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Detection of hepatitis C virus (HCV) negative strand RNA and NS3 protein in peripheral blood mononuclear cells (PBMC): CD3+, CD14+ and CD19+

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Abstract

Background

Although hepatitis C virus (HCV) is primarily hepatotropic, markers of HCV replication were detected in peripheral blood mononuclear cells (PBMC) as well as in ex vivo collected tissues and organs. Specific strains of HCV were found to be capable to infect cells of the immune system: T and B cells and monocytes/macrophages as well as cell lines in vitro. The direct invasion of cells of the immune system by the virus may be responsible for extrahepatic consequences of HCV infection: cryoglobulinemia and non-Hodgkin’s lymphoma.

The aim of the present study was to determine the prevalence of markers of HCV infection: negative strand HCV RNA and non-structural NS3 protein in PBMC subpopulations: CD3+, CD14+ and CD19+. The presence of virus and the proportion of affected cells within a particular PBMC fraction could indicate a principal target cell susceptible for HCV.

Methods

PBMC samples were collected from 26 treatment-free patients chronically infected with HCV. PBMC subpopulations: CD3+, CD14+, CD19+ were obtained using positive magnetic separation. The presence of negative strand RNA HCV and viral NS3 protein were analyzed by strand-specific RT-PCR and NS3 immunocytochemistry staining.

Results

Negative strand HCV RNA was detectable in 7/26 (27%), whereas NS3 protein in 15/26 (57.6%) of PBMC samples. At least one replication marker was found in 13/26 (50%) of CD3+ cells then in 8/26 (30.8%) of CD14+ and CD19+ cells. The highest percentage of cells harboring viral markers in single specimen was also observed in CD3+ (2.4%), then in CD19+ (1.2%), and much lower in CD14+ (0.4%) cells.

Conclusions

Our results indicate that CD3+ cells are a dominant site for extrahepatic HCV replication, although other PBMC subpopulations may also support virus replication.

Background

Multiple studies showed that hepatitis C virus (HCV) is not a strictly hepatotropic pathogen [14]. In recent years, the evidence of the extrahepatic HCV replication by detection of positive and negative strand HCV RNA and viral proteins were shown in peripheral blood mononuclear cells (PBMC); [58], bone marrow [9] and in the central nervous system [10, 11] as well as in vitro in cell culture models: macrophages, cell lines MT2, Huh7, Jukat, Molt-4 [12].

Molecular markers of extrahepatic HCV replication were detected frequently in subjects with severely impaired immunity, in particular due to advanced HIV infection [2, 3, 5, 13]. In these patients cells supporting HCV replication were T and B lymphocytes and monocytes/macrophages [6, 14].

The clinical consequences of HCV extrahepatic replication are known, as the role of viral infection in the induction of type II mixed cryoglobulinemia and B-cell non-Hodgkin lymphoma (B-NHL) is well ascertained [1518]. However, the pathogenetic mechanisms underlying these phenomena are poorly understood. They may include functional defects, abnormal proliferation and differentiation of lymphocytes due to chronic inflammatory process and/or direct cell infection by the virus [1922].

To characterize the extrahepatic sites of HCV replication and virus reservoirs in the organism the studies of separate markers of HCV replication in PBMC were performed [2, 8, 23, 24], however, there is no complex study detecting both viral genetic material and viral proteins in separated cell subpopulations, as well as determining the frequency of cell infection with HCV. While presence of negative strand HCV RNA indicates virus RNA replication, NS3 HCV production indicates the presence of viral mRNA translation and polyprotein processing [23]. Non structural protein (NS3) as an essential component of the HCV replication life cycle, and plays an important role in the pathogenesis of HCV.

The aim of the present study was to determine the prevalence of HCV infection in separated PBMC fractions: T cells (CD3+), B cells (CD19+) and monocytes (CD14+). The presence of HCV intermediate replication product (negative strand RNA) as well as the presence of viral NS3 protein were analyzed in different cell subpopulations.

Results and discussion

The mechanisms of HCV replication in cells of the immune system are far from clear. Invasion of cells by this virus may be consequential as previous in vivo and in vitro studies showed modified multiple gene expression and apoptotic pathways in HCV infected cells [14, 25, 26]. Thus, it is important to recognize the principal target population for HCV within cells of the immune system and further determine the role of the virus in cell dysfunction, particularly in the light of the were described detrimental effect of HIV/HCV coinfection [14].

