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Conceived and designed the experiments: NN KMC. Performed the experiments: NN HC. Analyzed the data: NN HC GJF KMC. Contributed reagents/materials/analysis tools: HC AS KO MEV MK EG DAP GJF EJW KMC. Wrote the paper: NN DAP GJF EJW KMC.
Viral persistence is associated with hierarchical antiviral CD8 T cell exhaustion with increased programmed death-1 (PD-1) expression. In HCV persistence, HCV-specific CD8 T cells from the liver (the site of viral replication) display increased PD-1 expression and a profound functional impairment that is not reversed by PD-1 blockade alone. Here, we report that the inhibitory receptor cytotoxic T lymphocyte-associated antigen-4 (CTLA-4) is preferentially upregulated in PD-1+ T cells from the liver but not blood of chronically HCV-infected patients. PD-1/CTLA-4 co-expression in intrahepatic T cells was associated with a profound HCV-specific effector dysfunction that was synergistically reversed by combined PD-1/CTLA-4 blockade in vitro, but not by blocking PD-1 or CTLA-4 alone. A similar effect was observed in circulating HCV-specific CD8 T cells with increased PD-1/CTLA-4 co-expression during acute hepatitis C. The functional response to combined blockade was directly associated with CTLA-4 expression, lost with CD28-depletion and CD4-independent (including CD4+FoxP3+ Tregs). We conclude that PD-1 and CTLA-4 pathways both contribute to virus-specific T cell exhaustion at the site of viral replication by a redundant mechanism that requires combined PD-1/CTLA-4 blockade to reverse. These findings provide new insights into the mechanisms of virus-specific T cell dysfunction, and suggest that the synergistic effect by combined inhibitory receptor blockade might have a therapeutic application against chronic viral infection in vivo, provided that it does not induce autoimmunity.
Hepatitis C virus (HCV) is an important human pathogen with a high rate of persistence associated with chronic liver disease that can progress to cirrhosis and hepatocellular carcinoma. Chronic HCV infection occurs in the setting of impaired antiviral T cells that over-express an inhibitory receptor PD-1 (programmed death-1 receptor). Recent studies showed that in vitro inhibition of the PD-1 pathway via an inhibitory antibody can reverse the functional impairment in HCV-specific CD8 T cells from blood but not the liver (the site of viral infection and disease progression). In this study, we show that a second co-inhibitory receptor, CTLA-4, is upregulated in HCV-specific CD8 T cells from the liver and that combined PD-1/CTLA-4 blockade (but not single blockade of PD-1 or CTLA-4) can synergistically enhance their function. This functional enhancement was CD28-dependent but CD4-independent. This effect also differed between viruses, tissue compartments (liver vs. periphery) and clinical status (acute vs. chronic). We conclude that PD-1, CTLA-4, and CD28 expression profiles define a novel hierarchy in HCV-specific CD8 T cell exhaustion than can be synergistically reversed by combined inhibitory receptor blockade. These findings have potential immunotherapeutic applications, provided that no autoimmunity is induced.
Virus-specific CD8 T cells become progressively exhausted during chronic viral infection due to increased level or duration of antigenic stimulation without sufficient CD4 help. Among the CD28 family of costimulatory molecules, programmed death-1 (PD-1) is an immune inhibitory receptor that is highly expressed on both exhausted and activated T cells. Interactions between PD-1 and its ligands PD-L1/PD-L2 can inhibit antigen-specific T cell proliferation and effector function,. Importantly, blockade of PD-1 signaling can restore function to exhausted virus-specific CD8 T cells with reduced viral load in mice with chronic lymphocytic choriomeningitis virus (LCMV) infection in vivo, thereby raising the possibility that immune exhaustion can be reversed with potentially therapeutic antiviral effects. A role for PD-1 pathway in viral persistence and antiviral T cell exhaustion has been shown in various chronic viral infections including hepatitis B virus (HBV), human immunodeficiency virus (HIV), simian immunodeficienty virus (SIV) and hepatitis C virus (HCV),,,,.
In particular, HCV is a highly persistent human pathogen that infects the liver and causes significant morbidity and mortality due to chronic liver disease. Patients with chronic HCV infection harbor dysfunctional antiviral T cells with increased PD-1 expression in circulating blood, and PD-1 blockade can restore their antigen-specific effector function in vitro ,,,,. However, HCV-specific CD8 T cells in the liver (the site of HCV infection) display markedly increased PD-1 expression compared to peripheral blood ,, and a profound functional impairment that is refractory to PD-1 blockade alone. Similarly, highly activated circulating HCV-specific CD8 T cells in acute evolving hepatitis C show markedly increased PD-1 expression with a deep functional impairment that is unresponsive to PD-1 blockade. These results suggested the existence of additional inhibitory mechanisms that contribute to virus-specific CD8 T cell exhaustion in HCV-infected patients, particularly in PD-1high cells.
