Mediators of Inflammation

Mediators of Inflammation / 2013 / Article

Research Article | Open Access

Volume 2013 |Article ID 425915 | 10 pages | https://doi.org/10.1155/2013/425915

High Intestinal and Systemic Levels of Interleukin-23/T-Helper 17 Pathway in Chinese Patients with Inflammatory Bowel Disease

Academic Editor: Anshu Agrawal
Received14 Jul 2013
Revised07 Nov 2013
Accepted08 Nov 2013
Published05 Dec 2013

Abstract

Interleukin-23/T-helper 17 (IL-23/Th17) pathway plays a key role in the pathogenesis of inflammatory bowel disease (IBD), but little is known about its expression in Chinese population. In this study, we investigated the mRNA and protein levels of IL-12p40, tumor necrosis factor-like cytokine 1A (TL1A), Janus kinase 2 (JAK2), and IL-23R both locally and systemically in Chinese IBD patients. Our results indicated that the mRNA levels of IL-12p40 and TL1A were increased in ulcerative colitis (UC) patients. Furthermore, serum IL-12p40 and TL1A levels were higher in active UC patients, especially in patients with disease course less than 1.25 years or initial onset. No correlation was found between the genotype and serum levels of IL-12p40 or TL1A in UC patients. Additionally, the mRNA and protein expression of JAK2 and IL-23R were increased in UC and Crohn’s disease (CD) patients. Taken together, our results provided evidence that IL-23/Th17 pathway genes may represent important biomarkers of active stage of IBD and serve as novel therapeutic targets for IBD in Chinese population.

1. Introduction

Inflammatory bowel disease (IBD) is a chronic, relapsing inflammatory disorder of the gastrointestinal tract which includes ulcerative colitis (UC) and Crohn’s disease (CD). IBD is caused by complex interactions of genetic, immunoregulatory factors, intestinal microbiota, and environmental factors. Of these, genetic susceptibility of IBD has been demonstrated as a key factor by traditionally epidemiological studies [1]. Genome-wide association (GWA) studies have discovered some IBD susceptibility genes in interleukin-23/T-helper 17 (IL-23/Th17) pathway, such as IL-12B, IL-23R, Janus kinase 2 gene (JAK2), signal transducer and activator of transcription 3 (STAT3) and tumor necrosis factor (ligand) superfamily member 15 (TNFSF15) [25].

So far, little is known about the IL-23/Th17 pathway in Chinese IBD patients, and many studies illustrate that genetic mutations that predispose to IBD appear to vary between different geographical and racial groups [6, 7]. Thus, our previous study examined the distribution of 26 SNPs of UC and 18 SNPs of CD in the IL-23/Th17 pathway genes in Chinese IBD patients and found that the polymorphisms of IL-12B, IL23R, JAK2, and TNFSF15 are strongly associated with Chinese IBD patients. It is illustrated that the IL-23/Th17 pathway is a key regulator of intestinal homeostasis and proinflammatory response in defense of microbial infection [810]. IL-12B encodes the IL-12p40 subunit shared by IL-12 and IL-23 cytokine on the genetic level [11]. Functionally, the proinflammatory cytokines IL-12 and IL-23 play critical roles in bridging the innate and adaptive immune systems in IBD, while IL-23R may play more important role than IL-12/23p40 in the genetic susceptibility to IBD [8, 12, 13].

The interplay of IL-23 and IL-23 receptor complex activates the JAK2/STAT3 signaling pathway and ultimately leads to a variety of downstream immune responses. Recently, JAK2 is demonstrated to be associated with increased risk of UC and CD in a large study across the United Kingdom [14]. Meanwhile, the first GWA study provides evidence that the variation in TNFSF15 leads to both CD and UC in the European population [15]. Moreover, the cytokine, tumor necrosis factor-like cytokine 1A (TL1A), encoded by the TNFSF15, is involved in the IBD pathogenesis [16]. Accumulating evidence demonstrates that the IL-23R SNPs might lead to a variant in the 39-untranslated region of IL-23R mRNA and affect its response to anti-TNF therapy in UC [17, 18]. So this association between single nucleotide polymorphisms (SNPs) and IBD may be explained by the effects on the gene function and/or expression leading to dysregulation of intestinal inflammation.

