Chronic inflammation is a complex process that promotes carcinogenesis and tumor progression; however, the mechanisms by which specific inflammatory mediators contribute to tumor growth remain unclear. We and others recently demonstrated that the inflammatory mediators IL-1β, IL-6, and PGE2 induce accumulation of myeloid-derived suppressor cells (MDSC) in tumor-bearing individuals. MDSC impair tumor immunity and thereby facilitate carcinogenesis and tumor progression by inhibiting T and NK cell activation, and by polarizing immunity toward a tumor-promoting type 2 phenotype. We now show that this population of immature myeloid cells induced by a given tumor share a common phenotype regardless of their in vivo location (bone marrow, spleen, blood, or tumor site), and that Gr1highCD11bhighF4/80−CD80+IL4Rα+/−Arginase+ MDSC are induced by the proinflammatory proteins S100A8/A9. S100A8/A9 proteins bind to carboxylated N-glycans expressed on the receptor for advanced glycation end-products and other cell surface glycoprotein receptors on MDSC, signal through the NF-κB pathway, and promote MDSC migration. MDSC also synthesize and secrete S100A8/A9 proteins that accumulate in the serum of tumor-bearing mice, and in vivo blocking of S100A8/A9 binding to MDSC using an anti-carboxylated glycan Ab reduces MDSC levels in blood and secondary lymphoid organs in mice with metastatic disease. Therefore, the S100 family of inflammatory mediators serves as an autocrine feedback loop that sustains accumulation of MDSC. Since S100A8/A9 activation of MDSC is through the NF-κB signaling pathway, drugs that target this pathway may reduce MDSC levels and be useful therapeutic agents in conjunction with active immunotherapy in cancer patients.
Chronic inflammation increases the risk for the development of transformed cells and aggravates the development of established malignancies (1, 2). Some of the properties of inflammation that contribute to these processes are understood, such as the promotion of angiogenesis (3), the induction of tumor-promoting cytokines (4), the up-regulation of anti-apoptotic genes (5), and uncontrolled feed-forward signaling in tumor cells through cell surface receptors such as the receptor for advanced glycation end-products (RAGE)3 (6). Many of these mechanisms are due to perturbations in the tumor microenvironment that co-opt innate immunity to favor tumor initiation and progression (7). We (8, 9, 10), and others (11, 12), recently reported that inflammation also promotes tumor progression by blocking adaptive immunity through the induction of myeloid-derived suppressor cells (MDSC), which prevent the activation of CD4+ and CD8+ T cells. The inflammatory stimuli in these studies were either the proinflammatory cytokines IL-1β and IL-6, or PGE2. In these studies, mice with heightened levels of IL-1β or IL-6 in the tumor microenvironment accumulated MDSC with enhanced suppressive activity (8, 9, 11), and bone marrow stem cells cultured with PGE2 or other E-prostanoid receptor agonists differentiated into MDSC (10). However, MDSC also accumulated in the absence of overtly elevated levels of IL-1β, IL-6, or PGE2, suggesting that there may be additional inflammatory mediators that induce the accumulation and retention of MDSC.
Three members of the S100 family of calcium binding proteins, S100A12, S100A8, and S100A9, are inflammatory mediators released by cells of myeloid origin. These intracellular molecules are released to extracellular compartments in response to cell damage, infection, or inflammation, and function as proinflammatory danger signals (13, 14, 15). Elevated serum levels of S100A8 and S100A9 proteins are hallmarks of inflammatory disorders and recurrent infections (16), and increased S100A8 and S100A9 expression is seen in tumor-infiltrating cells in many epithelial tumors (reviewed in Refs. 6 ,17). The proteins function predominantly as S100A8/A9 heterodimers and are chemotactic for leukocytes, thereby amplifying the local proinflammatory microenvironment. Similar to IL-1β, IL-6, and PGE2, S100A8/A9 proteins mediate their effects by binding to plasma membrane receptors on their target cells. These receptors include heparan sulfate (18), TLR4 (19), and carboxylated N-glycans (20). Carboxylated N-glycans are constitutively expressed on endothelial cells, macrophages, and dendritic cells and are recognized by the mAbGB3.1 (21, 22). Carboxylated N-glycans on RAGE play an important role in HMGB1-RAGE-mediated signaling (23). Interaction of RAGE with S100A12 was the first described receptor-ligand model for an S100 protein (24). Although direct binding of S100A8/A9 to RAGE was not previously demonstrated, recent studies show that such interactions are likely (25, 26). In addition, we found that S100A8/A9 bind to a subpopulation of RAGE modified by carboxylated glycans (27). A glycan-specific Ab, mAbGB3.1, blocks the onset of inflammation and reverses its early stage progression in a T cell model of colitis (22), a model in which RAGE and S100A8/A9 are up-regulated in colon and secondary lymphoid organs. The Ab also reduces the incidence of colitis-associated colon cancer (CAC) (27).