Since intrahepatic PD-1+ CD8 T cells also express increased levels of immune inhibitory receptor cytotoxic T lymphocyte-associated antigen-4 (CTLA-4), we asked if CTLA-4 might contribute to virus-specific T cell dysfunction in HCV-infected patients. We show that CTLA-4 is preferentially co-expressed in PD-1high CD8 T cells (particularly HCV-specific CD8 T cells) in peripheral blood during acute hepatitis C and in the liver during chronic HCV infection. PD-1/CTLA-4 co-expression was associated with marked antigen-specific effector T cell dysfunction that was dramatically and synergistically reversed by combined PD-1/CTLA-4 blockade in vitro. The response to combined PD-1/CTLA-4 blockade was directly associated with CTLA-4 expression, independent of CD4 T cells including FoxP3+ Tregs and dependent on CD28 expression. Collectively, these findings suggest that both CTLA-4 and PD-1 pathways contribute to HCV-specific T cell exhaustion in a distinct manner in HCV infection and that combined inhibition of CTLA-4 and PD-1 pathways may have potential therapeutic application in reversing immune exhaustion.
In chronically HCV-infected patients (C), CTLA-4 expression was greater in CD8 T cells from liver infiltrating lymphocytes (LIL) compared to peripheral blood lymphocytes (PBL) (p<0.0001) (Figure 1A). This compartmental difference was further amplified in HCV-specific CD8 T cells both in MFI (p=0.023) and percentages (p=0.005), but not in CD8 T cells specific for influenza virus (Flu), cytomegalovirus (CMV) or Epstein-Barr virus (EBV) epitopes (p>0.3) (Figure 1B). These expression patterns mirrored PD-1 expression, which is also upregulated in intrahepatic HCV-specific CD8 T cells,,,. Of note, CTLA-4 expression was low in CD8 T cells from liver explants of two HCV-seronegative patients with nonalcoholic steatohepatitis and alcoholic liver disease (Figure S1). In peripheral blood, CTLA-4 expression levels were uniformly low in total, HCV-specific and non-HCV-specific CD8 T cells during chronic or resolved (R) HCV infection; this contrasts with PD-1 expression, which is elevated in circulating HCV-specific CD8 T cells from chronic compared to resolved patients. CTLA-4 expression was also upregulated in total and HCV-specific (but not non-HCV-specific) CD8 T cells from the peripheral blood of patients with acute hepatitis C (Figure 1A/B). Figure 1C shows the representative PD-1 and CTLA-4 expression for peripheral blood and intrahepatic CD8 T cells specific for HCV and non-HCV epitopes detected by HLA-A2/peptide tetramers. Of note, CTLA-4 was preferentially expressed in PD-1-high, but not PD-1-intermediate or PD-1-negative CD8 (Figure 1D) and CD4 T cells (data not shown) with a strong association between PD-1 MFI and CTLA-4 expression in percentage (R=0.81, p<0.0001) (Figure 1E) as well as MFI (R=0.69, p<0.0001, data not shown). Taken together, CTLA-4 expression is induced early with PD-1 in HCV-specific CD8 T cells during acute hepatitis C but becomes compartmentalized to the liver with chronic infection.
Intrahepatic CD8 T cells were further examined for expression levels of additional CD28 family receptors. As shown (Figure 2A), CD28 was highly expressed in PD-1+CTLA-4+ subset, compared to PD-1+CTLA-4− or PD-1−CTLA-4− subsets (median 62% vs 49% vs 33%, p<0.0001). By contrast, ICOS and BTLA expression levels were generally low, although a slight increase in ICOS expression was observed in PD-1+CTLA-4+ subset compared to others (median 2.4% vs 0.5% vs 0.1%, p=0.049). Thus, intrahepatic CD8 T cells may be subject to inhibitory signals from PD-1 and CTLA-4 as well as a positive signal from CD28 with little contribution from ICOS or BTLA.
CTLA-4 expression was also increased in CD4 T cells from the liver compared to peripheral blood (p<0.0001) (Figure S3A). Since CD4+FoxP3+ Tregs are upregulated in HCV-infected patients and they co-express CTLA-4, we asked whether FoxP3+ Tregs accounted for increased CTLA-4 expression in intrahepatic CD4 T cells. However, FoxP3+ Treg frequencies did not differ between the liver and blood compartments (p=0.209) (Figure S3B/C); furthermore, FoxP3−CTLA-4+ CD4 T cells were enriched by 2–3 fold in the liver compared to blood (Figure S3D). Thus, intrahepatic CD4 and CD8 T cells in HCV-infected patients display increased CTLA-4 expression without increased FoxP3+ Treg frequency.
