Background
Allogeneic hematopoietic stem cell transplantation (allo-HSCT) remains the only curative option for many hematologic malignancies. Unfortunately, a serious complication is frequently developed after allo-HSCT: graft-versus-host disease (GvHD). GvHD occurs when donor T lymphocytes recognize as foreign and destroy patient’s healthy tissues. Despite the immunosuppressive regimens administered, GvHD remains the major cause of morbidity and mortality after allo-HSCT. Thus, new therapeutic strategies are needed.
One of the key signaling pathways involved in T cell activation and function is phosphatidylinositol 3-kinase/AKT/mammalian target of rapamycin (PI3K/AKT/mTOR) [
1]. This pathway controls numerous cellular processes, including proliferation, survival, migration, and metabolism [
2]. In particular, PI3K activation in T cells promotes survival [
3] and cell cycle progression [
4], modulates differentiation [
5,
6], and controls the acquisition of effector and memory phenotypes [
7]. Thus, inhibitors of PI3K/AKT/mTOR pathway can interfere with T cell activation and function.
The use of PI3K/AKT/mTOR inhibitors has been scantily explored in the allo-HSCT context. Only the utility of the mTORC1 inhibitor rapamycin (Sirolimus) has been extensively studied, providing promising results [
8]. In addition, it has been suggested that the beneficial effects observed in patients with chronic GvHD treated with tyrosine kinase inhibitors could be due, in part, to their ability to inhibit PI3K signaling in T cells [
9]. However, few studies have evaluated the immunosuppressive effect of PI3K inhibitors on T lymphocytes [
10‐
12] and their ability to prevent GvHD development [
13,
14]. Herein, we have analyzed the effects of two novel antitumor drugs, the pan-class I PI3K inhibitor BKM120 and the dual PI3K/mTOR inhibitor BEZ235, on T cell activation and evaluated the utility of BEZ235 in a murine model of GvHD.
Methods
Drugs
BEZ235 was kindly provided by Novartis Pharma (Basel, Switzerland). BKM120 was purchased from Selleck Chemicals (Houston, TX, USA). For in vitro studies, BKM120 and BEZ235 were reconstituted in DMSO at 10 mM and stored frozen at −20 °C until use. For in vivo assays, BEZ235 solution was prepared fresh before administration. In brief, BEZ235 was dissolved in one volume of N-methyl-2-pyrrolidone (Sigma-Aldrich, St. Louis, MO) and then nine volumes of polyethylene glycol 300 (Sigma-Aldrich) were added. The application volume was 10 ml/kg body weight.
Cell isolation and culture
Peripheral blood mononuclear cells (PBMCs) were isolated from buffy coats of volunteer healthy donors by density gradient centrifugation using Ficoll–Paque solution (GE Healthcare Bio-Sciences, Uppsala, Sweden). Buffy coats were provided by the Centro de Hemoterapia y Hemodonación de Castilla y León, after written informed consent obtention. The research was approved by the Clinical Research Ethics Committee (CEIC) of “Area de Salud de Salamanca” (2012/11/132).
For Western blot analysis, PBMCs were allowed to adhere to tissue culture flasks (Corning, NY, USA) O/N at 37 °C and thereafter, non-adherent cells (T cell-enriched PBMCs) were collected. For cell cycle, apoptosis, and cytokine secretion assays, T cells were isolated from PBMCs by immunomagnetic selection, using the Pan T Cell Isolation Kit (Miltenyi Biotec, Bergisch Gladbach, Germany). The purity of isolated populations was routinely >95 %.
PBMCs or isolated T cells were cultured in well plates (Greiner Bio-One, Frickenhausen, Germany) at a density of 1 × 106 cells/ml in RPMI 1640 medium supplemented with 2 mM l-glutamine, 100 U/ml penicillin, 100 μg/ml streptomycin (all from Gibco-Invitrogen, Paisely, UK), and 10 % human AB serum (Sigma-Aldrich). Cells were stimulated or not with plate-bound anti-CD3 (5 μg/ml) and soluble anti-CD28 (2.5 μg/ml) monoclonal antibodies (mAbs) (BD Biosciences, San Jose, CA, USA) and treated with different doses of BKM120 or BEZ235 (0–10 μM).
