Inhibitors of PD-1 signaling have revolutionized cancer therapy. PD-1 and PD-L1 antibodies have been approved for the treatment of cancer. To date, therapeutic PD-1 inhibitors have not been compared in a functional assay. We used an efficient T cell reporter platform to evaluate the efficacy of five clinically used PD-1 inhibitors to block PD-1 signaling. The half maximal effective concentrations (EC50) for nivolumab and pembrolizumab were 76.17 ng/ml (95% CI 64.95–89.34 ng/ml) and 39.90 ng/ml (34.01–46.80 ng/ml), respectively. The EC50 values of the PD-L1 inhibitors were 6.46 ng/ml (5.48–7.61 ng/ml), 6.15 ng/ml (5.24–7.21 ng/ml) and 7.64 ng/ml (6.52–8.96 ng/ml) for atezolizumab, avelumab, and durvalumab, respectively. In conclusion, a functional assay evaluating antibodies targeting PD-1 inhibition in vitro revealed that pembrolizumab is a slightly more effective PD-1 blocker than nivolumab, and that PD-L1 antibodies are superior to PD-1 antibodies in reverting PD-1 signaling.
Programmed cell death-1 (PD-1), an important inhibitory receptor, is critical for the maintenance of central and peripheral T cell tolerance. However, PD-1, which is upregulated on activated and exhausted T cells, also limits productive immune responses against pathogens and cancer cells. PD-1 signaling is induced upon binding of its ligands, PD-1 ligand-1 (PD-L1) and PD-1 ligand-2 (PD-L2). The expression of PD-L2 is mainly restricted to professional antigen presenting cells (APCs) like macrophages and dendritic cells (DCs), whereas PD-L1 is also expressed in non-hematopoietic tissues and can thus be regarded as the major PD-1 ligand. Importantly, PD-L1 is also upregulated in the tumor microenvironment and is found in a large variety of tumor cells. Tumor infiltrating lymphocytes frequently express PD-1, providing a rationale for therapeutically disrupting the PD-1/PD-L1 interaction to improve anti-tumor responses. Currently, several PD-1 and PD-L1 antibodies are in clinical use for the treatment of various solid cancers and lymphomas, and blocking of the PD-1 pathway was shown to induce impressive response rates across a broad spectrum of tumor types1,2.
Although the clinical indications for which regulatory authorities have approved antibodies targeting PD-1 and PD-L1 only partially overlap, the mode of action of these drugs is blocking PD-1 signaling. Therefore, it is evident that the ability of these agents to disrupt the function of PD-1 critically impacts their clinical efficacy. As with other drugs, dose response curves and half maximal effective concentrations (EC50) provide valuable information on the efficacy of these antibodies. However, these values are not available for therapeutic PD-1 and PD-L1 antibodies, and the ability of these agents to block PD-1 signaling have not been compared in a functional assay. We have previously developed and described an efficient, robust and cost-effective fluorescent T cell reporter platform for the evaluation of immune checkpoint inhibitors (ICIs) targeting different inhibitory receptors, including PD-13.
Here, we have exploited this system to determine the EC50 values of five antibody-drugs used in the clinic to block the PD-1/PD-L1 interaction, namely atezolizumab, avelumab, durvalumab, nivolumab and pembrolizumab. In addition, we used flow cytometry-based binding assays on the cells in our reporter system to explore whether it can be used to predict the functional potency of blocking antibodies.
Characterization of PD-1 reporter cells and T cell stimulator cells expressing PD-1 ligands
PD-1 expressing NF-κB::eGFP reporters and control reporters based on the human Jurkat T cell line JE6.1 were used in this study3. High levels of PD-1 were detected on the PD-1 reporters, whereas the control reporters were PD-1-negative. Both, the PD-1 and control reporters, expressed similar levels of the costimulatory receptor CD28 and of CD3 on their surface (Fig. 1A). To stimulate our reporters in the absence and presence of PD-1 ligands, we used T cell stimulators (TCS) based on the murine thymoma cell line BW51474. TCS express a membrane-bound anti-human CD3 single chain antibody fragment that can functionally engage the CD3-TCR complex on our T cell reporters. TCS, which express high levels of human PD-L1 or PD-L2, were generated to trigger PD-1 on the PD-1 expressing reporter cells (Fig. 1B). In addition, we generated TCS expressing the costimulatory ligand CD86 and TCS co-expressing CD86 and PD-L1 (Fig. 1C).