We previously showed that PD-1 blockade failed to restore function to highly PD-1+ HCV-specific CD8 T cells from HCV-infected liver, although it enhanced the functionality of PD-1 intermediate CD8 T cell from blood. As CTLA-4 was preferentially expressed in PD-1high CD8 T cells (Figure 1D), we asked if CTLA-4 blockade might reverse their dysfunction, either alone or combined with αPD-L1. To this end, intrahepatic and peripheral lymphocytes from HCV-infected patients were cultured with 15mer peptides spanning the entire HCV NS3 or Flu matrix protein in the presence of blocking αPD-L1 and/or αCTLA-4 or isotype control antibodies. On day 7, the cultures were examined for antigen-specific IFN-γ and TNF-α expression by intracellular cytokine staining. As shown in Figure 3A, there was little to no HCV-specific CD4 or CD8 T cell cytokine expression in intrahepatic lymphocytes cultured with αPD-L1 or isotype control antibodies, although low level responses were occasionally seen with αCTLA-4 alone. Remarkably, combined blockade with αPD-L1 and αCTLA-4 resulted in a marked enhancement of intrahepatic HCV NS3-specific CD8 and CD4 T cell cytokine production from 4/6 patients. The comparison of total NS3-specific cytokine responses showed a significant difference between combined PD-1/CTLA-4 blockade and single PD-1 blockade (2.3% vs 0%, p=0.0037 by Mann Whitney U). However, in blood, HCV-specific CD8 T cell cytokine response was augmented by αPD-L1 without further enhancement by αCTLA-4. Thus, combined PD-1/CTLA-4 blockade resulted in marked HCV-specific cytokine response in LIL but not PBL in HCV-infected patients: LIL 4/6 patients (67%) vs PBL 0/8 patients (0%), p=0.015 by Fisher's Exact. The effect of inhibitory receptor blockade is shown in representative flow cytometry plots for intrahepatic CD8 (Figure 3B); notably, the intrahepatic Flu-specific cytokine response was readily detectable without blockade and not enhanced by PD-1/CTLA-4 blockade (Figure 3B, right panels).
The effect of combined PD-1/CTLA-4 blockade on HCV-specific CD8 T cell function was more directly examined in HLA A2+ patients using HLA-A2/peptide tetramers. As shown in Figure 4A, αPD-L1 alone did not enhance intrahepatic HCV NS3 1073-specific CD8 T cell expansion compared to isotype in patient C57, and a 2-fold enrichment was observed with αCTLA-4. However, combined PD-1/CTLA-4 blockade induced a dramatic increase in the HCV NS3 1073 tetramer+ CD8 T cell frequency compared to isotype control or single blockades with aPD-L1 or aCTLA-4. In peripheral blood, αPD-L1 enhanced HCV-specific CD8 T cell expansion as expected while αCTLA-4 provided only an additive effect (Figure 4B). As for antigen-specific effector function, the frequency of tetramer+ CD8 T cells with HCV-specific IFN-γ production, CD107a mobilization and perforin expression increased with αCTLA-4 and combined αPD-L1/αCTLA-4 but not with αPD-L1 alone; in peripheral blood, the functional enhancement also occurred with αPD-L1 alone. Overall, the combined PD-1/CTLA-4 blockade enhanced the expansion and effector function of liver-derived HCV tetramer+ CD8 T cells compared to isotype control in 2/3 patients (Figure 4C). By contrast, intrahepatic CMV-specific CD8 T cells displayed little to no PD-1 or CTLA-4 expression ex vivo and were highly functional without further enhancement by PD-1/CTLA-4 blockade (Figure 4D). Collectively, these results show that combined PD-1/CTLA-4 blockade can restore proliferative capacity and effector function to deeply exhausted intrahepatic HCV-specific CD8 T cells in a synergistic manner.
