Background Several mechanisms are present in the tumor microenvironment (TME) to impair cytotoxic T cell responses potentially able to control tumor growth. Among these, the accumulation of adenosine (Ado) contributes to tumor progression and represents a promising immunotherapeutic target. Ado has been shown to impair T cell effector function, but the role and mechanisms employed by Ado/Ado receptors (AdoRs) in modulating human peripheral and tumor-infiltrating lymphocyte (TIL) function are still puzzling.
Methods CD8+ T cell cytokine production following stimulation was quantified by intracellular staining and flow cytometry. The cytotoxic capacity of tumor infiltrating lymphocytes (TILs) was quantified by the chromium release assay following co-culture with autologous or anti-CD3-loaded tumor cell lines. The CD8+ T cell metabolic fitness was evaluated by the seahorse assay and by the quantification of 2-NBDG uptake and CD71/CD98 upregulation upon stimulation. The expression of AdoRs was assessed by RNA flow cytometry, a recently developed technology that we validated by semiquantitative RT-PCR (qRT-PCR), while the impact on T cell function was evaluated by the use of selective antagonists and agonists. The influence of Ado/AdoR on the PKA and mTOR pathways was evaluated by phosphoflow staining of p-CREB and p-S6, respectively, and validated by western blot.
Results Here, we demonstrate that Ado signaling through the A2A receptor (A2AR) in human peripheral CD8+ T cells and TILs is responsible for the higher sensitivity to Ado-mediated suppression of T central memory cells. We confirmed that Ado is able to impair peripheral and tumor-expanded T cell effector functions, and we show for the first time its impact on metabolic fitness. The Ado-mediated immunosuppressive effects are mediated by increased PKA activation that results in impairment of the mTORC1 pathway.
Conclusions Our findings unveil A2AR/PKA/mTORC1 as the main Ado signaling pathway impairing the immune competence of peripheral T cells and TILs. Thus, p-CREB and p-S6 may represent useful pharmacodynamic and efficacy biomarkers of immunotherapies targeting Ado. The effect of Ado on T cell metabolic fitness reinforces the importance of the adenosinergic pathway as a target for next-generation immunotherapy.
- CD8 T cells
Beatris Mastelic-Gavillet and Blanca Navarro Rodrigo contributed equally to this work.
- Adenosine receptor
- Effect:target (ratio)
- Peripheral blood mononuclear cells
- Protein kinase A
- Phorbol 12-myristate 13-acetate
- Semiquantitative real-time PCR
- Rapid expansion protocol
- T central memory cells
- T cell receptor
- Tumor-infiltrating lymphocytes
- Tumor microenvironment
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
Statistics from Altmetric.com
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Beatris Mastelic-Gavillet and Blanca Navarro Rodrigo contributed equally to this work.
Recently, it was discovered that activated T cells undergo a pronounced mTOR-mediated metabolic switch [1–3], and failure to reprogram metabolic activities leads to a hyporesponsive state, including exhaustion and anergy [4, 5]. In the tumor microenvironment (TME), multiple mechanisms such as overexpression of immune checkpoint molecules  and loss of nutrients [7, 8] were recently shown to impair T cell metabolic fitness, thus impairing immune control of tumor growth [9, 10]. However, it remains largely unexplored whether and how immunosuppressive molecules, such as adenosine (Ado), impair T cell functions by subverting their metabolic activity.
Extracellular Ado is produced by the sequential dephosphorylation of ATP catalyzed by two cell surface ectonucleotidases, CD39 and CD73. In the TME, the ATP released by cell death, the increased expression of CD39 and CD73 and the decreased expression of the adenosine deaminase (ADA)/CD26 complex lead to the accumulation of Ado [11, 12]. The persistent high concentration of Ado may become detrimental, generating an immunosuppressive microenvironment [13–18]. Mechanistically, Ado mediates multiple effects by binding the G-protein-coupled receptors A1, A2A, A2B and A3 . Signaling of A2A and A2B adenosine receptors (A2AR, A2BR) through Gs proteins increases cyclic AMP levels and protein kinase A (PKA) activity [19–21]. Studies with selective agonists/antagonists have revealed the key role of A2AR in the suppression of T cell functions [15–17, 20]. However, the relative sensitivity of T cell subsets to Ado and the relevant mediators downstream of Ado receptors (AdoRs) have not yet been determined.
Here, we demonstrate that Ado immunosuppressive effects on human CD8+ T cells are primarily exerted on T central memory cells (TCM), likely due to their higher levels of A2AR expression. Selective blockade of A2AR, but not A2BR, restored CD8+ T cell functionality. Triggering A2AR increased PKA activation (i.e., CREB phosphorylation), resulting in impaired TCR signaling, the mTORC1 (but not mTORC2) pathway (i.e., S6 phosphorylation), cytokine production and metabolic fitness, both in the context of T cell polyclonal stimulation and of tumor cell recognition and killing by autologous tumor infiltrating lymphocytes (TILs).
Our findings unveil the A2AR/PKA/mTORC1 pathway as the main axis for the Ado-mediated impairment of T cell function and metabolic fitness. In line with other studies evaluating the Ado pathway as a relevant target for immunotherapy [13, 14, 16, 21], we corroborate that blockade of A2AR has great potential for next-generation immunotherapy, and we propose p-CREB and p-S6 as potential biomarkers of efficacy for validation in future clinical studies.
Subjects and specimen preparation
Human blood samples from healthy donors were collected at the local Blood Transfusion Center Lausanne, Switzerland, under IRB approval (Ethics Committee, University Hospital of Lausanne-CHUV). Written informed consent was obtained from all healthy subjects and patients, in accordance with the Declaration of Helsinki. Fresh anticoagulated blood diluted at a 1:2 ratio in PBS was layered on lymphoprep (ratio of diluted blood:lymphoprep 1.5:1). Mononuclear cells were isolated by density gradient centrifugation (1800 rpm, 20 min centrifugation without break, room temperature), washed twice and immediately cryopreserved in 90% fetal calf serum (FCS) and 10% DMSO.
Informed consent from the cancer patients was obtained based on the procedures approved by the same IRB as mentioned above. Clinical characteristics are described in Additional file 2: Table S2.
Freshly resected tumors not needed for histopathologic diagnosis were transferred in transport media (RPMI + 2% penicillin-streptomycin) in sterile containers at 4 °C. Tumors were then cut into 1–2 mm2 pieces and used freshly or cryopreserved in 90% human serum+ 10% DMSO.
