Mediterranean Journal of Hematology and Infectious Diseases Cytokine Response Associated with Hepatitis C Virus Clearance in Hiv Coinfected Patients Initiating Peg Interferon- Based Therapy Results: High Pretreatment Concentrations of Ip-10 (cxcl-10) and Mcp-1 (ccl-2) Were Associated with a Poor An

Background: Treatment of hepatitis C virus (HCV) infection based on peginterferon- (pegIFN) and ribavirin induces important changes in cytokine release and T cell activation. Objective: Immune response to pegIFN-ribavirin therapy was explored in patients coinfected by HCV and HIV. Methods: Concentrations of 25 cytokines and CD8 + T cell activation were monitored in HCV/HIV coinfected patients classified as sustained virological responders (SVR, n=19) and non-responders (NR, n=11). This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Introduction. Infection by hepatitis C virus (HCV) and HIV shared common routes of transmission and thus confections with the two viruses are frequent. HCV infection is seen in 15–30% of HIV-infected patients in Western Europe, with almost 20 000 HIV-infected individuals chronically infected with HCV in France. 1,2 Since the introduction of antiretroviral

levels in serum. 6 Finally, ART-related adverse events are more frequent in HCV/HIV coinfected individuals, with increased difficulties in optimally treating HIV infection. 7,8 Until recently, a combination of pegIFN and ribavirin has been the standard-of-care for treatment of chronic HCV patients. In coinfected individuals -ribavirin therapy is less efficacious than in single HCV infection. 9,10 Approximately 30% of patients receiving a combination of ribavirin with pegIFN have a sustained virological response when infected with HCV genotype 1 and 4. 9 This rate increases to 60% when genotype 2 and 3 are involved. 10 Most of the current anti-HCV therapeutic options remained based on pegIFN and/or ribavirin in addition to protease inhibitors or NS5A or NS5B inhibitors. 11 PegIFN constitutes an active immunotherapy triggering innate immune response and T cell activation. The cytokine response to pegIFN-based regimens plays probably an important role in treatment outcome. IFN stimulates Th1 cells and limits secretion of Th2 related cytokines such as IL-4 or IL-10. 12 IFN signals through Janus kinase signal transducer, an activator of transcription pathway, and induction of IFN-stimulated genes. 13 Ribavirin synergies this effect by reducing IL-10 production, enhancing autocrine IFN- and IL-8 secretion. [14][15][16] Several immune factors are predictive of virological response on pegIFN-ribavirin-based therapy: pretreatment concentration of IFN-inducible protein 10 (IP-10, also called CXCL-10), polymorphisms near the interleukin-28B gene coding for the IFN-3, and CD4 + T cell count in HIV/HCV coinfected individuals. 18,19 Progressive impairment of immune functions and T cell exhaustion induced by prolonged exposure to virus antigens are fundamental features of HIV infection. Inhibitory networks, such as the programmed cell death protein-1 (PD-1) and IL-10 play a key role in this process. 20,21 PD-1 is upregulated on CD8 + and CD4 + T cells and mediates a dysfunction partially reversible on ART. 22-24 PD-1 signalling impacts the expression of both Th1 and Th2 cytokines but limits particularly the capacity of Th1 and IFN secretion by CD4 + and CD8 + T cells. 21 Although HCV clearance depends on immune response induced by pegIFN-ribavirin therapy, the dynamics of cytokine response and T cell activation in individuals coinfected with HIV and HCV remain poorly characterized. 25 In this study, we monitor serum concentration of 25 cytokines alongside with the level of CD8 + T cell activation in HIV/HCV coinfected patients initiating anti-HCV therapy.

