Effect of haptoglobin on the treatment of chronic hepatitis B with interferon
- Authors:
- Published online on: June 11, 2019 https://doi.org/10.3892/etm.2019.7661
- Pages: 1417-1425
Abstract
Introduction
Chronic hepatitis B (CHB) is the most common infectious chronic liver disease in humans, with a total of 240 million patients suffering from chronic hepatitis. CHB causes >600,000 mortalities each year from complications of end-stage liver disease and hepatocellular carcinoma (1). Antiviral treatments approved and available in China for CHB infection include standard or pegylated (Peg-) interferon (IFN) and nucleos(t)ide analogs (NAs), including an L-nucleoside analog (lamivudine), acyclic nucleoside phosphonates (adefovirdipivoxil and tenofovirdisoproxilfumarate) and a D-cyclopentane class nucleoside analog (entecavir). However, drug resistance and high cost of these drugs limits their long-term efficacy (2).
IFN, including Peg-IFN and unmodified IFN, has direct antiviral activity and immune stimulating properties. As a result, it has been widely used in recent decades. Studies have indicated that patients who received IFN therapy had a lower risk of decompensated liver diseases (3,4). However, the available clinical data suggest that the antiviral efficacy of IFN therapy is currently not satisfactory. In clinical observation, the rate of effective IFN treatment was reported to be only 30–42% (5–7). Therefore, it is important to identify the factors that affect the treatment outcomes of patients with CHB who receive IFN therapy.
In the present study, isobaric tags for relative and absolute quantitation (iTRAQ)-based mass spectrometry (MS) was performed to quantify differentially expressed proteins (DEPs) between plasma samples from virological response (VR) patients before and after IFN therapy. DEPs are also sometimes referred to as ‘aberrantly expressed proteins’ in the present study when we wish to emphasize their biological and/or clinical relevance. The present iTRAQ analysis verified the likely importance of downregulated haptoglobin (Hp) expression after 48 weeks of IFN therapy. Serum Hp levels were lower in the VR group than in the non-VR group. Further in vitro experiments were conducted to verify the effects of Hp on IFN and on the clearance of hepatitis B virus (HBV). The present results suggest that Hp is a potentially useful target for the treatment of HBV and a marker for predicting the efficacy of IFN therapy.
Materials and methods
Subjects and plasma collection
In the present study, 38 patients with CHB who received 48 weeks of Peg-IFN monotherapy (180 µg/week) were followed up for ≥48 weeks from September 2014-November 2015 at the Department of Infectious Diseases, The Second Affiliated Hospital, Chongqing, China. These patients were hepatitis B surface antigen (HBsAg) positive for >6 months and were currently HBsAg and/or DNA HBV positive at the time of treatment. Following 48 weeks of Peg-IFN treatment, for hepatitis B envelope antigen (HBeAg)-positive patients with CHB, virological response (VR) was defined as HBeAg seroconversion and an HBV DNA level <2,000 IU/ml. For HBeAg-negative patients with CHB, VR was defined as an HBV DNA level <2,000 IU/ml, in accordance with American Association for the Study of Liver Diseases guidelines (7). Following 48 weeks of IFN treatment, 10 VR patients and 28 non-VR patients were identified. The Ethics Committee of Chongqing Medical University (Chongqing, China) approved the present study. Written informed consent was obtained from all participants prior to treatment. Table I presents the patient demographics and clinical pathological data. Serum samples were collected, according to the guidelines set forth by the Human Proteome Organization Plasma Proteome Project (8), at the initiation, midpoint and end of therapy (weeks 0, 24 and 48, respectively), and stored at −80°C.
iTRAQ labeling
A total of 10 individual samples from VR patients taken at 0, 24 and 48 weeks were mixed following treatment to create three sample pools. A ProteoPrep 20 Plasma Immunodepletion Kit (GE Healthcare Life Sciences, Shanghai, China) was used to deplete the most abundant proteins. A 2-D Quant kit (GE Healthcare Life Sciences) was used to measure the protein concentration of the immune depleted plasma. Protein samples were acetone precipitated at −20°C for 1 h and dissolved in lysis buffer, denatured at 60°C for 1 h and blocked in 1 µl cysteine at room temperature for 10 min. Each sample was digested with trypsin solution at 37°C overnight, and then labeled with the iTRAQ tags with iTRAQ reagents (Applied Biosystems; Thermo Fisher Scientific, Inc., Waltham, MA, USA) as follows: week 0, 113 tag; week 24, 114 tag; and week 48, 115 tag. The labeled samples were pooled prior to further analysis (9).