Antibodies and reagents
Anti-CCR7 (CD197) Alexa Fluor 488 (clone G043H7), anti-CCR7 (CD197) PE/Cy7 (clone G043H7), anti-CD107a (LAMP-1) Brilliant Violet 510 (clone H4A3), anti-CD16 Alexa Fluor 700 (clone 3G8), anti-CD19 Brilliant Violet 650 (clone HIB19), anti-CD3 Brilliant Violet 605 (clone UCHT1), anti-CD3 APC/Fire750 (clone SK7), anti-CD4 Brilliant Violet 421(clone RPA-T4), anti-CD4 PE/Dazzle 594 (clone RPA-T4), anti-CD45RA Alexa Fluor 700 (clone Hl100), anti-CD56 PE (clone NCAM), anti-CD71 PE/Cy7 (clone CY1G4), anti-CD73 PE/Dazzle 594 (clone AD2), anti-CD8 PE/Cy7 (clone RPA-T8), anti-CD8 Brilliant Violet 650 (clone RPA-T8), CD8 FITC (clone SK1); anti-IL2 PE (clone MQ1-17H12), anti-PD1 (CD279) Brilliant Violet 421 (clone EH12.2H7), and anti-TNF-α PE/Cy7 (clone Mab11) were purchased from BioLegend. Anti-CD39 Brilliant Violet 711 (clone TU66), anti-CD4 BUV496 (clone SK3), anti-CD45RA Brilliant Violet 510 (clone Hl100), anti-CD8 Pacific Blue (clone RPA-T8), anti-CD98 PE (clone UM7F8), and anti-IFN-γ APC (clone B27) were purchased from Becton Dickinson. The Anti-phospho-CREBSer133 Alexa Fluor 647 (clone 87G3), unconjugated anti-phospho-S6Ser235/236, and unconjugated anti-phospho-AktSer473 (clone 193H12) were purchased from Cell Signaling Technology. The secondary antibody goat anti-rabbit IgG H&L Alexa Fluor 488 was purchased from Abcam. Stable adenosine (Ado), A2AR agonist CGS 21680, A2AR inhibitor ZM 241385, A2BR inhibitor PSB 1115, PKA inhibitor KT 5720, rapamycin and AKT1/2 inhibitor MK 2206 were purchased from Sigma-Aldrich. Anti-CD3 used for the redirected cytotoxicity assay was generated by a hybridoma in house.
A peptide pool of CMV-EBV-Flu-specific peptides optimal for CD8+ T cells has been purchased from JPT Peptide Technologies. The following HLA-A2-restricted single peptides have been synthetized by the peptide facility at the Ludwig Cancer Institute of Lausanne: CMV-NLVPMVATV, EBV-GLCTLVAML, and Flu-GILGFVFTL.
The EBV-transformed B-cell line (generated in house), human leukemic lines: THP1, (catalog number (cn): TIB-202, ATCC) and HL60 (cn: CCL-240, ATCC), prostate cancer lines: DU145 (cn: HTB-81, ATCC) and PC3 (cn: CRL-1435, ATCC), LNCaP (cn: CRL-1740, ATCC), breast cancer cell line MCF-7 (cn: HTB-22, ATCC) and the mastocytoma cell line P815 (cn: TIB-64, ATCC) were maintained in tissue culture flasks in RPMI supplemented with 10% FCS, amino acids and HEPES. All cell lines were periodically tested for mycoplasma contamination and confirmed negative by PCR with mycoplasma-specific primers (5′-ACTCCTACGGGAGGCAGCAGTA-3′ and 5′-TGCACCATCTGTCACTCTGTTAACCTC-3′).
Human peripheral blood mononuclear cells (PBMCs)
PBMCs were cultured in RPMI supplemented with 5% penicillin-streptomycin, 25 mM HEPES, and 8% heat-inactivated FBS. When mentioned, assays were performed in glucose-free RPMI supplemented with 5% penicillin-streptomycin.
Tumor-infiltrating lymphocytes (TILs)
For TILs expansion, tumor tissues were dissected into fragments of approximately 2 mm3. Each fragment was plated individually in a single well of a 24-well plate and stimulated with 6000 IU/ml rhIL-2 for 3 weeks. A rapid expansion protocol (REP) was performed by stimulating TILs with PHA 1 μg/ml, 3000 IU/ml rhIL2 (Proleukin, Roche) and feeders. TIL culture media was RPMI supplemented with 5% penicillin-streptomycin (Gibco), 25 mM HEPES, 1% L-glutamine (Gibco), 1% nonessential amino acids (Gibco), 1% Na pyruvate (Gibco), 0.1% 2β-mercaptoethanol (Gibco), and 8% heat-inactivated, pooled human serum.
Melanoma cell lines
Autologous tumor cell lines were established from three melanoma samples. Tissue was mechanically dissociated, with a clamp and scalpel, and enzymatically dissected using collagenase type I (Sigma-Aldrich) and deoxiribonuclease I (Roche) for 45–60 min at 37 °C. Tumor cell suspensions were cultured in RPMI, 10% fetal bovine serum (Gibco), and 1% penicillin-streptomycin (Gibco), dispensed into 10-cm petri dishes, and transferred to T-25 and T-75 flasks as cells expanded.
TIL/autologous tumor cell line cocultures
When described, cells were preincubated with the A2AR antagonist ZM 241385 (30 μM) or the A2BR antagonist PSB 1115 (100 μM) for 1 h and 30 min and then with nothing or Ado (30 μM) for 2 h. After preincubation, 200,000 TILs/well were dispensed into a 96-well plate containing, or not, the same number of autologous melanoma tumor cells. Intracellular staining for cytokine production, the cytotoxic assay or p-CREB and p-S6 flow cytometry staining were then performed.
Cytokine production assay and intracellular staining
Cryopreserved blood mononuclear cells were stimulated with anti-CD3/CD28 beads (bead-to-cell ratio = 1:2; Miltenyi) or CMV−/EBV−/Flu-specific peptides (1 μM). TILs were stimulated by anti-CD3/CD28 beads (bead-to-cell ratio = 1:2; Miltenyi) or autologous tumor cell lines. Stimulation was performed overnight at 37 °C in the presence of GolgiPlug (1 μg/ml; BD) and anti-CD107. When described, cells were preincubated with the A2AR antagonist ZM 241385 (30 μM), the A2BR antagonist PSB 1115 (100 μM), or the PKA inhibitor KT 5720 (30 μM) for 1 h 30 min and then with nothing, Ado (30 μM), or the A2AR agonist CGS 21680 (30 μM) for an additional 2 h. The time of incubation for Ado was chosen as the time giving the lowest reduction in IFN-γ production with no impact on cell survival. The time of incubation of antagonists was chosen as the time needed by ZM 241385 to fully prevent Ado inhibition of IFN-γ production. Then, the cells were washed with PBS-2 mM EDTA and stained extracellularly. First, cells were stained for the surface markers CCR7 and CD45RA and with a viability dye (Zombie UV, Biolegend) for 20 min at 4 °C. Cells were then washed and permeabilized with Cytofix/Cytoperm solution (30 min 4 °C, Fix and Perm buffer, Becton Dickinson), washed with wash buffer (Becton Dickinson) and stained with antibodies directed to CD3, CD4, CD8, IFN-γ, TNF-α and IL-2 (20 min, 4 °C). After washing, the cells were resuspended in PBS and analyzed by flow cytometry.