Methods.
Patient samples: Patients coinfected by HIV/HCV followed at Montpellier University Hospital and initiating anti-HCV therapy were included consecutively between January 2007 and January 2010 after providing written informed consent. The study was approved by the local institution ethical committee (DC-2011(DC- -1405. Chronic hepatitis was proved by the presence of serum HCV antibodies and detectable viral RNA. HCV genotype, HCV and HIV-1 viral loads, CD4 + T cell count, and liver enzyme levels were all determined using standard procedures. All patients received pegIFN2a 180 microg/week plus ribavirin 800 to 1,200 mg daily; patients infected with HCV genotype 2 and 3 received 800 mg daily and genotype 1 and 4 received a weight based dose: 1,000 mg/day for persons less than 75 kg and 1200 mg/day over 75 kg. Subjects were ranged into two distinct groups based on HCV response to therapy: i) Sustained virological responders (SVR) when serum HCV RNA was undetectable 24 weeks after completing therapy, and ii) non responders (NR) when HCV RNA decrease was < 2 log copies/mL at week 12 or when HCV RNA was detectable at the end of treatment. iii) Patient relapsing in the 24 weeks period after therapeutic cessation were excluded from the study.
Routine laboratory testing: Serum HCV RNA was quantified using COBAS AmpliPrep/COBAS TaqMan HCV assay (Roche Diagnostic Systems). HCV genotypes were determined using INNO-LiPA HCV II test (Innogenetics). Alanine aminotransferase (ALT) dosages were executed using standard methods.

Quantitation of serum cytokine concentrations:
Cytokines were quantified in serum samples obtained before initiation of treatment, and four weeks after the start of PegIFN-based therapy. A multiplexed microbead assay was used according to manufacturer's instructions (cytokine twenty-five-plex kit, Life Technologies Ltd, Paisley, UK) and an FIDIS™ apparatus (BMD). Twenty five cytokines were expression of CD38 bright on CD8 + T cells was analyzed as previously described using a two-colour staining with anti-CD8 and anti-CD38 conjugated to fluorescein isothiocyanate (FITC) and phycoerythrin (PE), respectively (Beckman Coulter). 26 The positive threshold for CD38 bright analysis was established using the CellQuant CD38/CD8 kit for quantitation of CD38 cell surface expression (BioCytex, Marseille, France) and was defined as 8,500 CD38 binding sites/cells. The CD8 + /CD38 bright values were expressed as the percentage of CD38 bright cells from the CD8 + T cell populations.
Statistical Analysis: The Mann-Whitney U test and Kruskal-Wallis test were used to analyze continuous variables where appropriate. The Friedman test was used to evaluate changes in serum cytokine levels over time. A mixed model was used to analyze the association between T cell activation during anti-HCV therapy and therapeutic response. Statistical analyses were done using SPSS software version 18.0J.

Results.
Clinical characteristics at baseline: Thirty HCV/HIV coinfected patients receiving pegIFN-ribavirin therapy were included in the study. Nineteen (63%) were classified as SVR and eleven (37%) as NR. Patient characteristics are shown in Table 1.
Pretreatment levels of soluble and cellular inflammatory markers: IP-10 levels were higher in the NR group than in the SVR group, P = 0.021 ( Table 2). Individuals from the NR group also had higher pretreatment concentrations of MCP-1, P = 0.0009. A trend for a higher serum concentration of IL-8 was also observed in patients of the NR group compared to the SVR group, P = 0.106.
Cytokines change after therapeutic initiation of HCV treatment: Initiation of anti-HCV treatment elicited IFN rise in both SVR and NR patients (Figure 1 and Supplemental Table 1). This enhancement of IFN in serum was similar in the two groups. Besides IFN, the anti-HCV therapy induced a significant increase in the serum levels of eleven cytokines in SVR patients, including cytokines related to Th1-dominant immune responses (IL-12p40/70, IP-10), Th2-type cytokines (IL-4, IL-5, and IL-13), and pro-inflammatory *Seven subjects had a reduction of less than 2 log 10 in HCV RNA after 12 weeks of therapy (null responders), and four subjects had a reduction of more than 2 log 10 (partial responders).  Table 1). Finally, when results were analyzed without consideration of the HCV therapeutic response (combining SVR and NR patients), we also

Comparison of the cytokine level changes induced by pegIFN-ribavirin between SVR and NR group:
Changes in cytokines were compared among SVR and NR using the ratio between baseline and four weeks of treatment (Figure 1). A sharp increase of MCP-1 and MIP-1 concentration was observed after initiation of anti-HCV therapy in the SVR group whereas the value decreased or remained stable in the NR group (p=0.0024 and p=0.029, respectively). Furthermore, the IL-8 concentration remains stable after a one-month period of pegIFN-ribavirin therapy in most of the patients responding to anti-HCV treatment, whereas this concentration declined in NR patients (p=0.052).

