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T-cell immunotherapies are promising options in relapsed/refractory B-precursor acute lymphoblastic leukemia (ALL). We investigated the effect of co-signaling molecules on T-cell attack against leukemia mediated by CD19/CD3-bispecific T-cell engager. Primary CD19+ ALL blasts (n≥10) and physiologic CD19+CD10+ bone marrow precursors were screened for 20 co-signaling molecules. PD-L1, PD-1, LAG-3, CD40, CD86, CD27, CD70 and HVEM revealed different stimulatory and inhibitory profiles of pediatric ALL compared to physiologic cells, with PD-L1 and CD86 as most prominent inhibitory and stimulatory markers. PD-L1 was increased in relapsed ALL patients (n=11) and in ALLs refractory to Blinatumomab (n=5). Exhaustion markers (PD-1, TIM-3) were significantly higher on patients' T cells compared to physiologic controls. T-cell proliferation and effector function was target-cell dependent and correlated to expression of co-signaling molecules. Blockade of inhibitory PD-1-PD-L and CTLA-4-CD80/86 pathways enhanced T-cell function whereas blockade of co-stimulatory CD28-CD80/86 interaction significantly reduced T-cell function. Combination of Blinatumomab and anti-PD-1 antibody was feasible and induced an anti-leukemic in vivo response in a 12-year-old patient with refractory ALL. In conclusion, ALL cells actively regulate T-cell function by expression of co-signaling molecules and modify efficacy of therapeutic T-cell attack against ALL. Inhibitory interactions of leukemia-induced checkpoint molecules can guide future T-cell therapies.
Acute lymphoblastic leukemia (ALL) is the most common childhood malignancy. Children with standard risk ALL have excellent survival rates with further improvement over the last decades . However, refractory B-precursor ALL and especially relapsed ALL after hematopoietic stem cell transplantation (HSCT) is still associated with a dismal prognosis [2-4]. Immunotherapy and targeted therapy are novel approaches that undergo implementation into treatment strategies in pediatric ALL . The bispecific anti-CD3/CD19 T-cell engager (BiTE) antibody Blinatumomab or T cells expressing chimeric antigen receptors (CARs) can successfully recruit the forces of T cells and guide them against lymphoblastic cells. These polyclonal T cells induce perforin/granzyme-mediated lysis of malignant target cells [5-7] and have the potential to induce hematological remission in adult and pediatric patients with relapsed/refractory B-precursor ALL [2, 8-11]. Despite the encouraging results, it is unknown why T cells could attack malignant blasts in some cases or remained paralyzed in others. There is emerging evidence that loss of co-stimulatory molecules and expression of co-inhibitory molecules have a pivotal role in tumor immune escape . Sustained inhibitory signaling mediated by expression of numerous co-signaling molecules on T cells such as TIM-3, LAG-3, PD-1 or CTLA-4 correlates with a stage of T-cell exhaustion, marked by a reduced T-cell effector function, proliferative potential and cytotoxicity [13, 14]. Since T-cell function is essential for tumor control [15, 16], efforts are made to increase T-cell function and to reverse T-cell exhaustion for induction of a sustained tumor immune surveillance and efficient elimination of malignant cells . Recent advances were achieved by targeting immune escape checkpoints such as CTLA-4 or PD-1 [13, 18, 19]. Antitumor activity of checkpoint blockade was demonstrated in various tumors [18, 20-23], but has not been evaluated in ALL until now. In this study, we examined T-cell attack against pediatric lymphoblastic target cells by analysis of effector-target cell interactions in co-culture experiments with Blinatumomab. As co-inhibitory signaling might interfere with the clinical benefit of T-cell immunotherapy, we examined functional relevance of leukemia-related co-signaling molecules on lymphoblasts for T-cell activity and investigated combined immunotherapy approaches with checkpoint inhibitory antibodies to increase efficacy of T-cell attack against ALL (Table (Table1).1). Feasibility of combined treatment with Blinatumomab and PD-1 blocking antibody Pembrolizumab was analyzed in a 12-year-old patient with refractory ALL.