Because S100A8/A9 proteins are elevated in inflammation and cancer and are chemotactic, we hypothesized that they may contribute to the recruitment and retention of MDSC. We report here that MDSC from tumor-bearing mice not only have receptors for S100A8/A9, but also synthesize and secrete these proteins, providing an autocrine pathway for MDSC accumulation. Treatment of tumor-bearing mice with the mAbGB3.1, which binds to carboxylated N-glycans on cell surface receptors, blocks S100A8/A9 binding and signaling, reduces serum levels of S100A8/A9, and reduces the accumulation of MDSC in the blood and secondary lymphoid organs. Therefore, S100A8/A9 proteins are another class of proinflammatory mediators that complicate cancer immunotherapy strategies by promoting the accumulation of MDSC that block tumor immunity.
Materials and Methods
BALB/c and transgenic DO11.10 (I-Ad-restricted, OVA peptide 323–339-specific) (28) and clone 4 (H-2Kd-restricted, hemagglutinin (HA) peptide 518–526-specific) (28) mice were bred in the University of Maryland Baltimore County animal facility. All animal procedures were approved by the University of Maryland Baltimore County Institutional Animal Care and Use Committee.
Abs and flow cytometry
Fluorescently coupled Gr1, CD11b, IL-4Rα, CD80, arginase, inducible NO synthase (iNOS), Ly-6G, Ly-6C, and isotype control Abs were purchased from BD Pharmingen. F4/80 and Fc block Ab were purchased from Caltag Laboratories. S100A8 and S100A9 Abs were from Santa Cruz Biotechnology. Commercial Abs were used at a concentration of 4–10 μg/ml. mAbGB3.1 and isotype control Ab (21) were used at 40 μg/ml. Intracellular and cell surface staining were performed as described (28). Stained samples were run on a Beckman Coulter XL flow cytometer and analyzed using FCS-Express analysis software.
Tumor cells, tumor cell inoculation, tumor growth, surgery, and Ab treatment
4T1 mouse mammary carcinoma cells were maintained as described (29). For tumor progression experiments, BALB/c mice were inoculated in the abdominal mammary gland with 7000 4T1 cells, and tumor progression, surgical removal of primary tumors, and quantification of metastatic disease were performed as described (29). mAbGB3.1 or isotype control Ab treatment (10 μg protein/gm body weight, i.v.) was started 3 days after removal of primary tumor and continued once weekly. Seventy-two h after each treatment, mice were tail bled into 500 μl of a 0.008% heparin solution, and RBCs were removed by lysis (30). Remaining white cells were identified by flow cytometry (28). Ab treatment was terminated when mice were moribund and spleens, lymph nodes, and lungs were cryopreserved for immunohistochemistry.
MDSC purification, phenotype, morphology, and T cell suppression assay
Spleens, lungs, and femurs were obtained from 4T1 tumor-bearing mice on day 33 after inoculation of 7000 4T1 tumor cells. Femurs were flushed with excess PBS using a syringe fitted with a 27-g needle. Spleens and lungs were dissociated to single-cell suspensions as described (29). Splenocytes, bone marrow, and lung cells were depleted of RBCs, and MDSC were isolated by magnetic bead sorting of Gr1+cells using Miltenyi Biotec magenetic beads, as described (28). For blood MDSC, tumor-bearing mice were bled into 500 μl of a 0.008% heparin solution, and RBC removed by lysis as described (28). Remaining white blood cells that were >90% Gr1+CD11b+ were used in experiments. MDSC were phenotyped using fluorescent-conjugated Abs and stained with Wright-Giemsa stain using Diff-Quik (Dade Behring) (28). T cell suppression was assessed by coculturing DO11.10 or clone 4 splenocytes with irradiated-blood MDSC or MACS-purified MDSC and specific peptide as described (28).
Real-time RT-PCR analysis
MDSC from tumor-bearing mice were isolated as described. To obtain sufficient Gr1+CD11b+ cells from tumor-free mice, mice were bled as described and Gr1+CD11b+ cells were purified using Gr1 Ab and Miltenyi Biotec magnetic beads (28). The resulting cells were washed once with PBS, and the pellets were frozen in dry ice and sent to SuperArray (http://www.superarray.com/) for RT-PCR analysis. Results are expressed as the number of threshold cycles (Ct) needed to detect product, or the fold change of tumor MDSC vs naive MDSC as calculated by the ΔΔCt method (31) using the following formulas:
ΔCt = average Ct (experimental) − average Ct (housekeeping genes).