The effect of PD-1/CTLA-4 blockade was examined in 2 HLA-A2+ patients (A29, A35) with acute hepatitis C characterized by markedly elevated serum alanine aminotransferase (sALT) activities and viral titers. As shown (Figure 5A/B), circulating HCV-specific CD8 T cells displayed increased PD-1 (A29: 95%; A35: 92%) and CTLA-4 (A29: 28%; A35: 14%) expression. As we previously reported, HCV-specific CD8 T cells expanded poorly in vitro when stimulated in the presence of αPD-L1 alone. With αCTLA-4 alone, small increases in HCV tetramer+ CD8 T cell frequencies were observed in both patients, with proliferation directly measured by CFSE dilution in A35 (Figure 5B). However, a marked enhancement of HCV-specific CD8 T cell expansion occurred with combined PD-1/CTLA-4 blockade, mirroring the scenario with intrahepatic T cells. Notably, HCV-specific CD8 T cell dysfunction during acute infection did not persist after spontaneous (A29) or treatment-induced (A35) viral clearance (data not shown), suggesting that PD-1 and CTLA-4 inhibitory pathways can downregulate immune function upon active antigenic encounter, but without necessarily defining the ultimate virological outcome.
The HCV-specific cytokine response to combined PD-1/CTLA-4 blockade was tightly correlated with CTLA-4 expression in CD8 T cells directly ex vivo (R=0.83, p=0.0026) (Figure 6A); a similar positive trend was noted with PD-1 expression, although this did not reach a statistical significance (R=0.36, p=0.20). Notably, the HCV-specific cytokine response during combined PD-1/CTLA-4 blockade did not correlate with the Foxp3+ Treg frequency directly ex vivo. Moreover, the functional restoration by PD-1/CTLA-4 blockade persisted after CD4-depletion that resulted in complete loss of CD4+FoxP3+ Tregs (Figure 6C); these data indicate that the functional response to inhibitory receptor blockade is independent of CD4+FoxP3+ Tregs. Among tetramer+ CD8 T cells, increased PD-1 expression associated with poor augmentation in antigen-specific expansion with the addition of αPD-L1 (data not shown), as previously reported. However, the addition of αCTLA-4 to αPD-L1 resulted in marked expansion of tetramer+ CD8 T cells in direct correlation with CTLA-4 expression ex vivo (Figure 6B), suggesting that αCTLA-4 acts directly on effector CD8 T cells expressing CTLA-4.
Since CD28 is over-expressed in PD-1+CTLA-4+ CD8 T cells (Figure 2A) and mediates positive costimulatory signaling for T cell activation ,, we asked if the functional response to PD-1/CTLA-4 blockade is mediated by CD28+ T cells. To this end, the effect of PD-1/CTLA-4 blockade on the HCV-specific CD8 T cell IFN-γ response was examined in CD4-depleted lymphocyte subsets with and without CD28-depletion in 3 patients (2 chronic HCV patients with liver-derived lymphocytes, 1 acute HCV patients in peripheral lymphocytes). As shown (Figure 7A), the HCV-specific CD8 T cell IFN-γ response was markedly enhanced by combined PD-1/CTLA-4 blockade even in CD4-depleted cells. However, this response was lost with CD28-depletion in all 3 patients, suggesting that the functional response to combined blockade in CD28-dependent.
The role of CD28 in the functional response to PD-1/CTLA-4 blockade was further examined in an HLA-A2+ patient with acute hepatitis C using an HLA-A2/peptide tetramer. As shown in Figure 7B, circulating HCV 1073 tetramer+ CD8 T cells in this patient showed 28% CD28 expression in addition to increased PD-1 (97%) and CTLA-4 (21%) expression ex vivo. Further subset analysis of HCV 1073 tetramer+ CD8 T cells based on PD-1/CTLA-4 expression showed that CD28 was preferentially expressed in PD-1+CTLA-4+ (50%) compared to PD-1+CTLA-4− (19.5%) or PD-1−CTLA-4− (12.2%) subsets (far right histogram on Figure 7B), similar to intrahepatic CD8 T cells (Figure 2A). As shown in the upper panel (Figure 7C), combined PD-1/CTLA-4 blockade markedly enhanced HCV-specific CD8 T cell proliferation in CD4-depleted lymphocytes. With CD28-depletion, this proliferative response was largely lost, even though HCV tetramer+ CD8 T cells remained detectable (Figure 7C). Taken together, our results show that both PD-1 and CTLA-4 can co-inhibit HCV-specific CD8 T cell function and that this effect can be reversed by combined PD-1/CTLA-4 blockade. We further show that this functional effect is mediated by CD28+ CD8 T cells, independently from CD4+ FoxP3+ Tregs.