Western blot analysis
Unstimulated or stimulated T cell-enriched PBMCs were treated with different concentrations of BKM120 or BEZ235. After 48 h, cells were lysed and cell extracts were electrophoresed, transferred onto PVDF membrane (Millipore, Bedford, MA, USA), and immunoblotted with antibodies against caspase 3, phosphorylated AKT (p-AKT) (T308 and S473), total AKT, phosphorylated 4E-BP1 (p-4E-BP1) (T37/46), total 4E-BP1, phosphorylated RPS6 (p-RPS6) (S235/236), total RPS6, phosphorylated p38 MAPK (p-p38) (T180/Y182), total p38 MAPK, phosphorylated ERK1/2 (p-ERK1/2) (T202/Y204) (all from Cell Signaling Thechnology®, Leiden, Netherlands), or total ERK2 (Santa Cruz Biotechnology, Heidelberg, Germany); antibodies to GAPDH (Cell Signaling Thechnology®) and calnexin (Enzo® Life Science, Plymouth Meeting, PA, USA) were used as loading controls. Anti-rabbit or anti-mouse antibodies conjugated to horseradish peroxidase (GE Healthcare, Buckinghamshire, UK) were used as secondary antibodies. Proteins were visualized with an ECL detection system (GE Healthcare).
Proliferation assays
PBMCs were stained with PKH-67 green fluorescent dye (Sigma-Aldrich) following manufacturer’s instructions. Thereafter, PKH-stained cells were seeded in the absence or in the presence of anti-CD3/anti-CD28 mAbs as described above and treated with different concentrations of the drugs. After 5 days, cells were stained with 7-amino-actinomycin D (7AAD) and anti-CD3-APC and acquired in a FACSCalibur flow cytometer (all from BD Biosciences). Percentage of proliferating T cells (CD3+PKHlow) was calculated using the Infinicyt software (Cytognos, Salamanca, Spain).
Cell cycle analysis
Unstimulated or anti-CD3/anti-CD28 stimulated isolated T cells were cultured in the presence of different concentrations of BKM120 or BEZ235. After 4 days, cells were stained with propidium iodide, using the CycleTEST™ PLUS DNA Reagent Kit (BD Biosciences) and acquired on a FACSCalibur flow cytometer. The distribution of cells along the cell cycle phases was analyzed using ModFit LT™ Macintosh program (Verity Software House, Topsham, ME, USA).
Apoptosis assessment
Unstimulated or anti-CD3/anti-CD28 stimulated isolated T cells were cultured in the presence of different concentrations of the compounds. After 2 days, cells were stained with Annexin V-PE (BD Pharmingen™, San Diego, USA). Samples were acquired on a FACSCalibur flow cytometer and analyzed using the Infinicyt software.
Cytokine assays
Isolated T cells were stimulated with anti-CD3/anti-CD28 mAbs in the presence of several concentrations of BKM120 or BEZ235. After 48 h, concentration of different cytokines in culture supernatants was analyzed on a FACSCalibur flow cytometer using the Human Th1/Th2 Cytokine Cytometric Bead Array (CBA) kit and BD CBA software (all from BD Biosciences).
Immunophenotypic analysis
Unstimulated or anti-CD3/anti-CD28 stimulated PBMCs were treated with different concentrations of BKM120 or BEZ235. After 48 h, cells were stained with the following combination of mAbs: anti-CD45RA-FITC/anti-IFN-γ-PE/anti-CD8-PerCP-Cy5.5/anti-CD25-PE-Cy7/anti-Granzyme B-Alexa Fluor® 647/anti-CD4-APC-Alexa Fluor® 750/anti-CD27-Brillant Violet 421/anti-CD3-Brillant Violet 510. For intracellular staining of IFN-γ and granzyme B, brefeldin A (10 μg/ml) (Sigma-Aldrich) was added for the last 4 h prior to acquisition and the IntraStain Kit (Dako Cytomation, Denmark) was used. Acquisition was performed on a FACSCanto flow cytometer (BD) and analyzed using the Infinicyt software.
