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BioMed Research International
Volume 2014 (2014), Article ID 710642, 8 pages
Impact of Immunogenetic IL28B Polymorphism on Natural Outcome of HCV Infection
1Bio-Proteomics Facility, Department of Translational Research, CRO, National Cancer Institute, 33081 Aviano, Italy
2Interdepartmental Center for Systemic Manifestations of Hepatitis Virus MASVE, Department of Experimental and Clinical Medicine, University of Florence, 50121 Florence, Italy
3Hepatobiliary Unit, National Cancer Institute “Fondazione Pascale”, 80138 Naples, Italy
4Liver Unit, IRCCS Casa Sollievo della Sofferenza Hospital, 71013 San Giovanni Rotondo, Italy
5Cytogenetics and Molecular Biology Unit, Santa Maria degli Angeli Hospital Pordenone, 33170 Pordenone, Italy
6Internal Medicine-Liver Unit, Santa Maria degli Angeli Hospital Pordenone, 33170 Pordenone, Italy
7Immunology Section, Department of Biomedical Sciences and Human Oncology, University of Bari Medical School, 70121 Bari, Italy
8Clinic of Rheumatology, Department of Medical and Biological Sciences, University Hospital Santa Maria della Misericordia, 33100 Udine, Italy
9Hematology and Transplant Unit, San Gerardo Hospital, University of Milano-Bicocca, Monza, Italy
10Medical Oncology, Centro di Riferimento Oncologico, 33081 Aviano, Pordenone, Italy
11Epidemiology and Biostatistics, Centro di Riferimento Oncologico, IRCCS, 33081 Aviano, Italy
12Molecular Biology and Viral Oncology, National Cancer Institute “Fondazione Pascale”, 80138 Naples, Italy
Received 27 September 2013; Revised 19 November 2013; Accepted 20 November 2013; Published 26 February 2014
Academic Editor: Maria Lina Tornesello
Copyright © 2014 Valli De Re 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.
With the aim of investigating whether interleukin 28B gene (IL28B) rs1297860 polymorphism is associated with different hepatitis C (HCV) infection statuses, we compared IL28B allelic distribution in an Italian case series of 1050 patients with chronic infection and different outcomes, 47 individuals who spontaneously cleared HCV, and 178 blood donors. Furthermore, we compared IL28B variants among 3882 Caucasian patients with chronic infection, 397 with spontaneous clearance, and 1366 blood donors reported in PubMed. Overall data confirmed a relation between IL28B C allele and HCV spontaneous clearance. Furthermore, we found that IL28B T allele had a weak relation with chronic HCV progression to hepatocellular carcinoma. Study findings are in accordance with the hepatocellular carcinogenic model where IL28B TT genotype, by promoting a persistent chronic hepatitis which leads to both hepatocyte injury and chronic inflammation, could facilitate HCC development. Conversely, patients with lymphoproliferative disorders had not any significantly different IL28B rs1297860 allelic distribution than those with chronic HCV, but, like all chronic HCV-related diseases, they showed a lower CC frequency than patients who spontaneously cleared HCV. Study results confirmed the model of persistent HCV infection as a risk factor for the pathogenesis of both liver and lymphoproliferative disorders.
Hepatitis C virus (HCV), a positive-strand RNA virus widely diffused (about 2-3%) around the world, is a major causative agent of chronic liver diseases, including hepatitis, cirrhosis, and hepatocellular carcinoma (HCC) [1, 2]. HCV infection is also associated with lymphoproliferative disorders, represented by mixed type II cryoglobulinemia (MC) and B-cell non-Hodgkin’s lymphomas (NHLs) [3–6]. The reason for such different outcome of HCV infection among patients is still largely unknown.
Traditional therapy for treatment of chronic HCV involves pegylated type I IFN (PEG-IFN) in combination with ribavirin. This treatment eradicates HCV infection in only 40%–50% of patients infected with genotypes 1 or 4 and 75%–90% of those infected with genotypes 2 or 3 [7, 8]. However, adverse effects due to this treatment regimen frequently lead to poor tolerance.
Recent studies have reported that human genetic variants, in particular rs1297860 single nucleotide polymorphism (SNP), within or near the interleukin 28B gene (IL28B) are significantly associated with spontaneous HCV clearance as well as different outcomes of treatment with IFN/ribavirin therapy for chronic HCV infection [9–19]. The relation is more evident for HCV genotype 1 infection. These observations suggest an important role of IL28B against HCV infection and natural history of HCV outcomes.
IL28B is a member, along with IL-29 and IL-28A, of type III interferons, also termed interferon-lambda (IFN-λ). They have in common a strong antiviral function and induction of interferon stimulated genes (ISGs) [20–24].
IFN-λ signals through interferon-lambda receptor1 (IFNLR1) and interleukin-10 receptor2 (IL-10R2) result in STAT phosphorylation, dimer formation, nuclear translocation, and then induction of ISG expression and upregulation of major histocompatibility complex (MHC) class I .