To functionally validate our reporter platform, control and PD-1 reporter cells were stimulated by TCS expressing PD-1 ligands or control TCS. In the control reporter cells similar levels of reporter activation were induced by control TCS and TCS expressing PD-1 ligands. In contrast, eGFP expression on the PD-1 reporters was strongly reduced upon stimulation with TCS-PD-L1 or TCS-PD-L2 (Fig. 1D). This effect was completely abolished upon the addition of the therapeutic PD-1 antibodies nivolumab or pembrolizumab, whereas the therapeutic PD-L1 antibodies avelumab and durvalumab blocked PD-L1 but not PD-L2 inhibition (Fig. 1D). In a next set of experiments, we analyzed the effects of PD-1 on reporter cells that received costimulatory signals. For this we used TCS co-expressing PD-L1 and CD86, a ligand for the primary costimulatory receptor CD28. As expected, stimulation with TCS-CD86 resulted in strong activation of both reporters, and the presence of PD-L1 on these cells inhibited eGFP expression by the PD-1 reporters (Fig. 1E). This reduction in reporter gene expression was abolished by the presence of therapeutic PD-1 and PD-L1 antibodies (Fig. 1F). Taken together, our results indicate that PD-1 strongly suppressed reporter gene expression in the presence or absence of CD28 costimulation. Moreover, these experiments demonstrate that our reporter platform is an intrinsically controlled system well-suited to evaluate and compare clinically used antibodies targeting PD-1 inhibition.
Determination of functional EC50 values for atezolizumab, avelumab, durvalumab, nivolumab and pembrolizumab
In order to assess the functional efficacy of ICIs in blocking PD-1 signaling, we set out to determine the EC50 values for each of these antibodies using our reporter system. Two recent studies suggest that CD28 signaling is the preferred target of PD-1 inhibition5,6. Consequently, we have used TCS-CD86/PD-L1 to stimulate PD-1 reporter cells. Nivolumab, pembrolizumab, atezolizumab, avelumab, and durvalumab were added at concentrations ranging from 1 µg/ml to 976 pg/ml, and reporter gene expression was measured after 24 h by flow cytometry. An increase in eGFP expression was observed in the PD-1 reporter cells in the presence of PD-1 or PD-L1 antibodies in a dose-dependent manner and PD-1 inhibition was completely abolished at higher concentrations of antibodies (Fig. 2). Normalized reporter gene expression values from three independently performed experiments were combined and used to calculate the EC50 values for each antibody. The EC50 values calculated for all three PD-L1 antibodies were very low at 6.46 ng/ml for atezolizumab, 6.15 ng/ml for avelumab and 7.64 ng/ml for durvalumab. The PD-1 antibodies were less effective with nivolumab having the highest EC50 value (76.17 ng/ml), while pembrolizumab (39.90 ng/ml) was slightly more effective (Fig. 2). In additional experiments, we evaluated avelumab and nivolumab using different T cell stimulator cells based on the human myelogenous leukemia cell line K562. The EC50 values obtained from these experiments were similar to those obtained with the TCS based on the BW5147 murine cell line (Fig. S1).
