Effective activation of dendritic cells (DCs) toward T helper (Th)-1 cell polarization would improve DC-based antitumor immunotherapy, helping promote the development of immunotherapeutic vaccines based on T-cell immunity. To achieve this goal, it is essential to develop effective immune adjuvants that can induce powerful Th1 cell immune responses. The pathogenic organism Mycobacterium tuberculosis includes certain constitutes, such as heparin-binding hemagglutinin (HBHA), that possess a strong immunostimulatory potential. In this study, we report the first clarification of the functions and precise mechanism of HBHA in immune stimulation settings relevant to cancer. HBHA induced DC maturation in a TLR4-dependent manner, elevating expression of the surface molecules CD40, CD80, and CD86, MHC classes I and II and the proinflammatory cytokines IL-6, IL-12, IL-1β, TNF-α, and CCR7, as well as stimulating the migratory capacity of DCs in vitro and in vivo. Mechanistic investigations established that MyD88 and TRIF signaling pathways downstream of TLR4 mediated secretion of HBHA-induced proinflammatory cytokines. HBHA-treated DCs activated naïve T cells, polarized CD4+ and CD8+ T cells to secrete IFN-γ, and induced T-cell–mediated cytotoxicity. Notably, systemic administration of DCs that were HBHA-treated and OVA251–264-pulsed ex vivo greatly strengthened immune priming in vivo, inducing a dramatic regression of tumor growth associated with long-term survival in a murine E.G7 thymoma model. Together, our findings highlight HBHA as an immune adjuvant that favors Th1 polarization and DC function for potential applications in DC-based antitumor immunotherapy. Cancer Res; 71(8); 2858–70. ©2011 AACR.
Owing to the immunosuppressive environment within a tumor, effective antitumor therapy requires the powerful induction of appropriate immune responses. Dendritic cell (DC)-based antitumor immunotherapy is mediated by specialized interactions between DCs and T lymphocytes (1).
For all DC-based antitumor immunotherapeutic strategies, several factors that relate to the in vitro manipulation of DCs are important for the induction of a powerful immune response in patients. These factors include DC lineage, amount and type of antigen (Ag) loading on DCs, maturation stage of DCs, and route of injection (2). Evidence has suggested that immunostimulatory adjuvants are critical for the maturation of immature DCs, which boosts the activity of DCs as well as enhances T-cell–mediated immune responses. Therefore, the use of poorly immunogenic Ags combined with effective adjuvants can enhance specific T helper (Th)-1 cell responses. Although many adjuvants have been discovered, the use of adjuvant(s) for DC-based antitumor immunotherapy is limited due to safety concerns and unforeseen inappropriate immune responses (3).
Because Toll-like receptor (TLR) activation usually induces Th1 responses, TLR ligands are potential candidates for immunostimulatory adjuvants in anticancer therapy (4). On recognition of their ligands, TLRs mediate signals via 2 intracytoplasmic adaptor molecules, myeloid differentiation primary response protein (MyD88) and Toll/IL-1R domain-containing adaptor inducing IFNβ (TRIF), which are used by all TLRs except TLR3 (5). In the recent years, synthetic agonists of TLR3, TLR4, TLR5, TLR7, TLR8, and TLR9 have been identified as suitable immunostimulants (6–11). In fact, based on the efficacy of TLR agonists, the use of TLR ligands as adjuvants in humans is likely to increase in the near future. Furthermore, DC activation by various microbial components through TLRs' signaling is a critical link between innate and adaptive immunity and is crucial for the generation of protective immune responses.
Adjuvants inducing Th1-type responses are essential for effective immunotherapeutic strategies. Because some components expressed by organism of the genus Mycobacterium and related genera, showed strong Th1-type adjuvancity, a significant effort has been focused on identifying and characterizing these mycobacterial proteins (12). Although an immunotherapeutic approach using mycobacterial Ags appears to be clinically effective, the precise mechanism by which these Ags mediate immune stimulation has not been adequately clarified (12).
To date, it is known that M. tuberculosis interacts with Ag-presenting cells, specifically DCs (13). In addition, we recently showed that the Mycobacterium avium protein fibronectin attachment protein induces DC maturation and Th1 polarization (14). These reports provide direct evidences for the potential use of mycobacterial proteins in DC-based antitumor immunotherapies to induce the activation of T-cell–mediated cytotoxicity.