Previous studies have reported evidence for extrahepatic replication of HCV in peripheral blood mononuclear cells (PBMCs) [27]. However, discrepancies exist regarding the main cell populations infected [8, 13, 21, 23]. Other studies have reported evidence for HCV replication in granulocytes and dendritic cells as well as in extrahepatic tissues [23]. While extrahepatic replication is gaining wide acceptance some authors consider it to be controversial [27, 28].

Replicative forms of HCV were detected in all studied subpopulations: CD3+, CD14+, CD19+.

The negative strand HCV RNA was detected in 7/26 (27%) PBMC samples with similar frequency in all separated CD3+, CD14+ and CD19+ cells, 3/26 (11.5%), 2/26 (7.6%) and 4/26 (15.3%) respectively (Table 1). The presence of genomic (positive) HCV RNA strand was detectable in all cell specimens studied (data not shown). The measurement of positive to negative strand ratio was not performed due to the limited amount of material and low viral loads. However, our previous studies indicated that the genomic RNA strand is typically detectable at a level 1–2 logs higher than the negative strand [29].

Table 1 Demographic, clinical and laboratory data of the patients

The presence of HCV NS3 protein was observed in more than half 15/26 (57%) of the examined PBMC samples, most frequently in CD3+ cells: 11/26 (42.3%), followed by CD14+ and CD19+ cells: 6/26 (23%). The observed prevalence of HCV infection was higher than reported in other studies performed in immunocompetent patients, probably due to the application in the current analysis of two different viral replication markers [3, 7, 13].

Previous studies showed that CD3+ cells harboured the virus more often than the remaining PBMC subpopulations [3, 14, 15, 19, 30].

In our study we found that half of CD3+ samples (13/26) were NS3 HCV positive, whereas in CD14+ and CD19+ the prevalence reached 30.8%. In two patients, NS3 HCV was observed in all three examined cell subpopulations (Table 1; Figure 1).

Figure 1
figure1

Detection of NS3 HCV in PBMC subpopulations: CD3+, CD14+ and CD19+ (Pt 1). Negative control CD3+, CD14+ and CD19+ subpopulations were collected from HCV - negative patient. Liver tissue control: liver biopsy samples from HCV positive patient (HCV pos.) and HCV negative patient (HCV neg.).

Proportion of NS3 positive cells within cell subsets was highest for CD3+ cells (range: 1–17; mean: 2.4 ± 4.2), whereas for CD14+ (range: 1–20; mean: 4 ± 0.7), and CD19+ (range: 1–23; mean: 1.2 ± 4.5); (Table 1).

No correlation between NS3 HCV and HCV RNA negative strand was found, which could be due to low level of the virus replication [5, 24]. While in some other studies the presence of HCV proteins was correlated with HCV RNA, however, this was based on the analysis of the genomic, not negative strand RNA [1, 8, 31, 32].

The prevalence of NS3 - positive cells is lower than observed in the liver were proportion infected cells varies from 0.04% to more than 80% [31, 33]. Results of the current study are similar to those published by Rodriguez-Inigo et al. who used in situ hybridization in unselected PBMC. In that study infected cells constituted 0.08% to 4% of all PBMC [8].

Conclusions

Our results indicate that CD3+ cells are a dominant site for extrahepatic HCV replication, although other PBMC subpopulations may also support virus replication.

Methods

Blood samples were collected on EDTA, from 26 consecutive chronically HCV infected patients (male/female 17/9; mean age 54.69 ± 8.12) treated at Clinic of Hepatology and Acquired Immune Deficiencies, Medical University of Warsaw.

Twenty five patients were infected with genotype 1b, one with genotype 3a.

Eleven patients (42%) were diagnosed with crioglobulinemia. Demographic and clinical characteristics of the studied patients are shown in Table 1[34].

The study was approved by the Internal Review Board at the Warsaw Medical University (ref. no. KB/17/2013) and each patient provided a written consent.