Evaluation of therapeutic PD-1 and PD-L1 antibodies in a flow cytometry-based binding assay
We hypothesized that the binding of blocking antibodies to their target antigens would correlate with their activity in our functional assay. To test this, we used reporter cells and T cell stimulator cells to perform binding assays with therapeutic antibodies targeting PD-1 and PD-L1, respectively. Atezolizumab, avelumab, and durvalumab binding was analyzed on PD-L1 expressing TCS, whereas PD-1 expressing reporter cells were used to test nivolumab and pembrolizumab binding. Target cells were probed with antibodies at a wide range of concentrations, and binding was detected with an APC-labeled anti-human IgG antibody and measured by flow cytometry. These experiments revealed comparable EC50 values for the PD-L1 antibodies atezolizumab (15.08 ng/ml), avelumab (12.69 ng/ml) and durvalumab (13.76 ng/ml) (Fig. 3A). The EC50 values for the PD-1 antibodies nivolumab (7.27 ng/ml) and prembrolizumab (7.89 ng/ml) were also similar (Fig. 3B).
Comparison of EC50 values obtained in binding assays and functional assays
The EC50 values and the 95% CI from the functional assays and the binding assays are summarized in Table 1. A statistical comparison of these values is shown in Table 2. Our data show that among the therapeutic PD-1 antibodies, pembrolizumab is the most effective at blocking PD-1 signaling (Table 2). The functional EC50 values of the therapeutic PD-L1 antibodies were very similar and were significantly lower than the EC50 values of the therapeutic PD-1 antibodies (Tables 1 and 2). The results of the binding studies yielded similar EC50 values for the binding of both therapeutic PD-1 antibodies to PD-1 and for the binding of the three PD-L1 antibodies to PD-L1 (Table 1). The EC50 values of the PD-1 antibodies were significantly lower than the EC50 values of the PD-L1 antibodies (Table 2). Interestingly, neither the higher blocking ability of pembrolizumab compared to nivolumab nor the better performance of PD-L1 antibodies compared to PD-1 antibodies were reflected by the binding studies. This indicates that testing PD-1 blockers in standard flow cytometry-based binding assays may be of little use in appraising their ability to block PD-1 signaling in a functional assay.
T cell-expressed inhibitory receptors like CTLA-4, LAG-3, BTLA, TIM-3 and PD-1 function as immune checkpoints, which limit and terminate immune responses. We have recently highlighted that each of these molecules has unique properties and that many aspects of the roles of these molecules in immunity are currently not fully understood7. Immune checkpoint inhibition with therapeutic antibodies is a very effective mean to enhance T cell responses and it has been successfully exploited to treat patients suffering from different types of cancers8,9,10. Several antibodies targeting PD-1 or PD-L1 have received clinical approval as first and second line treatments for different malignancies and numerous clinical trials are ongoing to test the efficacy of these drugs when used alone or in combination with conventional anti-cancer drugs as well as targeted therapies10. Clinicians can choose from several ICIs to disrupt PD-1 signaling and a thorough characterization of these drugs is warranted to ensure their optimal use. Their efficacy in blocking the interaction of PD-1 with its major ligand PD-L1 is of great interest in this context. However, to our knowledge this information was not available for the PD-1 and PD-L1 antibodies that are currently used in the clinic.