Peptide fractionation
The pooled iTRAQ labeled trypsin peptide samples were dissolved in 1% Pharmalyte and 8M urea and evenly coated on prehydrated immobilized pH gradient (IPG) strips (18 cm; pH 3–10). Samples were placed in an IPGphor system (GE Healthcare, Chicago, IL, USA)and subjected to isoelectric focusing at 68 kV/h. The adhesive strip was then cut into 36 sections (thickness, 0.5 cm). The peptides were extracted by incubating the gel sections in buffer A (2% acetonitrile, 0.1% formic acid) for 1 h at room temperature (10). These isolated peptides were freeze-dried, purified on a Discovery DSC-18 SPE column (Sigma-Aldrich; Merck KGaA, Darmstadt, Germany) and cryopreserved at −80°C prior to further use.
MS
The purified peptides were dissolved in buffer A at room temperature for 20 min with vortex oscillation and loaded on to a C18-PepMap (Dionex; Thermo Fisher Scientific, Inc.) column (100 µm × 3 cm, 3 µm, 150A) of a Dionex Ultimate 3000 system. The peptides were eluted with the following concentration gradient: 4% buffer B (98% acetonitrile, 0.1% formic acid) and 96% buffer A, 3 min; 4–10% buffer B, 7 min; 10–35% buffer B, 55 min; 35–100% buffer B, 25 min; 100% buffer B, 15 min; 96% buffer A, 20 min. The control flow rate was 0.3 µl/min and the eluted fractions were automatically injected for MS analysis. The mass spectrometer was set in the positive ion mode at a mass range of 300–1,800 m/z. The switching time between MS scan and MS/MS event acquisition was set to 2 sec. The two most intensely charged peptides >20 counts were selected for MS/MS. Dynamic exclusion criteria was set to 30 sec.
Protein identification and quantification was performed using Protein Pilot v2.0 (AB SCIEX, Framingham, MA, USA). MS/MS data were processed by searching the International Protein Index Human database v3.77 (11). Methyl methanethiosulfonate was set as a fixed modification. Proteins with ≥2 unique peptides were considered to be differentially expressed. The peak area of the iTRAQ tag molecule represents the relative quantification of the identified proteins in different samples, with a 95% confidence interval and a P-value <0.05.
ELISA
Commercial ELISA kits were used to measure the serum levels of Hp, hemoglobin subunit β (HBB) and isoform 1 of fibrinogen α chain (FGA) according to the manufacturer's instructions. Human Hp ELISA kit (cat. no. ab108856), human HBB ELISA kit (cat. no. ab137972) and human FGA ELISA kit (cat. no. ab19079) were purchased from Abcam (Cambridge, UK).
Cell line
The HepG2.2.15 cell line, which was derived from the hepatoblastoma-derived cell line HepG2 and contains >1-unit length of the HBV genome integrated into the host genomes (12), was used in the present study. Cells were cultured at 5% CO2 and 37°C in high-glucose Dulbecco's modified Eagle's medium (DMEM; GE Healthcare Life Sciences, Logan, UT USA) supplemented with 100 µg/ml streptomycin, 0.1% non-essential amino acids, 100 IU/ml penicillin, 1.0 mM sodium pyruvate, 2 mM glutamine and 10% fetal bovine serum (FBS; Gibco; Thermo Fisher Scientific, Inc.) (13).