Magnetic cells sorting

PBMC were isolated by density gradient centrifugation on Histopaq (Sigma, Missouri, USA) from 10 ml of blood collected into a tube containing EDTA. The PBMC subpopulations: CD3+, CD14+, CD19+ were isolated by positive selection by IMag (magnetic cell separation system, BD IMagnet™; San Jose, USA). For separation of particular cell subpopulations, the following antibodies were used: anti-CD3 (anti-human CD3 magnetic Particles-DM, BD IMag™, San Jose, USA), anti-CD19 (anti-human CD19 magnetic Particles-DM, BD IMag™; San Jose, USA), anti-CD14 (anti-human CD14 magnetic Particles-DM, BD IMag™; San Jose, USA).

Purity of each population was verified by flow cytometry (Canto II, BD) using the antibodies: PE mouse anti-human CD3 (BD Pharmingen™, San Jose, USA), PE mouse anti-human CD14 (BD Pharmingen™; San Jose, USA), APC mouse anti-human CD19 (BD Pharmingen™; San Jose, USA), and isotype control: PE and APC mouse IgG1ĸ (BD Pharmingen™; San Jose, USA).

The purity of the separated CD3+, CD14+ and CD19+ cells was no lower than 92.4%, 97.5% and 96.7%, respectively (Figure 2).

Figure 2
figure2

The purity of CD3 + (A), CD14 + (B) and CD19 + (C) cell subpopulations separated from PBMC collected from HCV positive patient.

Detection of negative strand HCV RNA

HCV RNA was extracted from 1×106 PBMC and 2-3×104 of separated CD3+, CD14+and CD19+ subpopulations, as described elsewhere [1]. Qualitative detection of the negative-strand HCV RNA, spanning 5’UTR viral region was accomplished by specific synthesis of cDNA in 70°C using the thermostable enzyme Tth (Applied Biosystem, Life Technologies, Carlsbad, USA).

For Tth-based RT-PCR detection of the negative strand, cDNA was synthesized in 20 μl of reaction mixture containing 50 pM sense primer, 1x RT buffer (Applied Biosystem, Life Technologies, Carlsbad, USA), 1 mM MnCl2, 200 mM (each) dNTP, and 5 U of Tth (Applied Biosystem, Life Technologies, Carlsbad, USA). After 30 min at 72°C, Mn2+ was chelated with 8 μl of 10x EGTA chelating buffer (Applied Biosystem, Life Technologies, Carlsbad, USA), 50 pM antisense primer was added, the volume was adjusted to 100 μl, and the MgCl concentration was adjusted to 2.2 mM. To increase the specificity and sensitivity of assay, wax beads (Ampliwax; Applied Biosystem) were routinely employed for “hot start”. The amplification was performed in Perkin Elmer GenAmp PCR System 9600 thermocycler (Perkin Elmer, Waltham, Massachusetts, USA). The sequence of primers and reaction conditions are shown in Table 2. The PCR products were analyzed on 2% agarose gel.

Table 2 Sequences of primers and PCR conditions

All PCR runs included positive controls, consisting of end point dilutions of the respective RNA strands. The titers were determined by analyzing 10-fold serial dilutions of the template. To prevent contamination, pre-PCR steps were carried out in separate room. Negative controls consisting of PBMC from HCV negative patients were included in all reaction series: one negative sample was processed for every 3 to 4 tested specimens. Under these conditions, none of the negative controls was positive [35].

The strand specific assay used in the study was capable of detect 100 viral genomic eq/ml of the correct negative strand or HCV genomic strand, while ≥ 108 genomic equal of the incorrect strand. The amount of used RNA was 1–4 μg RNA per reaction [5].

The results were reported as positive or negative.

Detection of HCV NS3 in PBMC and separated cell subpopulations

PBMC smears preserved in acetone/chloroform were incubated with primary monoclonal anti-NS3 antibody (Novocastra™, Leica, Newcastle, UK), following incubation with Alexa 488 goat anti-mouse secondary antibody (Life Technologies, Carlsbad, USA). To stain the cell nuclei, preparations were incubated with Hoechst reagent (Molecular Probes, Carlsbad, USA) and analyzed by fluorescent microscope Eclipse 80i (Nikon, Tokio, Japan) using 330–380 nm (Hoechst) and 450 – 490 nm (Alexa 488) UV-2A filter.