First, we addressed the question if the difference in T-cell responses against ALL is due to effector- or target-related factors. For analysis of T-cell effector function and proliferation capacity, PBMC from healthy donors were incubated with lymphoblastic cells (Raji) as target cells and exposed to subphysiological, physiological and supraphysiological levels of Blinatumomab. T-cell function was analyzed in terms of proliferation, CD107a expression, cytokine production and GrB/Perforin expression - with variable E/T cell ratios and incubation times (Figures (Figures11 and Supplementary Figure S1). In all cases, T-cell function was shown to be strictly target cell- and dose-dependent. After stimulation with physiological in vivo serum levels of 100pg/ml-1ng/ml Blinatumomab , high T-cell proliferation rates were induced, as determined by flow cytometry after 5 days – with a mean CD4+ T-cell proliferation of 97.1%±3.5 (mean±SD, n=10) after stimulation with Blinatumomab 1ng/ml (Supplementary Figure S1A). In contrast, proliferation of T cells was low when PBMC were incubated with high dose of 0.1μg/ml Blinatumomab without addition of target cells or with Raji cells without addition of Blinatumomab (Figures (Figures11 and Supplementary Figure S1A). Despite variable E/T cell ratios, different incubation times and doses of Blinatumomab, there was no significant difference in analyzed T-cell function between different donors (Figures (Figures11 and Supplementary Figure S1). Analysis of different cell populations confirmed dose-dependent recruitment of T cells as effector cells whereas NK-cell activity remained independent of Blinatumomab (Supplementary Figure S1A).
To analyze whether effector cells or target cells determine T-cell attack against leukemic blasts, we compared T-cell function from patients responding to Blinatumomab treatment, non-responders and healthy donors. Results of T-cell proliferation and CD107a expression were compared within the group of patients (in vivo responders vs in vivo non-responders) and to T-cell function of healthy donors (Figures (Figures1B1B and Supplementary Figure S1D). Patients and controls both showed target cell- and dose-dependent CD107a expression and proliferation of T cells as detected by CFSE assay and flow cytometry. There was neither a significant difference of T-cell function between responders (n=3) and non-responders (n=3), nor between patients and healthy donors (Figure (Figure1),1), with a mean CD4+ T-cell proliferation of 98.2%±1.7 (mean±SD, n=5) among patients as compared to 96.7%±3.8 (mean±SD, n=8) among controls under 1ng/ml Blinatumomab. As in vivo responders and non-responders to treatment with Blinatumomab both showed similar results regarding induced T-cell function (Figure (Figure1B),1B), there was no correlation of in vivo and in vitro results when irradiated Raji cells were used as target cells.
For analysis of bone marrow blasts, at least 10 pediatric ALL patients were screened for expression of a variety of co-inhibitory and co-stimulatory molecules by flow cytometry (Table (Table1).1). Results were compared to expression pattern on physiologic CD19+CD10+ cells in healthy bone marrow samples (Figures (Figures2A2A and Supplementary Figure S2A). We especially aimed to identify markers with interindividual differences as these molecules might be candidates explaining functional differences. Ex vivo expression pattern of inhibitory molecules PD-L1, LAG-3 and PD-1, the bi-functional molecule HVEM and of co-stimulatory molecules CD86, CD40, CD27 and CD70 revealed interindividual differences on patients blasts' as compared to consistent low or absent expression on CD19+CD10+ cells of controls (Figure (Figure2A).2A). The most prominent inhibitory marker on primary pediatric blasts was PD-L1. The stimulatory marker CD86 was significantly higher expressed on malignant lymphoblastic cells compared to physiologic CD19+CD10+ bone marrow precursors. Expression pattern of co-signaling molecules BTLA, CD80, PD-L2, B7H3, B7H4, CD160, Galectin9, CD137L, CD278, CTLA-4 and TIM-3 was similar for patients and controls, with uniform low or absent expression on the surface of CD19+CD10+ bone marrow cells. The co-inhibitory molecule CD200 was expressed in high levels on patients' blasts (mean±SD CD200 expression= 90%±17) and on controls, with no significant intra- and interindividual difference between the two groups (Supplementary Figure S2A).