Changes in T cell activation over the three-months period of therapy initiation:
The impact of pegIFNribavirin on T cell activation was explored at day 0, week 4 and week 12 (Figure 2). CD8 + T cell activation before the treatment tends to be higher in NR patients compared to the SVR patients, (p=0.066, Figure 2). CD38 bright expression on CD8 T + cells in the two groups of patients (p<0.001). No significant differences were observed between the two groups in the slope of CD38 cell surface expression of CD8 + T cells suggesting that the over time changes of this activation marker not be associated with a better immune response to therapy.

Discussion.
Although the virological response to pegIFNribavirin-based therapy is intimately associated with the host immunity, the monitoring of HCV treatment is based on the serum HCV-RNA level decay regardless of the immune response. In this study, CD8 + T cell activation and levels of 25 cytokines were analyzed in HIV/HCV coinfected patients with favourable versus unfavourable therapeutic outcome.
PegIFNribavirin administration induced a dramatic change in serum cytokine concentrations and CD8 + T-cell activation level. We observed that the HCV clearance under pegIFN/ribavirin therapy was associated with broader and higher cytokine responses in SVR than in NR.
Multianalyte assays make possible to analyze a wide an array of cytokines using a small sample volume rapidly. In the present study, the level of 25 cytokines and CD8 + T-cell activation were analyzed at baseline and week four after the initiation of pegIFN/ribavirin therapy. Comparison between different multiplex bead assays has shown variable agreement among kits evidencing that absolute cytokine concentrations differ across commercial assays. 27,28 As a consequence, multisite comparisons between cytokine concentrations obtained with different methods are difficult to interpret because of the lack of standardization. However, these methods are useful for longitudinal studies, and a similar rank order of cytokine concentrations between samples is preserved between the different commercial kits. Hence, we considered comparisons based on fold change under pegIFN-ribavirin therapy as a valuable method for identifying a predictor of therapeutic success or failure. Even if interferon-free regimen progressively substitute pegIFN-containing regimen for treatment of hepatitis C it remains of particular importance to describe immune response after initiation of pegIFNIndeed, IFNremains the only drug approved for treatment of chronic hepatitis D and the only treatment used for a limited period for hepatitis B.
Baseline serum concentration of IP-10 and MCP-1 (monocyte chemotactic protein 1) were higher in NR than in SVR. A significant increase was observed after treatment initiation in 15 out of 25 soluble biomarkers tested. The strongest increased was observed for IFN as an expectable consequence of the anti-HCV therapy, with more than 4-fold rise between week 0 and week 4. Increase in cytokine concentrations after pegIFNribavirin administration was observed for proinflammatory-and Th1-related cytokines such as IL-12 or IP-10, but also for Th2-related cytokines such as IL-4 or IL-13. Activation of T cells accompanied this phenomenon as shown by the increased cell surface expression of CD38 on CD8 + T cells.
Based on therapeutic outcome distinct cytokine patterns were identified. Differences in cytokine concentrations were observed at baseline and following anti-HCV initiation. In agreement with previous studies in individuals coinfected we observed the pretreatment serum level of IP-10 was higher in the NR group than in the SVR group. 19 Circulating IP-10 concentration is well correlated with intrahepatic IP-10 messenger RNA expression during chronic HCV infection. 29 The high baseline hepatic IFN-stimulated genes expression is associated with a lower chance to be SVR to IFN-based therapy when HIV-uninfected. [30][31][32][33] Interestingly, the pre-treatment MCP-1 concentration was also found at a higher concentration in the NR group. This proinflammatory chemokine is involved in the migration and infiltration of monocytes and CD4 + memory T lymphocytes. Intra-hepatic and serum MCP-1 levels are associated with liver inflammation and fibrosis during chronic HCV infection. 34,35 MCP-1 plays a significant role in the recruitment of monocytes by interacting with their cell-surface adhesion-molecules that are over expressed during chronic HCV infection. 