The control material included PBMC samples collected from uninfected patients and liver biopsy samples from HCV infected patients (positive samples) and uninfected patients (negative control). The specificity of the method was verified by an “internal” reaction control without a primary antibody (Figure 1).

Statistical analysis

Statistical analysis was performed using one-way analysis of variance (ANOVA) and chi square test (Install 07). Spearman’s correlation test was used to investigates the linear relationships between presence of NS3 HCV in individual cell subpopulations: CD3+, CD14+, CD19+, and negative strand level HCV RNA. P values > 0.05 was considered to be statistically significant. The analysis was performed by use of Statistica software, version 10.

References

  1. 1.

    Laskus T, Radkowski M, Wang LF, Vargas H, Rakela J: Search for hepatitis C virus extrahepatic replication sites in patients with acquired immunodeficiency syndrome: specific detection of negative- strand viral RNA in various tissues. Hepatology 1998, 28: 1398-1401. 10.1002/hep.510280531

  2. 2.

    Laskus T, Radkowski M, Wang LF, Vargas H, Rakela J: The presence of active hepatitis C virus replication in lymphoid tissue in patients coinfected with human immunodeficiency virus type 1. J Infect Dis 1998, 178: 1189-1192. 10.1086/515682

  3. 3.

    Pal S, Sullivan DG, Kim S, Kae J, Cotler SJ, Carithers RL Jr, Wood BL, Perkins JD, Gretch DR: Productive replication of hepatitis C virus in perihepatic lymph nodes in vivo : implications of HCV lymphotropism. Gastroenterology 2006, 130: 1107-1116. 10.1053/j.gastro.2005.12.039

  4. 4.

    Stamataki Z: Hepatitis C infection of B lymphocytes: more tools to address pending questions. Expert Rev Anti Infect Ther 2010, 8: 977-980. 10.1586/eri.10.86

  5. 5.

    Laskus T, Operskalski EA, Radkowski M, Wilkinson J, Mack WJ, deGiacomo M, Al-Harthi L, Chen Z, Xu J, Kovacs A: Negative-strand hepatitis C virus (HCV) RNA in peripheral blood mononuclear cells from anti-HCV-positive/HIV-infected women. J Infect Dis 2007, 195: 124-133. 10.1086/509897

  6. 6.

    Laskus T, Radkowski M, Piasek A, Nowicki M, Horban A, Cianciara J, Rakela J: Hepatitis C Virus in Lymphoid cells of patients coinfected with human immunodeficiency Virus Type 1: evidence of active replication in Monocytes/Macrophages and Lymphocytes. J Infect Dis 2000, 181: 442-448. 10.1086/315283

  7. 7.

    Müller HM, Pfaff E, Goeser T, Kallinowski B, Solbach C, Theilmann L: Peripheral blood leukocytes serve as a possible extrahepatic site for hepatitis C virus replication. J Gen Virol 1993, 74: 669-676. 10.1099/0022-1317-74-4-669

  8. 8.

    Rodriguez-Inigo E, Casqueiro M, Navas S, Bartolome J, Pardo M, Carreno V: Fruorescent in situ hybridization of hepatitis C virus RNA in peripheral blood mononuclear cells from patients with chronic hepatitis C. J Med Virol 2000, 60: 269-274. 10.1002/(SICI)1096-9071(200003)60:3<269::AID-JMV4>3.0.CO;2-1

  9. 9.

    Radkowski M, Kubicka J, Kisiel E, Cianciara J, Nowicki M, Rakela J, Laskus T: Detection of active hepatitis C virus and hepatitis G virus/GB virus C replication. Blood 2000, 95: 3986-3989.

  10. 10.

    Bürgel B, Friesland M, Koch A, Manns MP, Wedemeyer H, Weissenborn K, Schulz-Schaeffer WJ, Pietschmann T, Steinmann E, Ciesek S: Hepatitis C virus enters human peripheral neuroblastoma cells - evidenve for extra hepatic cells sustaining hepatitis C virus penetration. J Viral Hepat 2011, 18: 562-570. 10.1111/j.1365-2893.2010.01339.x

  11. 11.

    Wilkinson J, Radkowski M, Laskus T: Hepatitis C virus neuroinvasion: identification of infected cells. J Virol 2009, 83: 1312-1319. 10.1128/JVI.01890-08

  12. 12.