Functional avidity assessment
The functional avidity of virus-specific CD8+ T cell responses was assessed by performing limiting peptide dilutions (ranging from 1 μM to 10 pM) and measuring cytokine production by flow cytometry. The peptide concentration required to achieve a half-maximal IFN-γ response (EC50) was determined as described . Peptide stimulation and antibody staining were performed as described in the cytokine production assay.
Functional sensitivity to ado assessment
Functional sensitivity to Ado of peripheral or expanded tumor-infiltrating or peripheral CD8+ T cells was assessed by stimulating cells overnight with anti-CD3/anti-CD28-coated beads in the presence of decreasing doses of Ado (ranging from 0 μM to 100 μM) and measuring cytokine production by flow cytometry. The Ado concentration required to achieve a half-maximal cytokine response (IC50) was determined. Stimulation and antibody staining were performed as described in the cytokine production assay.
P-CREBSer133, p-S6Ser235/236 and p-AktSer473 flow cytometry staining
Peripheral or expanded tumor-infiltrating CD8+ T cells were preincubated with the A2AR antagonist ZM 241385 (30 μM), the A2BR antagonist PSB 1115 (100 μM), or the PKA inhibitor KT 5720 (10 μM) for 1 h and 30 min and then with nothing, Ado (30 μM), or the A2AR agonist CGS 21680 for 2 h (30 μM). Rapamycin (RAPA, 20 μM) was used as a positive control for mTORC1 (p-S6Ser235/236) inhibition, and MK2206 (100 nM) was used as a positive control for mTORC2 (p-AktSer473) inhibition. To evaluate p-S6Ser235/236 or p-AktSer473, CD8+ T cells were stimulated for 3 h with anti-CD3/anti-CD28-coated beads or autologous tumor cell lines. Then, the cells were washed with PBS-2 mM EDTA and stained extracellularly. First, cells were stained for the surface markers CCR7, CD45RA and/or CD98, CD71 and with a viability dye (Zombie, Biolegend) for 20 min at 4 °C. Cells were then washed and fixed/permeabilized with the Transcription Factor Staining Buffer Set (eBioscience). Cells were stained with antibodies directed to p-CREBSer133, p-S6Ser235/236 and p-AktSer473 (20 min, 4 °C). p-S6Ser235/236 and p-AktSer473 were not conjugated to a fluorochrome; therefore, after washing, a preadsorbed secondary goat anti-rabbit IgG H&L antibody Alexa Fluor® 488 (Abcam) was added. After washing, the cells were resuspended in PBS and analyzed by flow cytometry.
Measure of metabolic parameters by flow cytometry
The following assays were performed in glucose-free medium. 2-[N-(7-Nitrobenz-2-oxa-1,3-diazol-4-yl)amino]-2-deoxy-d-glucose (2-NBDG, Invitrogen) uptake, CD98 and CD71 upregulation were carried out with magnetically isolated CD3+ T cells (Pan T Cell Isolation Kit, Miltenyi), which were preincubated with ZM 241385 (30 μM), PSB 1115 (100 μM), and KT 5720 (Sigma) for 1 h and 30 min and then with nothing, Ado (30 μM), CGS 21680 or BAY 60–6583 (Sigma) for 2 h and finally activated overnight by anti-CD3/CD28 beads. T cells were then stained with antibodies directed to CD3, CD4, CD8, CCR7, and CD45RA and when needed CD98 and CD71 (20 min 4 °C). To evaluate glucose uptake, cells were washed and incubated with 100 μM 2-NBDG at 37 °C for 20 min prior to fluorescence measurement by flow cytometry.
Detection of AdoR mRNA by RNA flow cytometry (Prime Flow RNA, Affymetrix)
Human PBMCs were thawed, and when needed, total CD3+ cells were isolated by negative selection with a Pan T Cell Isolation Kit (MACS technology, Miltenyi). Cells were transferred to RNA Flow staining tubes (RNAse free; provided with the kit). Mouse splenocytes were also taken as a negative control and stained for anti-mCD45. Cells were first stained at the surface for CD3, CD4, CD8, CD56, CD16, CD19, CD14, CCR7, and CD45RA (20 min 4 °C) and then stained for AdoR mRNA following the manufacturers’ instructions . Briefly, tubes were centrifuged at 2500 rpm for 5 min. Cells were then fixed and permeabilized in the presence of RNAse inhibitors. A second step of fixation was performed for 1 h at room temperature. Mouse cells were added to each human sample as an internal negative control or in a separate tube. Cells were then washed twice in wash buffer, and target probes for AdoRs were added and incubated for 2 h at 40 °C. After centrifugation, the cells were left overnight at 4 °C. PreAmp-mix and Amp-mix were then added successively with an incubation time of 1 h and 30 min at 40 °C each and two washes between each incubation step. Finally, labeled custom probes directed against ADORA2A, ADORA2B, ADORA1 and ADORA3 were added, and the cells were washed before flow cytometry analysis.
Flow cytometry analysis
Flow cytometry acquisition was performed with an LSRFortessa flow cytometer (BD Biosciences). Flow cytometry analysis was performed with FlowJo software (Version 10.2, Treestar). Data were analyzed by Prism v7.