Enzyme-linked immunospot (ELISPOT) assays
PBMCs from cytomegalovirus (CMV)-positive donors (responder cells) were stimulated with irradiated (25 Gy) PBMCs from a second donor (allogeneic cells) in a 2:1 ratio. Different doses of BKM120 or BEZ235 were added. After 96 h, responder cells were collected and cultured, in the absence of drugs, in an IFN-γ ELISpot plate (Mabtech, Nacka Strand, Sweeden): (a) in the absence of stimulation (control), (b) re-stimulated with allogeneic cells from the same donor of the primary culture, or (c) re-stimulated with CMV-pp65 recombinant protein (Miltenyi Biotec). After 36 h, ELISPOT was performed following manufacturer’s instructions. Spots corresponding to IFN-γ secreting cells were quantified using an Immunospot ELISPOT reader (CTL, Aale, Germany). The percentage of IFN-γ secreting cells was determined by subtracting, from the number of spots counted in allogeneic or CMV-pp65 re-stimulated wells, the background spots in the corresponding unstimulated (control) wells. These values were normalized with respect to those obtained from the samples pre-stimulated in the absence of drugs (0 μM) and re-stimulated with allogeneic cells or CMV-pp65, respectively, considered as 100 %.
GvHD murine model
Female recipient Balb/c (H2d) and male donor C57BL/6 (H2b) mice (12 weeks old) were purchased from Harlan Laboratory (Carshalton, UK). Animal experiments were approved by the ethical committee of Salamanca University (N°201300004045).
Balb/c mice received total body irradiation (8.5 Gy in two fractions) from a Cs137 source and then an intravenous injection of 10 × 106 C57BL/6 bone marrow cells without (BM group) or with 5 × 106 splenocytes. Mice receiving splenocytes were either untreated (GvHD group) or treated orally with BEZ235 (GvHD + BEZ235 group) once a day, from day +1 to day +60 post-transplantation. Different concentrations of BEZ235 (5–50 mg/kg/day) were tested and, finally, the best results were observed at a dose of 5 mg/kg/day.
Four experiments were performed with at least two mice per group. A control mouse receiving irradiation without stem cell support (Total Body Irradiation, TBI group) was also included in each experiment.
Balb/c mice were monitored daily for survival and for the following clinical signs of GvHD: weight loss, posture (hunching), activity, fur texture and skin integrity. Each parameter received a score of 0 (normal), 1 (mild to moderate), or 2 (severe) and a clinical GvHD index was generated subsequently by summation of the five criteria scores (maximum index = 10), as previously described [
15]. All moribund mice were humanely killed.
For histopathological analysis of GvHD target organs (large intestine, skin and liver), at least one animal of each group was killed in the third week post-transplantation and once treatment was completed. Tissues were fixed in 10 % neutral-buffered formalin (Sigma-Aldrich), embedded in paraffin, and sectioned and stained with hematoxylin and eosin (both from Merck KGaA, Darmstadt, Germany). Slides were examined under a BX41 light microscope and images were captured using a DP50 digital camera and the software Cell^A 2.6 (all from Olympus Optical Co. Ltd., Tokyo, Japan). Details of the scoring system are summarized in Table
1.
Table 1
Histologic criteria for GvHD score
0 | Normal | Normal | Normal |
0.5 | | Focal mild portal lymphoid infiltrate | Occasional or rare necrotic cells in glands or crypts |
1 | Basal vacuolar change | Widespread mild portal lymphoid infiltrate | Isolated apoptotic epithelial cells, without crypt loss |
2 | Dyskeratotic cells in the epidermis and/or follicle, dermal lymphocytic infiltrate | Focal bile duct invasion or cellular injury | Individual crypt loss. Regeneration changes |
3 | Fusion of basilar vacuoles to form clefts and microvesicles | Multiple foci of bile duct injury and regeneration | Contiguous area of multiple crypt loss |
4 | Separation of the epidermis from the dermis | Widespread injury and destruction of bile ducts | Extensive crypt dropout with denudation of epithelium |
Statistical analysis
Most statistical analyses were performed using IBM SPSS Statistics 20 (Chicago, IL, USA). Differences between the effects of different doses of a drug and between both drugs were analyzed by the Kruskal–Wallis multiple-comparison Z value test. Pairwise comparisons were performed using the Mann–Whitney test with Bonferroni correction. Survival curves were plotted using Kaplan–Meier estimates and a log-rank test was used to compare survival rates.
For statistical analysis of weight variation and clinical scores, curves of each mouse along time from transplantation were fitted by cubic splines using the program “Compare” in the SIMFIT statistical package (
http://simfit.org.uk), applying unweighted least square fitting. Areas under the curve (AUCs) from the replicate curves of mice in each group were compared by a one-way ANOVA followed by the Tukey’s post hoc test.
Statistical significance in all tests was concluded for values of p < 0.05.