The M. tuberculosis protein, heparin-binding hemagglutinin (HBHA) was recently identified as surface-exposed and secreted Ag. This protein is a virulence factor that promotes bacterial aggregation, adhesion to heparin sulfate proteoglycans of nonphagocytic cells, and dissemination of tubercle bacilli from the lungs to other tissues in patients with tuberculosis (15, 16). HBHA induces protective immunity against M. tuberculosis by triggering the interferon (IFN)-γ production in CD4+ and CD8+ T lymphocytes (17). Thus, it could serve as an immnoadjuvants to design and develop immunotherapies against various diseases including if the detailed elucidation of the cellular immune responses to HBHA. However, very little is known about the antitumor activity of HBHA mediated by inducing DC maturation and, hence, promoting T-cell immunity.
To clarify the action mechanism of HBHA and its potential use as an adjuvant in DC-based antitumor immunotherapies, we investigated whether HBHA exhibits an antitumor effect in DC-based vaccination in a mouse model.
Materials and Methods
Male 6–8-week old C57BL/6 (H-2Kb and I-Ab) mice were purchased from the Korean Institute of Chemistry Technology (Daejeon, Korea). C57BL/6 OT-1 T-cell receptor (TCR) transgenic mice, C57BL/6J TLR2 knockout mice (TLR2−/−; B6.129-Tlr2tm1Kir/J), and C57BL/10 TLR4 knockout mice (TLR4−/−; C57BL/10ScNJ) were purchased at 6–8 weeks of age from the Jackson Laboratory (Bar Harbor, ME). The TLR9-knockout mice, originally from Dr. Shizuo Akira (Osaka, Japan), were obtained from Dr. Seong-Kug Eo (Chonbuk National University, Korea). All mice were housed in a specific pathogen-free environment and used in accordance with the institutional guidelines for animal care.
The cell lines EL4, a thymoma-derived cell line from the C57BL/6 (H-2Kb and I-Ab) mouse, and E.G7, an ovalbumin (OVA)-expressing EL4 variant, were purchased from ATCC and cultured in RPMI 1640 supplemented with 10% heat-inactivated FBS, 100 U/mL penicillin, 100 μg/mL streptomycin, and 10 mmol/L l-glutamine (all purchased from Invitrogen) at 37°C with 5% CO2.
Reagents and antibodies
Recombinant mouse granulocyte-macrophage colony-stimulating factor (GM-CSF), interleukin (rmIL)-4, chemokine ligand (CCL) 19, and the fluorescein isothiocyanate (FITC)-annexin V/propidium iodine kit were purchased from R&D Systems. Dextran-FITC (40,000 Da) was purchased from Sigma-Aldrich. Lipopolysaccharide (LPS, from Escherichia coli O111:B4) was purchased from Invivogen. Peptron synthesized the OT-I peptide (OVA257–264) and OT-II peptide (OVA323–339). The following FITC- or phycoerythrin (PE)-conjugated monoclonal antibodies (Abs) were purchased from BD Biosciences: CD11c (HL3), CD40 (HM40–3), CD80 (16–10A1), CD86 (GL1), Iab β-chain (AF-120.1), H-2Kb (AF6–88.5), CCR7 (CD197), IL-10 (JESS-16E3), and IL-12p40/p70 (C15.6). Alexa568 and Alexa488 conjugated anti-mouse IgG Abs as secondary Abs were purchased from Invitrogen. FITC-conjugated mouse IgG Abs and cytokine ELISA kits for murine IL-1β, IL-2, IL-6, IL-10, IL-12p70, tumor necrosis factor (TNF)-α, and IFN-γ were purchased from eBiosciences.
Expression and purification of recombinant HBHA
Dr. G. Delogu (University of Sassari, Sassari, Italy) kindly provided the pMV3–38 plasmid (pMV206-based construct) containing the full-length HBHA open reading frame. Methylated-recombinant HBHA expressed in Mycobacterium smegmatis was purified as previously described (18). Preparation of M. smegmatis competent cells and electroporation procedures were performed as previously described (19). A Detoxi-Gel™ Endotoxin Removing Gel (Pierce) was used to remove endotoxin. Finally, the protein concentration was determined using a BCA Protein Assay Kit (Pierce) and the purified protein was stored at −80°C in aliquots until use in the subsequent experiments. To evaluate the purity of rHBHA, SDS-PAGE followed by Coomassie blue (CB) staining, immunoblot assay using antihistidine antibody and silver nitrate staining as previously described (PMID: 17487168).
Generation and culture of DCs
Bone marrow-derived DCs were isolated and cultured as recently described (20). In certain experiments, DCs were labeled with bead-conjugated anti-CD11c mAb and positively selected (>90%) according to the manufacturer's instructions (LS columns; Miltenyi Biotec).