Fold change = 2^ (tumor MDSC ΔCt − naive MDSC ΔCt).
The HG panel included glucuronidase β, Hprt1, Hsp90ab1, Gapdh, and actin β cytoplasmic.
Cryosections (6 μm) were air-dried, fixed in cold acetone for 2 min at room temperature, rehydrated in PBS, stained with anti-mouse Abs to CD11b and Gr-1 (BD Pharmingen), followed by Alexa 594- or Alexa 488-conjugated secondary Abs (Invitrogen), cover-slipped with VectaShield DAPI mounting medium (Vector Laboratories), and examined using an inverted TE300 Nikon wide field fluorescence microscope and photographed with a CCD SPOT RT Camera (Diagnostic Instruments). Cells in three high power fields were counted for quantitation.
22) and anti-HMGB-1 (Abcam), respectively, and bands were visualized using corresponding alkaline phosphatase-conjugated secondary Abs (Jackson ImmunoResearch Laboratories) followed by BCIP/NBT substrate (Sigma-Aldrich).
S100A8 and S100A9 quantification
Secreted S100A8 and S100A9 proteins were quantified by ELISA as described (3230) or 4T1 tumor or serum from tumor-bearing mice were diluted in HBSS containing 0.05% Tween 20. Polyclonal rabbit anti-mouse S100A8 Ab (33) was biotinylated using normal human serum-biotin as per the manufacturer’s protocol (Pierce) and used at a dilution of 1/1000. Incubation with biotinylated anti-S100A8 Ab was for 2 h at room temperature, followed by streptavidin alkaline phosphatase (Promega; 1/2000) for 1 h at room temperature. Wells were developed with p-nitrophenyl phosphate substrate and read at 405 nm. Purified S100A8/A9 (34) served as standard.
S100A8/A9 protein binding
Cell membranes were generated from 108 blood MDSC by homogenization in 10 mM Tris-HCl (pH 7.4), containing 200 mM sucrose and protease inhibitors (mixture of EDTA-free serine and cysteine protease inhibitors; Roche). Nuclei and cell debris were removed by centrifugation at 900 × g for 10 min at 4°C. Resulting supernatants were ultracentrifuged at 110,000 × g for 75 min at 4°C, and pellets resuspended in 200 μl of 10 mM Tris-HCl (pH 7.4) with 150 mM NaCl and protease inhibitors. Endogenous S100A8/A9 proteins were stripped by incubation in 50 mM glycine and 100 mM NaCl (pH 3.0) for 3 min at 4°C followed by neutralization with cold HBSS. Membranes were incubated with increasing concentrations of Na125I-labeled purified S100A8/A9 (labeled using Iodobeads (Pierce) as per the manufacturer’s protocol to a specific activity of 2 × 105 cpm/pmol) for 1 h at 4°C in HBSS, washed twice with 1 ml of HBSS, recovered by ultracentrifugation, solubilized in 0.2 ml of 0.5 M NaOH, and cell-bound radioactivity was counted. Nonspecific binding was determined by binding in the presence of 100-fold molar excess of cold ligand. Where required, binding was conducted in the presence of 10-fold molar excess of mAbGB3.1, anti-RAGE, anti-S100A8, or isotype-matched irrelevant mAb. Saturation binding kinetic analyses were performed using GraphPad Prism. Values were normalized for number of cells.
Blood MDSC (108/ml) were cultured with S100A8/A9 (5 μg/ml) or TNF-α (20 ng/ml), with or without mAb GB3.1 or control irrelevant mAb (10 μg/ml) in 250 μl of serum-free DMEM in 24-well plates. At the indicated times, MDSC were washed with cold PBS and lysed in 200 μl lysis buffer (Cell Signaling Technology) containing PMSF (1 mM) and protease inhibitors (1 tab/10 ml lysis buffer). Cell lysates were centrifuged at 4°C and supernatants stored at −80°C until analyzed by PathScan Inflammation MultiTarget Sandwich ELISA Kit or PathScan phospho-NF-κB p65 (Ser536) Sandwich ELISA Kit according to the manufacturer’s protocol (Cell Signaling Technology). Percentage increase in pNF-κB = (100%) × [(MDSC with inducer) − (MDSC without inducer)/(MDSC without inducer)].