Overall, our laboratory illustrated the polymorphism of IL-23/Th17 pathway genes, while the phenotypic functions and potential genotype-phenotype interactions are mainly unknown in Chinese IBD patients. Here we investigate the mRNA and protein expression of IL-12B, TNFSF15, JAK2, and IL23R both locally (intestinal mucosal) and systemically (peripheral blood) in Chinese IBD patients to provide a revealing insight into their roles in IBD pathogenesis.

2. Materials and Methods

2.1. Subjects

In this study, 118 patients with UC and 30 patients with CD were studied, which were previously genotyped IL-23/Th17 genes polymorphisms (Table 1). The diagnosis was based on conventional clinical, radiological, endoscopic, and histological criteria. The extent of colonic disease was determined by endoscopy and reported according to the Montreal classification [19]. Disease activity was assessed by the Truelove and Witts activity index in UC patients [20], while CD patients were determined by the Crohn’s disease activity index (CDAI) [15]. Comparison was made with 93 healthy controls while individuals with infectious colitis, ischemic colitis, intestinal tuberculosis, and autoimmune diseases were excluded. This study was approved by the ethics committee of Zhongnan Hospital of Wuhan University.


CharacteristicsUC
( (%))
CD
( (%))
Healthy controls
( (%))

Male54 (45.76)19 (63.33)65 (69.89)
Age (years) mean ± SD (range)   (10–67) (17–61) (21–88)
Course of disease (years)
Mean ± SD (range)
  (1.25, 0.003–23) (1.29, 0.08–16)
Smoke habit24 (20.34)7 (23.33)
Family history13 (11.02)0
Extraintestinal manifestations33 (27.97)16 (53.33)

Disease location
UCCD
 Left sided colitis Colon35 (29.66)7 (23.33)
 Extensive colitis Ileocolon36 (30.51)9 (30.00)
 Proctitis Ileum47 (39.83)14 (46.66)

Disease behavior
UCCD
 Initial onset Stricturing54 (45.76)4 (13.33)
 Chronic relapse Nonstricturing,  Nonpenetrating57 (48.31)19 (63.33)
 Chronic continuous Penetrating7 (5.93)7 (23.33)
Active disease90 (76.27)20 (66.67)
Inactive disease28 (23.73)10 (33.33)

Treatment
5-ASA/SASP103 (87.29)23 (76.67)
Steroid52 (44.07)9 (30.00)
Antibiotics28 (23.73)2 (6.67)
Immunosuppressive9 (7.63)5 (16.67)
Infliximab1 (0.85)4 (13.33)
Operation05 (16.67)

SD: standard deviation; 5-ASA: 5-aminosalicylate; SASP: sulfasalazine.
2.2. Quantitative Real-Time PCR Analysis

For mRNA expression analysis, intestinal mucosal biopsies were obtained during colonoscopic investigation in 31 UC patients, 30 CD patients, and 28 healthy controls. Real-time PCRs were performed with the real-time PCR kit (Takara, Shiga, Japan) and amplified in the LightCycler instrument (BioRad, Hercules, CA, USA). The reaction conditions were initial denaturation at 95°C for 30 s, followed by 40 cycles of denaturing at 95°C for 5 sec and annealing at 54°C (IL-12B), 58°C (TL1A), 55°C (JAK2), or 56°C (IL-23R) for 40 sec. All samples were processed in triplicate. Relative units were calculated by the method [21]. The primer sets used for PCR amplification were shown (Table 2).


GenePrimer setsLength (bp)

IL-12B
 ForwardGACAAGTAGTTATGGCTAAGGACATGA102
 ReverseAGGGATTCCAGATTTTCTTTGCA
TNFSF15
 ForwardGAGGCCTGTGTGCAGTTCCA182
 ReverseCCTAGTTCATGTTCCCAGTGCAGA
JAK2
 ForwardGTGTTCCATTTGATAGAACTTTTGAAGA105
 ReverseATTATTGTTCCAGCATTCTGTCATGA
IL-23R
 ForwardTGGGTCCAAGCAGCAAACGCAC105
 ReverseCTCAGCCCTGGAAATGACGGCTG
-actin
 ForwardCTCCATCCTGGCCTCGCTGT268
 ReverseGCTGTCACCTTCACCGTTCC

2.3. Detection of Soluble IL-12p40 and TL1A by ELISA

Blood was collected from 118 UC patients and 93 healthy controls in serum separator tubes, and serum was separated, aliquoted, and stored at −80°C. Serum IL-12B (Mabtech, Stockholm, Sweden) and TL1A (Enzo, Farmingdale, NY, USA) levels of UC patients and healthy controls were measured by enzyme-linked immunosorbent assay (ELISA), according to the manufacturer’s protocol.