Therapeutic implanted tumor experiments
Mice were injected subcutaneously (s.c.) into the right lower back with EL4 or E.G7 thymoma cells (2 × 106), followed by intravenous injection of immature DCs and HBHA-treated DCs (1 × 106) pulsed with or without OVA (1 μg/mL) via the tail vein on days 1, 3, and 5 after tumor inoculation. Groups of tumor-bearing mice were treated with PBS, iDCs (untreated immature DCs), DCs-OVA (DCs pulsed with OVA peptide), or HBHA-DCs-OVA (HBHA-treated DCs pulsed with OVA peptide). Tumor size was measured every 2 days, and tumor mass was calculated as: V = (2A × B)/2, where A is the length of the short axis and B is the length of the long axis.
Confocal laser scanning microscopy
Cells were permeabilized with 1% saponin for 3 minutes, stained with anti-mouse HBHA followed by Alexa568-conjugated anti-mouse IgG antibody overnight at 4°C, and then stained with Alexa488-conjugated anti-mouse TLR2 or TLR4/MD2 for 3 hours at room temperature. Cell morphology and fluorescence intensity were analyzed using a confocal laser scanning microscope (Zeiss LSM510 Meta). Images were acquired using the LSM510 Meta software and processed using the LSM image examiner.
Immunoprecipitation and immunoblotting
DCs (5 × 106) were incubated with 1 μg/mL HBHA for 24 hours, and cell pellets were lysed with lysis buffer (10 mmol/L Tris-HCl, 150 mmol/L NaCl, 1.0 mmol/L EDTA, 1.0% NP-40, 2.0 mmol/L sodium orthovanadate, 1 mmol/L PMSF, 10 μg/mL aprotinin, and 10 μg/mL leupeptine). Total cell lysates were precleared with protein G Sepharose for 2 hours at 4°C. HBHA-associated proteins were immunoprecipitated by incubation with protein G Sepharose for 24 hours at 4°C after incubation with anti-goat as control Ab for anti-TLR2, anti-TLR2, anti-rat as control Ab for anti-TLR4, or anti-TLR4 Abs for 1 hour at 4°C. Samples were eluted, and immunoblot analysis was performed using an anti-HBHA mAb.
Antigen uptake quantification
Ag uptake was performed as recently described (14). Briefly, DCs (2 × 105) were equilibrated at 37°C or 4°C for 30 minutes and pulsed with 1 mg/mL FITC-conjugated dextran for 45 minutes, and then the action was stopped with cold staining buffer. Washed cells were stained with PE-conjugated anti-CD11c and analyzed using a FACSCalibur flow cytometer.
In vitro and in vivo migration of DCs
In vitro chemotaxis was performed as previously reported (21). For the in vivo migration test, DCs were labeled with 0.5 μmol/L carboxyfluorescein diacetate succinimidyl ester (CFSE; Molecular Probes). Labeled cells (1 × 106) were injected s.c. in the hind-leg footpad. Popliteal lymph nodes (LNs) were removed 72 hours later, mechanically disaggregated, and treated with collagenase A (1 mg/mL; Boehringer Mannheim) and DNase (0.4 mg/mL; Roche) for 30 minutes. The enzymatically treated cell suspension was evaluated for the percentage of CFSE+ DCs by FACScan (Becton Dickinson).
In vivo imaging
Nude mice were preinjected with TNF-α in the hind-leg footpad (30 ng/leg). A total of 1 × 106 labeled DCs in 50 μL PBS was injected s.c. in the hind-leg footpad. After 2 days, mice were anesthetized with an intramuscular (i.m.) injection of 100 μL/kg zoletil 50 solution (Virbac Korea). In vivo imaging was performed using the Maestro in vivo imaging system (CRI, ex = 797 nm; em = 830 nm long-pass).
Mixed lymphocyte reaction
OVA-specific CD8+ T cells, derived from C57BL/6 OT-1 TCR transgenic mice, were negatively selected using a mouse CD8+ T-cell kit (Miltenyi Biotec). Mixed lymphocyte reaction (MLR) was performed as recently described (22).
ELISA for IFN-γ and IL-2
BALB/c mice were injected with PBS, untreated DCs, DCs-pulsed with OVA257–264, or HBHA-treated DCs-pulsed with OVA257–264 on days 1 and 7. Seven days following the final injection, splenocytes (2 × 106 per well) were isolated and restimulated for 24 hours with 10 μg/mL OVA257–264, and the culture supernatant was used for the detection of IFN-γ and IL-2 by using ELISA.