Preparation of cellular extracts and western blot analysis
Whole-cell extracts were prepared using RIPA buffer (50 mM Tris, 150 mM NaCl, 1% Triton X-100, 1% sodium deoxycholate, 0.1% sodium dodecyl sulfate (SDS), 1 mM phenylmethylsulfonyl fluoride (PMSF), 1 mM Na3VO4, 5 mM NaF, and 1% cocktail protease inhibitors; Sigma). The protein concentration was measured using the Pierce™ BCA Protein Assay Kit (Thermo Scientific). Equal amounts of protein (40 μg/sample) were separated by electrophoresis in a 12% denatured polyacrylamide gel and blotted onto nitrocellulose membranes (Bio-Rad). The membranes were blocked for 1 h in 5% low-fat milk in PBS with 0.1% Tween 20 (PBST) at room temperature. Then, the filters were incubated with the following primary antibodies overnight at 4 °C: Phospho-CREB (Ser133) (9198, Cell Signaling, USA; diluted 1:1000); CREB (9197, Cell Signaling, USA; diluted 1:1000); Phospho-p44/42 MAPK (Erk1/2) (Thr202/Tyr204) (9101, Cell Signaling, USA; diluted 1:1000); p44/42 MAPK (Erk1/2) (9102, Cell Signaling, USA; diluted 1:1000); Phospho-Akt (Ser473) (4058, Cell Signaling, USA; diluted 1:1000); Akt (pan) (2920, Cell Signaling, USA; diluted 1:2000); Phospho-S6 Ribosomal Protein (Ser235/236) (2211, Cell Signaling, USA; diluted 1:1000); S6 Ribosomal Protein (2317, Cell Signaling, USA; diluted 1:1000); and α-Tubulin (3873, Cell Signaling, USA; diluted 1:1000). The membranes were washed 3 times with PBST and then incubated with (HRP)-conjugated anti-rabbit or anti-mouse antibodies for 2 h at room temperature. The membranes were then washed 3 times (10 min in PBST), and proteins were visualized by the ECL chemiluminescence method. The immunoreactive bands of proteins were acquired by using the GBOX Chemi XX6 system (Syngene).
When described, TILs were preincubated with the A2AR antagonist ZM 241385 (30 μM) for 1 h and 30 min and then with nothing or Ado for 2 h (30 μM). TILs were then dispensed into a 96-well plate, in triplicate, at decreasing densities: from 100,000 to 1000 cells/well.
Autologous melanoma cell lines or P815 cell lines (unloaded or loaded with anti-CD3) were labelled with 51chromium for 45 min at 37 °C, and after 3 washing steps, 1000 cells were dispensed into each TIL-containing well. In addition, for calculation of specific lysis, 1000 cells were also dispensed into four wells containing only tumor medium (spontaneous release) and into four wells containing 1 M HCL (maximum release).
Effector and target cells were incubated in a total volume of 200 μl of RPMI 10% FBS or HCL for 4 h at 37 °C, 5% CO2. The plates were centrifuged for 3 min at 230×g. Forty microliters of the culture supernatants was transferred to a LumaPlate-96 (PerkinElmer, Turku, Finland) and, after drying the plates, read on a TopCount NXT (Packard, Meriden, USA). The percentage lysis was calculated by the following formula:
Semiquantitative RT-PCR (qRT-PCR) (SYBR GREEN)
To measure AdoR expression, CD8+ T cells were isolated from cryopreserved blood mononuclear cells by magnetic activated cell sorting (MACS technique) using a CD8+ T Cell Isolation Kit (Miltenyi Biotech) according to the manufacturer’s instructions. The MCF-7, EBV-B, PC3, THP-1 and HL-60 cell lines were also used as internal controls for validation. AdoR and HIF-1α expression were measured in total TILs. Total cellular RNA was isolated by the RNeasy Micro kit (Qiagen). cDNA was synthesized from 250 ng of total RNA using the Superscript II system according to the manufacturer’s protocol (Life Technologies). PCR reactions contained cDNA, 2x qPCR Master Mix (KAPA Biosystems), and 2 μM of forward and reverse primers. qRT-PCR was performed on an Applied Biosystems® 7500 Fast Real-Time PCR instrument. Each reaction was performed in three replicates, with beta-2-microglobulin (β2M) as an internal control gene for normalization. Raw Ct values were imported into Excel, and the expression levels of the PCR products relative to β2M were calculated using the 2 − ΔCt method.
The primer sequences used were as follows: β2M sense, 5′-CCAGCAGAGAATGGAAAGTC-3′; antisense, 5′-GATGCTGCTTACATGTCTCG-3; ADORA1 sense, 5′-CCTCCATCTCAGCTTTCCAG-3′ (DOI: 10.1182/blood-2013-02-482406); antisense, 5′-AGTAGGTCTGTGGCCCAATG-3′, ADORA2A sense, 5′- CTCCGGTACAATGGCTTGGT-3′; antisense, 5′- TGGTTCTTGCCCTCCTTTGG-3′, ADORA2B sense, 5′-ATGCCAACAGCTTGAATGGAT-3′; antisense, 5′-GAGGTCACCTTCCTG GCAAC-3′, ADORA3 sense, 5′-TTGACCAAAAGGAGGAGAAGT-3′; antisense, 5′- AGTCACATCTGTTCAGTAGGA G-3′. HIF-1α sense, 5′-GGC AGC AAC GAC ACA GAA ACT GA-3′; antisense, 5′-TGA TCC TGA ATC TGG GGC ATG GT-3′ (DOI: 10.1038/s41598-017-00508-x).
The efficiency of each primer set was tested by generating a standard curve using relative positive control samples for each primer (MCF-7, EBV-B, PC3 and HL-60 for adenosine receptor A1, A2A, A2B and A3, respectively). All primers were tested by qRT-PCR using a two-fold serial dilution of cDNA and water as a nontemplate control to determine the amplification efficiency and specificity. The amplification efficiency for each primer was determined from the linear slope of the standard curve; only primers with a standard curve slope between − 3.1 and − 3.4 were used for further quantification.
Analysis of the relative changes (arbitrary units) in gene expression required calculations based on the threshold cycle (Ct: the fractional cycle number at which the amount of amplified target reaches a fixed threshold). The threshold cycles of the cell subsets were then normalized based on the threshold cycle of the housekeeping gene (β2M) to obtain the ΔCt.
Measure of glycolytic and phospho-oxidative metabolism (seahorse assay)
Magnetically isolated CD3+ T cells were left unconditioned or incubated with ZM 241385 (30 μM) and/or Ado (30 μM). Cells were then stimulated overnight with anti-CD3/CD28 beads, and the seahorse assay was performed. For the extracellular flux assay, the sensor cartridge was hydrated overnight in Seahorse XF Calibrant at 37 °C in a non-CO2 incubator. A total of 4 × 105 human T cells with different treatment conditions were seeded in a Seahorse Bioscience culture plate for 30 min. OCR and ECAR were then measured by an XF96 Seahorse Extracellular Flux Analyzer following the manufacturer’s instructions. During the seahorse assay, cells were treated with oligomycin (0.5 μM), FCCP (2 μM), rotenone (0.5 μM), antimycin A (0.5 μM) and 2-DG (50 mM). Each condition was performed in 3–6 replicates.
Statistical analysis was performed with Prism software (Version 7, GraphPad) using nonparametric and parametric paired (Friedman or Wilcoxon or t test) and unpaired (Kruskal-Wallis or Mann-Whitney) tests as indicated. For multiple comparisons, adjusted P-values were calculated by one-way ANOVA followed by Dunn’s test. Correlations were assessed by the nonparametric Spearman’s test.