CTLA-4 is an immune inhibitory receptor within the CD28 family of costimulatory molecules,,. Induced in activated T cells and constitutively expressed in FoxP3+ Tregs,, CTLA-4 shares its ligands B7-1 and B7-2 with CD28 but binds them with differential kinetics,,. CTLA-4 inhibits T cell activation by engaging specific signaling pathways and by outcompeting the positive costimulatory receptor CD28,. A critical immune regulatory role for CTLA-4 is evident from the massive and fatal lymphoproliferation that occurs in CTLA-4-deficient mice,. Antibody-mediated blockade of CTLA-4 signaling can augment antigen-specific CD8 T cell responses in a CD4-independent manner, promoting anti-tumor and autoimmune effects,. CTLA-4 also contributes to immune regulation and pathology in animal models of bacterial or parasitic infection,. CTLA-4 may play a more variable role in viral infections. For example, in LCMV-infected mice, the disruption of CTLA-4 signaling fails to modify the course of infection or antiviral T cell responses in vivo,, unlike PD-1 blockade. By contrast, increased CTLA-4 expression on HIV-specific CD4 (but not CD8) T cells is strongly associated with disease progression and reversible immune dysfunction in HIV-infected patients. Little is known about the relevance of CTLA-4 in HCV infection. We show here that CTLA-4 (together with PD-1) contributes to HCV-specific T cell dysfunction in HCV-infected liver that can be dramatically reversed by combined CTLA-4 and PD-1 blockade.
There are several notable findings in our study. For example, CTLA-4 was upregulated in deeply exhausted, HCV-specific PD-1high CD8 T cells at the site of viral replication (i.e. liver). The increased CTLA-4 and PD-1 expression was functionally relevant, since intrahepatic HCV-specific CD8 T cells regained their function with combined PD-1/CTLA-4 blockade, although not with single-blockade of PD-1 or CTLA-4. Overall, combined PD-1/CTLA-4 blockade strongly enhanced the HCV-specific CD8 T cell response in vitro in 6/9 patients from the liver (4/6 HLA-A2−; 2/3 HLA-A2+), compared to the peripheral blood response which was enhanced in none of the 11 chronically infected patients (p=0.0016). The combined blockade enhanced antigen-specific T cell cytokine production (e.g. IFN-γ and TNF-α) and cytolytic potential (e.g. perforin expression and CD107a degranulation) as well as their expansion. Thus, PD-1/CTLA-4 blockade promoted a polyfunctional HCV-specific T cell response, perhaps acting beyond the inhibition of cellular apoptosis which is increased in highly PD-1+ CD8 T cells in the liver or during acute hepatitis C,. Interestingly, while combined blockade enhanced both HCV-specific T cell IFN-γ and TNF-α production (Figure 3), the increase was particularly evident for TNF-α, suggesting that PD-1/CTLA-4 blockade may promote a cytokine profile that differs from a preferential (albeit weak) IFN-γ rather than TNF-α production by dysfunctional HCV-specific CD8 T cells in chronic hepatitis C. The combined PD-1/CTLA-4 blockade also enhanced intrahepatic HCV-specific CD4 T cell function, an important consideration given the relevance of CD4 T cells in immune regulation,.
Although HCV persistence is associated with increased levels of circulating CD4+FoxP3+ Tregs that constitutively express CTLA-4,,,, the level of functional restoration in CD8 T cells by PD-1/CTLA-4 blockade correlated directly with the frequency of CTLA-4+ CD8 T cells but not FoxP3+CD4+ Tregs ex vivo. Furthermore, while the functional response to combined blockade differed between the liver and blood, FoxP3+ Treg frequencies did not differ between the two compartments ex vivo or following in vitro culture with PD-1/CTLA-4 blockade (data not shown). Finally, the response to combined blockade persisted after CD4 T cells (including CD4+FoxP3+ Tregs) were depleted. These results suggest that PD-1/CTLA-4 blockade targets effector T cells directly in a manner independent of CD4 T cells including FoxP3+ Tregs.
PD-1 and CTLA-4 inhibit T cell activation through distinct mechanisms that converge on Akt: PD-1 inhibits CD28-mediated activation of phosphatidylinositol 3-kinase (PI3K) and CTLA-4 activates the type II serine/threonine phosphatase PP2A, both leading to the inhibition of Akt phosphorylation. By competing with CD28 for B7-1 and B7-2,, CTLA-4 can reduce CD28-mediated PI3K activation, further enhancing the negative signaling through PD-1. Since PD-L1 also interacts with B7-1, both αPD-L1 and αCTLA-4 can increase the accessibility of B7-1 to CD28. In our study, HCV-specific CD8 T cells co-expressing PD-1 and CTLA-4 (e.g. from HCV-infected liver) were deeply exhausted and resistant to PD-1 blockade alone, whereas combined PD-1/CTLA-4 blockade had a synergistic effect in restoring their function. However, the two negative regulators may act redundantly to inhibit T cell function in this setting, such that both must be blocked to regain normal functions. The PD-1+CTLA-4+ phenotype with a functional response to PD-1/CTLA-4 blockade also occurred in circulating HCV-specific CD8 T cells during acute hepatitis C. By contrast, circulating HCV-specific CD8 T cells from chronic HCV patients (e.g. with intermediate PD-1 expression without CTLA-4 co-expression) were functionally augmented by PD-1 blockade alone. These findings suggest that the CTLA-4 and PD-1 pathways are induced early in HCV infection to co-regulate HCV-specific CD8 T cell function in a redundant manner that differs between tissue compartments over the course of infection.