We have previously developed a fluorescent transcriptional reporter system based on the human Jurkat T cell line3,11,12. When PD-1 is expressed in these cells, transcriptional activation is inhibited in the presence of PD-1 ligands. Analysis of PD-1 signaling in a multiparameter reporter line that simultaneously measures three transcription factors that play major roles in T cell activation, NF-κB, NFAT and AP-1, revealed that NF-κB and NFAT activation were both strongly inhibited by PD-1 engagement and are thus well-suited as a readout for PD-1 blocking11. In the current study, we used a highly sensitive NF-κB::eGFP JE6.1 reporter cell line expressing PD-1 to determine the EC50 values for the five antibodies that are currently used in the clinic to disrupt PD-1 signaling3. T cell stimulator cells expressing human PD-L1 and providing CD28 costimulation via CD86 were used to activate these reporters in presence of different concentrations of the ICIs. We found that the PD-1 antibody pembrolizumab is slightly more effective than nivolumab and that the PD-L1 antibodies atezolizumab, avelumab and durvalumab have significantly lower EC50 values than the PD-1 antibodies. Experiments with the PD-L1 antibody avelumab and the PD-1 antibody nivolumab using different T cell stimulator cells based on the human K562 cell line yielded similar EC50 values and confirmed that the PD-L1 antibody had a higher blocking efficiency than the PD-1 antibody (Fig. S1). K562 cells are devoid of CD80 or CD86 so these results also suggest that CD28 costimulation does not have a major influence on the functional EC50 values for PD-1 and PD-L1 antibodies. One potential explanation for the lower functional EC50 values of PD-L1 antibodies compared to PD-1 antibodies is that ligands are more effectively blocked than receptors, but more work is required to address this possibility. We hypothesized that the binding activity of the blocking antibodies to their target antigens would correlate with their activity in our functional assay. We thus used the reporter cells and T cell stimulator cells to perform flow cytometry-based binding assays with ICIs targeting PD-1 and PD-L1. Surprisingly these experiments did not indicate that flow cytometry-based binding assays performed under standard conditions are informative regarding the EC50 values of PD-1 blockers.
Therapeutic antibodies targeting PD-1 inhibition have not been compared in clinical trials. Although analysis of published data on non-small-cell lung carcinoma (NSLC) patients did not reveal differences in the efficacy between PD-1 and PD-L1 antibodies, such studies have many limitations as pointed out by the authors13,14. Our results demonstrate a superior blocking capacity of therapeutic PD-L1 antibodies, but the distinct properties and functions of ICIs binding PD-1 and PD-L1 have to be considered when evaluating their clinical use. In the priming phase, T cells interact with dendritic cells which express both PD-1 ligands, PD-L1 and PD-L215. Although there is ample evidence that blocking PD-L1 enhances the response of human T cells interacting with APCs, PD-1 antibodies, which block PD-1 binding to both ligands, are likely to be more effective at promoting the priming of tumor specific T cells15,16,17,18. It should be stressed however, that PD-1 expression does not selectively mark dysfunctional cells as it is not limited to chronically stimulated T cells, which enter a state often referred to as “exhaustion”19,20. All T cells upregulate this immune checkpoint upon activation and therefore PD-1 prevents the activation of self-reactive or pathognomonic T cells21,22,23. Thus, blockade of both PD-1 ligands on DCs and other APCs, mediated by PD-1 antibodies, could potentially be associated with more severe side effects than the use of PD-L1 antibodies, which do not prevent the binding of PD-1 to PD-L2. In line with this, there is some evidence that PD-1 antibodies induce higher rates of immune adverse events like pneumonitis than PD-L1 antibodies13,14. In the tumor microenvironment and on tumor cells, PD-L1 is the predominant PD-1 ligand and thus blocking PD-L1 and PD-1 is likely to be equally efficient in the effector phase of tumor specific T cells. Therapeutic PD-1 and PD-L1 antibodies currently in use also have different isotypes. PD-1 antibodies are IgG4, whereas the PD-L1 antibodies harbor unmodified (avelumab) or modified IgG1 Fc sequences (durvalumab and atezolizumab).
In addition to PD-1, PD-L1 also binds CD80, a molecule which has an important role as a costimulatory ligand24,25. Therapeutic PD-L1 antibodies also disrupt the binding of PD-L1 to CD80, and therefore PD-L1 antibodies could potentially also augment T cell responses by blocking this pathway.
PD-L1 blockers are used at much higher doses than PD-1 antibodies, while the results of our study reveal that PD-L1 antibodies have a superior blocking capacity. The serum half-life of IgG1 and IgG4 antibodies is 21 days and the reported half-lives of nivolumab, pembrolizumab, atezolizumab, and durvalumab were in this range, while a much lower half-life was reported for avelumab (Table 3). It is possible that other factors like the higher density of PD-L1 compared to PD-1 or the faster clearance of PD-L1-IgG1 antibodies in the tissues via Fc-receptor mediated mechanisms warrant a higher dosage of PD-L1 antibodies compared to PD-1 antibodies. Nevertheless, the results of our study may provide a rationale for testing PD-L1 antibodies at lower doses.