In vitro migration of MDSC was evaluated in 24-well plates with transwell polycarbonate permeable supports (8.0 μm) (Costar Corning). One million MDSC (>90% Gr1+CD11b+ cells) were plated in 100 μl of serum-free IMDM in the upper compartment and 500 μl of chemoattractant (tumor-conditioned media (CM) ± 10 μg of Abs to S100A8 or S100A9, or IgG control Ab) were added to the lower compartment. Plates were incubated at 37°C with 5% CO2 for 3 h, and the number of MDSC in the bottom compartment counted. For CM, supernatants were harvested from confluent cultures of 4T1 tumor cells cultured in medium IMDM containing 3% serum and 1% antibiotics. CM was filter sterilized and stored at −80°C as single-use aliquots. Percentage increase in migration of Gr1+CD11b+ cells = (100%) × [(MDSC migration with inducer ± Ab) − (MDSC migration in media control)/(MDSC migration in media control)].
Student’s two-tailed t test was performed using Microsoft Excel 2000.
MDSC in the blood, spleen, and bone marrow of 4T1 tumor-bearing mice, and metastatic 4T1 tumors, have a similar phenotype and suppressive activity
MDSC accumulate at the site of tumor and are elevated in the blood, bone marrow, and spleens of tumor-bearing mice. To confirm that MDSC within a given individual are homogeneous regardless of location, splenocytes, circulating leukocytes (blood), bone marrow cells, and lungs containing metastases were isolated from BALB/c mice that had been inoculated in the mammary fat pad 33 days earlier with 7000 4T1 tumor cells. The resulting cells were analyzed by immunofluorescence and flow cytometry for the canonical MDSC markers Gr1 and CD11b, and gated Gr1+CD11b+ cells were further analyzed for F4/80, IL-4Rα, and CD80, markers that are differentially expressed on MDSC isolated from mice with histologically distinct tumors (35, 36). The percentage of Gr1+CD11b+ cells differed in each tissue; however, Gr1+CD11b+ cells from all locations shared a similar phenotype (Gr1highCD11bhighF4/80−CD80+IL-4Ra+/−Arginase+) (Fig. 1⇓A). Previous studies have classified Gr1+CD11b+ cells as either “neutrophil-like” or “monocyte-like” based on the expression of Ly6G (immature neutrophil marker) or Ly6C (monocyte/macrophage marker), respectively, and nuclear morphology (35, 37, 38, 39). To determine whether differentially localized Gr1+CD11b+ cells are distinguished by either of these categories, CD11b+ cells were gated and analyzed for Ly6G and Ly6C (Fig. 1⇓), and Gr1+CD11b+ cells were Wright-Giemsa stained and examined histologically (Fig. 1⇓C). All MDSC express Ly6C and Ly6G, although MDSC from bone marrow and spleen of 4T1 tumor-bearing mice have small subpopulations (9 and 7%, respectively) of Ly6Chigh cells. As previously reported for blood MDSC (30), 4T1-induced Gr1+CD11b+ cells from all locations are a mixture of cells with single- and multilobed nuclei (Fig. 1⇓C). To confirm that MDSC are consistently suppressive regardless of their location, MDSC from blood, spleen, bone marrow, and lung (all ≥ 85% Gr1+CD11b+) were cocultured at varying ratios with splenocytes from transgenic D011.10 (CD4+) or Clone 4 (CD8+) mice and their respective peptides, and T cell proliferation was measured by uptake of [3H]thymidine (Fig. 1⇓D). These results combined with previous studies demonstrating that splenic MDSC from tumor-free mice are equally suppressive on a per cell basis as splenic MDSC from tumor-bearing mice (28), demonstrate that MDSC from different anatomical locations have approximately equivalent suppressive activity. Therefore, anatomical location does not affect the phenotype or function of MDSC, and subsequent experiments performed with blood MDSC are representative of MDSC from all locations.