Human CD8+ T cell memory subsets are differentially affected by ado
Activated naïve CD8+ T cells differentiate in memory subsets with distinct phenotypic and functional properties . The differentiation and maintenance of murine naïve CD8+ T cells is negatively impacted by A2AR signaling . However, the differences in the sensitivity to Ado of memory subsets in human CD8+ T cells have not yet been explored. We identified the major CD8+ T cell memory subsets according to their differential expression of CCR7 and CD45RA (i.e., T central memory-TCM, T effector memory-TEM, T terminally differentiated-TEMRA; Additional file 1: Figure S1a, Additional file 2: Table S1), and we assessed the relative sensitivity to Ado by measuring cytokine production following polyclonal or antigen-specific stimulation (Fig. 1a-b, Additional file 2: Table S1). Exposure to Ado decreased cytokine production (i.e., IFN-γ, TNF-α, and IL-2) and partially decreased the degranulation activity (i.e., CD107a mobilization) in CD8+ T cells (Fig. 1a-b and Additional file 1: Figure S1 b-d), consistent with previous studies [14, 16, 17, 20]. Ado mediated suppression of responses to both polyclonal stimulation (i.e., anti-CD3/anti-CD28-coated beads) (Fig. 1a-b and Additional file 1: Figure S1b-d) and viral epitopes (Fig. 1b and Additional file 1: Figure S1c) but not stimulation with ionomycin or phorbol-12-myristate-13-acetate (PMA) (Additional file 1: Figure S1b,e). Of interest, among the distinct T cell subsets, TCM were more sensitive to Ado, with deeper suppression of cytokine production than those of the TEM and TEMRA subsets (Fig. 1b and Additional file 1: Figure S1f).
The functional avidity of CD8+ T cells, also called antigen sensitivity, is measured as the peptide concentration able to mobilize 50% of the maximal response (EC50). The functional avidity of T cells is independent of the magnitude of a response measured at saturating antigen concentrations  and is usually associated with superior control of virus replication or tumor growth [22, 27]. We evaluated the functional avidity of a panel of virus-specific polyclonal CD8+ T cells exposed to decreasing peptide concentrations. We observed that Ado significantly reduced the functional avidity of all virus-specific CD8+ T cells (Fig. 1c-d), with the strongest effect observed in the TCM subset (Fig. 1c-d). These data indicate that Ado limits the ability of T cells to respond to targets expressing cognate antigens.
A2AR expression levels dictate ado sensitivity in human CD8+ T cells
Our data suggest that TCM cells are the most sensitive subset to functional blunting by Ado. To substantiate this further, we quantified the functional sensitivity to Ado of each memory subset by determining the Ado concentration inhibiting 50% of the maximal response (IC50 of the cytokine production). We confirmed that CD8+ TCM cells displayed higher sensitivity to Ado than TEM and TEMRA cells (Fig. 2a-b and Additional file 1: Figure S2a).
We therefore hypothesized that the differential sensitivity to Ado may be explained by TCM cells expressing higher AdoR levels than the other memory subsets. Due to the lack of antibodies for flow cytometry analyses for A1R and A3R, we established RNA staining for flow cytometry (PrimeFlow RNA assay)  (Additional file 1: Figure S2b) to determine the expression of all four ADORs (i.e., ADORA1, ADORA2A, ADORA2B and ADORA3) in primary human CD8+ T cells. Moreover, we used semiquantitative real-time PCR (qRT-PCR) as a validation tool. To include positive controls for each receptor tested, we evaluated AdoR expression in distinct cell lines: EBV-transformed B cell line, human leukemic lines (THP-1 and HL-60), prostate cancer lines (DU-145 and PC-3, LNCaP) and a breast cancer cell line (MCF-7) (Additional file 1: Figure S2c). AdoR expression data obtained from qRT-PCR analysis correlated with flow cytometry values in both cell lines and primary CD8+ T cells (Additional file 1: Figure S2d-e). A correlation was also found in CD8+ T cells when only A2AR expression was considered (Additional file 1: Figure S2e). Overall, these data indicate that the PrimeFlow RNA assay is a suitable technology for the relative quantification of AdoR expression in human CD8+ T cells. We also measured A2AR and A2BR expression with antibodies by flow cytometry in CD8+ T cells and found a correlation with A2AR expression measured by PrimeFlow RNA (Additional file 1: Figure S2f-g). Moreover, we confirmed the lower/undetectable expression of A2BR by CD8+ T cells (Additional file 1: Figure S2f, h).
We then evaluated AdoR expression in total CD8+ T cells and in different memory subsets ex vivo. Of interest, A2AR was expressed at a higher percentage than other AdoRs in total CD8+ T cells (Fig. 2c). Among the memory subsets, it was predominantly expressed by CD8+ TCM cells, similar to naïve CD8+ T cells (Fig. 2d). These data strongly suggest that the high sensitivity of CD8+ TCM cells to Ado is associated with their high expression of A2AR. In addition, our results not only support the role of A2AR as a critical player in Ado-mediated suppressive effects in CD8+ T cells but also indicate that A2AR expression quantitatively dictates sensitivity to Ado. This was further corroborated by the positive correlation between A2AR expression in CD8+ T cells and the Ado-mediated fold change (i.e., decrease) in IFN-γ production (Fig. 2e), which was not observed for A2BR (Additional file 1: Figure S3a).
Furthermore, we evaluated whether blocking A2AR or A2BR with selective inhibitors (ZM 241385 and PSB 1115, respectively) would prevent the Ado-mediated reduction of cytokine production. The blockade of A2AR, but not A2BR, was able to circumvent the immunosuppressive effects of Ado on CD8+ T cells (Fig. 2f). The selective A2AR agonist CGS 21680 was also able to reduce IFN-γ production in CD8+ T cells (Fig. 2f). Consistent with what was already shown in the presence of Ado (Fig. 1b), CGS 21680 primarily affected the TCM subset (Additional file 1: Figure S3b). The preventive action of A2AR- or A2BR-selective inhibitors was equal in all the differentiation subsets evaluated (data not shown). The blockade of A2AR or A2BR alone did not affect cytokine production significantly (Additional file 1: Figure S3c). Finally, selective A2AR blockade also efficiently prevented Ado-mediated immunosuppression of virus-specific CD8+ T cells (Fig. 2g).
Taken together, these data not only confirm A2A as the main receptor responsible for Ado-mediated immunosuppression but also highlight the relevance of A2AR expression levels in quantitatively determining Ado suppressive effects in primary human CD8+ T cells.