2.4. Western Blot

Proteins were extracted from colon tissues which we used for quantitative PCR mentioned above. Protein samples were separated on 10% SDS-PAGE gel electrophoresis and transferred to a polyvinylidene fluoride membrane (Millipore, Billerica, MA, USA), and then immunoblotted with primary antibodies: human JAK2 (Cell Signaling Technology, Beverly, MA, USA), human IL-23R (Millipore, Billerica, MA, USA), and β-actin (Cell Signaling Technology, Beverly, MA, USA), respectively. The blots were developed by enhanced chemiluminescence (ECL) Western Blotting Substrate (Pierce, Rockford, Illinois, USA) and imaged using an ECL system (Fusion FX7, Vilber Lourmat, Torcy, France). The band intensity was determined using Quantity One Software (Bio-Rad, Hercules, CA, USA).

2.5. Immunohistochemical Staining

After the colon tissues were paraffin-embedded and sectioned, immunohistochemical analyses were performed according to the method described. Briefly, goat polyclonal anti-human JAK2 and IL-23R antibodies were used as the primary antibody. Corresponding areas of sections were marked and high-power fields were counted at 200x magnification.

2.6. Statistical Analysis

Due to the individuals highly skewed distributions, comparison of values for all dates between IBD subgroups and control was performed by Mann-Whitney U test (2 groups compared) or Kruskal-Wallis test (more than 2 groups compared). All data were analyzed with Statistical Product and Service Solutions Vision 17.0 (SPSS, Chicago, Illinois, USA). Results were considered statistically significant only if the value was less than 0.05.

3. Results

3.1. Levels of IL-12p40 and TL1A mRNA Were Upregulated in the Inflamed Intestinal Mucosa of UC Patients

Previously, we found that IL-12B and TNFSF15 genes polymorphisms were associated with UC in Chinese patients, which clearly showed that these two genes were involved in human susceptibility to UC.

To further understand their biological functions, here we compared the relative IL-12p40 and TL1A mRNA expression between samples obtained at endoscopy from the UC patients and healthy controls. The relative level of IL-12p40 transcripts in colonic mucosa was significantly different between UC and healthy controls (mean ± SD: versus , resp.; ; see Figure 1(a)). In comparison to IL-12p40, we also observed a clear difference between UC and healthy controls regarding TL1A expression (UC: , healthy controls: ; ; see Figure 1(b)).

3.2. Serum IL-12B and TL1A Levels Were Increased in Patients with UC

Since our tissue data clearly showed the local increase of IL-12p40 and TL1A, we then compared their serum concentrations in UC individuals and the healthy controls in the systemic levels. We found that the serum IL-12p40 levels were elevated in UC patients than that in healthy controls (255.59, 68.16–4756.60 versus 164.43, 0.1–986.43 pg/mL; ; median, 95% CI; see Figure 2(a)) and serum TL1A concentrations were also increased in UC patients (354.24, 172.78–7113.24 pg/mL) compared with healthy controls (218.95, 0–2032.06 pg/mL, ; see Figure 2(b)).

To our knowledge, previous studies suggested that genotype-phenotype association played an important role in IBD, so we suspected that, whether the increase in serum IL-12p40 and TL1A levels was due to the genotype-phenotype association, the serum concentrations should be varying in different genotype. We investigated the effect of the distribution of rs6887695 or rs4263839 SNP on the serum levels of IL-12p40 and TL1A in UC patients, respectively. There were 71 of 118 UC patients genotyped allele C and 87 of 118 UC patients genotyped allele G for rs6887695, while 82 of 118 UC patients were genotyped allele A and 84 of 118 UC patients were genotyped allele G for rs4263839 (Figure 3). Results showed that there was no statistical difference among three genotype groups ( ; see Figure 3). Thus, the differences in IL-12p40 and TL1A expression are not related to their genotype.