IFN-λ responsiveness is restricted to specific cell types , partially because IFNLR1 tissue distribution is highly restricted . In contrast to the epithelial-like cells, fibroblasts and endothelial cells were completely unresponsive to IFN-λ. A good IFN-λ-induced response was shown in hepatic cells, with an increased IFNLR1 expression after viral infection . Naïve B and T cells, lymphocytes, and monocytes, although express adequate amounts of IFNLR1 receptor, respond poorly or not at all to IFN-λ . This implies the presence of specific mechanisms on the lymphoid tissues that may inhibit the IFN-λ response. This important functional difference in tissue response to IFN-λ may provide a clinical advantage from IFN-α as a treatment for chronic HCV infection, as IFN-λ is less likely to induce the leucopenia most often associated with IFN-α therapy and may be used in HCV patients who are resistant to IFN-α. Moreover, it was found that IFN-λ upregulates the production of cytokines by natural killer (NK) and T cells  and reduces the proliferation of regulatory T cells ; thus  it is supposed that lymphoid cells respond to IFN-λ by different signals than hepatic cells. Due to the responsiveness of most cell types to IFN-λ and a limited toxicity, IFN-λs are under study for clinical use not only for anti-HCV therapy but also as anticancer and antiviral drug .
The aim of this paper is to investigate whether a relation between IL28B rs12979860 polymorphism and severity of liver or lymphoproliferative diseases exists.
2. Material and Methods
We identified and reviewed papers published from 2009 to 2013 analyzing Caucasian HCV-infected patients for distribution of IL28B genetic variants, using the online database pubMed. Selected studies included in the analysis along with inclusion criteria were reported in Table 1.
We also analyzed the IL28B rs12979860 polymorphism in a case series of 1050 HCV-infected patients, 47 individuals who experienced spontaneous HCV clearance, and 178 blood donors, from a cohort of HIV- and HBV-negative Italian patients, referred to the following centers: MASVE Center, University of Florence, Florence; “Santa Maria degli Angeli” General Hospital, Pordenone; National Cancer Institute “Fondazione Pascale”, Naples; “Casa Sollievo della Sofferenza” Hospital, San Giovanni Rotondo; “Azienda Ospedaliero-Universitaria Consorziale Policlinico”, Bari; University Hospital “Santa Maria della Misericordia”, Udine; Ospedale san Gerardo-University of Milano-Bicocca, Monza; and National Cancer Institute “Centro di Riferimento Oncologico”, CRO Aviano National Cancer Institute. Our series of 1050 patients with chronic HCV infection included group of patients with absence of HCC or any sign/symptom of definite MC or NHL (CHC, ), patients with HCC (), patients with a definite MC syndrome, according to previously described criteria  (), and presence of a definite malignant B-cell NHL ().
2.2. IL28B Genotyping
Genomic DNA was extracted from peripheral blood which has been previously stored at −80°C.
IL28B genotyping was performed using a specific customized TaqMan SNP-genotyping Assay (rs12979860; Applied Bosystem, Foster City, CA, USA) based on allele-specific labeled probes on a Rotor Gene 6000 (Corbett Research, Sidney, Australia). Amplicon sequencing was used to validate the genotyping techniques.
2.3. Statistical Analysis
Frequencies (f) of IL28B rs12979860 C and T alleles and genotypes polymorphisms were determined individually by direct counting of the positive individuals for a specific genotype/allele polymorphism. The observed and expected genotype frequencies among the study groups were analyzed using the Hardy-Weinberg equilibrium theory. Differences in f between groups of selected patients were evaluated using Fisher’s exact test, Pearson’s chi-square () test (with Yates correction), or Cochran-Armitage test for trend in frequencies as appropriate . A two-sided value <0.05 was considered as statistically significant.
Reviewed data on IL28B variant distribution in different HCV outcomes and limited to Caucasian subjects were reported in Table 2. The genotype frequencies of the IL28B rs12979860 polymorphism were found in Hardy-Weinberg equilibrium in the blood donors group (Pearson’s = 0.09; df = 1; ). The IL28B rs12979860 C allele was related to a significant increase in spontaneous clearance of the virus in a dominant genetic model (CC versus CT + TT) employed to compare HCV+ patients presenting spontaneous viral clearance versus all other HCV+ subjects (Pearson’s = 148.9; ). Data indicates that C allele had an important role in the control of infection (Fisher’s test, , Figure 1).
A significant negative linear trend was detected in the order of the CC genotype frequencies of patients with an increasing severity of liver diseases (from 40% in CHC to 17% in HCC, Figure 2; Cochran-Armitage’s = 22.38, ), whereas a significant positive linear trend emerged for TT genotype frequencies (from 12.0% in CHC to 22.8% in HCC, Figure 2; Cochran-Armitage’s = 8.42, ), suggesting an important role of CC allele in the control of liver disease progression.