Ado/A2AR triggers PKA, impairing TCR/mTORC1 signaling and metabolic/effector functions in CD8+ T cells
Ado-mediated activation of A2AR increases intracellular cAMP levels , and many of the downstream effects of cAMP elevation are dependent upon PKA activation [19, 29]. Of interest, the selective inhibition of the PKA pathway in CD8+ T cell clones can prevent Ado-induced suppression of cytokine production . We therefore investigated whether molecular mediators of PKA signaling were activated by Ado in primary human CD8+ T cells. Basal p-CREB levels increased in the presence of Ado or CGS 21680, which is a selective A2AR agonist (Fig. 3a and Additional file 1: Figure S4a-b). This effect was prevented by both the PKA-specific inhibitor KT 5720 (Fig. 3a and Additional file 1: Figure S4a-b) and the selective A2AR antagonist ZM 241385 (Fig. 3a and Additional file 1: Figure S4a-b), while it was not affected by the selective A2BR antagonist (PSB 1115, Fig. 3a). All memory T cell subsets were influenced by Ado (Additional file 1: Figure S4c), while CGS 21680 mostly affected the TCM subset (Additional file 1: Figure S4c), mirroring the functional data (Fig. 1).
Consistent with the increase in PKA activation and previous observations [21, 30], we observed that Ado reduces TCR-dependent ERK phosphorylation in primary human CD8+ T cells, reflecting impaired TCR signaling. Notably, this effect was dependent upon A2AR/PKA signaling (Additional file 1: Figure S4d-e).
Since the mTOR pathway is pivotal for complete T cell activation and induces potent effector functions [4, 31, 32], we evaluated whether Ado/A2AR signaling could affect mTOR triggering in a PKA-dependent manner. To this end, we assessed the phosphorylation of downstream effectors of mTORC1 and mTORC2, i.e., S6 (p-S6; Additional file 1: Figure S5a-b) and AktSer473 (p-AktSer473; Additional file 1: Figure S5c-d) after polyclonal CD8+ T cell stimulation. Ado signaling markedly impaired phosphorylation of S6 (Fig. 3b and Additional file 1: Figure S5a-b) but not of AktSer473 (Additional file 1: Figure S5c-e). These data indicate that the mTORC1, but not the mTORC2, complex is a target of Ado-mediated signaling in primary human CD8+ T cells. Importantly, this effect was mediated by A2AR activation since the selective A2AR agonist CGS 21680 also reduced S6 phosphorylation (Fig. 3b), and the selective inhibitor of A2AR (ZM 241385), but not A2BR (PSB 1115), was able to prevent both Ado and CGS 21680 effects (Fig. 3b). Interestingly, S6 phosphorylation was reduced in both TCM and TEM subsets but not in the TEMRA subset (Additional file 1: Figure S5f). Additionally, the selective agonist of A2AR (CGS 21680) predominantly affected the TCM compartment (Additional file 1: Figure S5f), mirroring the functional data (Fig. 1). Finally, blockade of the PKA pathway prevented Ado-mediated inhibition of mTORC1 activation (Fig. 3b), thus indicating that Ado impaired mTORC1 signaling through PKA activation. These data strongly suggest that Ado/A2AR signaling impairs mTORC1 activation in human CD8+ T cells through PKA, likely due to the PKA-dependent inhibition of TCR signaling.
mTOR is the main complex responsible for both metabolic rewiring [3, 33] and augmented effector functions following TCR-mediated activation [34, 35]; thus, we assessed whether Ado also impaired CD8+ T cell metabolic fitness. Upon CD8+ T cell activation, Ado impaired metabolic activity of both OXPHOS and glycolysis in an A2AR-dependent manner (Fig. 3c). However, Ado induces more severe impairment of ECAR, suggesting that cells prefer to utilize oxygen consumption to sustain metabolic needs in this condition.
This was further confirmed by the Ado-mediated impairment of CD71/CD98 expression and of 2-NBDG (glucose analog) uptake (Fig. 3d and Additional file 1: Figure S6a). The selective inhibition of A2AR, but not of A2BR, prevented the Ado-mediated effects (Fig. 3d). Among the memory CD8+ T cell subsets, TCM cells were the most affected (Additional file 1: Figure S6b). Notably, both PKA and A2AR inhibition were able to prevent Ado-mediated impairment of metabolic fitness and cytokine production (Fig. 3d-e).
Taken together, these results strongly suggest that the Ado/A2AR-mediated increase in PKA activation in primary human CD8+ T cells leads to subsequent impairment in metabolic fitness and effector functions, likely due to the reduction in TCR signaling and mTORC1 activation.
Ado suppresses TILs activation and tumor recognition
Ado is a mediator of TME immunosuppression and may limit the success of immunotherapy, notably the adoptive cell transfer of tumor infiltrating lymphocytes (TILs) [13, 36]. Since little is known regarding the susceptibility of human TILs to Ado-mediated suppression and the Ado receptors involved , we evaluated the capacity of selective A2AR and A2BR inhibitors to prevent Ado immunosuppression in human TILs. TILs were expanded with the REP (rapid expansion protocol) from tumoral or inflamed/normal prostate (n = 8), colon cancer metastasis (n = 4) and metastatic melanoma (n = 6) (Additional file 2: Table S2); cell cultures with heterogeneous CD4+/CD8+ T cell ratios were obtained according to the tumor evaluated (Additional file 1: Figure S7a). Although heterogeneous (Additional file 1: Figure S7b), the cytokine production capacity of CD8+ TILs was consistently suppressed by Ado (Additional file 1: Figure S7c). In line with the effects of Ado on peripheral T cells, inhibitors of A2AR prevented the Ado-mediated suppression of CD8+ TILs (Fig. 4a and Additional file 1: Figure S7c). Surprisingly, in prostate-derived samples, A2BR blockade was also able to prevent the Ado effect (Fig. 4a and Additional file 1: Figure S7c). However, we did not find any impact of A2AR or A2BR inhibitors on the TIL expansion capacity (data not shown). We also evaluated the sensitivity of CD8+ TILs to Ado and compared it to circulating CD8+ T cells from healthy donors and cancer patients in resting conditions (ex vivo) or after in vitro expansion. Despite high variability, we observed that CD8+ TILs and circulating CD8+ T cells had an overall similar sensitivity (IC50) to Ado (Fig. 4b). To gain further insight into the AdoR responsible for Ado-mediated immunosuppression in TILs, we evaluated AdoR expression by qRT-PCR in total TIL products. As for the REP-expanded healthy peripheral T cells, TILs predominantly expressed A2AR and lacked A1R and A3R (Additional file 1: Figure S7d). However, TILs showed higher expression of A2BR in some cases, in particular the ones derived from prostate tissues (Additional file 1: Figure S7d). Notably, we found a correlation between A2BR expression and the capacity of the A2BR antagonist to prevent the Ado-mediated reduction in IFN-γ production (Fig. 4c). The higher expression of A2BR can only be partially explained by the T cell activation status. Indeed, CD8+ T cells stimulated moderately and transiently upregulated A2BR in vitro at day 3 (Additional file 1: Figure S7e).