Hp small interfering (si)RNA transfection
For functional studies, three siRNA duplexes against human Hp (SR302217A, 5′-GACCAGACCAAUGCAUAAGGCATT-3′; SR302217B, 5′-GGAGUGUACACACCUUAAACAAUGAGA-3′; and SR302217C, 5′-CGGAUAUCGCAGAUGACGGCUGCCC-3′) and a negative control (SR30004) were purchased from OriGene Technologies, Inc. (Rockville, MD, USA). Briefly, siRNA and Lipofectamine 2000 (Invitrogen; Thermo Fisher Scientific, Inc.) were diluted inmoderate Opti-MEM I medium (Gibco; Thermo Fisher Scientific, Inc.) for 5 min and incubated together for 20 min at room temperature. Subsequently 30–50% cells were plated into a 6-well plate and the transfection mixture added. The HepG2.2.15 cells were transfected with 20 nM of Hp-specific siRNA and a negative control. Following 6 h of transfection, the medium was replaced with DMEM medium containing 10% FBS and continued in culture for an additional 42 h. Cells were harvested 48 h following transfection for western blot analysis and reverse transcription-quantitative polymerase chain reaction (RT-qPCR) analysis. All experiments were performed at least in triplicate.
Western blotting
Cells were lysed at 4°C with non-ionic detergent lysis buffer (50 mM, pH 7.5 Tris-HCl; 0.5% IGEPAL; 150 mM NaCl; 1 mM, pH 8.0 EDTA; 0.5% Triton X; 50 mM sodium fluoride; 1 mM sodium orthovanadate; and protease inhibitors). The lysates were centrifuged at 15,294 × g at 4°C for 30 min. A 2-D Quant kit was used to determine the protein concentration. A total of 40 µg protein/lane was separated by 10% SDS-PAGE and transferred to polyvinylidene difluoride membranes. The membranes were blocked at room temperature for 1 h with 5% non-fat milk in Tris-buffered saline solution with Tween-20 (TBS-T) and incubated overnight with the primary antibodies (all 1:500) in TBST plus 5% bovine serum albumin (Beijing Solarbio Science & Technology Co., Ltd., Beijing, China) at 4°C. After washing three times with TBS-T buffer for 5 min, the membranes were incubated with a horseradish peroxidase-conjugated goat anti-rabbit IgG as the secondary antibody (1:5,000) for 1 h at room temperature. Proteins were visualized with an enhanced chemiluminescencedetection system (Bio-Rad Laboratories, Hercules, CA, USA) (9,14). The densitometry was analysed by ImageJ v1.51 (National Institutes of Health, Bethesda, MD, USA). Anti-Hp antibody(cat. no. ARG55106) was purchased from Arigo Biolaboratories (Taiwan, R.O.C. China), anti-GAPDH antibody (cat. no. ab181602) was purchased from Abcam, and the secondary antibody (cat. no. ATA0011) was purchased from ATgene Biotech (Chongqing, China).
RT-qPCR
Total RNA was isolated from the transfected cells using TRIzol reagent (Gibco; Thermo Fisher Scientific, Inc.) and reversed-transcribed using a Revert Aid First Strand cDNA Synthesis kit (Thermo Fisher Scientific, Inc.) according to the manufacturer's protocol. cDNA was quantified via qPCR with a KAPA SYBR FAST qPCR kit Master Mix (2X) Universal HBV detection kit (Roche Diagnostics, Basel, Switzerland) on a Roche LightCycler instrument (Roche Molecular Diagnostics, Pleasanton, CA, USA). The gene-specific primers used were as follows: Actin, Hp (cat. no. HP208336; forward, 5′-TGGCTAGTGGAGCACTCGGTT-3′, reverse, 5′-CAGGAAGTTTATCTCCAACAGCC-3′), MX dynamin like GTPase 1 (MX1; cat. no. HP206142; forward, 5′-GGCTGTTTACCAGACTCCGACA-3′, reverse, 5′-CACAAAGCCTGGCAGCTCTCTA-3′), RNASEL (cat. no. HP214068; forward, 5′-AAGGCTGTTCAAGAACTACACTTG-3′, reverse, 5′-TGGATCTCCAGCCCACTTGATG-3′), hepatic