    Tariq H, Manzoor S, Parvaiz F, Javed F, Fatima K, Qadri I: An overview: in vitro model sof HCV replication in different cell cultures. Infec Genet Evol 2012, 12: 13-20. 10.1016/j.meegid.2011.10.009

  13. 13.

    Chary A, Winters MA, Eisen R, Knight TH, Asmuth DM, Holodniy M: Quantitation of hepatitis C virus RNA in peripheral blood mononuclear cells in HCV-monoinfection and HIV/HCV-coinfection. J Med Virol 2012, 84: 431-437. 10.1002/jmv.23210

  14. 14.

    Laskus T, Radkowski M, Jablonska J, Kibler K, Wilkinson J, Adair D, Rakela J: Human immunodeficiency virus facilitates infection/replication of hepatitis C virus in native human macrophages. Blood 2004, 103: 3854-3859. 10.1182/blood-2003-08-2923

  15. 15.

    Fazi C, Dagklis A, Cottini F, Scarfò L, Bertilaccio MT, Finazzi R, Memoli M, Ghia P: Monoclonal B cell lymphocytosis in hepatitis C virus infected individuals. Cytometry B Clin Cytom 2010,78(Suppl 1):S61-S68.

  16. 16.

    Jadali Z: Hepatitis C virus cryoglobulinemia and non-Hodgkin lymphoma. Hepat Mon 2012, 12: 85-91. 10.5812/hepatmon.4905

  17. 17.

    Ramos-Casals M, Forns X, Brito-Zerón P, Vargas A, Ruiz M, Laguno M, Yagüe , Sánchez-Tapias JM, Gatell JM, Font J: Cryoglobulinemia associated with hepatitis C virus: influenze of HCV genotypes, HCV-RNA viraemia and HIV coinfection. J Viral Hepat 2007, 14: 736-742.

  18. 18.

    Sansonno D, Tucci FA, Montrone M, Troiani L, Sansonno L, Gatti P, Lauletta G: B-cell depletion in the treatment of mixed cryoglobulinemia. Dig Liver Dis 2007, 39: 116-121.

  19. 19.

    Ayers CL, Firan M, Pillai V, Lee WM, Karandikar NJ: Viral interactions with B-cells contribute to increased regulatory T-cells during chronic HCV infection. Viral Immunol 2011, 24: 119-129. 10.1089/vim.2010.0077

  20. 20.

    Fourniller A, Freida D, Defrance T, Merle P, Trépo C, Inchauspé G: Analysis of B-lymphocyte differentiation in patients infected with hepatitis C virus. J Med Virol 2004, 72: 566-574. 10.1002/jmv.20039

  21. 21.

    Ito M, Murakami K, Suzuki T, Mochida K, Suzuki M, Ikebuchi K, Yamaguchi K, Mizouchi T: Enhanced expression of lymphomagenesis-related genes in peripheral blood B cells of chronic hepatitis C patients. Clini Immunol 2010, 135: 459-465. 10.1016/j.clim.2010.02.002

  22. 22.

    Talamini R, Montella M, Crovatto M, Dal Maso L, Crispo A, Negri E, Spina M, Pinto A, Carbone A, Franceschi S: Non-Hodgkin’s lymphoma and hepatitis C virus: a case–control study from northern and southern Italy. Int J Cancer 2004, 110: 380-385. 10.1002/ijc.20137

  23. 23.

    Blackard JT, Smeaton L, Hiasa Y, Horiike N, Onji M, Jamieson DJ, Rodriguez I, Mayer KH, Chung R: Detection of hepatitis C virus (HCV) in serum and peripheral-blood mononuclear cells from HCV-monoinfected and HIV/HCV- coinfected persons. J Inf Dis 2005, 192: 258-265. 10.1086/430949

  24. 24.

    Liao WH, Tung SY, Shen CH, Lee KF, Wu CS: Tissue expression of the hepatitis C virus NS3 protein does not correlate with histological or clinical features in patients with chronic hepatitis C. Chang Gung Med J 2011, 34: 260-267.

  25. 25.

    Duberg A, Nordström M, Törner A, Reichard O, Strauss R, Janzon R, Bäck , Ekdahl K: Non-Hodgkin’s Lymphoma and other nonhepatic malignancies in Swedish patients with hepatitis C virus infection. Hepatology 2005, 41: 652-659. 10.1002/hep.20608

  26. 26.