Discussion
In the last decade, numerous class I PI3K inhibitors with various profiles, such as pan-Class I PI3K, isoform-specific PI3K or dual PI3K/mTOR inhibitors, have been developed for clinical applications, especially in the field of oncology. In the current study, we have evaluated the ability of the pan-Class I PI3K inhibitor BKM120 and the dual PI3K/mTOR inhibitor BEZ235 to block T cell activation and shown for the first time the potential utility of BEZ235 in the context of allo-HSCT.
Although largely demonstrated on tumor cells [
18,
19], the antiproliferative effect of these drugs on T cells had been scantily evaluated [
11,
20]. We have confirmed the ability of BKM120 and BEZ235 to inhibit activated T cell proliferation and, in the case of BEZ235, we have shown for the first time the induction of cell cycle arrest in G0/G1 phase.
Cell proliferation is strongly associated with PI3K/AKT/mTOR pathway, since components such as AKT, RPS6 and 4E-BP1 drive the synthesis and activity of cell cycle-related proteins [
21‐
26]. In this regard, we have shown that the degree of T cell proliferation correlated to phosphorylation levels of AKT, 4E-BP1 and RPS6, and that simultaneous inhibition of PI3K and mTOR was effective at lower concentrations than PI3K inhibition alone.
On the other hand, the inhibitors reduced not only RPS6 and 4E-BP1 phosphorylation, but also their expression. It has been reported that the expression of ribosomal protein genes, such as RPS6, is cell cycle-dependent and, therefore, levels of RPS6 remain low during the G0 phase [
27], as we observed in resting T cells. Thus, the decrease of RPS6 expression could be linked to the antiproliferative effect of the inhibitors. Regarding 4E-BP1, it has been shown that its expression is downregulated by the activity of MAPKs ERK and p38 [
16]. Interestingly, both drugs induced an increase in p38 phosphorylation, that could contribute to the 4E-BP1 expression decrease. However, as we had previously shown for BKM120, neither of the drugs enhanced ERK phosphorylation on stimulated T cells [
11].
On the other hand, BKM120 and BEZ235 induced a dose-dependent decrease in Th1/Th2 cytokine secretion, according to studies performed with PI3K [
10,
12] and mTOR inhibitors [
28,
29]. Once more, BEZ235 was more potent than BKM120 at intermediate doses. This could be due to the direct effect of BEZ235 on mTOR kinase, which regulates the activity of T-bet and GATA-3, key transcription factors in Th1/Th2 cytokine production [
5,
6,
30]. Nevertheless, despite an IL-2 decrease at low doses of BEZ235, concentrations ≥1 μM led to a tendency to recover IL-2 secretion. Probably, the potent inhibition of PI3K/mTOR signaling by BEZ235 leads to upregulation of other pathways that drive IL-2 synthesis, such as Ca
2+/calcineurin/NFAT, NF-κB or RAS pathways. In this sense, it is known that after T cell stimulation, initial high IL-2 production is followed by its decline, due to the repression of NF-κB and NFAT by T-bet activity [
31,
32]. Therefore, mTORC1 inhibition exerted by BEZ235 would decrease mTORC1-dependent expression of T-bet [
5], leading to IL-2 secretion maintenance. In addition, inhibition of mTOR and PI3K can increase RAS signaling as a compensatory mechanism, leading to an increase in ERK phosphorylation [
33,
34]. However, we have not observed a higher ERK phosphorylation in treated T cells. In any case, the increase in IL-2 levels does not induce an increase in T cell proliferation, probably due to the downregulation of IL-2 receptor alpha chain (CD25) observed in the presence of the drug.
Regarding IFN-γ and granzyme B, their expression is dependent on T-bet and EOMES [
35,
36], which are regulated by mTORC1 and mTORC2 activity [
37]. Accordingly, intracellular expression of these molecules decreased in the presence of BKM120 and, specially, of BEZ235.
With respect to apoptosis, we have observed that BEZ235 does not induce significant apoptosis, neither among resting nor among stimulated T lymphocytes, as we had previously shown for BKM120 [
11,
12]. Moreover, caspase 3 activation, generally considered to be an apoptosis indicator, decreased with the addition of BKM120 and BEZ235. This could indicate that the drugs reduce apoptosis in activated lymphocytes. However, it should be noted that the inhibitors prevent activation and, therefore, activation-induced cell death [
38]. In addition, it has been reported that T cell activation induces cleavage of caspase 3 in the absence of apoptosis [
39,
40], what could be reversed by activation inhibition achieved by the drugs. In any case, neither BKM120 nor BEZ235 seems to induce apoptosis in stimulated T cells. Other authors have also shown limited toxicity of BKM120 and BEZ235 toward normal PBMCs [
41‐
43].