We show here, that the ICIs that are currently used to target the PD-1/PD-L1 interaction are extremely efficient blockers of PD-1 inhibition. Cmax values for pembrolizumab measured in sera of treated patients were more than three orders of magnitudes higher than the EC50 values measured in our in vitro assays26. Based on studies in mice, the concentration of these antibodies in the tumor microenvironment can be expected to be much lower than the Cmax values27. Information on the concentrations of PD-1 or PD-L1 antibodies in the tumors of treated patients is not available, and thus it is not known whether they are indeed higher than the EC50 values obtained in our in vitro assays. Nevertheless, the results of our study may provide a rationale for testing antibodies targeting PD-1 inhibition and in particular PD-L1 antibodies at lower doses. Various factors, such as hypoxia or difficulty in tumor stroma penetration, restrict the immunotherapy effects and measures to overcome these limitations; for instance, using antibody drug conjugates or prodrugs based disruption of hypoxia were shown to have utility in improving immune checkpoint blockade28,29.
Currently, there are intense efforts to develop novel ICIs targeting inhibitory pathways like LAG-3, TIM-3, TIGIT, BTLA or VISTA7,10,30,31. Selecting ICIs that are highly effective at blocking these pathways will greatly increase the prospects of such endeavors. Cellular reporter platforms such as the one used here are well-suited to discern ICIs with high potential.
Material and Methods
Antibodies, cell culture and flow cytometry
The Jurkat E6.1 cells and the BW5417 cell line, which is a murine thymoma cell line (short designation in this work: BW) were derived from inhouse stocks and cultured as previously described11,32. The generation and validation of Jurkat E6.1 NF-κB::eGFP, and Jurkat E6.1 NF-κB::eGFP-PD1 reporter T cell lines have been previously reported3. T cell stimulator cells (TCS), which are BW cells engineered to stably express an anti-human CD3 single chain fragment have previously been described in detail4. TCS expressing high levels of PD-L1, PD-L2, CD86 and co-expressing PD-L1 and CD86 or no human costimulatory molecule (TCS-control) were generated by retroviral transduction. Surface expression was confirmed by flow cytometry. All cell lines were tested for the absence of mycoplasma using a method described recently33. The cells were stained with a panel of antibodies to authenticate them, and the reporter and stimulator cells were kept in culture for up to three months without perceptible loss of functionality. The following antibodies from Biolegend (San Diego, CA) were used: APC-conjugated PD-1 (#EH12.2H7), APC-conjugated PD-L1 (#29E.2A3), APC-conjugated CD86 (#IT2.2), PE-Cy7-conjugated CD3 (#UCHT-1), PE-conjugated PD-L2 (#24 F.10C12), PE-conjugated CD28 (#28.2), and the PE-conjugated isotype antibody control. A DyLight-649-conjugated goat-anti-mouse IgG (H + L) antibody (Jackson ImmunoResearch, West Grove, PA) was used to detect the membrane-bound anti-CD3 fragment. An APC-conjugated antibody to mouse CD45 (#104, Biolegend) was used to exclude TCS in reporter assays.
The PD-1 antibodies, nivolumab (Opdivo®, Bristol-Myers Squibb GmbH & Co) and pembrolizumab (Keytruda®, MSD Sharp & Dohme GmbH), and the PD-L1 antibodies, avelumab (Bavencio®, Merck), durvalumab (Imfinzi®, AstraZeneca), and atezolizumab (Tecentriq®, Roche) were used at the indicated final concentrations.
Flow cytometry was performed on a FACSCalibur flow cytometer (Becton Dickinson Immunocytometry System, San Jose, CA) using CellQuest software. Data were analyzed with FlowJo (version 10.0.6, Tree Star, Ashland, OR) and GraphPad Prism (version 5, GraphPad Software, Inc., La Jolla, CA).