Previous data support the hypothesis that hypoxia could induce the activation of the CD73-A2AR adenosine pathway and that A2AR expression was positively correlated in head and neck squamous cell carcinoma tissues [18, 37, 38]. However, we did not find a correlation between the expression of HIF-1α and A2AR in the expanded TILs (Additional file 1: Figure S7f).
Ado can inhibit the ability of TILs to recognize and kill target cells loaded with the melanoma differentiation antigen MART125–36 peptide . However, the effect of Ado on autologous tumor cell recognition was not addressed. We first characterized AdoR expression in 6 autologous melanoma cell lines (Additional file 2: Table S2) by qRT-PCR and compared it to AdoR expression in TILs expanded from the same lesion. In contrast to TILs, tumor cells expressed A2AR at lower levels than A2BR and at levels comparable to A1R and A3R (Additional file 1: Figure S8a). We then evaluated whether Ado could impair the ability of TILs to respond to autologous tumor cells in vitro. Of interest, Ado was able to reduce cytokine production, cytotoxic activity and metabolic fitness of melanoma-derived TILs cocultured with autologous tumor cells (Fig. 4d-g and Additional file 1: Figure S8b-c). In the redirected killing assay, the maximum frequency of cell lysis was 100% for all patients tested, and the suppressive effect of Ado on cytotoxic function was almost undetectable (less than 20% reduction for any ratio considered) (Additional file 1: Figure S8d). In contrast, in the autologous setting, Ado inhibition was more pronounced, reaching a 50% reduction for some of the ratios tested where the maximum level of cell lysis was approximately 20% (Mel002, Mel007, and Lau1015) (Fig. 4e). The lowest effect was observed for patients Mel0011 and Lau50, where the cytotoxicity was naturally very high (91 and 100%). We could not test the effect of Ado in patient Lau1660 due to a low overall killing capacity (less than 10%). In the autologous setting, when the highest lysis values were considered (effector:target ratio E:T = 100:1), a significant reduction of cytotoxicity was observed in the presence of Ado, which was prevented by A2AR blockade (ZM 241385) (Fig. 4f). These observations suggest that in a physiological setting where tumor rejection antigens may be poorly expressed by tumors or when TILs contain limited frequencies of tumor antigen-specific T cells, then Ado may play an important role in preventing tumor cell killing by activating A2AR signaling. The variability in the Ado effect observed at different E:T ratios, however, indicates that further investigation is needed to confirm this evidence. Notably, Ado-mediated immunosuppression in the autologous setting was concomitant with a decrease in metabolic fitness (i.e. CD71 and CD98 upregulation, Fig. 4g), an increase in p-CREB and a decrease in p-S6 activation (Fig. 4h and Additional file 1: Figure S8e-f); these effects were also prevented by the selective inhibition of A2AR (Fig. 4d-h). These data suggest a predominant role of Ado in mediating the suppression of human expanded TILs through A2AR signaling, thus potentially jeopardizing the efficacy of adoptive cell transfer.
Several targets, such as CD39, CD73 and AdoRs, contributing to the accumulation of Ado and its immunosuppressive effects in the TME are under evaluation in preclinical and clinical studies of cancer immunotherapy [40–43]. Ado is known to suppress tumor immunity by reducing immune cell infiltration, cytotoxicity and cytokine production [20, 43]. Moreover, CD8+ T cell effector functions and metabolic fitness are dramatically impaired in the TME [9, 10]; thus, understanding the mechanisms of action of immunosuppressive molecules is pivotal to restoring an efficient anti-tumor immune response. However, mediators of Ado signaling are not fully understood, and biomarkers of efficacy for therapies targeting the adenosinergic pathway remain unknown. Our study unveils new mechanisms of Ado-mediated suppression in CD8+ T cells and highlights potential new biomarkers to monitor during Ado-targeted immunotherapies.
The inhibition of T cell activation in early-differentiated cells can preclude the regeneration of the effector cells that will die after exerting their cytotoxic/inflammatory function. TCM cells have a longer half-life than effector cells and an enhanced ability to divide and differentiate into more differentiated subsets . We found that human CD8+ TCM cells are the most sensitive to Ado due to their high expression of A2AR. A high concentration of Ado in the TME may therefore negatively affect the renewal of fully differentiated effector cells. Studies in both mice and, to a lesser extent, humans support the main role of A2AR in mediating Ado-dependent T cell immunosuppression and exhaustion in the TME [16, 17, 20, 21]. We identified A2AR as the main mediator of the Ado immunosuppressive effect in peripheral and tumor-infiltrating human CD8+ T cells, strengthening the importance of this target in next-generation immunotherapy. As previously suggested [20, 21], we confirmed that the Ado/A2AR-mediated suppression in human CD8+ T cells relies on PKA activation and inhibition of TCR signaling. To evaluate the expression of the 4 AdoRs, we used RNA flow technology due to the lack of anti-A1R and anti-A3R antibodies available for flow cytometry. We found consistent expression of A2A and A2B receptors measured by RNA flow and by antibodies. However, these antibodies are not optimal for flow cytometry since both were developed for western blotting; anti-A2AR is against an intracellular epitope, thus requiring permeabilization of the cells and not allowing the distinction between the surface and the intracellular compartment, while the anti-A2BR is polyclonal, thus affecting his affinity and specificity. Finally, these antibodies cannot be combined in the same panel since A2BR staining is erased by cell permeabilization.
Independent studies have reported the Ado inhibitory effect on the mTORC pathway and chemotaxis in neutrophils  and the presence of a PKA-dependent manner of mTORC1 inhibition in nonimmune cells that was unrelated to the classical mTORC1 activators (i.e., TSC2, Rheb and Rag GTPases) [45, 46]. However, there is no previous evidence demonstrating that Ado impairs mTORC1 activation in an A2AR/PKA-dependent manner in CD8+ T cells. Herein, we demonstrate that Ado reduces TCR-dependent mTORC1 activation by triggering A2AR and PKA. Although mTORC1-independent effects cannot be excluded, the importance of this complex in mediating effective T cell activation [1, 4, 31, 32] strongly suggests that, among the targets of TCR signaling, impairment of mTORC1 activation is responsible for most of the Ado/A2AR/PKA-mediated suppressive effects in human CD8+ T cells. Notably, we show that Ado signaling in both peripheral CD8+ T cells and TILs exposed to autologous tumors or to polyclonal stimulation not only impaired cytokine production but also metabolic fitness. The impairment in mTORC1 activation is presumably the leading cause of the impairment in CD8+ T cell metabolism. From a translational standpoint, this evidence implies that Ado/A2AR-mediated immunosuppression may be reverted as well by molecules aiming at improving mTOR activation and metabolism selectively in T cells [47, 48]. On the other hand, the Ado pathway may be key in leading to T cell metabolism uncoupling in the TME, and thus, targeting this signaling may restore the metabolic fitness of infiltrating T cells.
