Journal of Immunology Research

Journal of Immunology Research / 2017 / Article
Special Issue

Genetic Factors of Autoimmune Diseases 2017

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Research Article | Open Access

Volume 2017 |Article ID 2185083 | 5 pages | https://doi.org/10.1155/2017/2185083

Polymorphisms of IL12RB2 May Affect the Natural History of Primary Biliary Cholangitis: A Single Centre Study

Academic Editor: Nancy Agmon-Levin
Received14 Sep 2016
Accepted30 Jan 2017
Published19 Feb 2017

Abstract

Background. Recent GWAS in primary biliary cholangitis (PBC) showed strong associations with SNPs located within interleukin-12 receptor (IL12R) beta-2 (IL12RB2) gene. Aims. We assessed whether genetic variation of IL12RB2 is associated with laboratory and clinical features of PBC. Methods. Genomic DNA was isolated from 306 patients with PBC and 258 age/gender-matched controls. PBC-specific anti-mitochondrial antibodies (AMA) were tested in all subjects by ELISA. Two SNPs, rs3790567 and rs6679356, of IL12RB2 were genotyped using the MGB-TaqMan SNP assay. Results. Despite comparable age at diagnosis of cirrhotic and noncirrhotic PBC patients, allele A of rs3790567 and allele C of rs6679356 were overrepresented in the former rather than the latter group ( and , resp.). The risk of cirrhosis at presentation increased when allele A and allele C coexisted. AMA-M2 titres were significantly higher in AA homozygotes of rs3790567 compared to GG homozygotes ( versus , ) and in rs6679356 when C allele was present (). There were no other significant associations between IL12RB2 polymorphisms and laboratory or clinical features. Conclusion. In this first study analyzing phenotypic features of PBC carriers of the IL12RB2 polymorphisms, we found that carriers are more frequently cirrhotic at diagnosis and have significantly higher titres of AMA.

1. Introduction

Interleukin-12 (IL-12) belongs to the IL-12 family cytokines along with IL-23, IL-27, and IL-35. IL-12 is a heterodimer comprised of two subunits: a 35 kDa (p35) light chain encoded by IL12A gene and a 40 kDa heavy chain (p40), encoded by IL12B gene. The synthesis and secretion of IL-12 occur via stimulation of Toll-like receptors expressed by antigen presenting cells (APCs) in response to microbial constituents [1, 2]. IL-12 exerts its immunobiological action through its binding to specific IL-12 receptors (IL-12Rs), termed IL-12Rβ1 and IL-12Rβ2, which are mapped on chromosomes 19p13.1 and 1p31.2, respectively [13]. Secreted IL-12 targets naive T cells, NK cells, and NKT cells and promotes their proliferation and differentiation. The most significant function of IL-12 is its involvement in the differentiation of T-helper 1 from naive CD4+ T cells resulting in the secretion of the proinflammatory interferon-γ (IFN-γ) cytokine [14].

Primary biliary cholangitis (PBC), formerly known as primary biliary cirrhosis [5, 6], is an autoimmune cholestatic liver disease, affecting up to 1 in 1000 women over 40 years of age with complaints such as fatigue and/or pruritus [79]. The hallmark of PBC is the presence of high-titre anti-mitochondrial autoantibodies (AMA) and the accumulation of antigen-specific autoreactive B and (CD4+ and CD8+) T cells targeting biliary epithelial cells [10]. Studies on patients with PBC, experimental work on animal models, and in vitro studies indicate a potential role of the IL-12 pathway in the development of autoimmune cholangitis [11, 12]. There is evidence for a pathogenic role for IL-12B in experimental murine model of PBC. It has been demonstrated that deletion of the IL-12B on the transforming growth factor β receptor II dominant negative (dnTGFβRII) murine model of PBC results in the amelioration of cholangitis [13].

Genetic studies provided additional support in favour of the instrumental role of IL-12 in the immunopathogenesis of PBC. Genome wide association studies (GWAS) provided evidence that PBC displays a strong association with SNPs located within the IL12A as well as within IL12RB2 gene [14, 15]. The involvement of the IL-12 pathway in PBC could be indirectly supported by associations found between PBC and several SNPs across the STAT4 gene, which encodes an effector that is essential for interleukin-12 signaling [16]. To better understand the extent of involvement of IL-12 in PBC, we analyzed the potential association between two SNPs located in the IL-12R2 gene and phenotypic features of PBC in a well-defined cohort of patients with PBC.