Reporter cells (5 × 104) and TCS (2 × 104) were cocultured in 96-well flat bottom plates for 24 h in the presence or absence of antibodies to PD-1 (nivolumab; pembrolizumab) or PD-L1 (avelumab; durvalumab; atezolizumab) at 1000, 500, 250, 125, 62.5, 31.25, 15.63, 7.81, 3.91, 1.95, and 0.98 ng/ml (two-fold dilution steps). Subsequently, reporter gene expression (eGFP) was analyzed by flow cytometry as previously described in detail3. Briefly, cells were harvested and TCS were excluded using mCD45 mAb. The geometric mean of the fluorescence intensity (gMFI) of viable reporter cells was used for further analysis. To estimate EC50 values, three independent PD-1 reporter stimulation experiments were performed in duplicate. For each stimulation experiment, reporter gene induction in response to stimulation in presence of PD-L1 (stimulation with TCS-CD86/PD-L1) was normalized to reporter gene expression in the respective control (stimulation with TCS-CD86) and expressed as fold induction of the (gMFI).
PD-1 expressing reporter cells (1 × 105) were incubated for 30 minutes at 4 °C with the PD-1 antibodies nivolumab or pembrolizumab at final concentrations of 3.16 µg/ml, 1 µg/ml, 316 ng/ml, 100 ng/ml, 31.6 ng/ml, 10 ng/ml, 3.16 ng/ml, 1 ng/ml, 316 pg/ml, 100 pg/ml, 31.6 pg/ml, and 10 pg/ml. All the PD-L1 antibodies, avelumab, durvalumab, and atezolizumab were incubated with PD-L1 expressing TCS at final concentrations of 10 µg/ml, 3.16 µg/ml, 1 µg/ml, 316 ng/ml, 100 ng/ml, 31.6 ng/ml, 10 ng/ml, 3.16 ng/ml, 1 ng/ml, 316 pg/ml, 100 pg/ml, 31.6 pg/ml and 10 pg/ml. Binding was detected using an APC-conjugated goat-anti-human IgG (Fc-specific) antibody (Jackson ImmunoResearch) measured via flow cytometry. Three independent PD-1 and PD-L1 antibody binding experiments were performed in triplicate. The geometric mean of the fluorescence intensity of viable reporter cells was used for further analysis.
A 4-parameter logistic function was fitted to assess the relationship between log concentration (mg/ml) and binding (gMFI) or normalized stimulation. The fit was excellent with a pseudo-R² above 0.9. EC50 values were estimated from the intercept and slope of the logistic function and 95% confidence intervals were computed by applying Fieller’s theorem. EC50 values for different monoclonal Abs were statistically compared using Walsh tests. P-values for pairwise comparisons were Bonferroni-Holm corrected. Analyses were done using SPSS 25.0 (IBM, Amonk, N.Y.).
Gong, J., Chehrazi-Raffle, A., Reddi, S. & Salgia, R. Development of PD-1 and PD-L1 inhibitors as a form of cancer immunotherapy: a comprehensive review of registration trials and future considerations. J Immunother Cancer 6, 8, https://doi.org/10.1186/s40425-018-0316-z (2018).
Zou, W., Wolchok, J. D. & Chen, L. PD-L1 (B7-H1) and PD-1 pathway blockade for cancer therapy: Mechanisms, response biomarkers, and combinations. Sci Transl Med 8, https://doi.org/10.1126/scitranslmed.aad7118 (2016).
Jutz, S. et al. A cellular platform for the evaluation of immune checkpoint molecules. Oncotarget 8, 64892–64906, https://doi.org/10.18632/oncotarget.17615 (2017).
Leitner, J. et al. T cell stimulator cells, an efficient and versatile cellular system to assess the role of costimulatory ligands in the activation of human T cells. J Immunol Methods 362, 131–141 (2010).
Kamphorst, A. O. et al. Rescue of exhausted CD8 T cells by PD-1-targeted therapies is CD28-dependent. Science 355, 1423–1427 (2017).
