS Grant P30 DK0789392, Department of Defense, Food Allergy Project, the Buckeye Foundation and the Campaign Urging Research for Eosinophilic Disease (CURED) Foundation. J.D.S. is supported by a T32 NIH training grant (HL091805). M.E.R. has proprietary interest in reslizumab, a drug being developed by Cephalon.

We would like to thank all of the participating families, patients, physicians, and nurses as well as members of the clinical research team (A. Ahrens, B. Buckmeier Butz, A. Ellison, A. Greenberg, A. Greenler, T. Grotjan, S. Jameson, E. Stucke, and M. Mingler) at the Cincinnati Center for Eosinophilic Disorders for assistance with patient enrollment, DNA preparation and/or database management. We are also grateful to S. Hottinger for her editorial assistance with this review.

Abbreviations used


EoE	eosinophilic esophagitis

hpf	high-powered field

GERD	gastroesophageal reflux disease

IL-13	interleukin 13

EDC	epidermal differentiation complex

TSLP	thymic stromal lymphopoietin

CCL26	chemokine (C-C motif) ligand 26

TGF-β1	transforming growth factor, beta 1

HLA	human leukocyte antigen

FLG	filaggrin

DSG1	desmoglein-1

POSTN	periostin

WDR36	WD repeat domain 36

SNP	single-nucleotide polymorphism

GWAS	genome-wide association study

Glossary


BASAL ZONE HYPERPLASIA (BZH), PAPILLARY ELONGATION	Histological findings in EoE that are caused by active basal cell proliferation and increased extension of the vascular papillae and subepithelial lamina propria into the epithelial space. Other typical histologic features of EoE include dilated intercellular spaces and lamina propria fibrosis

CCR3 and EOTAXINS	C-C Chemokine Receptor-3 (CCR3) binds eotaxins. While eotaxins-1, −2 target eosinophils to the lung and lower gastrointestinal tract, eotaxin-3 is present only in humans and functions as a chemoattractant for esophageal eosinophils

CHROMATIN IMMUNOPRECIPITATION	ChIP technology uses antibodies to precipitate a protein bound to DNA. The bound DNA sequence can be analyzed to look for, e.g. target sequences for transcription factors or histone associated regions of DNA

EPIGENETICS	The study of changes in DNA configuration that allow for changes in gene expression independent of sequence changes. For example, DNA methylation can cause DNA closing, making specific genetic regions inaccessible to RNA polymerase, transcription factors thus silencing gene expression. Histone acetylation can allow DNA to open and can increase transcription. Creb binding protein (CBP, p300) is a histone acetylase implicated in EoE pathogenesis

FILAGGRIN	INVOLUCRIN, Involucrin is present in the cytoplasm of keratinocytes and is cross linked to cell membrane proteins via transglutaminase. This allows the formation of a strong epithelial barrier and decreases skin invasion by microorganisms. The usual function of filaggrin is to function as a natural moisturizing factor. Loss of function in the filaggrin gene causes ichthyosis vulgaris and predisposes to eczema, asthma, and eosinophilic esophagitis

GENOME WIDE ASSOCIATION STUDY (GWAS)	GWAS uses gene chip technology and bioinformatics to analyze the human genome for single nucleotide polymorphisms in diseased and non-diseased states. Haplotypes (in blocks) that vary between diseased and non-diseased subjects are considered to be associated with the disease state

INTERLEUKIN 13	IL-13 is a Th2 cell-derived interleukin capable of inducing multiple aspects of eosinophil- associated tissue remodeling. IL-13 overexpression in target organs of transgenic animals is associated with pulmonary, esophageal, and cutaneous fibrosis as well as angiogenesis

LAMBDA (λ)	The familial relative risk is defined by the statistic λ which assesses the risk of disease in an individual with a diseased first degree biological relative to the risk in the population at large. The larger the λ, the stronger the genetic effect is on the disease

LINEAR FURROWING, WHITE EXUDATES	Typical endoscopic findings in EoE include esophageal lichenification, linear furrowing, pallor, and white exudates/plaques (histologically comprised of eosinophils), strictures, and concentric rings due to motility or fibrosis

SINGLE NUCLEOTIDE POLYMORPHISM (SNP)	Genetic variant in single nucleotide that may be normally present in the population and associated with risk for certain complex polygenic diseases

TARC	Thymus and activation regulated chemokine (TARC), also known as CCL17 induces migration of CCR4+ T cells to the skin in eczema patients and can be elevated in the periphery of some EoE patients

TRANSFORMING GROWTH FACTOR- Beta (TGFβ)	TGFβ is produced by epithelial cells, and inflammatory cells including eosinophils, and mast cells and has pro-fibrotic effects. TGFβ1, 2, and 3 reside on distinct chromosomes but utilize the same signaling pathway and receptors

TRANSCRIPTOMES	PROTEOMES, Gene expression microarray defines transcriptional differences among subjects with and without a disease state. Gene chip technology and bioinformatics are utilized to analyze the level of gene expression (referred to as the “transcriptome”) across the genome in diseased versus control populations. Proteomes are the protein expression pattern of an organism. Proteomic analysis can use techniques such as 2D gel analysis and peptide sequencing or antibody arrays to find both previously known and unknown proteins associated with a particular disease state

Footnotes

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