2. Methods

2.1. Patients and Controls

All patients with PBC fulfilled the diagnostic criteria established by the European Association for the Study of Liver (EASL) [17]. The study was performed in a homogenous group of Caucasian patients with PBC who were treated in two Polish liver transplant centres, in Szczecin and in Warsaw. Patients recruited at both sites did not differ in terms of demographic, clinical, and biochemical characteristics (data not shown). One hundred and seven (36.5%) subjects were diagnosed with liver cirrhosis, by either liver biopsy or imaging screening. Data on cirrhosis status were not available in 28 patients. Clinical and laboratory features of analyzed subjects are summarized in Table 1. Health-related quality of life (HRQoL) was assessed with disease-specific questionnaires (PBC-40 and PBC-27) [18]. PBC-specific AMA were tested by ELISA (Inova Diagnostics, San Diego, CA, USA).


PBCPBCp value
(cirrhotic versus noncirrhotic)
NoncirrhoticCirrhotic

Age (years)NS
Gender (female/male)277/29152/689/18
Liver cirrhosis (yes/no/unknown)107/158/41158107
Death or OLTx (yes/no/unknown)66/214/2617/13342/61
UDCA response (yes/no/unknown)81/120/10546/4724/56
ALP (IU/l; mean ± SD; normal: 30–120)NS
ALT (IU/l; mean ± SD; normal: 3–30)NS
AST (IU/l; mean ± SD; normal: 3–30)NS
γ-GT (IU/l; mean ± SD; normal: 3–30)NS
Bilirubin (mg/dl; mean ± SD; normal: 0.2–1.0)NS

Control group was comprised of 258 age- and gender-matched subjects without liver diseases. These controls were also tested for AMA using the same ELISA.

2.2. Genotyping

Genomic DNA from peripheral blood mononuclear cells was isolated using the DNeasy Blood & Tissue Kit (Qiagen). Oligonucleotide primers and TaqMan probes for IL-12R2 polymorphisms (rs3790567, rs6679356) were designed and synthesized by Applied Biosystems. The fluorescence data were analyzed with allelic discrimination 7500 Software v.2.0.2.

2.3. Ethics

Appropriate informed consent was obtained from each patient included in the study. The study protocol was approved by the Ethics Committee of Pomeranian Medical University and Medical School of Warsaw. They conformed to the Ethical Guidelines of the 1975 Declaration of Helsinki (6th revision, 2008).

2.4. Statistical Analysis

Data are shown as means and standard deviations. All statistical analyses (chi-square, odds ratios, and confidence intervals) were carried out using StatView software (Cary, NC, USA). The genotype and allelic frequencies were compared between patients and controls using Fisher’s PLSD test. The analysis of genotype frequency within PBC patients in regard to the clinical characteristics was performed using Fisher’s PLSD test. The general genotype-dependent survivals were estimated using the Kaplan-Meier survival curves.

3. Results

3.1. Distribution of IL12RB2 Polymorphisms in Patients with PBC and Controls

The allele A of rs3790567 and allele C of rs6679356 were overrepresented in PBC patients compared to controls, 30.4% versus 20.7% () and 25% versus 17.2% (), respectively, confirming a significant impact of IL12RB2 polymorphisms on PBC susceptibility (Table 2).


SNPGenotypeCount of alleles/genotypesFisher exact
value
OR
Control () (%)PBC () (%)

rs3790567A/G107/409 (20.7/79.3)186/426 (30.4/69.6)0.000911.51.7 [1.3–2.2]
AA11 (4.2)29 (9.5)0.025.82.3 [1.1–4.8]
AG85 (33)128 (42)0.024.71,5 [1.0–2.1]
GG162 (62.8)149 (48.5)0.000911.30.6 [0.4–0,8]

rs6679356C/T89/427 (17.2/82.8)153/459 (25/75)0.0029.51.6 [1.2–2.1]
CC11 (4.2)22 (7.2)NS2.21,7 [0.8–3.6]
CT67 (26)109 (35.6)0.016.11,6 [1.1–2.3]
TT180 (69.8)175 (57.2)0.035.10,6 [0.4–0.8]