3.3. Association of Serum IL-12p40 and TL1A Levels with Clinical Features of Patients with UC

We then examined whether the concentrations of IL-12p40 and TL1A were associated with clinical features of patients with UC. We analyzed serum IL-12p40 and TL1A levels in patients with UC after stratification by gender, age, course of disease, smoke habit, family history, extraintestinal manifestations, location, behavior, and treatments of disease (Table 3). Our results showed that the disease characteristics revealed no association on serum IL-12p40 or TL1A ( ), including the gender, age, smoke habit, and family history. Serum TL1A levels were higher in UC patients without extraintestinal manifestations ( ), which exhibited no statistically significant difference in serum IL-12p40 levels.


CharacteristicsUC
IL-12p40 (pg/mL)
Median (range)
TL1A (pg/mL)
Median (range)

Gender
 Male54275.12
(82.54–4756.60)
353.17
(178.15–5989.46)
 Female64252.84
(68.16–4581.92)
355.85
(172.78–7113.23)
Age (years)
 ≤4060251.21
(68.16–4482.94)
339.75
(172.78–5425.89)
 >4058256.91
(79.33–4756.60)
386.99
(182.45–7113.23)
Course of disease (years)
 ≤1.2562306.21
(79.33–4756.60)*
433.65
(172.78–7113.23)*
 >1.2556214.40
(68.16–3355.24)
319.35
(176.00–5425.89)
Smoke habit
 Yes24291.60
(82.54–4756.60)
385.38
(218.95–5989.46)
 No94252.84
(68.16–4581.92)
353.17
(172.78–7113.23)
Family history
 Yes13246.33
(79.33–1131.80)
318.81
(207.14–5425.89)
 No105257.01
(68.16–4756.60)
358.54
(172.78–7113.23)
Extraintestinal manifestations
 Yes33229.34
(79.33–3355.24)
310.22
(172.78–2198.54)*
 No85258.43
(68.16–4756.60)
388.60
(176.00–7113.23)
 Active disease90290.04
(68.16–4756.60)**
390.75
(172.78–7113.23)*
 Inactive disease28185.60
(80.91–3193.59)
293.04
(176.00–2305.60)
Disease location
 Extensive colitis36280.63
(82.54–4756.60)
347.26
(172.78–6831.63)
 Distal colitis82252.84
(68.16–4581.92)
361.22
(176.00–7113.23)
Disease behavior
 Initial onset54361.95
(79.33–4756.60)**
545.21
(207.14–7113.23)**
 Chronic relapse/chronic continuous64214.39
(68.16–3355.24)
312.90
(172.78–5425.89)
Treatment
 SASP/5-ASA monotherapy66239.69
(79.33–4581.92)
359.51
(176.00–6831.63)
 Other drugs52268.61
(68.16–4756.60)
353.17
(172.78–7113.23)

, .

Among UC patients, serum IL-12p40 and TL1A levels were influenced by disease course, exhibiting higher values in UC patients with disease course less than 1.25 years (IL-12p40, ; TL1A, ). Comparisons among serum IL-12p40 and TL1A levels of UC patients with different disease behaviors exhibited significant differences (IL-12p40, ; TL1A, ), which were elevated in patients with initial onset than those with chronic relapse or chronic continuous IBD. Moreover, serum IL-12p40 and TL1A levels were higher in active disease compared with inactive disease (IL-12p40, ; TL1A, ). No association was established between disease location, treatments, and serum IL-12p40 or TL1A levels.

3.4. JAK2 and IL-23R mRNA Were Highly Expressed in IBD Patients

As for mRNA, different levels of JAK2 were observed in UC, CD, and healthy controls ( versus versus , resp.; ; see Figure 1(c)). Meanwhile, the relative average IL-23R mRNA expression was in UC patients and in CD patients, which were significantly elevated compared with healthy controls ( ; ; see Figure 1(d)).

3.5. The Protein Expression of JAK2 and IL-23R Was Significantly Elevated in IBD Patients

To confirm the expression of JAK2 and IL-23R, western blot and immunohistochemical analyses were performed on intestinal mucosal biopsies of 31 UC, 30 CD, and 28 healthy controls using primary antibodies that recognize the bioactive forms of JAK2 and IL-23R. The significant increase of JAK2 and IL-23R was found in UC and CD compared with healthy controls in colon tissues (Figure 4).

4. Discussion

Our study identified the abnormal IL-23/Th17 pathway expression levels both locally and systemically in IBD patients. The results indicated that UC patients had higher mRNA and serum levels of IL-12B and TL1A, while JAK2 and IL-23R levels were higher in UC and CD patients. Moreover, genotype-phenotype analysis showed that there was no significant correlation between the serum levels and different genotype groups of IL-12B or TL1A in UC patients. Nonetheless, some association was found between serum IL-12p40 and TL1A with the extraintestinal manifestations, disease course, and behavior of UC in our study.