MDSC have receptors for the S100A8/A9 proinflammatory proteins
Several observations circumstantially link S100 proinflammatory proteins with MDSC. Inflammation is an inducer of MDSC (8, 10, 11). Proinflammatory S100 proteins are present in the tumor environment of mammary carcinomas (40, 41), and over-expression of S100A8/A9 heteromeric complexes is associated with poor prognosis in invasive ductal carcinoma of the breast (42). We therefore examined whether MDSC induced by the 4T1 mammary carcinoma express receptors for S100 proteins. Blood was collected from tumor-free mice and from BALB/c mice 31 days after 4T1 inoculation, when metastatic disease was established and primary tumors were 9.41 ± 0.3 mm in diameter. We found that Gr1+CD11b+ leukocytes from both tumor-free and tumor-bearing mice stained with mAbGB3.1, which detects carboxylated N-glycans expressed on cellular receptor(s) for S100A8/A9 proteins (20, 21) (Fig. 2⇓A). In addition, cell membranes prepared from blood MDSC (>90% Gr1+CD11b+) had specific saturable binding sites for 125I-S100A8/A9 with a Kd of 37.43 ± 6.99 nM and a Bmax of 1.882 ± 0.142 pmols/million cells (Fig. 2⇓B). 125I-S100A8/A9 binding was displaced by molar excess of cold ligand or by anti-S100A8 Abs (Fig. 2⇓C). To ascertain that the S100A8/A9 heterodimers were binding to carboxylated N-glycans on cell surface receptors, MDSC membranes were incubated with 125I-S100A8/A9 proteins in the presence of mAbGB3.1. Binding was significantly reduced in the presence of mAbGB3.1 (Fig. 2⇓C), while an isotype control Ab had no effect on binding. Interestingly, anti-RAGE also partially blocked binding, consistent with our earlier reports that RAGE is modified by carboxylated N-glycans (23) and that S100A8/A9 proteins bind to RAGE (27). Therefore, MDSC from tumor-free mice and from mice with primary and metastatic mammary carcinoma contain carboxylated N-glycan receptors that bind S100A8/A9, consistent with the concept that proinflammatory S100 proteins are part of the inflammatory milieu that induces the accumulation of MDSC.
MDSC synthesize and secrete S100A8/A9 heterodimers
Since S100A8/A9 proteins are synthesized by cells of the myeloid lineage, we reasoned that MDSC may also contribute to the inflammatory milieu by producing these proinflammatory mediators. To test this hypothesis, we bled mice on day 36 after 4T1 inoculation when Gr1+CD11b+ cells were >90% of the circulating white cells (Fig. 3⇓A, left panel), primary tumors were 9.70 ± 0.21 mm in diameter, and metastatic disease was established. Tumor-free mice were also bled and Gr1+CD11b+ cells, comprising <10% of the circulating white cells, were purified to >90% purity (Fig. 3⇓A, right panel). Real-time RT-PCR was performed and the number of cycles required to amplify these messages was compared with that required for a panel of five HG and the poorly expressed CXCL1 gene (Fig. 3⇓B, left panel). Gr1+CD11b+ cells from both tumor-free and tumor-bearing mice expressed elevated levels of S100A8/A9 relative to the HG (Fig. 3⇓B). RAGE and HMGB1 transcripts were also expressed; however, at somewhat lower levels than the HG. S100A8 and RAGE were increased 2- to 3-fold in Gr1+CD11b+ cells from tumor-bearing mice vs tumor-free mice (Fig. 3⇓B, right panel).
To confirm the PCR results, lysates of the purified MDSC were analyzed by Western blotting for S100A8/A9, HMGB1, and RAGE (Fig. 3⇑C). S100A8 and S100A9 monomers and low levels of HMGB1 were present in Gr1+CD11b+ cells from both tumor-bearing and tumor-free mice. HMGB1 levels in MDSC increase in the presence of tumor, and multimers of S100A8/A9, which are the active forms, were only present in MDSC from tumor-bearing mice. In contrast to mRNA levels, S100A9 protein level is greatly increased in tumor MDSC in relation to S100A8. This could be related to inefficient translation of S100A8 mRNA and/or stability of S100A8 protein (43, 44). Collectively, the PCR and protein data suggest that expression of S100A8 is S100A9-dependent and that S100A8 acquires stability by S100A8/A9 heterocomplex formation (42). In fact, S100A8/A9 heterodimer is extremely protease resistant relative to the homodimers (45). Therefore, MDSC from tumor-bearing mice, but not from tumor-free mice, contain functionally active S100A8/A9 proteins, consistent with the concept that these proinflammatory mediators and receptors of MDSC are regulated by tumor.
Upon cellular activation, S100A8/A9 are secreted into the extracellular milieu where they mediate leukocyte recruitment and other functions that promote inflammation (15). If MDSC contribute to the inflammatory milieu, then they may secrete S100A8/A9 proteins. To test this possibility, equal numbers of circulating white blood cells from BALB/c mice with advanced 4T1 tumors (>95% Gr1+CD11b+ cells) and purified MDSC from tumor-free mice (>95% Gr1+CD11b+) were cultured for 24 h and the supernatants assayed by ELISA for S100A8/A9 proteins. MDSC from both tumor-bearing and tumor-free mice released significant amounts of S100A8/A9 proteins on a per cell basis (Fig. 3⇑D). Therefore, MDSC not only have the capacity to respond to S100A8/A9 proteins, but they may also sustain an autocrine stimulatory pathway by secreting active S100A8/A9 proteins.