PD-L1 expression was significantly higher on patients' blasts of non-responders to Blinatumomab (median PD-L1 expression: 14.6%, n=5) as compared to responders (median PD-L1 expression: 5.0% n=5) and to controls (p = 0.0022; n=6) (Figure (Figure2C).2C). Median PD-L1 surface expression was higher on patients' ALL blasts at relapse (median PD-L1 expression: 9.5%; n=11) as compared to patients with primary diagnosis (median PD-L1 expression: 1.1%; n=8) and to controls (median PD-L1 expression: 0.49%, n=6) (Figure (Figure2D).2D). Samples for analysis of PD-L1 surface expression at diagnosis and relapse did not originate from the same patients. The findings of increased PD-L1 surface expression at relapse compared to expression levels at diagnosis might contain an intrinsic element of heterogeneity and therefore have to be confirmed in further analyses of leukemic blasts originating from the same patients.
Expression of PD-L1 on ALL blasts could be upregulated during the course of treatment and was shown to be inducible after 24-44h stimulation with Th1 cytokines TNF-α and IFN-γ (Figures 2E, 2F and 2G). Expression pattern of co-signaling molecules on CD19+CD10+ cell lines demonstrated preponderance of co-stimulatory molecules on target cells susceptible to T-cell attack (Raji, Supplementary Figure S3) as compared to less immunogenic lymphoblasts (NALM-6, NALM-16 and MHH-CALL-4) with predominantly absent co-stimulatory molecules (data not shown). PD-L1 expression on B lymphoblastic cells (e.g. NALM-16) was shown to be inducible after stimulation with Th1 cytokines IFN-γ or TNF-α plus IFN-γ. Thus, surface expression of co-signaling molecules on CD19+CD10+ cells can strongly differ between individuals. A range of co-signaling molecules are variably expressed on patients' blasts with gradual differences in expression levels and concomitant absence on CD19+CD10+ bone marrow cells of controls. In contrast, analysis of intracellular PD-L1 expression showed consistently high expression in B-cell malignancies (cell lines) and patients' ALL blasts. Immunohistochemical analysis of PD-L1 expression on bone marrow smears of patients' blasts confirmed interindividual differences in expression levels of PD-L1 (Figure (Figure2B2B).
Since target cell analyses demonstrated differences in the expression of co-signaling molecules, we analyzed effector T cells for expression of the corresponding binding partners. Blinatumomab-induced recognition of target cells led to a dose- and target cell-dependent increase in expression of T-cell exhaustion markers CTLA-4, PD-1, TIM-3 and LAG3 (Figures 3A-3C, 3E-3F and Supplementary Figure S2B). Mean PD-1 expression of CD4+ T cells was 1.9%±1.3 (mean±SD, n=6) after 48h-incubation of PBMC with irradiated Raji cells and could be significantly increased up to 77.4%±3.8 (mean±SD, n=7) after addition of Blinatumomab 1ng/ml (Figure (Figure3B).3B). Dose-dependent induction of PD-1 expression could be confirmed at different effector/target cell ratios (data not shown). Surface expression of exhaustion markers PD-1+, TIM-3+ and PD-1+TIM-3+ on CD3+ T cells in the bone marrow was significantly higher among leukemia patients as compared to physiological bone marrow T cells (Figure (Figure3D).3D). Expression of exhaustion markers PD-1, LAG-3 and TIM-3 on T cells could be further upregulated in leukemia patients after addition of Blinatumomab (Figures (Figures3E3E and and3F3F).