Recent studies suggested that the genetic polymorphisms were associated with gene expressions and functions in IBD, which indicated that genetic variants could regulate individual’s susceptibility to IBD [2225]. Our unpublished data found that IL-12B, IL-23R, JAK2, and TNFSF15 genes polymorphisms were strongly associated with IBD in Chinese population. In this study we first demonstrated that their levels were elevated in IBD and then investigated whether genetic polymorphism could affect the expression of IL-23/Th17 pathway genes which led to different clinical features in Chinese IBD patients.

Since we found that IL-12B polymorphisms were involved in human susceptibility to UC in Chinese population, we observed a remarkable increase in the mRNA and protein level of IL-12p40 in mucosal biopsies and serum of UC patients. Currently, there was limited data about the phenotypic effects of IL-12B in Chinese population. However, recent studies suggested that IL-12p40 homodimer may have higher affinity for the IL-23 receptor than IL-12 receptor, and IL-12p40 delivery ameliorated dextran sulfate sodium-induced colitis by suppressing IL-17A production and inflammation in the intestinal mucosa [26]. Moreover, the secreted IL-12p40 was able to inhibit IL-23-mediated immune responses [22]. Therefore, it showed that IL-12p40 could be another novel target.

Our unpublished results found that the SNP rs6887695 of IL-12B was associated with UC pathogenesis. From a genotype-phenotype interaction standpoint, our results showed that the rs6887695 SNP polymorphism might be unable to fully affect the IL-12p40 serum levels, which suggested that the genetic polymorphisms located within these genes did not thoroughly explain the variations in disease phenotypes or IBD pathogenesis. Furthermore, we evaluated the possible relationship between serum IL-12p40 levels and clinical features of UC patients. Our results suggested that the elevation of serum IL-12p40 levels was only affected by disease course and behavior which suggested that the active UC patients with shorter course or initial onset had higher expression of serum IL-12p40. The similar results were also observed in the onset phase of autoimmune arthritis [27, 28]. Our results suggested that IL-12p40 may act as a molecular marker to indicate active disease on the early onset of UC patients, and therapy against IL-12p40 may delay the onset and reduce the UC severity.

TL1A, which represented a ligand for the death domain receptor 3 (DR3), was involved in clinical and experimental intestinal inflammation [16, 29]. TL1A induced Th17 immune response in cooperation with IL-23 in the CD pathogenesis [30]. Recent studies reported that the soluble TL1A levels increased in UC [31, 32]. Herein, we corroborated these findings by showing the increase of soluble TL1A levels in UC as well as the mucosal TL1A mRNA expression. It was the first evidence that the TL1A mRNA and protein expression levels were increased in Chinese UC patients.

Our results implied that the rs4263839 SNP polymorphism of TNFSF15, which was associated with UC patients in our previous data, might be unable to fully affect the serum TL1A levels. Then we evaluated the possible relationship of serum TL1A levels with clinical features of UC patients. Like IL-12p40, there was a significant correlation between serum TL1A levels and course or disease behavior. The polymorphism of decoy receptor 3 (DcR3), another TL1A receptor, was also associated with the pediatric onset UC [33]. Our results also suggested that serum TL1A level may act as a risk factor on the onset phase of active UC patients. Different from IL-12p40, we found that serum TL1A levels were higher in UC patients without extraintestinal manifestations, presumably because the patients in the cohort was limited and/or serum TL1A levels may be affected by the UC patient distribution.

As we know, IL-23/IL-23R activated JAK2/STAT3 to induce Th17 cell differentiation and this pathway contributed to the IBD pathogenesis [810]. Various studies delineated the effect of JAK2 on mediating intestinal inflammation [14, 34, 35]. Our unpublished results found that polymorphisms of IL-23R and JAK2 were associated with UC and CD, so we further demonstrated that the mRNA and protein levels of IL-23R and JAK2 were increased in intestine mucosa of IBD patients. Similarly, it was also reported that IL-23R-positive cells were significantly increased in NK cells and some kinds of T cells in IBD patients while the JAK2 mRNA expression was upregulated in CD patients [36, 37].