On the other hand, standard GvHD prophylaxis is associated with high risk of life-threatening opportunistic infections [
44]. Thus, GvHD prophylactic strategies should induce tolerance of alloreactive T cells but maintain an adequate immune response against pathogens, such as cytomegalovirus (CMV). Previous studies have shown that mTORC1 inhibition with rapamycin can induce T cell anergy in vitro [
45,
46] and reduce GvHD incidence [
8] as well as CMV reactivation [
47] after allo-HSCT. In addition, we had proved that mTOR inhibition during allogeneic PBMC stimulation induced tolerance of alloreactive T cells while preserving immune response against CMV [
48]. In the present study, we have shown that not only mTOR inhibition but also PI3K inhibition provides these results.
In general, in vitro studies have shown that BEZ235 exerts a strong inhibitory effect at lower concentrations than BKM120, what is logical since BEZ235 inhibits more potently the different PI3K isoforms and simultaneously targets mTOR. However, it is worthy to note that the concentrations above which BKM120 achieves similar inhibition to BEZ235 (≥5 μM) are precisely those in which it drastically decreases phosphorylation of mTOR targets (4EBP1, RPS6, AKT S473), that is, between 1 and 10 μM, as shown by Western blot. Moreover, BKM120 non-specific activity against mTOR has been described at concentrations greater than 2 μM [
49]. Thus, it is possible that the potent effect observed at high concentrations of BKM120 is due to a direct effect on mTOR as well. This would indicate that simultaneous targeting of PI3K and mTOR achieve a better inhibitory capacity than PI3K inhibition alone. On the other hand, we had previously observed that dual mTORC1/mTORC2 targeting exerts a more potent T cell inhibition than mTORC1 blockade [
48], and similar to PI3K/mTOR targeting. Thus, we could conclude that to effectively block PI3K/AKT/mTOR pathway in T cells, we should block, at least, both mTORC1 and mTORC2 complexes, accompanied or not by PI3K inhibition.
Importantly, BEZ235 reduced more effectively than BKM120 the percentage of T
EE cells, which arise from naïve T cells after stimulation [
50]. This ability to prevent naïve T cell activation is important, given the key role played by this T cell population in GvHD induction [
51,
52].
Finally, we selected BEZ235 to evaluate its utility on GvHD prophylaxis. BEZ235 significantly improved mice survival and ameliorated GvHD-associated signs. On the other hand, it is probable that the damage observed in BEZ235-treated animals is not entirely caused by GvHD, but possibly to drug-induced toxicity as well. In this sense, it has been reported that the use of PI3K/AKT/mTOR pathway inhibitors is associated with metabolic disorders and damages in skin, liver or gastrointestinal mucosa [
53]. Thus, the tissue damage observed at third week post-transplantation could be due, at least in part, to a toxic effect of the drug difficult to discern from GVHD-induced damage in early post-transplant phases [
54,
55]. In addition, BEZ235 administration in murine tumor models induces a weight loss associated with a lower food intake [
56]. Thus, further studies are warranted to optimize BEZ235 dosing in order to reduce toxicity.
Our results show the ability of novel PI3K inhibitors to control T cell activation and confirm their potential utility as a therapeutic alternative in GvHD management. Nevertheless, two questions must be addressed. On the one hand, the concern arises about their potential negative effect on anti-leukemia T cells, which would have a negative impact on relapse incidence. Previous [
42,
43,
57‐
59] and future studies analyzing their antitumor activity on hematologic malignancies will help to elucidate if their administration could counterbalance this negative effect and reduce the incidence of relapse. On the other hand, it should be noted that the overall in vivo impact of PI3K inhibitors on T cells will also depend on their effect on other immune cells that modulate or contribute to T cell activation, such as antigen-presenting cells. In this sense, both pro- and anti-inflammatory effects of PI3K inhibitors on monocytes and DCs have been described [
60‐
62]. In our hands, the use of PI3K inhibitors in total PBMC cultures induced an immunosuppressive effect on T lymphocytes similar to that observed in isolated T cell cultures (present work and data not shown).