Next, we analyzed how different target cells can modify functional T-cell characteristics during T-cell attack (numbers are given as mean±SD). T-cell proliferation capacity and IFN-γ secretion were markedly reduced when PBMC of healthy donors were incubated with primary patients' blasts instead of Raji cells under the same experimental conditions (Figure (Figure4).4). Incubation of PBMC from healthy donors with irradiated Raji cells led to a mean IFN-γ secretion of 3.3%±0.9 (n=3) and to a mean T-cell proliferation of 50.5%±12.0 (n=7) among CD3+ T cells under 48h-presence of Blinatumomab. In contrast, incubation of the same donor PBMC with primary patients' ALL blasts led to a significant reduction in IFN-γ secretion and T-cell proliferation (0.3%±0.0 IFN-γ+CD3+ T cells (n=3) and CD3+ T-cell proliferation of 12.7%±8.6; n=7). Similar results were obtained when patients' PBMC were incubated with their autologous ALL blasts – with a mean IFN-γ secretion of 0.3%±0.2 (n=3) and a mean T-cell proliferation of 9.86%±8.67 (n=7) among CD3+ T cells. Besides, target cell-dependent differences in T-cell function could be demonstrated when PBMC of the same donors were incubated with different cell lines as target cells (Supplementary Figure S2B). We could confirm that target-cell related co-signaling factors determine the effect of T-cell attack against leukemic blasts by luciferase-based cytotoxicity assays. In order to evaluate the impact of co-signaling molecules on Blinatumomab-mediated cytolytic activity, we consistently used GFP/luciferase expressing NALM-6 as target cells as well as their retrovirally transduced sublines expressing either PD-L1 or CD80 (cells were kindly provided by Dr. Michel Sadelain, MSKCC, New York) (Figure (Figure6A).6A). We could show that cytolytic activity mediated by Blinatumomab was significantly decreased under inhibitory influence of PD-L1 and significantly increased when target cells provided co-stimulatory signaling via the CD80-CD28 axis (Figure (Figure66).
In order to analyze influence of co-signaling interactions on T-cell function, we performed functional T-cell assays with addition of blocking antibodies against either CD80 and CD86 to block co-stimulatory CD80/CD86-CD28 interactions or against PD-1 and/or CTLA-4 for blockade of inhibitory PD-1–PD-L or CTLA-4–CD80/CD86 signaling (numbers are given as mean±SD; Figure Figure5).5). For analysis of CD80/CD86-CD28 blockade (Figures (Figures5E5E and and5F),5F), PBMC of healthy donors (n≥15) were incubated with irradiated CD80+CD86+ Raji cells and stimulated with Blinatumomab 1ng/ml for 48 hours. Addition of CD80/CD86-blocking antibodies led to a significant decrease in T-cell proliferation, IL-2 and IFN-γ secretion when Raji cells were used as target cells whereas control experiments with CD80−CD86− NALM-6 cells or addition of anti-CD80/CD86 antibodies to unstimulated co-cultures of PBMC and Raji cells showed no significant differences. Co-culture experiments with PBMC and Raji cells showed a reduction of CD3+ T-cell proliferation from 37.8%±14 under stimulation with 1ng/ml Blinatumomab to 24.6%±11.6 after addition of CD80/CD86 blocking antibodies (n=16, Figure Figure5E).5E). In order to examine the influence of co-inhibitory signals mediated by the PD-1–PD-L and CTLA-4-CD80/CD86 axis, PBMC of healthy donors or patients were incubated with irradiated Raji cells or patients' blasts and stimulated with Blinatumomab in the presence or absence of PD-1 and/or CTLA-4 blocking antibody. Experiments with Raji cells as target cells demonstrated significant increase of IFN-γ secretion by CD4+ and CD8+ T cells under PD-1 blockade at different E/T ratios and concentrations of Blinatumomab (Figure (Figure5D).5D). When patients' ALL blasts were used as target cells, proliferation of T cells could be significantly increased under PD-1 blockade or under combined blockade of PD-1 and CTLA-4 (Figure (Figure5A):5A): CD3+ T-cell proliferation was 19.8%±14.9 after stimulation of PBMC with irradiated ALL blast cells and 1ng/ml Blinatumomab (n=13) and was increased to a mean CD3+ T-cell proliferation of 24.4%±15 after addition of PD-1 blocking antibody and of 31.1%±15.1 after PD-1 and CTLA-4 antibody blockade. These results could be confirmed for patients' PBMC and for PBMC of healthy donors as effector cells (Figures 5A-5B). IFN-γ secretion was also increased by blocking PD-1–PD-L interactions and reached statistical significance for CD8+ T cells (Figure (Figure5C).5C). Moreover, Blinatumomab-mediated cytotoxicity could be significantly increased under PD-1 blockade when PD-L1-expressing NALM-6 luciferase-GFP cells served as targets. Consistently, cytolytic capacity was significantly decreased by inhibition of co-stimulatory CD28-CD80 interactions when CD80-transduced NALM-6 luciferase-GFP cells were used as targets. There was no effect of PD-1 or CD80 blockade when PD-L1−CD80− NALM6 luciferase-GFP cells served as targets (Figures (Figures6D6D and and6E6E and there was no relevant allo-reactive cytotoxicity in control experiments without addition of Blinatumomab (Figure (Figure6C).6C). Therefore, we proved that stimulatory and inhibitory interactions between effector cells and lymphoblastic target cells guide T-cell function against leukemia through CD80/86–CD28/CTLA-4 as well as PD-1–PD-L interactions.