Finally, besides IL-12p40, TL1A, IL-23R, and JAK2 mentioned in this research, IL-23/Th17 pathway cytokines in IBD also included IL-23p19, STAT3, IL-17, and IL-22 [2, 3]. Our unpublished study did not find their polymorphisms to be associated with IBD in Chinese population. However, it was reported that Th17 cells may be responsible for the deleterious effects through IL-17 expression and/or the beneficial effects through IL-22 production, which meant that these cytokines may play potential roles in IBD [38, 39]. Moreover, IL-17 could activate stromal, endothelial, and epithelial cells to produce cytokines and chemokines, which not only help neutrophil recruit into tissues, but also induce inflammatory cytokine production by macrophages [40]. Thus, further investigations on the mechanisms of IL-23/Th17 cytokines are still needed.

5. Conclusion

Taken together, our data was the first comprehensive finding to evaluate the relationship between IL-23/Th17 pathway and IBD in Chinese population. We found that the expression of IL-23/Th17 pathway genes was both locally and systemically elevated in IBD patients. Furthermore, we demonstrated that the serum IL-12p40 and TL1A levels were not associated with the gene polymorphism but were highly expressed in the early onset and active condition of UC patients. Together, IL-23/Th17 pathway genes may represent important biomarkers of active inflammation in Chinese IBD patients, and they were new potential therapeutic targets for IBD.

Conflict of Interests

All authors declare no conflict of interests.

Acknowledgments

The authors thank all individuals who participate in this study. This work was supported by the National Natural Science Foundation of China (no. 81070280) and the Fundamental Research Funds for the Central Universities of China (nos. 201130302020004 and 2012303020201).