Notably, CD28 was highly expressed in intrahepatic PD-1+CTLA-4+ CD8 T cells compared to CTLA-4− CD8 T cells. CD28 expression may be induced to counter the inhibitory signals mediated by PD-1 and CTLA-4. Conversely, CTLA-4 may be induced in CD28+PD-1+CD8 T cells to downregulate the active inflammation at the site of viral replication. In either case, increased CD28 expression may enable greater functional enhancement upon PD-1/CTLA-4 blockade due to unhampered positive signaling through CD28. Indeed, the functional response to PD-1/CTLA-4 blockade was abolished in HCV-specific CD8 T cells by CD28-depletion in our study. Along these lines, direct CD28 costimulation enhanced HCV-specific CD8 T cell IFN-γ response in HCV-monoinfected patients but not in HIV/HCV-coinfected patients with reduced CD28 expression on CD8 T cells in one study. Since loss of CD28 expression is a marker of T cell senescence and functionality, detection of CD28 expression in PD-1+CTLA-4+ CD8 T cells provides an additional marker for reversible functional exhaustion. Collectively, these costimulatory receptors may define a dynamic and complex functional hierarchy for antigen-specific CD8 T cells at various stages and types of viral infections that may respond to distinct therapeutic modulation. If this is correct, combined blockade could have potential therapeutic implications in chronic viral infection, provided it does not trigger autoimmunity.
There are distinct differences between our study and those in human HIV or murine LCMV infections,. In peripheral blood of HIV-infected patients, increased CTLA-4 expression with a functional response to CTLA-4 blockade was limited to HIV-specific CD4 but not CD8 T cells. This difference may be explained by the reduced CTLA-4 and CD28 expression in HIV-specific CD8 T cells, since the functional response to combined PD-1/CTLA-4 blockade depended on both CTLA-4 and CD28 expression in our study. Alternatively, HIV-specific CD8 T cells might exhibit compartmental differences (e.g. between blood and tissue compartments) similar to HCV. In LCMV-infected mice, LCMV-specific CD8 T cells displayed increased CTLA-4 and PD-1 expression, but responded only to PD-1 but not CTLA-4 blockade in vivo. Furthermore, HIV-specific and LCMV-specific T cells were functionally augmented by αPD-L1, without a synergistic response to combined αPD-L1/αCTLA-4,. Thus, PD-1 may play a more universal role in antiviral T cell exhaustion whereas the effect of CTLA-4 may differ between viral infections, T cell subsets and even anatomical locations.
In conclusion, both CTLA-4 and PD-1 contributes to HCV-specific T cell exhaustion in a redundant manner in human HCV infection, particularly in HCV-infected liver; this intrahepatic virus-specific T cell dysfunction can be synergistically reversed by combined PD-1/CTLA-4 blockade in vitro in a CD4-independent and CD28-dependent manner. These findings provide new insights to the mechanisms that regulate virus-specific T cell dysfunction and suggest that immune exhaustion at the site of antigen expression may be reversed by combined inhibitory receptor blockade.
All subjects were recruited with informed consent approved by the Institutional Review Boards. All investigations have been conducted according to the principles expressed in the Declaration of Helsinki. Patients were recruited at the Philadelphia Veterans Affairs Medical Center (PVAMC) and the Hospital of the University of Pennsylvania. A total of 47 patients with chronic hepatitis C without HIV coinfection (group C) were examined, including 33 cirrhotic patients undergoing liver transplantation and 14 patients with chronic stable HCV infection. Control groups included 10 healthy HCV-seronegative subjects (group N), 4 HCV-seropositive but RNA-negative patients with spontaneous resolution of HCV infection without prior antiviral therapy (group R) and 6 patients with acute hepatitis C (group A) diagnosed by acute serum alanine amino-transferase (sALT) elevation with documented HCV-seroconversion and/or viremic fluctuations greater than 10-fold without prior liver disease as described previously. The patient characteristics are shown in Table 1.