3.2. Association of rs3790567 and rs6679356 with Liver Cirrhosis

The frequency distributions of the rs3790567 and rs6679356 genotype in cirrhotic and noncirrhotic patients are shown in Table 3. Allelic analysis demonstrated that allele A of rs3790567 and allele C of rs6679356 were overrepresented in patients with histological and/or clinical features of liver cirrhosis (38% versus 25%, and 31% versus 20.8%, , resp.). Moreover, subjects who were GG homozygote of the rs3790567 were overrepresented in noncirrhotic group (), similarly to subjects who were TT homozygote of rs6679356 (). The risk of cirrhosis increased when A (rs3790567) allele and C (rs6679356) allele coexisted ().


SNPGenotype Cirrhosis ()Fisher exact 
value
OR
No (%)Yes (%)

rs3790567A/G83 (25%)/247 (75%)84 (38%)/138 (62%)0.00110.121.8 [1.3–2.6]
AA12 (7.3%)16 (14.4%)NS3.712.1 [0.9–4.7]
AG59 (35.7%)52 (46.9%)NS3.391.6 [0.9–2.6]
GG94 (57%)43 (38.7%)0.0038.820.5 [0.3–0.8]

rs6679356C/T69 (20.8%)/263 (79.2%)68 (31%)/152 (69%)0.0137.271.7 [1.1–2.5]
CC10 (6%)12 (10.9%)NS2.151.9 [0.8–4.6]
CT49 (29.5%)44 (40%)NS3.251.6 [0.9–2.6]
TT107 (64.5%)54 (49.1%)0.0096.430.5 [0.3–0.9]

3.3. The Association of rs3790567 and rs6679356 with Features of PBC

A positive association between IL12RB2 polymorphisms and the PBC-specific AMA-M2 concentration was found in patients with PBC. The AA-carriers of rs3790567 were characterized by an increased concentration of AMA-M2 in comparison to GG-carriers () (Table 4). The association of rs6679356 genotypes with higher AMA-M2 concentrations has not been observed. However, higher serum AMA-M2 was associated with the presence of allele C (). No other associations between polymorphism distribution and clinical or laboratory features of PBC were found.


SNPGenotypeCount of genotypes ()AMA level-mean [IU/l]

rs3790567A/G177/413NS
AA27AA versus GG
AG123
GG145

rs6679356C/T147/4430.0384
CC21CC versus TT
NS
CT105
TT169

AMA: anti-mitochondrial antibody.

4. Discussion

IL-12 activates through its receptor’s subunits a cascade of signaling factors such as NFKβ and STAT4 to promote the production of proinflammatory Th1-type cytokines including TNFα and IFNγ, as well as to enhance the cytotoxic response of NK, NKT, and CD8+ T cells [19]. Genetic association data that have emerged from GWAS highlighted a relationship between the IL-12/STAT4/Th1 pathway and PBC [14, 15, 20, 21]. Two SNPs, namely, rs3790567 and rs6679356, in the intronic regions downstream of IL12RB2 showed strong associations with PBC in a Canadian PBC cohort when compared to controls [20]. Another GWAS on Italian PBCs confirmed disease’s association with rs3790567 [14].

Such GWAS are by nature unable to assess whether SNPs are associated with features of the disease, namely, presence of cirrhosis at diagnosis, fibrosis stage, liver biochemical indexes, and response to treatment or magnitude of autoantibody response. In the present study, we evaluated the association between IL12RB2 polymorphisms and PBC in a cohort of Caucasian individuals with PBC and unaffected controls. As clinicians are more interested to know whether specific genetic markers are associated with features of the disease, we analyzed the potential association between rs3790567 and rs6679356 and clinical or laboratory features of the disease in our PBC cohort.

Our study, including a homogenous cohort of more than 300 Caucasian patients with PBC, confirmed the GWAS findings; the allele A of rs3790567 and allele C of rs6679356 are indeed overrepresented in PBC compared to disease-free controls. In view of the aforementioned associations, we considered our cohort an adequate population to further investigate the potential relationship between such polymorphisms and laboratory as well as clinical features of the disease.