S100A8/A9 signal through the NF-κB pathway in MDSC
To determine whether S100A8/A9 proteins activate MDSC after binding to cell surface receptors, we examined potential signaling pathways in the Gr1+CD11b+ cells. Circulating white blood cells were obtained from BALB/c mice on day 31 after 4T1 inoculation (>95% Gr1+CD11b+ cells) and were purified from tumor-free mice (>95% Gr1+CD11b+), cocultured with endotoxin-free S100A8/A9 proteins, and cell lysates assayed by ELISA for phosphorylated NF-κB and MAPK pathway signaling molecules, two pathways activated by inflammation. None of the molecules in the MAPK pathway were affected (data not shown). However, NF-κB was phosphorylated in MDSC from both tumor-bearing and tumor-free mice within the first 10 min of incubation at a level comparable to activation by TNF-α, a NF-κB-dependent gene that is known to be activated by S100A8/A9 (22) (Fig. 3⇑E). S100A8/A9-induced activation was reduced in the presence of mAbGB3.1. Therefore, S100A8/A9 proteins activate the NF-κB pathway in MDSC, and this activation is mediated in part by binding to cell surface receptors expressing carboxylated glycans.
S100A8/A9 proteins are chemotactic for MDSC
In addition to myeloid cells and MDSC, S100A8/A9 proteins are produced by many tumor cells (40, 41, 46, 47, 48, 49) and are chemotactic for target cells expressing their receptor (20, 50), raising the possibility that tumor cell and/or MDSC-secreted S100A8/A9 proteins attract MDSC to tumor sites. To test this concept, supernatants from 4T1 cultures were assayed for S100A8/A9 and MDSC were tested for migration in response to 4T1 supernatants, using transwell chambers. We found that 4T1 cells secrete S100A8/A9 proteins (Fig. 3⇑F) and 4T1 supernatants are chemoattractants for MDSC (Fig. 3⇑G). Chemotaxis was mediated by S100A8/A9 in the culture supernatants, since migration was reduced in the presence of Abs to S100A8 or S100A9.
Blocking of S100A8/A9 binding reduces the levels of MDSC and S100A8/A9 proteins in the blood of tumor-bearing mice
If S100A8/A9-mediated signaling promotes recruitment of MDSC, then inhibition of S100A8/A9 binding in vivo may reduce MDSC levels. To test this possibility, mAbGB3.1 or irrelevant control mAb was administered to BALB/c mice with established metastatic disease whose primary 4T1 tumors were surgically removed. This experimental design was used for two reasons: (i) we previously demonstrated that MDSC levels decrease with removal of primary tumor, and rapidly increase thereafter unless there is therapeutic intervention (30, 51). (ii) This setting closely models the conditions under which immunotherapy would be administered clinically and we wanted to see whether mAbGB3.1 could facilitate a reduction in MDSC in a clinically relevant situation. Mice were inoculated on day 0 with 4T1 tumor cells, primary tumors were surgically resected on day 20, and mAbGB3.1 or irrelevant isotype control Ab treatment was started on day 24. Primary tumor diameters (5.09 ± 0.76 and 5.36 ± 0.68 mm) and percent MDSC in blood (41.25% ± 3.98 and 44.65% ± 6.60) were matched at the time of surgery for mAbGB3.1 and control Ab treated groups, respectively. Mice were bled 3 days after each Ab treatment, and their circulating white blood cells were stained for Gr1 and CD11b. Consistent with previous observations, removal of primary tumor temporarily reduced MDSC levels in the blood (28). Treatment with mAbGB3.1 significantly decreased the accumulation of MDSC relative to treatment with control mAb (Fig. 4⇓A), and did not affect the levels of other peripheral blood monocytes, dendritic cells, T cells, or B cells (data not shown).
If MDSC production of S100A8/A9 proteins contributes to the overall inflammatory milieu in tumor-bearing individuals, then these proteins should be elevated in tumor-bearing mice and reduction of MDSC should result in a concomitant decrease in serum S100A8/A9. To test this hypothesis, we measured the levels of S100A8/A9 proteins in the serum of tumor-free and tumor-bearing mice treated with mAbGB3.1 or control mAb. Treatment with mAbGB3.1 significantly reduced serum levels of S100A8/A9 in tumor-bearing mice (Fig. 4⇑B), and the level of serum S100A8/A9 in tumor-bearing mice was roughly proportional to the quantity of MDSC in the blood (Fig. 4⇑C). mAbGB3.1 treatment did not affect the amount of S100A8/A9 released per cell in culture (not shown). Therefore, the accumulation of S100A8/A9 in the serum of tumor-bearing mice may be at least partially due to the production of these molecules by MDSC.