References

  1. G. Bouma and W. Strober, “The immunological and genetic basis of inflammatory bowel disease,” Nature Reviews Immunology, vol. 3, no. 7, pp. 521–533, 2003. View at: Publisher Site | Google Scholar
  2. C. W. Lees, J. C. Barrett, M. Parkes, and J. Satsangi, “New IBD genetics: common pathways with other diseases,” Gut, vol. 60, no. 12, pp. 1739–1753, 2011. View at: Publisher Site | Google Scholar
  3. M. S. Silverberg, J. H. Cho, J. D. Rioux et al., “Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study,” Nature Genetics, vol. 41, no. 2, pp. 216–220, 2009. View at: Publisher Site | Google Scholar
  4. M. Parkes, J. C. Barrett, N. J. Prescott et al., “Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility,” Nature Genetics, vol. 39, no. 7, pp. 830–832, 2007. View at: Publisher Site | Google Scholar
  5. R. Thiébaut, S. Kotti, C. Jung et al., “TNFSF15 polymorphisms are associated with susceptibility to inflammatory bowel disease in a new European cohort,” The American Journal of Gastroenterology, vol. 104, no. 2, pp. 384–391, 2009. View at: Publisher Site | Google Scholar
  6. S. C. Ng, K. K. Tsoi, M. A. Kamm et al., “Genetics of inflammatory bowel disease in Asia: systematic review and meta-analysis,” Inflammatory Bowel Diseases, vol. 18, no. 6, pp. 1164–1176, 2012. View at: Publisher Site | Google Scholar
  7. Z. Chen, S. R. Brant, C. Li et al., “CTLA4-1661A/G and 3′UTR long repeat polymorphisms are associated with ulcerative colitis and influence CTLA4 mRNA and protein expression,” Genes and Immunity, vol. 11, no. 7, pp. 573–583, 2010. View at: Publisher Site | Google Scholar
  8. R. H. Duerr, K. D. Taylor, S. R. Brant et al., “A genome-wide association study identifies IL23R as an inflammatory bowel disease gene,” Science, vol. 314, no. 5804, pp. 1461–1463, 2006. View at: Publisher Site | Google Scholar
  9. S. Brand, “Crohn's disease: Th1, Th17 or both? The change of a paradigm: new immunological and genetic insights implicate Th17 cells in the pathogenesis of Crohn's disease,” Gut, vol. 58, no. 8, pp. 1152–1167, 2009. View at: Publisher Site | Google Scholar
  10. C. Abraham and J. Cho, “Interleukin-23/Th17 pathways and inflammatory bowel disease,” Inflammatory Bowel Diseases, vol. 15, no. 7, pp. 1090–1100, 2009. View at: Publisher Site | Google Scholar
  11. C. Parham, M. Chirica, J. Timans et al., “A receptor for the heterodimeric cytokine IL-23 is composed of IL-12Rβ1 and a novel cytokine receptor subunit, IL-23R,” Journal of Immunology, vol. 168, no. 11, pp. 5699–5708, 2002. View at: Google Scholar
  12. C. L. Langrish, B. S. McKenzie, N. J. Wilson, R. de Waal Malefyt, R. A. Kastelein, and D. J. Cua, “IL-12 and IL-23: master regulators of innate and adaptive immunity,” Immunological Reviews, vol. 202, pp. 96–105, 2004. View at: Publisher Site | Google Scholar
  13. C. A. Anderson, G. Boucher, C. W. Lees et al., “Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47,” Nature Genetics, vol. 43, no. 3, pp. 246–252, 2011. View at: Publisher Site | Google Scholar
  14. C. A. Anderson, D. C. Massey, J. C. Barrett et al., “Investigation of Crohn’s disease risk loci in ulcerative colitis further defines their molecular relationship,” Gastroenterology, vol. 136, no. 2, pp. 523–529, 2009. View at: Publisher Site | Google Scholar
  15. W. R. Best, J. M. Becktel, J. W. Singleton, and F. Kern Jr., “Development of a Crohn's disease activity index. National cooperative Crohn's disease study,” Gastroenterology, vol. 70, no. 3, pp. 439–444, 1976. View at: Google Scholar
  16. G. Bamias, M. Mishina, M. Nyce et al., “Role of TL1A and its receptor DR3 in two models of chronic murine ileitis,” Proceedings of the National Academy of Sciences of the United States of America, vol. 103, no. 22, pp. 8441–8446, 2006. View at: Publisher Site | Google Scholar
  17. A. Zwiers, L. Kraal, T. C. van de Pouw Kraan, T. Wurdinger, G. Bouma, and G. Kraal, “Cutting edge: a variant of the IL-23R gene associated with inflammatory bowel disease induces loss of microRNA regulation and enhanced protein production,” Journal of Immunology, vol. 188, no. 4, pp. 1573–1577, 2012. View at: Publisher Site | Google Scholar
  18. M. Jürgens, R. P. Laubender, F. Hartl et al., “Disease activity, ANCA, and IL23R genotype status determine early response to infliximab in patients with ulcerative colitis,” The American Journal of Gastroenterology, vol. 105, no. 8, pp. 1811–1819, 2010. View at: Publisher Site | Google Scholar
  19. M. S. Silverberg, J. Satsangi, T. Ahmad et al., “Toward an integrated clinical, molecular and serological classification of inflammatory bowel disease: Report of a Working Party of the 2005 Montreal World Congress of Gastroenterology,” Canadian Journal of Gastroenterology, vol. 19, supplement A, pp. 5A–36A, 2005. View at: Google Scholar
  20. S. C. Truelove and L. J. Witts, “Cortisone in ulcerative colitis; final report on a therapeutic trial,” British Medical Journal, vol. 2, no. 4947, pp. 1041–1048, 1955. View at: Google Scholar