In PBC, small and medium-size intrahepatic bile ducts are destroyed by an autoimmune attack which if left untreated could lead to liver cirrhosis in a proportion of patients with PBC. At times, patients present with cirrhosis and a diagnosis of PBC is made at presentation, based on laboratory, immunological, and clinical features compatible with the autoimmune cholestatic nature of the disease. Our allelic analysis demonstrated that the allele A of rs3790567 and the allele C of rs6679356 significantly increased risk of cirrhosis at the diagnosis. The IL-12 signaling pathway is a key player in the effector mechanisms that lead to biliary destruction and subsequent liver cirrhosis. IL-12Rβ2 is upregulated by IFNγ triggered by IL-12; thus in this case cytokine-receptor interaction provides a positive feedback loop further promoting biliary epithelial cell damage. Since IL-12-dependent, self-perpetuating autoimmune mechanism appears to be responsible for cholangiocyte destruction, it is reasonable to expect a more progressive pace of the disease in patients who carry specific IL12RB2 polymorphisms.

The characteristic immunological hallmark of PBC is the presence of disease-specific M2-AMA in serum of affected patients [22]. More than 90% of PBC patients have detectable AMA, but their titres vary amongst affected individuals. Our data show that analyzed IL12RB2 polymorphisms were associated with significantly higher AMA-M2 titres. IL-12 is secreted by activated APCs. It is likely that their activation occurs via release of E2 subunit mitochondrial pyruvate dehydrogenase autoantigen (PDC-E2) during apoptosis of biliary epithelial cells (BECs) [23, 24]. PDC-E2 is endocytosed by APC and this endocytosis leads to APC maturation and IL-12 secretion which provides the cytokine milieu which is essential for the maintenance of the continuum of proinflammatory T-helper type 1 (Th1) induction arising from naive CD4+ T through antigen presentation; such antigen-specific CD4 T cells help plasmocytes to produce high-titre AMA targeting PDC-E2. IL-12Rβ2 appears to be pivotal for the continuation of this deleterious positive feedback. Though our study is the first to identify IL12RB2 polymorphisms positively associated with the magnitude of AMA response, this is not the first time that an association between IL12RB2 and high-titre autoantibodies has been found in autoimmune diseases, providing a link between the IL-12/IL-12R axis and the scale of the autoimmune attack at the humoral level. This is not the first time that an association between autoantibody status and IL12-IL12R/STAT4 polymorphisms has been reported. In fact, Joshita et al. [16] have found an association between three STAT4 PBC risk alleles (rs7574865, rs8179673, and rs10181656) with ANA status (but not with AMA positivity) in Japanese patients with PBC; IL12R polymorphisms do not appear to be risk alleles in non-Caucasian patients, and in particular those originated from Japan, and this may explain why associations were not reported by the former study between AMA or ANA with IL12R alleles. In systemic lupus erythematosus, the presence of anti-dsDNA antibodies is also associated with rs7574865 within STAT4, further highlighting the close relationship between the immunogenetic make-up of the autoimmune disease and pathognomonic immunological features, such as disease-related autoantibodies [25].

We found no association between analyzed polymorphisms and liver biochemistry indexes; this is not unexpected as liver cirrhosis is a “burnt out” condition characterized by low aminotransferase levels. We have recently published that patients with PBC have impaired HRQoL, irrespectively of whether they are cirrhotic or not [18]; thus an association between the analyzed polymorphisms and HRQoL measures depicted by the PBC-40 or PBC-27 questionnaires would be rather unlikely; this appears to be the case, as our analysis failed to identify significant associations.

In conclusion, we have confirmed the relationship of IL12RB2 polymorphisms with PBC susceptibility. Moreover, we have provided evidence that IL12RB2 polymorphisms are associated with liver cirrhosis and an increased concentration of disease-specific AMA in sera of PBC patients. Larger, multicentre studies are warranted to assess the diagnostic and prognostic significance of our findings in a more comprehensive manner.

Competing Interests

The authors declare that there is no conflict of interests regarding the publication of this paper.

Acknowledgments

Piotr Milkiewicz was supported by Grant no. 2011/02/A/NZ5/00321 from National Science Centre, Poland.

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Copyright © 2017 Urszula Wasik 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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