Combined treatment approach with Blinatumomab and PD-1 blocking antibody Pembrolizumab was applied to a 12-year-old girl with refractory ALL after 2nd HSCT and previous non-response to monotherapy with Blinatumomab. Immunohistochemical staining prior to treatment start revealed PD-L1 expression of nearly all bone marrow blasts (Figure (Figure7C).7C). Pembrolizumab was administered at a dose of 1mg/kg body weight one day after transfusion of CD45RA-depleted T cells from her haploidentical stem cell donor. Blinatumomab was added one day later at a dose of 15μg/m2/d without previous steroid application. Further applications of Pembrolizumab were given after 18 and 29 days. Additional CD45RA-depleted T cells from her HSCT donor were infused at time of third Pembrolizumab administration. Leukemia load prior to treatment start revealed 45% bone marrow blasts. Treatment with Blinatumomab and Pembrolizumab was safe without acute toxicities, but with expected inflammatory response associated with high fever and transient increase of inflammatory parameters IL-6, soluble IL-2 receptor, CRP, procalcitonin, D-dimer and ferritin (Figures (Figures7A7A and and7B).7B). Antileukemic response was confirmed by flow cytometric detection of T-cell expansion and reduction of blast load in peripheral blood under treatment (Figure (Figure7D).7D). Ex vivo analysis predicted a low effector T-cell function against patient's ALL blasts (co-culture experiment: T cells plus primary blasts plus Blinatumomab), but an increased T-cell function after addition of PD-1 blocking antibody (data not shown). Bone marrow analysis 34 days after treatment start showed morphological remission of ALL blasts to <5% (Figure (Figure7D,7D, right plot). Treatment with Blinatumomab ended 2 days later and there was no further administration of Pembrolizumab. The patient is still alive, although relapse occurred 2 months after this combined treatment.
Despite considerable improvement in survival rates of pediatric patients with acute B-lymphoblastic leukemia (B-ALL), relapsed and refractory ALL is still associated with a poor prognosis [3, 4]. Novel approaches focus on T-cell therapy, e.g. ex vivo genetic modification of T cells to express chimeric antigen receptors (CARs) targeting leukemic antigens or by antibody-mediated activation of patients' T cells . The CD19/CD3-bispecific T-cell engager antibody Blinatumomab is a successful example of antibody-based T-cell treatment with the potential to induce long-term clinical benefits in patients with refractory B-ALL [8, 10, 11]. Despite this promising data, some patients do not respond to these novel immunotherapeutic approaches. It is therefore important to uncover parameters that determine the fate of a T-cell response against leukemia cells. With functional assays we addressed the question whether factors on the target side (ALL blasts) or effector side (T cells) are responsible for differences in the Blinatumomab-mediated interaction between leukemia and T cells. Significant differences in T-cell function were found to be target-cell dependent whereas ex vivo T-cell function itself was consistent between patients with clinical response to Blinatumomab treatment and non-response. To uncover the mechanisms how pediatric ALL blasts manipulate T-cell responses, we investigated phenotypic and functional relevance of stimulatory and inhibitory co-signaling in primary blasts. Use of different target cells characterized by variable expression of co-signaling molecules on their cell surface resulted in differences of T-cell function. Co-signaling molecules PD-L1, PD-1, LAG-3, CD40, CD86, CD27, CD70 and HVEM showed significantly different expression on primary pediatric ALL blasts (n≥10) as compared to physiologic CD19+CD10+ bone marrow cells, confirming inter-individual differences in immune escape of ALL blasts. We demonstrate that co-signaling molecules influence T-cell attack against leukemic blasts and have a pivotal role for effector-target cell interactions in pediatric ALL. Most prominent T-cell inhibitory and stimulatory markers expressed on pediatric ALL blasts were PD-L1 and CD86 respectively. T-cell proliferation, cytokine secretion and cytotoxicity were increased when target cells showed high expression of mainly co-stimulatory molecules (e.g. CD80+CD86+) as compared to target cells with absence of co-stimulatory molecules or predominant expression of co-inhibitory molecules. Blockade of inhibitory PD-1–PD-L1 interactions and combined blockade of PD-1–PD-L1 and CTLA-4-CD80/86 interactions could further enhance effector T-cell function whereas blockade of the CD28-CD80/CD86 pathway led to significant reduction of T-cell response against ALL.