  21. K. J. Livak and T. D. Schmittgen, “Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method,” Methods, vol. 25, no. 4, pp. 402–408, 2001. View at: Publisher Site | Google Scholar
  22. O. Shimozato, S.-I. Ugai, M. Chiyo et al., “The secreted form of the p40 subunit of interleukin (IL)-12 inhibits IL-23 functions and abrogates IL-23-mediated antitumour effects,” Immunology, vol. 117, no. 1, pp. 22–28, 2006. View at: Publisher Site | Google Scholar
  23. S. A. McCarroll, A. Huett, P. Kuballa et al., “Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease,” Nature Genetics, vol. 40, no. 9, pp. 1107–1112, 2008. View at: Publisher Site | Google Scholar
  24. K. Asano, T. Matsushita, J. Umeno et al., “A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population,” Nature Genetics, vol. 41, no. 12, pp. 1325–1329, 2009. View at: Publisher Site | Google Scholar
  25. D. P. McGovern, A. Gardet, L. Törkvist et al., “Genome-wide association identifies multiple ulcerative colitis susceptibility loci,” Nature Genetics, vol. 42, no. 4, pp. 332–337, 2010. View at: Publisher Site | Google Scholar
  26. D. J. Kim, K. S. Kim, M. Y. Song et al., “Delivery of IL-12p40 ameliorates DSS-induced colitis by suppressing IL-17A expression and inflammation in the intestinal mucosa,” Clinical Immunology, vol. 144, no. 3, pp. 190–199, 2012. View at: Google Scholar
  27. K. Sato, A. Suematsu, K. Okamoto et al., “Th17 functions as an osteoclastogenic helper T cell subset that links T cell activation and bone destruction,” Journal of Experimental Medicine, vol. 203, no. 12, pp. 2673–2682, 2006. View at: Publisher Site | Google Scholar
  28. H. H. Uhlig, B. S. McKenzie, S. Hue et al., “Differential activity of IL-12 and IL-23 in mucosal and systemic innate immune pathology,” Immunity, vol. 25, no. 2, pp. 309–318, 2006. View at: Publisher Site | Google Scholar
  29. T.-S. Migone, J. Zhang, X. Luo et al., “TL1A is a TNF-like ligand for DR3 and TR6/DcR3 and functions as a T cell costimulator,” Immunity, vol. 16, no. 3, pp. 479–492, 2002. View at: Publisher Site | Google Scholar
  30. N. Kamada, T. Hisamatsu, H. Honda et al., “TL1A produced by lamina propria macrophages induces Th1 and Th17 immune responses in cooperation with IL-23 in patients with Crohn's disease,” Inflammatory Bowel Diseases, vol. 16, no. 4, pp. 568–575, 2010. View at: Publisher Site | Google Scholar
  31. G. Bamias, G. Kaltsa, S. I. Siakavellas et al., “High intestinal and systemic levels of decoy receptor 3 (DcR3) and its ligand TL1A in active ulcerative colitis,” Clinical Immunology, vol. 137, no. 2, pp. 242–249, 2010. View at: Publisher Site | Google Scholar
  32. G. Bamias, C. Martin III, M. Marini et al., “Expression, localization, and functional activity of TL1A, a novel Th1-polarizing cytokine in inflammatory bowel disease,” Journal of Immunology, vol. 171, no. 9, pp. 4868–4874, 2003. View at: Google Scholar
  33. S. Kugathasan, R. N. Baldassano, J. P. Bradfield et al., “Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease,” Nature Genetics, vol. 40, no. 10, pp. 1211–1215, 2008. View at: Publisher Site | Google Scholar
  34. A. Franke, T. Balschun, T. H. Karlsen et al., “Replication of signals from recent studies of Crohn's disease identifies previously unknown disease loci for ulcerative colitis,” Nature Genetics, vol. 40, no. 6, pp. 713–715, 2008. View at: Publisher Site | Google Scholar
  35. K. Wang, H. Zhang, S. Kugathasan et al., “Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn disease,” The American Journal of Human Genetics, vol. 84, no. 3, pp. 399–405, 2009. View at: Publisher Site | Google Scholar
  36. C. L. Noble, A. R. Abbas, C. W. Lees et al., “Characterization of intestinal gene expression profiles in Crohn's disease by genome-wide microarray analysis,” Inflammatory Bowel Diseases, vol. 16, no. 10, pp. 1717–1728, 2010. View at: Publisher Site | Google Scholar
  37. Z. Liu, P. K. Yadav, X. Xu et al., “The increased expression of IL-23 in inflammatory bowel disease promotes intraepithelial and lamina propria lymphocyte inflammatory responses and cytotoxicity,” Journal of Leukocyte Biology, vol. 89, no. 4, pp. 597–606, 2011. View at: Publisher Site | Google Scholar
  38. D. Yen, J. Cheung, H. Scheerens et al., “IL-23 is essential for T cell-mediated colitis and promotes inflammation via IL-17 and IL-6,” Journal of Clinical Investigation, vol. 116, no. 5, pp. 1310–1316, 2006. View at: Publisher Site | Google Scholar
  39. K. Sugimoto, A. Ogawa, E. Mizoguchi et al., “IL-22 ameliorates intestinal inflammation in a mouse model of ulcerative colitis,” Journal of Clinical Investigation, vol. 118, no. 2, pp. 534–544, 2008. View at: Publisher Site | Google Scholar
  40. J. K. Kolls and A. Lindén, “Interleukin-17 family members and inflammation,” Immunity, vol. 21, no. 4, pp. 467–476, 2004. View at: Publisher Site | Google Scholar

Copyright © 2013 Lu Song et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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