36 Association between MCP-1 baseline level, and response to pegIFN-ribavirin therapy has been recently reported in HIV-uninfected patients. 37 Both chronic HCV and HIV infections induce expression and release of MCP-1 in humans. 38,39 HIV proteins like gp120 40 and transactivator protein Tat 41,42 have shown strong immunomodulatory capacity through MCP-1 stimulation. MCP-1 has also been shown to promote Th2 responses by polarizing Th0 cells towards a Th2 phenotype 43 and is thought to be one of the key factors involved in HIV pathogenesis. 44 Hence, MCP-1 pretreatment level may be associated with the promotion of the Th1 dominant response and HCV clearance under pegIFN-ribavirin therapy in HIV/HCV coinfected patients.
Cytokine response to pegIFN/ribavirin therapy differed qualitatively between SVR and NR. The cytokine response appeared more restricted in NR than in SVR since only six versus 11 cytokines rise significantly following the commencement of anti-HCV therapy. As a possible consequence of high IP-10 and MCP-1 baseline level, the boost of circulating IP-10 and MCP-1 levels was not observed in the NR after four weeks of pegIFN-ribavirin treatment. Circulating IP-10 is considered as a marker of the pre-therapeutic activation level of IFN-stimulated genes. The defect in IP-10 response observed four weeks after starting pegIFN-ribavirin treatment can be viewed as a marker of the overexpression of IFN-stimulated genes leading to a poor capacity response to exogenous IFN injections.
Four weeks after initiation of pegIFN-ribavirin, a higher MIP-1β (macrophage inflammatory protein-1β) and MCP-1 secretions were observed in SVR when compared to NR. Of interest, a trend for a paradoxical decrease of MIP-1β was also observed at the same time in the NR group. The concentration of MIP-1β was halved in the NR group at week four compared to baseline whereas MCP-1β level tends to increase in the SVR group. This observation is consistent with a previous study showing that HCV clearance is more frequent in patients experiencing strong MIP-1 and MIP-1β response to pegIFN-based therapy. 45,46 MIP-1β (also named CCL4) is a chemokine linked to the Th1 response. MIP-1β is involved in T cell recruitment mediated by CCR5 and CCR1 in the liver of HCV infected patients. 38 The amplitude of MCP-1 variation in response to pegIFN/RBV is probably dependent on baseline MCP-1 level as for IP-10. IL-8 dynamic response to pegIFN-ribavirin therapy also appears different in the two groups. IL-8 serum levels tend to be elevated at baseline in NR and to diminish following pegIFN-ribavirin initiation. High IL-8 mRNA is involved in liver inflammation 47-49 and inhibition of the IFN antiviral response in vitro. 50 Pretreatment level of IL-8 has also been found associated with poor virological response to pegIFN-ribavirin therapy. 51 Evolution of IL-8 concentration may reflect the combined effect of pegIFN plus ribavirin since ribavirin induces its secretion through the activation of activator protein 1. 14 In this study, relapse patients were not included in the group of patients that did not recover from HCV under pegIFN-ribavirin. Subjects who experience relapse had patterns of virological response different from NR with a rapid decline in HCV RNA during the first week of treatment. 52,53 Hence, relapse patients should be explored a part from NR and SNR groups.
Our study had limitations related to its retrospective nature and the small number of subjects included. HCV genotypes and fibrosis stage were not taken into account in the analysis and IL-28 polymorphism, which is also known to predict the hepatic responsiveness to IFN-based therapy, was not assessed. The study was not designed to establish clinical performances of immunological markers useful for HCV therapeutic prediction and/or monitoring but showed that different ongoing trends of cytokine response to pegIFNribavirin can be observed in SVR and NR patients infected with HIV.
Conclusions. HIV/HCV coinfected patients, showing a high IP-10 and MCP-1 baseline level alongside with a reduced capacity to produce or to maintain broader secretion of cytokines, including MIP-1, IL-4, IL-6 or IL-8, may have a poor response to regimens based on Peg-IFN and ribavirin. Anti-HCV treatment based on drugs having immunomodulating activities may benefits from immunomonitoring using multiplex techniques.