brain-expressed X (HBEX; cat. no. HP213124; forward, 5′-GCATAGGCTTGGAGAACCACAG-3′, reverse, 5′-CCGCAGACTATGACTCAACTGC-3′), ISG15 (cat. no. HP208303; forward, 5′-CTCTGAGCATCCTGGTGAGGAA-3′, reverse, 5′-AAGGTCAGCCAGAACAGGTCGT-3′), 2′-5′-oligoadenylate synthetase (OAS)2 (cat. no. HK209134; forward, 5′-GCTTCCGACAATCAACAGCCAAG-3′, reverse, 5′-CTTGACGATTTTGTGCCGCTCG-3′), eukaryotic translation initiation factor (EIF)-2α (cat. no. HP215710; forward, 5′-CTGGACCTCATGCAGCTTTAGC-3′, reverse, 5′-CTCCATAGTAGGAAGCTCCTGTC-3′), IFNβ1 (cat. no. HP205913; forward, 5′-CTTGGATTCCTACAAAGAAGCAGC-3′, reverse, 5′-TCCTCCTTCTGGAACTGCTGCA-3′), OAS1 (cat. no. HP234311; forward, 5′-AGGAAAGGTGCTTCCGAG-3′, reverse, 5′-GGACTGAGGAAGACAACCAGGT-3′), IFNα1 (cat. no. HP214678; forward, 5′-AGAAGGCTCCAGCCATCTCTGT-3′, reverse, 5′-TGCTGGTAGAGTTCGGTGCAGA-3′) and OAS3 (cat. no. HP209172; forward, 5′-CCTGATTCTGCTGGTGAAGCAC-3′, reverse, 5′-TCCCAGGCAAAGATGGTGAGGA-3′; OriGene Technologies, Inc.). Relative quantification of gene expression were calculated using the 2−ΔΔCq method (15).
Statistical analysis
Statistical analyses were performed using GraphPad Prism 6 (GraphPad Software, Inc., La Jolla, CA, USA) and SPSS v22 software (IBM Corp., Armonk, NY, USA). Continuous variables are presented as the mean ± standard deviation. Differences between groups were analyzed using the Student's t-test and one-way ANOVA followed by Tukey's multiple comparison test. χ2 test or Fisher's exact test were used appropriately to compare categorical variables. P<0.05 was considered to indicate a statistically significant difference.
Results
iTRAQ analysis of DEPs
In order to explore the differential expression profile of the plasma proteome in the treatment of patients with CHB with IFN therapy, iTRAQ-based MS was utilized to analyze serum proteins at 0, 24 and 48 weeks from VR patients receiving IFN therapy. DEPs were defined using a 1.3 (1×1.3) and 0.77 (1/1.3) cut-off in accordance with commonly adopted iTRAQ-based MS conventions. This value has been employed in other large-scale protein identification and quantification studies using the iTRAQ approach (9,10,14,16,17). Briefly, proteins with iTRAQ ratios <0.77 were considered to be underexpressed, where as those >1.3 were considered overexpressed (10). A total of 522 non-extension proteins were identified. Based on the above values, 18 proteins were revealed to be differentially expressed between the groups, with 12 proteins being downregulated and 6 proteins being upregulated. Information on these proteins is presented in Table II.
Table II.Aberrantly expressed plasma proteins in virological response patients following 24 and 48 weeks of interferon therapy. |
Validation of DEPs
Hp, HBB and FGA were selected from the DEPs for further validation. ELISA assays were employed to determine the plasma levels of HP, HBB and FGA from the same sample set utilized for the iTRAQ analysis. The ELISA results were consistent with the results of iTRAQ, as the plasma levels of Hp were significantly decreased and HBB and FGA were increased following IFN therapy (Fig. 1A-C).
Hp reflects the efficacy of IFN in the treatment of CHB
The analysis indicated that Hp exhibited the greatest reduction among the DEPs. ELISA was utilized to detect the plasma levels of Hp in VR patients and non-VR patients following 48 weeks of treatment. The plasma levels of Hp in VR patients were significantly lower than in non-VR patients (Fig. 1D). Hp reflects the efficacy of IFN in the treatment of CHB.