Hui, E. et al. T cell costimulatory receptor CD28 is a primary target for PD-1-mediated inhibition. Science 355, 1428–1433 (2017).
De Sousa Linhares, A., Leitner, J., Grabmeier-Pfistershammer, K. & Steinberger, P. Not all immune checkpoints are created equal. Frontiers in immunology 9, 1909, https://doi.org/10.3389/fimmu.2018.01909 (2018).
Postow, M. A., Callahan, M. K. & Wolchok, J. D. Immune Checkpoint Blockade in Cancer Therapy. Journal of clinical oncology: official journal of the American Society of Clinical Oncology 33, 1974–1982 (2015).
Hargadon, K. M., Johnson, C. E. & Williams, C. J. Immune checkpoint blockade therapy for cancer: An overview of FDA-approved immune checkpoint inhibitors. Int Immunopharmacol 62, 29–39 (2018).
Marshall, H. T. & Djamgoz, M. B. A. Immuno-Oncology: Emerging Targets and Combination Therapies. Frontiers in oncology 8, 315, https://doi.org/10.3389/fonc.2018.00315 (2018).
Jutz, S. et al. Assessment of costimulation and coinhibition in a triple parameter T cell reporter line: Simultaneous measurement of NF-kappaB, NFAT and AP-1. J Immunol Methods 430, 10–20 (2016).
Rosskopf, S. et al. Creation of an engineered APC system to explore and optimize the presentation of immunodominant peptides of major allergens. Scientific reports 6, 31580, https://doi.org/10.1038/srep31580 (2016).
Khunger, M. et al. Incidence of Pneumonitis With Use of Programmed Death 1 and Programmed Death-Ligand 1 Inhibitors in Non-Small Cell Lung Cancer: A Systematic Review and Meta-Analysis of Trials. Chest 152, 271–281 (2017).
Pillai, R. N. et al. Comparison of the toxicity profile of PD-1 versus PD-L1 inhibitors in non-small cell lung cancer: A systematic analysis of the literature. Cancer 124, 271–277 (2018).
Brown, J. A. et al. Blockade of programmed death-1 ligands on dendritic cells enhances T cell activation and cytokine production. J Immunol 170, 1257–1266 (2003).
Selenko-Gebauer, N. et al. B7-H1 (programmed death-1 ligand) on dendritic cells is involved in the induction and maintenance of T cell anergy. J Immunol 170, 3637–3644 (2003).
Stecher, C. et al. PD-1 Blockade Promotes Emerging Checkpoint Inhibitors in Enhancing T Cell Responses to Allogeneic Dendritic Cells. Frontiers in immunology 8, 572, https://doi.org/10.3389/fimmu.2017.00572 (2017).
Blank, C. et al. Blockade of PD-L1 (B7-H1) augments human tumor-specific T cell responses in vitro. Int J Cancer 119, 317–327 (2006).
Haymaker, C., Wu, R., Bernatchez, C. & Radvanyi, L. PD-1 and BTLA and CD8(+) T-cell “exhaustion” in cancer: “Exercising” an alternative viewpoint. Oncoimmunology 1, 735–738 (2012).
Legat, A., Speiser, D. E., Pircher, H., Zehn, D. & Fuertes Marraco, S. A. Inhibitory Receptor Expression Depends More Dominantly on Differentiation and Activation than “Exhaustion” of Human CD8 T Cells. Frontiers in immunology 4, 455, https://doi.org/10.3389/fimmu.2013.00455 (2013).
Rosskopf, S., Jahn-Schmid, B., Schmetterer, K. G., Zlabinger, G. J. & Steinberger, P. PD-1 has a unique capacity to inhibit allergen-specific human CD4(+) T cell responses. Scientific reports 8, 13543, https://doi.org/10.1038/s41598-018-31757-z (2018).