In vivo treatment with mAbGB3.1 reduces the accumulation of MDSC
In addition to accumulating in the blood, spleen, bone marrow, and tumor sites, MDSC are also found in the lymph nodes of tumor-bearing mice (52). To determine whether blockade of S100A8/A9 receptors reduces MDSC levels in sites other than the blood, BALB/c mice were inoculated with 4T1, primary tumor was surgically resected on day 20, and mAbGB3.1 or control Ab treatment was started on day 24. Secondary lymphoid organs and metastatic lungs were cryo-preserved on day 41, when mice had established primary tumors and metastatic disease, and were stained for Gr1+CD11b+ cells. Gr1+CD11b+ cells were present in high numbers in the lymph nodes and spleens of untreated mice, and mAbGB3.1 treatment reduced accumulation of these cells at these sites (Fig. 5⇓, A and B) but not in the lungs (data not shown).
In addition to increasing the numbers of MDSC, S100A8/A9 proteins may increase MDSC suppressive activity. In this case, MDSC of tumor-bearing mice treated with mAbGB3.1 might be less suppressive on a per cell basis than MDSC of control Ab-treated mice. To test this hypothesis, mice were inoculated on day 0 with 4T1 cells, primary tumors were removed on day 26, mAbGB3.1 or control Ab treatment was started on day 29, and splenic MDSC were harvested, purified (>90% Gr1+CD11b+), and tested for their ability to suppress peptide-activation of CD4+ DO11.10 or CD8+ Clone 4 transgenic T cells (Fig. 5⇑C). Gr1+CD11b+ MDSC from mAbGB3.1-treated and from control-treated mice were equally suppressive on a per cell basis, and both MDSC cell populations used arginase to mediate their suppressive effects, as shown by restoration of T cell proliferation in the presence of the arginase inhibitor, Nw-hydroxy-nor-L-arginine diacetate salt. Therefore, S100A8/A9 proteins promote immune suppression by enhancing the recruitment and accumulation of Gr1+CD11b+ cells, but do not alter the suppressive activity of individual MDSC.
Myeloid cells with potent immune suppressive activity are present in most patients and mice with malignant tumors and have stimulated considerable interest as potential targets for therapy. In mice they are commonly characterized by expression of the cell surface markers CD11b and Gr1, which are characteristic of monocytes/macrophages and granulocytes, respectively. These so-called “MDSCs” (53) have also been associated with other cell surface markers such as IL-4Rα (35, 54), F4/80 (35, 37, 55), CD80 (56), Ly6C, and Ly6G (37). However, none of these markers is definitive since their expression varies based on the inducing tumor. In addition to cell surface markers, MDSC have been characterized by their content of suppressive molecules including arginase (10, 57, 58), iNOS (59), and other reactive oxygen species (58, 60), and have been classified as “neutrophil-like” or “monocyte-like” based on their nuclear morphology (38). Since MDSC are induced by multiple tumor and/or host cell-secreted factors (61, 62), it is likely that the MDSC phenotypes reported in different tumor systems are due to different combinations of factors produced by different tumors. Therefore, aside from the markers Gr1 and CD11b and the ability to suppress T cell activation, there is no unique or combination of phenotypic markers that unambiguously identifies mouse MDSC. In contrast to MDSC induced by different tumors, MDSC at different sites within an individual are homogeneous in their expression of phenotypic markers and they have the same suppressive activity, indicating that tissue localization does not alter MDSC phenotype or function. MDSC from 4T1 tumor-bearing mice have a consistent phenotype of Gr1+CD11b+F4/80−IL-4Rα+/−Arginase+iNOS−CD80+, contradicting some studies suggesting that IL-4Rα is a definitive marker for mouse MDSC (35, 54). Because blood MDSC are easily obtainable in high purity and MDSC localized to different sites do not differ, in our studies, we have used blood MDSC as a prototype and demonstrate here that MDSC from naive and tumor-bearing mice also express carboxylated glycans, RAGE, S100A8/A9, and HMGB1, and respond to S100A8/A9.