Flow cytometric and immunohistochemical staining confirmed variable PD-L1 expression patterns on patients' bone marrow blasts. All patients with clinical non-response to Blinatumomab-treatment showed high surface expression of PD-L1 on their leukemic blasts. Furthermore, median PD-L1 expression was higher on ALL blasts of patients at relapse as compared to patients at primary diagnosis. A role of PD-L1 in resistance to Blinatumomab was suggested for the first time in a recent case report of a patient with refractory B-precursor ALL . Our data demonstrate functional relevance of leukemic PD-L1 expression for T-cell inhibition and provide further insight into relevant mechanisms of co-signaling pathways for effector-target cell interactions, contributing to immune escape of pediatric ALL. As shown in other malignancies and models [12, 27-29], we now demonstrate that PD-L1 surface expression can also be dynamic in ALL. PD-L1 expression could be induced by stimulation with Th1 cytokines IFN-γ and TNF-α and could be upregulated in the course of disease.
Expression of exhaustion markers PD-1 and TIM-3 was significantly increased on patients' bone marrow infiltrating T cells as compared to healthy donors. Co-expression of both molecules has been shown to represent tumor infiltrating lymphocytes with the most exhausted T-cell phenotype as defined by dysfunctional proliferation potential and cytokine secretion which could be restored by combined antibody blockade [14, 30]. Expression of inhibitory checkpoint molecules PD-1, CTLA-4, LAG-3 and TIM-3  was induced and upregulated in a dose-dependent fashion through Blinatumomab. Concentrations of Blinatumomab were correlated to those achievable in vivo under continuous infusion [31, 32]. Our findings thus indicate that T-cell attack against ALL by itself induces suppressive interference of inhibitory regulators on leukemic ALL blasts with their binding partners expressed on T cells.
Based on this data, a 12-year-old patient with a pre-B-ALL refractory to Blinatumomab received combined treatment with Blinatumomab and PD-1 blocking antibody Pembrolizumab. The therapy induced an inflammatory response, was feasible and safe without acute toxicities. Flow cytometric analysis confirmed antileukemic response with detectable T-cell expansion and reduction of blast load in peripheral blood. Bone marrow analysis at the end of the therapy with Pembrolizumab and Blinatumomab (after a treatment period of 34 days) showed reduction of leukemic blasts from 45% to 1%. The case report shows that the combination of lymphocyte infusion, Blinatumomab and Pembrolizumab led to a successful induction of in vivo T-cell expansion and to reduction of ALL blasts. However, it does not allow a direct mechanistic conclusion to determine the relative contribution of the three components. Two of the three components have been shown unsuccessful before (donor cell infusion and Blinatumomab).