All fluorescent monoclonal antibodies (mAbs) were purchased from BD Bioscience (San Jose, CA) except for: (i) αFoxP3 and αCD28 from eBioscience (San Diego, CA); (ii) FITC-labeled αPD-1 (αCD279; clone EH12.2H7) from BioLegend (San Diego, CA); and, (iii) PE-labeled αPD-1 from the Dana Farber Cancer Institute (Boston, MA). Of note, PD-1 and CTLA-4 expression in all subjects was examined using FITC-labeled αPD-1 (clone M1H4, BD) and PE-labeled αCTLA-4 (αCD152; clone BNI3, BD). In selected subjects, the patterns of PD-1 (low/intermediate/high) and CTLA-4 expression in CD8 T cells were compared using FITC-labeled αPD-1 from BioLegend or PE-labeled αPD-1 from the Dana Farber Caner Institute combined with APC-labeled αCTLA-4 (BD). Dead cells were excluded with 7-AAD. For functional blockade, αPD-L1 mAb (clone 29E.2A3.C6) from the Dana Farber Cancer Institute, and αCTLA-4 mAb (clone BNI3; BD) were used.
The HCV-specific T cell response was measured using a pool of 105 overlapping 15mer peptides spanning the entire NS3 protein derived from HCV genotype 1a,,,. Similarly, the T cell response to influenza virus was examined using 49 overlapping 15mer peptides spanning the conserved matrix M1 protein (residues 1–252) based on the human A/PR/8/34 (H1N1) virus. For HLA-A2+ subjects, the following peptides corresponding to optimal CD8 epitopes were synthesized for antigenic stimulation and tetramer synthesis as described previously : (i) HCV NS3 1073 (CINGVCWTV), NS3 1406 (KLVALGINAV) and NS5B 2594 (ALYDVVSKL); (ii) influenza matrix (GILGFVFTL); (iii) EBV BMLF1 (GLCTLVAML); and, (iv) CMV pp65 (NLVPMVATV).
Cells were stained with fluorescent antibodies according to the manufacturer's instructions; events were acquired with a FACSCalibur or FACSCanto (Becton Dickinson, San Jose, CA) and analyzed with FlowJo software (Tree Star Inc., San Carlos, CA). Compensations were established using single color controls. As CTLA-4 is more readily detected in the cytoplasm due to rapid internalization,,, CTLA-4 expression was assessed by intracellular staining following permeabilization. Cutoffs for CTLA-4 expression was defined by isotype control where 99.9% of the events were negative. Figure S2 further confirms the preferential CTLA-4 expression on PD-1high CD8 T cells with corresponding isotype and unstained controls.
PBL were isolated by standard Ficoll-Histopaque (Sigma Chemical Co., St Louis, MO) density centrifugation,. LIL were isolated from 20–50 gm of fresh liver explant tissue that was transported in complete media and processed within 24 hours of explant (usually 1–3 hours) as described previously; briefly, this procedure incorporated careful dicing of liver into 5 mm3 pieces, incubation of the liver slurry at 37°C with 1 mg/ml collagenase (Type 1a; Roche Molecular) and 1 µg/ml DNase (Sigma Aldrich) for 30 minutes, further mechanical dissociation using the Seward Stomacher 400 Lab Blender (Brinkman Instruments, Westbury, NY), filtration through a 70 µm nylon filter and Ficoll-Histopaque density centrifugation. Control experiments showed that collagenase digestion for 30 minutes did not alter PD-1, CTLA-4, or CD28 expression (data not shown).
PBL and LIL (2×106 cells/ml/well) were stimulated on day 0 with overlapping HCV NS3 or influenza matrix 15mer peptides (2 µM) in complete media in the presence of isotype control antibodies, αPD-L1, αCTLA-4 or both αPD-L1 and αCTLA-4 (10 µg/ml for each mAb). Cell cultures were stimulated with rIL-2 (100 IU/ml) on day 4 and examined by flow cytometry on day 7 with CD107a, intracellular cytokine or perforin staining as previously described,. For intracellular cytokine staining, expanded PBL and LIL cultures were stimulated for 6 hours with HCV or Flu peptides in the presence of brefeldin A (10 µg/ml) before surface staining, permeabilization and intracellular staining with αIFN-γ and αTNF-α. Antigen-specific CD107a mobilization was quantified by adding FITC-labeled αCD107a before peptide stimulation. In selected HLA-A2+ subjects with available cells, PBL and LIL were stimulated with HLA-A2 restricted antigenic peptides (10 µg/ml) with the blocking conditions described above.
In select experiments, antigen-specific IFN-γ+ T cell response was quantified by IFN-γ ELISPOT assay in which cultured lymphocytes were stimulated for 45 additional hours with antigenic peptides or control media (200,000 cells/well in triplicates) as previously described,,. HCV-specific IFN-γ+ T cell frequency was calculated by subtracting the mean IFN-γ spot forming units (SFU) in control wells from the mean SFU in antigen-stimulated wells and expressed as IFN-γ SFU/106 cells.