Validation of interference effect
In order to explore the effect of the Hp protein on the hepatitis B virus, Hp-specific siRNA was used to inhibit the expression of the Hp gene in HepG2.215 cells. RT-qPCR and western blotting were utilized to verify the effect of siRNA knockdown at the gene and protein level. As presented in Fig. 2, the expression of Hp was significantly reduced at the gene and protein levels in the siRNA knockdown groups, compared with the control group.
Association of Hp with HBV replication
In order to explore whether Hp has an effect on the replication of HBV, the expression of Hp was inhibited with Hp-specific siRNA to observe changes in the levels of HBV DNA in HepG2.2.15 cell supernatants. Following 48 h of incubation, the Hp siRNA-transfected HepG2.2.15 cells exhibited reduced HBV DNA levels (Fig. 3).
Hp-mediated alteration of IFN and IFN-Induced downstream signaling pathways
In the treatment of hepatitis B with IFN, the level of Hp in the different response groups was varied. It was demonstrated that HBV levels decreased significantly when the expression of Hp was downregulated, and it was hypothesized that Hp may affect the production of IFN. Hp-specific siRNA was used to knockdown Hp expression and, following 48 h of culture, extracted mRNA from the cells was used to detect the levels of IFN RNA. The results indicated that IFNβ1 levels were significantly increased in comparison with the control group (Fig. 4). The expression levels of downstream IFN-stimulated genes in response to Hp inhibition were also detected and, as presented in Fig. 4, knockdown of Hp expression induced increased mRNA levels of five downstream IFN-stimulated genes (OAS1, OAS3, Mx1, ribonuclease Land HBEX). However, four other effectors (IFNα1, ISG15, EIF-2α and OAS2) exhibited only minimally altered mRNA levels in response to HP downregulation.
Discussion
Peg-IFN and nucleoside (acid) analogues are currently the two major antiviral drugs utilized for the treatment of hepatitis B. Although NAs are well tolerated, long treatment periods are required to halt the risk of relapse. Peg-IFN provides a greater likelihood of improved outcomes in a limited 48-week period and with a sustained viral response, but its tolerance is poor and Peg-IFN only exhibits efficacy for a number patients (18). Many factors may affect the Peg-IFN effect, such as baseline HBV DNA level, HBV genotype, alanine amino transferase (ALT) level, sex, age and patient genetic factor (19); however, the exact molecular mechanism is not well known. The efficiency of IFN therapy in the treatment of hepatitis B following 48 weeks is only 30–42% (77), and requires further investigation. HBV genotype, and pre-treatment HBV DNA and ALT levels have been developed to help select those patients best suited for Peg-IFN treatment (18,20).
An aim of the present study was to elucidate the factors that affect the efficacy of IFN therapy. A previous epidemiological study has indicated that the results of antiviral therapy are affected by many factors, such as viral and host factors (20). In order to explore these differences, many novel labeling methods such as iTRAQ have been recommended by the proteomics community to provide deeper proteome coverage and convenient biomarker discovery (21,22). In the present study, patients with CHB were treated with IFN. According to the effects of IFN treatment, patients were divided into the VR and non-VR groups. iTRAQ was utilized in order to screen the differential expression of proteins in the VR patients at 0, 24 and 48 weeks of IFN therapy.
Hp is a 2-glycoprotein acute phase reactant which binds to free hemoglobin and forms a stoichiometrically stable complex (23). Hpis expressed in many tissues and cell types, but the major source is the liver (24). Viagel electrophoresis, Hpis divided into three main types: Hp 1-1, Hp 2-1, and Hp 2-2 (25). The major biological function of Hp is to prevent hemoglobin-mediated renal parenchymal injury and the loss of iron following intravascular hemolysis by binding to hemoglobin with very high affinity in an equimolar ratio (26). Other functions include antioxidant activity, prevention of renal damage, antibacterial activity, inhibition of nitric oxide, inhibition of prostaglandins and angiogenesis (27).
The present analysis indicated that Hp was the most markedly reduced DEP. Following ELISA verification, it was also identified that Hp decreased significantly following treatment. Meanwhile, in patients with good response, the level of Hp also decreased significantly. This suggested that the level of Hp may reflect the efficacy of IFN treatment of CHB.