Although the proinflammatory S100A8/A9 proteins are up-regulated in many cancer patients and they have been proposed as prognostic markers (42, 63), a role for these molecules in tumor promotion and progression has not previously been demonstrated. The present study was based on the hypothesis that S100A8/A9 proteins contribute to tumor growth by inducing MDSC, which block tumor immunity and thereby facilitate tumor progression. We now report that S100A8/A9 not only induce the accumulation of MDSC, but they are also secreted by MDSC and by tumor cells, and bind to cell surface receptors leading to signaling within MDSC and MDSC migration. Thus, the S100A8/A9 proteins provide for a positive autocrine feedback loop that ensures the maintenance of functionally suppressive MDSC within an inflammatory tumor environment. We recently showed that MDSC expressing S100A8/A9 accumulate in all regions of dysplasia and adenoma in a CAC model (27), and that RAGE−/− mice are resistant to the onset of CAC. Up-regulation of S100A8/A9 in various tumors (17), their positive autocrine secretion, and promotion of a feed forward loop involving receptors such as RAGE suggest that these proteins play an important role in inflammation mediated cancer progression.
As reported earlier, Gr1+CD11b+ MDSC from tumor-free mice and from mice with 4T1 tumors are equally suppressive on a per cell basis (28). This observation combined with the current findings that MDSC from both sources share a common phenotype and are both activated by S100A8/A9 through NF-κB supports the concept that tumors regulate the expansion of a normal myeloid cell population rather than induce a novel myeloid population. Indeed, multiple proinflammatory mediators including S100A8/A9 (this report), IL-1β (8, 11), IL-6 (9), and PGE2 (10, 12) up-regulate MDSC, indicating that inflammation is an important contributing factor to the accumulation of MDSC in tumor-bearing individuals.
Our in vitro studies show that S100A8/9 binding to MDSC is dependent on carboxylated N-glycans and this binding is inhibited by mAbGB3.1, an Ab that recognizes carboxylated N-glycans. Carboxylated glycans are expressed on RAGE (23) and S100A8/A9 binds to a subpopulation of RAGE enriched for carboxylated glycans (27). The observation that inflammation-induced skin tumors in RAGE knockout mice have reduced levels of infiltrating MDSC also implicates RAGE in MDSC recruitment (6). Carboxylated glycans also bind Annexin I, S100A12, and HMGB1 (20, 23). Annexin I is anti-inflammatory. S100A12 and HMGB1 are ligands for RAGE, and our studies show that the binding of both ligands to RAGE is mediated by carboxylated glycans (20) (G. Srikrishna and H. Freeze, unpublished data). The role of S100A12 in our model is irrelevant since mice do not express S100A12 (64). However, the role of HMGB1 in mAbGB3.1-mediated effects on MDSC accumulation cannot be ruled out. Regardless of the nature and multiplicity of receptors and ligands, carboxylated glycan-mediated signaling in MDSC appears to converge with the activation of NF-κB.
In addition to S100A8/A9 proteins, MDSC are induced by other proinflammatory factors. Therefore, it is not surprising that in vivo blocking of S100A8/A9 binding reduces, but does not eliminate, MDSC accumulation in tumor-bearing mice. Since MDSC are a significant impediment to active T and NK cell immunotherapies (65), targeting of S100A8/A9 binding may improve immunotherapy with cancer vaccines and other immune strategies that require an immune-competent host. However, it is not clear what level of MDSC can be tolerated and still achieve active immunity, so optimal immunotherapy may require blocking or neutralizing all MDSC inducers. Interestingly, other proinflammatory mediators that activate MDSC also signal through the NF-κB pathway (S. Bunt, P. Sinha, V. Clements, and S. Ostrand-Rosenberg, unpublished observations), so drugs that target the NF-κB pathway may be particularly effective in reducing this tumor-promoting cell population.
We appreciate the technical support by Virginia K. Clements, the animal care by Terry King, the histology assistance of Robbin Newlin, and the illustrative contributions of Tim Ford. We thank Dr. Thomas Vogl, University of Münster, for the gift of S100A8/A9.
The authors have no financial conflict of interest.
The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.
↵1 These studies were supported by National Institutes of Health Grants NIH R01CA84232 and NIH R01CA115880, Susan G. Komen Foundation BCTR0503885 (to S.O.R.), and NIH R01CA92608 (to H.F. and G.S.).
↵2 Address correspondence and reprint requests to Dr. S. Ostrand-Rosenberg, Department of Biological Sciences, University of Maryland Baltimore County, 1000 Hilltop Circle, Baltimore, MD 21250. E-mail address:
↵3 Abbreviations used in this paper: RAGE, receptor for advanced glycation end-product; MDSC, myeloid-derived suppressor cell; HA hemagglutinin; HG, housekeeping gene; CM, conditioned media; CAC, colitis-associated cancer; iNOS, inducible NO synthase.
- Received May 7, 2008.
- Accepted August 5, 2008.
- Copyright © 2008 by The American Association of Immunologists