In conclusion, we examined the role of immune regulators as potential immunotherapeutic targets in pediatric ALL. We show that leukemic blasts can differentially express co-signaling molecules on their surface and that regulation of T-cell activation/inhibition by co-signaling molecules impacts effector-target cell interactions in pediatric ALL. Blinatumomab-induced inhibitory interactions between T cells and their counterparts expressed on target cells - such as PD-1-PD-L signaling or loss of co-stimulation through CD80 or CD86 - might contribute to in vivo resistance to therapy. Combined treatment approaches with checkpoint blocking antibodies could thus be a promising therapeutic strategy in pediatric refractory/relapsed B-ALL in order to increase antitumor T-cell activity. The efficacy of this treatment approach will have to be evaluated in larger patient cohorts in future studies. Immunotherapy targeting further negative regulators (e.g. CTLA-4, LAG-3, TIM-3) in single and combinatory treatment approaches has to be considered. Additional causes of immune escape will have to be identified in the future to recruit the full power of T-cell responses against B-lymphoblastic malignancies.
After obtaining informed consent, PBMC and/or blasts of pediatric patients with ALL were used for functional analysis. Expression of co-signaling molecules on CD19+CD10+ bone marrow cells and expression of exhaustion markers on bone marrow T cells were analyzed on physiological bone marrow samples as compared to samples from pediatric ALL patients. T-cell function was analyzed by detecting proliferation (CFSE), intracellular Th1-cytokines, Perforin, Granzyme and CD107a expression.
A 12-year-old patient with B-precursor ALL who had relapsed after 2nd allogeneic HSCT and did not respond to first cycle of Blinatumomab was treated with a combined treatment approach of Blinatumomab and Pembrolizumab (Keytruda®, Merck&Co, USA) in addition to CD45RA-depleted T cells from her haploidentical stem cell donor. Informed consent was given from the patients and the parents. Pembrolizumab was given as an off-label use. Inflammatory response during treatment was monitored by analysis of C-reactive protein (CRP), procalcitonin, ferritin, D-dimer, IL-6 and soluble IL-2 receptor (IL-2R) in peripheral blood of the patient. Flow cytometry was performed regularly to monitor blast load and T-cell count (CD3+CD4+ and CD3+CD8+) in peripheral blood. For evaluation of MRD, peripheral blood was analyzed and bone marrow puncture was performed on day 34 after treatment start.
Ex vivo T-cell proliferation under addition of Blinatumomab was analyzed for healthy donors and patients (in vivo responders and non-responders to treatment with Blinatumomab) with carboxyfluorescein diacetate succinimidyl ester (CFSE) as described previously . In brief, cells were labeled with 1.6μM CFSE (Molecular Probes; Invitrogen) and seeded (5×105 cells/mL/ well) in 48-well plates with non-irradiated or irradiated (60 Gy) malignant cells (primary ALL-blasts, Raji, NALM-6, NALM-16, MHH-CALL-4). PBMC were exposed ex vivo to variable doses of Blinatumomab (Amgen Inc., Thousand Oaks, CA, USA) in a 37°C humidified incubator. Incubation time and effector/target cell ratios (E/T) were changed according to experimental requirements. After incubation period, cells were collected, followed by extracellular antibody staining and analyzed by flow cytometry. Controls were performed with 5×105 CFSE-stained PBMC in co-culture with un-irradiated or irradiated malignant cells without addition of Blinatumomab. For functional analysis of cytokine secretion, PBMC were seeded with unirradiated or irradiated (60 Gy) target cells (Raji, NALM-6, NALM-16, MHH-CALL-4, patients' ALL blasts) in 48-well plates up to 48h and stimulated with Blinatumomab as described. Cells were counterstained by fluorochrome-labeled anti-CD3, anti-CD4 and anti-CD8 antibodies and flow cytometric assessment of IFN-γ+ and/or IL-2+ secretion of viable T cells was carried out by intracellular cytokine staining after addition of Brefeldin A (Sigma) for 4h. Subsequently, leukocytes were fixed with fix-and-perm solutions (Caltag Laboratories, Hamburg, Germany) according to the manufacturer's instructions.