IL28B rs12979860 genotype frequencies found in our case series were similar to those reported in the literature (Table 3). We found a slightly increasing trend in TT genotype frequency in HCC (18.9%) with respect to that of CHC (12.7%), but difference was not statistically significant (Fisher’s test, ) (Figure 3). Given the modest increase in HCC risk we found and the low number of HCC cases included in this study (35 from the literature and 95 in our case series), replication studied using larger series of HCV+ HCC would need to confirm this finding. However, carriage of TT genotype in blood donors (7.9%) and in patients who spontaneously cleared the virus (2.1%) was lower than that found in our HCC series (Fisher’s test, and 0.003, resp.). Moreover, similar to that found in data from the literature, the frequency of CC genotype was significantly higher among patients who spontaneously cleared the virus compared to patients with CHC (Fisher’s test, ) (Table 3 and Figure 3).
As regards the lymphoproliferative disorders associated with HCV infection, the literature reported only one study including patients with autoimmune MC syndrome  and no study on NHL. Data obtained in our case series were reported in Table 3.
In MC, IL28B CC genotype frequency was found similar to that in blood donors (Figure 3); nonetheless, the carriage of TT genotype in MC (15.1%) was weakly higher than that among blood donors (7.9%, Fisher’s test, ) but not significantly higher than that among CHC patients (12.9, Fisher’s test, ). HCV positive patients with NHL (11.9%) were very similar to CHC patients; in this case the carriage of TT genotype was not significantly different.
Several studies have indicated that IL28B rs12979860 polymorphism has a role in the response of HCV infection and liver disease risk, but the knowledge of its overall effect on the natural history of hepatitis viral infection remains partial and limited to certain aspect in individual studies. In addition, data regarding the IL-28B rs12979860 risk towards a HCV-related lymphoproliferative disorder (MC or NHL) is even less known. Thus we conducted this study to evaluate relations between IL-28B rs12979860 CT polymorphism and natural history of HCV infection by using the following inclusion criteria: Caucasian individuals affected by HCV infection (excluding HBV or HIV co-infection) and different liver or lymphoproliferative diseases related to HCV progression. The analysis of aggregated data from the literature clearly indicated that IL-28B rs12979860 allelic frequencies were significantly different in patients who spontaneously cleared HCV infection in comparison to patients with chronic HCV infection. HCV+ patients who spontaneously cleared the infection carried the CC genotype in 68.8% of cases, while patients with chronic HCV infection and liver diseases carried this genotype in a range from 39.6% to 17.1%. The IL-28B C allele was inversely related to the risk of chronic and liver diseases with respect to both blood donors and patients who spontaneously eliminated the virus when the dominant genetic model (CC versus CT + TT) was employed, in agreement with previous idea that C allele is implicated in the control of HCV infection. In addition, although resulting from a limited number of cases analyzed ( from literature , in our series), the carriage of TT genotype and the presence of T allele were slightly prevalent in the HCC group of patients. Due to the weak effect of IL28B T allele found on the progression to HCC, replication of this analysis in a large number of cases is required to confirm our study finding. Anyhow, this finding is in accordance with the HCC carcinogenic model where IL28B T allele carriage was much more favorable to persistence of a chronic HCV infection, which leads to both hepatocyte injury and chronic inflammation in the liver, thus facilitating the HCC development [35–37].
We presented for the first time a comparative analysis of IL28B rs12979860 allelic distribution in patients with chronic HCV infection and lymphoproliferative diseases (Table 3 and Figure 3). No statistically significant differences in IL28B rs12979860 allelic distribution emerged between patients with lymphoproliferative disorders and other groups of patients or blood donors. It should be noted, however, that CC genotype was more frequent in patients with MC (144/352, 40.9%) than in those with malignant tumors taken together (HCC + NHL, 50/162, 30.9%, Fisher’s test , data not shown in Tables). Moreover, TT genotype was slightly more frequent, without reaching statistical significance maybe because of low numbers, in patients with an HCC (18.9%) than in those with a NHL (11.9%, Figure 3). These findings could suggest that patients with MC syndrome carrying IL28B rs12979860 CC, a genotype more favorable to resolve the infection, should contrast both liver and lymphoproliferative malignant diseases and that patients with TT genotype could be more predisposed to evolve towards an HCC than a malignant lymphoma.
In conclusion, study results on overall data from the literature and our case series confirmed that all chronic HCV-related disorders presented a lower frequency of C allele as compared to patients who spontaneously eliminated HCV, thus supporting the model of persistent HCV infection as an important risk factor for the pathogenesis of both liver and lymphoproliferative disorders [3, 6]. Moreover, an additional risk factor related to TT homozygosis and liver disease progression emerged from this study. Of note, since recently a polymorphism (ss469415590) of a new interferon gene, IFNL4, was found strongly associated with HCV clearance and was in high linkage disequilibrium with IL28B ; further studies are needed regarding IFNL4 polymorphism and its possible involvement in the HCV-related malignancies.
Conflict of Interests
The authors declare that there is no conflict of interests regarding the publication of this paper.
The work was supported by the Italian Association for Cancer Research (AIRC no. 10266).
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