We also characterized AdoR expression in melanoma-derived tumor cell lines and in expanded TILs. Tumor cell lines show higher expression of A2BR than A2AR, possibly reflecting their metastatic origin . Expanded TILs, despite a minor increase in A2BR expression, show a prevalent and almost exclusive expression of A2AR along with results obtained in peripheral CD8+ T cells. In line with this evidence, we show that the sensitivity to Ado of CD8+ TILs derived from three different tumor types is not different from that of peripheral CD8+ T cells. However, TILs derived from prostate samples also express variable amounts of A2BR, and the selective inhibition of this receptor prevents Ado-mediated immunosuppression. This effect was quantitatively correlated with the level of A2BR expression. Although further investigation is needed, the monitoring of A2BR expression in TIL products may be of interest for next-generation personalized immunotherapy in the context of adoptive cell transfer.
Despite indications in the literature of a causal connection between hypoxia and the adenosine pathway, we did not find a correlation between the expression of HIF-1α and A2AR. This may be explained by the lack of a hypoxic environment in the in vitro TIL culture that is instead present in tumor tissues.
Remarkably, Ado is able to affect both polyclonal responses of TILs derived from multiple tumors and autologous tumor-cell recognition by melanoma TILs by reducing cytokine production and metabolic fitness. Ado is therefore able to exert systemic immune suppression as well as to impair antitumor activity. Along the same lines, we show a reduction in the killing capacity of autologous targets at some E:T ratios. This effect was barely observed in the redirected killing assay where killing was 100%. In vivo, however, tumor antigens are not expressed homogeneously throughout the tumor tissue, and their accessibility is limited to specific T cells. Thus, in this context, Ado may exert an inhibitory effect on killing capacity. Our data support this possibility; however, since the impairment in the in vitro cytotoxicity observed is dependent on the E:T ratio, further investigations are needed to explore this hypothesis. The blockade of A2AR abrogated Ado-mediated immunosuppression by preventing an increase in p-CREB and by restoring p-S6 activity. Finally, we did not find any effect of A2AR or A2BR inhibitors on the TIL expansion capacity. This may be due to the absence of a significant concentration of Ado in the culture or to the instability of the compound used that would not allow for observing a significant effect in long-term cultures. This should be better investigated by using drugs currently under investigation in clinical trials . Nevertheless, the AdoR expression and the susceptibility of expanded TILs to Ado immunosuppression described in our study strongly support the Ado/A2AR pathway as an important target for cancer immunotherapy with particular relevance for combinatorial T cell-based strategies.
The recent remarkable clinical success of immunotherapy brings along the need to discover predictive biomarkers of treatment efficacy and related adverse effects. This will help immune oncologists make decisions before and during therapy. To date, judgements are mainly based on the overall assessment of clinical improvement and treatment tolerance; however, early immunomodulation markers need to be unveiled to act faster and more specifically to improve clinical success rates. In this context, we observed that A2AR expression levels quantitatively dictate CD8+ T cell sensitivity to Ado and that A2AR blockade rapidly affected p-CREB and p-S6 levels during autologous tumor cell recognition. Therefore, in future preclinical or clinical studies testing therapies targeting the adenosinergic pathway, it will be relevant to monitor T cell expression of A2AR to predict their sensitivity to Ado but also of p-CREB and p-S6 to unveil their potential as biomarkers.
Overall, our data support the relevance of targeting the Ado/A2AR immunosuppressive pathway to restore both effector function and metabolic fitness of peripheral and tumor-derived CD8+ T cells. This could be of particular interest in combination with adoptive cell transfer to prevent TME immunosuppression and improve treatment efficacy. Finally, we postulate that the modulation of A2AR, p-CREB and p-S6 expression levels may be valuable efficacy biomarkers of A2AR blockade and T cell function recovery in the context of clinical studies.
The research leading to these results has received funding from the following:
The European Community’s Seventh Framework Program ([FP7/20013–2018] under grant agreement n°602200). The SNSF project grant (31003A_163204), the Institute for Experimental Cancer Research (26075483), and the Swiss Cancer Foundation (KFS-3949-08-2016) to P.-C.H. The Swisslife foundation project grant (2607011902) to S.V. The SNSF Ambizione grant (PZ00P3_161459) and the Swiss Cancer Foundation grant (KFS-3710-08-2015) to C.J. and SNSF grant 156469 to P.R.
We thank the immunomonitoring core team from CTE (Amandine Anastasio, Petra Baumgaertner, Aymeric Auger, and Anne-Christine Thierry) for sharing samples and knowledge and the members of the EU FP7-supported TumAdoR consortium that aims to bring anti-CD73 mAb candidates to clinical testing.
SV, BM-G, BNR, LD, HW, GE, RA, and LEL contributed to experimental execution. SV, BM-G, and BNR contributed to the experimental design and data analyses. AI, LD, MV, TT, PJ, TN-N, DS, GV, NG, OD, LK, and GK shared relevant material. SV, BM-G, BNR, CJ, CM-C, CC, P-CH, PR, and AH contributed to the scientific development of the project. SV drafted the manuscript. All authors reviewed the manuscript. All authors read and approved the final manuscript.
Availability of data and materials
The data generated and/or analyzed during the current study are available upon reasonable request to the corresponding author.
Ethics approval and consent to participate
Written informed consent was obtained from all healthy subjects and patients, in accordance with the Declaration of Helsinki. Ethics approval for sample collection was given by the University Hospital of Lausanne-CHUV IRB.
Consent for publication
The authors declare that they have no competing interests.
- Adenosine receptor
- Effect:target (ratio)
- Peripheral blood mononuclear cells
- Protein kinase A
- Phorbol 12-myristate 13-acetate
- Semiquantitative real-time PCR
- Rapid expansion protocol
- T central memory cells
- T cell receptor
- Tumor-infiltrating lymphocytes
- Tumor microenvironment
Electronic supplementary material The online version of this article (10.1186/s40425-019-0719-5) contains supplementary material, which is available to authorized users.