    Wang Q, Chen J, Wang Y, Han X, Chen X: Hepatitis C virus induced a novel apoptosis-like death of pancreatic beta cells through a caspase 3-dependent pathway. PLoS One 2012, 7: e38522. 10.1371/journal.pone.0038522

  27. 27.

    Sansonno D, Tucci FA, Lauletta G, De Re V, Montrone M, Troiani L, Sansonno L, Dammacco F: Hapatitis C virus productive infection in mononuclear cells from patients with cryoglobulinaemia. Clin Exp Imm 2006, 147: 241-248. 10.1111/j.1365-2249.2006.03272.x

  28. 28.

    Gowans EJ: Distribution of markers of hepatitis C virus infection throughout the body. Semin Liver Dis 2000, 20: 85-102. 10.1055/s-2000-9503

  29. 29.

    Laskus T, Radkowski M, Wang L, Vargas H, Rakela J: Detection of hepatitis G virus replication sites by using highly strand-specific Tth- based reverse transcriptase PCR. J Virol 1998, 72: 3072-3075.

  30. 30.

    Ito M, Kusunoki H, Mizuochi T: Peripheral B cells as reservoirs for persistent HCV infection. Front Microbiol 2011,2(177):1-3.

  31. 31.

    Rodriguez-Inigo E, Lopez-Alcorocho JM, Bartolome J, Ortiz-Movilla N, Pardo M, Carreno V: Percentage of hepatitis C virus-infected hepatocytes is a better predictor of response than serum viremia levels. J Mol Diagn 2005, 7: 535-543. 10.1016/S1525-1578(10)60585-5

  32. 32.

    Mahias K, Ahmed-El-Sayed N, Masante C, Bitard J, Staedel C, Darfeuille F, Ventura M, Astier-Gin T: Identification of a structural element of the hepatitis C virus minus strand RNA involved in the initiation of RNA synthesis. Nucleic Acids Res 2010, 38: 4079-4091. 10.1093/nar/gkq109

  33. 33.

    Laskus T, Radkowski M, Wang L, Cianciara J, Vargas H, Rakela J: Hepatitis C virus negative strand RNA is not detected in peripheral blood mononuclear cells and viral sequences are identical to those in serum: a case against extrahepatic replication. J Gen Virol 1997, 78: 2747-2750.

  34. 34.

    Michielsen PP, Haiben EI, Ramon AM, VanMarck EA, Pleckmans PA: Serum aminotransferase levels and histological disease in chronic hepatitia C. Acta Gastroenterol Belg 1997, 60: 11-14.

  35. 35.

    Rodriguez-Inigo E, Bartolome J, de Lucas S, Manzarbeitia F, Pardo M, Arocena C, Gosalvez J, Oliva H, Carreno V: Histological damage in chronic hepatitis C is not related to the extent of infection in the liver. Am J Pathol 1999, 154: 1877-1881. 10.1016/S0002-9440(10)65445-4

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Correspondence to Agnieszka Pawełczyk.

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Competing interests

The authors declare that they have no competing interests.

Authors’ contributions

AP for study design, laboratory work (immunohistochemistry, magnetic cell sorting flow cytometry), statistical analysis, interpretations of results and preparation of manuscript, NK for laboratory work (immunohistochemistry, magnetic cell sorting, flow cytometry), JJ for sample collection, analysis and interpretations of results analysis and interpretations of results, IBO for analysis and interpretations of results, KC for analysis and interpretations of results, MF for cell preparation, detection of negative strand HCV RNA. TL for interpretations of results preparation of manuscript, MR for study design, analysis and interpretations of results and preparation of manuscript. All authors read and approved the final manuscript.

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Pawełczyk, A., Kubisa, N., Jabłońska, J. et al. Detection of hepatitis C virus (HCV) negative strand RNA and NS3 protein in peripheral blood mononuclear cells (PBMC): CD3+, CD14+ and CD19+. Virol J 10, 346 (2013) doi:10.1186/1743-422X-10-346

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Keywords

  • HCV
  • PBMC
  • Extrahepatic replication
  • NS3 protein
  • Negative strand HCV RNA