A number of previous studies have demonstrated that inflammation, trauma, burns and tumors are often accompanied by an increase in plasma levels of Hp binding to the plasma protein (23,28). Therefore, Hp has antioxidant and anti-hemolytic function. Reduced levels of Hp maybe associated with hemolysis or liver injury (29). This is in accordance with the present research results. In the present study, it was demonstrated that ALT was lower in the VR group than the NON-VR group. If a significant difference had been observed in a comparison between the experimental group and another normal patient group, it would have been more convincing. The present study indicates that Hp was decreased significantly in the group with a good response to IFN therapy, which exhibited a decreased level of HBV-DNA. This suggests that Hp may have an inhibitory effect on viral clearance. It has been demonstrated that the Hp level in patients with hepatitis is different from that in normal subjects. In hepatitis C virus infection, increased levels of Hp1-1 have been reported (30). Patients with higher levels of Hp2-2 produce lower levels of hepatitis B antibody (30). In vitro cell experiments further verified that, in HepG2.215 cells, the amount of HBV-DNA in the supernatant was detected following inhibited expression of Hp. In cell experiments, where a lower expression of Hp was present, the amount of virus was demonstrated to decrease, indicating that Hp inhibited viral clearance.
It has previously been demonstrated that Hp functions as an immune system modulator (27). Hp establishes Th1-Th2 balance by enhancing the Th1 cellular response in vitro (31). Via the cluster of differentiation (CD)11b/CD18 (MAC 1) receptor, Hp binds to granulocytes, monocytes, T CD8 cells and natural killer cells, and can regulate the function of MAC 1 dependent cells (32). The Hp-hemoglobin complex is migrated by binding to the CD163 receptors on the surface of monocytes and macrophages (33,34). In the present study, the plasma levels of HP following IFN treatment were significantly lower than prior to treatment. It was hypothesized that the level of Hp may have some association with IFN. In vitro experiments demonstrated that the levels of IFN in HepG2.2.15 cells increased when Hp expression was inhibited. It was speculated that the presence of Hp may inhibit IFN, but it is not clear how specific pathways may affect it. The effects of Hp levels on the levels of downstream molecules of IFN were also explored. With the siRNA-meditated under expression of Hp, levels of IFNβ increased and the downstream molecules of IFN increased significantly. This data demonstrated that the presence of Hp not only inhibits the production of IFN, but also inhibits the production of downstream signaling molecules.
The present findings suggest the following: i) Hp was the most downregulated differential protein following IFN treatment, the level of Hp is decreased in patients with low HBV levels and the level of Hp may reflect the therapeutic effect of IFN. ii) Patients with low HBV levels exhibit a decreased level of Hp; in the in vitro experiments, the level of HBV-DNA was significantly decreased when Hp expression was inhibited, suggesting that Hp may promote the replication of HBV and inhibit the clearance of HBV. iii) Hp exhibited the greatest downregulation following IFN treatment, and affects the production of IFN and its downstream molecules; suggesting that there is an association between Hp and IFN. In future in vitro experiments, we may alter exogenous IFN levels to explore whether this inhibits the clearance of HBV.
The present study also had a number of limitations. Firstly, changes in serum protein levels following treatment with other drugs (nucleotide analogues) were not excluded. Secondly, there was a lack of normal patient control samples. A more rigorous experimental design is required in future experiments, as the present conclusions are valuable, and merit further exploration.
Acknowledgements
Not applicable.
Funding
The present study was supported by National Nature Science Foundation of China (grant no. 81172804).
Availability of data and materials
The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.
Authors' contributions
LL made substantial contributions to the design of the present study and to the acquisition, analysis and interpretation of the data. LL, TS and YY participated in the design of the study and in the acquisition, analysis and interpretation of data. All authors have read and approved the final manuscript.
Ethics approval and consent to participate
The Ethics Committee of Chongqing Medical University (Chongqing, China) approved this study. Written informed consent was obtained from all participants prior to treatment.
Patient consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
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