Zamani, M. R., Aslani, S., Salmaninejad, A., Javan, M. R. & Rezaei, N. PD-1/PD-L and autoimmunity: A growing relationship. Cell Immunol 310, 27–41 (2016).
del Rio, M. L., Buhler, L., Gibbons, C., Tian, J. & Rodriguez-Barbosa, J. I. PD-1/PD-L1, PD-1/PD-L2, and other co-inhibitory signaling pathways in transplantation. Transpl Int 21, 1015–1028 (2008).
Butte, M. J., Pena-Cruz, V., Kim, M. J., Freeman, G. J. & Sharpe, A. H. Interaction of human PD-L1 and B7-1. Mol Immunol 45, 3567–3572 (2008).
Butte, M. J., Keir, M. E., Phamduy, T. B., Sharpe, A. H. & Freeman, G. J. Programmed death-1 ligand 1 interacts specifically with the B7-1 costimulatory molecule to inhibit T cell responses. Immunity 27, 111–122 (2007).
Shimizu, T. et al. Phase 1 study of pembrolizumab (MK-3475; anti-PD-1 monoclonal antibody) in Japanese patients with advanced solid tumors. Invest New Drugs 34, 347–354 (2016).
Contreras-Sandoval, A. M. et al. Correlation between anti-PD-L1 tumor concentrations and tumor-specific and nonspecific biomarkers in a melanoma mouse model. Oncotarget 7, 76891–76901 (2016).
Jayaprakash, P. et al. Targeted hypoxia reduction restores T cell infiltration and sensitizes prostate cancer to immunotherapy. J Clin Invest 128, 5137–5149 (2018).
Sau, S., Petrovici, A., Alsaab, H. O., Bhise, K. & Iyer, A. K. PDL-1 Antibody Drug Conjugate for Selective Chemo-Guided Immune Modulation of Cancer. Cancers (Basel) 11, https://doi.org/10.3390/cancers11020232 (2019).
Nowak, E. C. et al. Immunoregulatory functions of VISTA. Immunol Rev 276, 66–79 (2017).
Le Mercier, I., Lines, J. L. & Noelle, R. J. Beyond CTLA-4 and PD-1, the Generation Z of Negative Checkpoint Regulators. Frontiers in immunology 6, 418, https://doi.org/10.3389/fimmu.2015.00418 (2015).
Leitner, J. et al. B7-H3 is a potent inhibitor of human T-cell activation: No evidence for B7-H3 and TREML2 interaction. Eur J Immunol 39, 1754–1764 (2009).
Battin, C. et al. A human monocytic NF-kappaB fluorescent reporter cell line for detection of microbial contaminants in biological samples. PLoS One 12, e0178220, https://doi.org/10.1371/journal.pone.0178220 (2017).
We wish to thank Claus Wenhardt and Hermann Denk for excellent technical support. Supported by the Austrian Science Fund, FWF (DK W 1248-B30), the Christian Doppler Society (https://www.cdg.ac.at; CD10262401), a grant of the Mayor of Vienna to KGP (18018/2018), and the Medical University of Vienna.
C. Hafner reports personal fees from Bristol-Myers Squibb, Amgen, Merck Sharp & Dohme, Roche, and Novartis and nonfinancial support from Bristol-Myers Squibb, Merck Sharp & Dohme, Roche and Pierre Fabre outside the submitted work. G.J. Zlabinger reports personal fees from Alexion, Bristol-Myers Squibb, MedAhead, the Austrian Chamber of Physicians, Pfizer, UCB Pharma, Merck Sharp & Dohme, GlaxoSmithKline, and AbbVie outside the submitted work. P. Steinberger reports personal fees from Bristol-Myers Squibb outside the submitted work. All other authors declare no potential conflicts of interest.
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De Sousa Linhares, A., Battin, C., Jutz, S. et al. Therapeutic PD-L1 antibodies are more effective than PD-1 antibodies in blocking PD-1/PD-L1 signaling. Sci Rep 9, 11472 (2019). https://doi.org/10.1038/s41598-019-47910-1
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