In order to evaluate the influence of co-signaling pathways for effector-target cell interactions, functional analysis of proliferation, IFN-γ and IL-2 secretion was performed after addition of blocking anti-human CD80 and anti-human CD86 antibodies (both Biolegend, San Diego, CA, USA) or anti-human PD-1 blocking antibody (Biolegend, San Diego, CA, USA) and/or CTLA-4 blocking human antibody Ipilimumab (Bristol-Myers Squibb GmbH & Co, New York, NY, USA). PBMC of healthy donors or ALL patients were seeded (5×105 cells/well) in 48-well plates with irradiated (60 Gy) CD80+CD86+ Raji cells, patients' bone marrow ALL blasts or with CD80−CD86− NALM-6 cells at an effector/target cell (E/T) ratio of 2:1, 10:1 or 100:1 for 48h. PBMC were stimulated with 100pg/ml or 1ng/ml Blinatumomab and incubated with 20μg/ml anti-CD80 and 20μg/ml anti-CD86 antibodies or 5μg/ml anti-PD-1 antibody and/or 10μg/ml Ipilimumab. Controls were performed with E/T cell co-cultures without addition of blocking antibodies and with unstimulated E/T cell co-cultures. After 48h, cells were collected without further restimulation, followed by intracellular and extracellular antibody staining as described above and analyzed by flow cytometry. Additional methods and details on functional assays are described in the Supplement.
Cytolytic activity was determined by a luciferase-based assay with NALM-6 expressing firefly luciferase-GFP as previously described as well as CD80 or PD-L1 expressing NALM-6 luciferase-GFP [45, 46] (kindly provided by Dr. Michel Sadelain, MSKCC, New York). PBMC and target cells were co-cultured at indicated E:T ratio and 1×105 target cells/ well in black-walled 96-well plates in a duplicate or triplicate manner. 100ul/well luciferase substrate (Gold Biotechnology, USA) was added after 46 hours and light emission was determined by luminescence plate reader. Target cells were seeded alone in order to determine the maximal luciferase expression (relative light unit; RLUmax) and lysis was determined as [1 − (RLUsample)/(RLUmax)] × 100. There was no relevant lysis detectable when PBMC and target cells were co-cultured without addition of Blinatumomab as compared to target cells alone. We demonstrated absence of lysis without Blinatumomab-stimulation in Figure Figure66 and compared Blinatumomab-induced lysis to same conditions (PBMC and target cells at same E:T ratio) without Blinatumomab for subsequent results.
Expression of co-signaling molecules PD-L1, PD-L2, PD-1, LAG-3, HVEM, BTLA, CD160, CD80, CD86, CD40, CD27, CD70, CD200, B7H3, B7H4, Galectin9, TIM-3, CD137L, CD278 (all: extracellular surface expression) and CTLA-4 (intracellular and extracellular expression) was analyzed by antibody staining and flow cytometry on ALL blasts and on physiologic CD19+CD10+ bone marrow cells of controls. In addition, expression of PD-L1, PD-1, LAG-3, HVEM, CD80, CD86, CD40, CD27, CD70 and CD200 was analyzed on CD19+CD10+ cell lines (Raji, NALM-6, NALM-16, MHH-CALL-4). Besides, PD-L1 expression on cell lines and patients' ALL bone marrow blasts was analyzed using intracellular flow cytometry as described above. Prior to analysis, functionality of all antibodies was tested on selected positive controls as previously described (s. Supplement) [12, 19, 34-44].
The experiments have been done by JF, SK, DG and MH. Patient treatment and sampling was done by TF, MD, FB, PS, PL and ME. Immunohistochemistry was done by HB and LQF. Concept and design of this work was done by TF, JF and SK and reviewed by RH. The manuscript was written by JF and TF and reviewed by all coauthors. All authors have no conflict of interest to disclose. We thank Susi Haase, Josef Leibold, Gerhard Zugmaier and Matthias Klinger for inspiring questions and helpful discussion and Sylvia Klein for excellent technical assistance.
CONFLICTS OF INTEREST
The authors declare that there is no conflict of interest.
This work was supported by the DFG (SFB685 to TF), by grants from the Stiftung für krebskranke Kinder Tübingen e.V., the José-Carreras Leukemia Foundation, the Care-for-Rare Foundation and the Stefan-Morsch-Stiftung.