Lymphocytes were labeled with 5 mM CFSE (Molecular Probes, Eugene, OR) as described previously, before 7 days of culture with antigenic peptides (10 µg/ml) in the presence of isotype control or blocking antibodies as described above. Cell cultures were stimulated with rIL-2 (100 IU/ml) on day 4 and examined by flow cytometry on day 7 for antigen-specific T cell expansion.
CD4 T cells were depleted from PBL and/or LIL using CD4 Dynabeads (Invitrogen, Oslo, Norway) as previously described. CD28+ T cells were depleted by sequentially staining with αCD28-PE (clone CD28.2, BD Pharmingen) and anti-PE Microbeads before separation by AutoMACS (Miltenyi Biotec Inc) as previously described . The efficiency of CD4 and CD28 depletion was >97% (data not shown).
Clinical and immunological parameters were compared using the Mann-Whitney U-test, the paired t-test and the Kruskal-Wallis test. Frequency differences were compared by Fisher's Exact test or the Chi-square test as appropriate. Correlations were tested for significance by the Spearman rank correlation test. P values below 0.05 were considered significant.
CTLA-4 and PD-1 expression in intrahepatic CD8 T cells from HCV-seronegative subjects. CTLA-4 and PD-1 expression in gated CD8 T cells from liver explants are shown for 2 HCV seronegative subjects (NC091, NC109) with nonalcoholic steatohepatitis (NASH) and alcoholic cirrhosis and 2 representative chronic HCV patients (C97, C08). Bottom plots show the isotype control staining of the intrahepatic lymphocytes.
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Preferential CTLA-4 expression in PD-1high CD8 T cells isolated from blood of an acute hepatitis C patient (A46). The sample on the far right was stained with αCTLA-4, aPD-1, αCD8 and 7-AAD. Two samples on the left were stained with the same antibody cocktail minus anti-CTLA-4 (unstained) or with the addition of the corresponding isotype antibody.
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Increased CTLA-4 expression in CD4 T cells is increased in HCV-infected liver. (A) %CTLA-4+ expression in CD4 T cells from peripheral blood and liver of 15 chronic (C) patients and blood of 4 HCV-seronegative controls (N). Median %CTLA-4+ in CD4 T cells (red horizontal lines): C-blood 6.9% vs. C-liver 17.9% (p<0.0001 by the Mann-Whitney U-test); N-blood 5.6%. Of note, examination of intrahepatic CD4 T cells from 3 HCV seronegative but cirrhotic patients showed similar level of CTLA-4 expression (10.4%, 4.8%, 1.4%) as those in normal control PBL. (B) %FoxP3+ in CD4 T cells from blood and liver of 30 chronic (C) HCV patients. Median %FoxP3+ in CD4 T cells (red horizontal lines): C-blood 7.6% vs. C-liver 6.3% (p=0.209 by the Mann-Whitney U-test). (C) Representative FoxP3 expression in CD4 and CD8 T cells from blood and liver of a chronic HCV patient (C97). (D) %FoxP3−CTLA-4+ CD4 T cells in the liver and blood in chronic HCV patients (blood, unfilled bars; liver, solid bars).
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The authors thank the members of the liver transplant team at the Hospital of the University of Pennsylvania for the liver sample procurement, Colleen Brensinger for statistics assistance, Geoffrey Dufrayne for technical assistance, and all of the study subjects. We acknowledge Drs. David E. Kaplan and Michael Betts for their support and helpful insights. We also thank Drs. James Riley and Francis V. Chisari for the thoughtful discussions and careful reading of the manuscript.
G.J.F. has a patent licensing arrangement for antibodies blocking the PD-1/PD-L pathways.
This study is supported by National Institutes of Health (NIH) grants AI47519, the American Gastroenterological Association Elsevier Research Initiative Award (K.M.C.); Philadelphia VA Medical Research, the NIH/National Institute of Diabetes and Digestive and Kidney Diseases Center of Molecular Studies in Digestive and Liver Diseases grant P30DK50306 and its Molecular Biology and Cell Culture Core Facilities, NIH Public Health Service Research grant M01-RR00040; a grant from the Foundation for the NIH through the Grand Challenges in Global Health Initiative, and NIH grant AI56299 (to G.J.F.); D.A.P. is a Medical Research Council (UK) Senior Clinical Fellow. Support for the Abramson Cancer Center Flow Cytometry and Cell Sorting Shared Resource of the University of Pennsylvania was funded through NIH grant P30 CA016520 from the National Cancer Institute.