In vivo CTL assay
C57BL/6 mice were injected with PBS, untreated DCs, DCs-pulsed with OVA257–264, or HBHA-treated DCs-pulsed with OVA257–264 on days 1 and 7. At the 7 days after last immunization, spleen cells from syngeneic mice were red blood cell lysed followed by pulsing with or without 10 μg/mL OVA257–264 for 45 minutes at 37°C. Then, the OVA257–264 pulsed and unpulsed populations were loaded with either 5 μM (high) or 0.5 μM (low) carboxyfluoroscein succinimidyl ester (CFSE; Molecular Probe) at 37°C for 10 minutes. The 2 cell populations were mixed 1:1 before tail vein injection to the immunized mice (107 cells per mouse). At 4 hours after injection, spleens from recipient mice were isolated and single cell suspensions were prepared prior to flow cytometric analysis using a FACScan (Becton Dickinson). The number of CFSEhigh and CFSElow population were determined and the in vivo OVA-specific lysis percentage was enumerated  A.M. Byers, C.C. Kemball, J.M. Moser and A.E. Lukacher, Cutting edge, J Immunol 171 (2003), pp. 17–21. View Record in Scopus | Cited By in Scopus (52).
All experiments were repeated at least 3 times. The levels of significance for comparison between samples were determined by Tukey's multiple comparison test by using GradPad InStat software (Ver 3.05, GraphPad). The data in the graphs are expressed as the mean ± SEM. Datasets of survival curves were analyzed by the Kaplan–Meyer log-rank test.
HBHA induces DC maturation
Soluble recombinant HBHA was expressed in M. smegmatis and characterized. Endotoxin levels in HBHA were undetectable (≤0.01 ng/mg; data not shown). The molecular mass of HBHA was approximately 29 kDa. The purity of HBHA was first assessed by sodium dodecyl SDS-PAGE, immunoblotting with an antihistidine Ab (Fig. 1A). In addition, the purity of rHBHA was quantified by Quantity-one software (Bio-Rad). The purity of HBHA was calculated by percentage of HBHA band against intensity/mm2 of the entire protein bands. The rHBHA revealed 84 and 96% purity after using Ni-NTA column only (left panel) and Ni-NTA followed by P11 column (right panel), respectively when 20 μg of each protein were assessed in silver nitrate staining (Supplementary Fig. 1). Apoptosis in DC cultures exposed to HBHA up to 1 μg/mL did not change significantly, as detected by Annexin V and PI staining (Fig. 1B).
To investigate whether HBHA induces DC maturation, we measured the expression of DC maturation markers involved in Th activation, such as CD40, CD80, CD86, major histocompatibility complex (MHC) classes I and II by flow cytometry. LPS served as a positive control. HBHA strongly induced the expression of various surface molecules in a dose-dependent manner (Fig. 1C).
We then tested whether HBHA-treated DCs produce pro- or antiinflammatory cytokines required for a Th response. DCs secreted IL-12 and IL-10, which stimulate the proliferation and development of Th1 and Th2 cells, respectively (23). The levels of IL-12 p40/p70 production in HBHA-treated DCs were significantly (P < 0.05–0.001) greater than those produced by untreated DCs (Fig. 1D). ELISA studies also revealed high levels of IL-12p70 in the supernatant of HBHA-treated DCs (Fig. 1E).
We also measured the production of IL-10, a pleiotropic cytokine that inhibits DC function and Th1 responses (24). Interestingly, unlike LPS, HBHA does not induce IL-10 in DCs (Fig. 1D and 1E). In addition, HBHA-treated DCs showed an enhanced secretion of proinflammatory cytokines (IL-1β, IL-6, and TNF-α) compared to untreated DCs (Fig. 1F). Similar to treatment with LPS, HBHA treatment significantly decreased the percentage of dextran+CD11c+ cells (Fig. 1G), as compared to untreated DCs. These results indicate that HBHA significantly enhances the phenotypic and functional maturation of DCs.
TLR4 signaling is required for HBHA-induced DC maturation
TLR2 and TLR4 have been reported to recognize M. tuberculosis in the context of activation and maturation of Ag-presenting cells in vitro (25). Therefore, we examined whether HBHA can be recognized by and acting through TLRs in DCs. To identify TLRs on DCs that interact with HBHA, wild type (WT), TLR2−/−, and TLR4−/− DCs were stimulated with HBHA, and HBHA on cell surface was detected with an Alexa568-conjugated anti-HBHA mAb (Fig. 2A and B). Anti-HBHA bound to the cell surface of WT, TLR2−/− DCs, but not TLR4−/− DCs. To confirm the interaction between HBHA and TLR, we performed immunoprecipitation studies with TLR2 or TLR4 and HBHA in DCs. HBHA bound to TLR4 but not TLR2 (Fig. 2C). This observation was also confirmed by confocal microscopy. As expected, co-localization of HBHA and TLR4 but not TLR2 was detected (Fig. 2D).
To test the ability of HBHA to activate DCs via TLR4, we measured the expression of surface molecules and proinflammatory cytokine (IL-12 p70, TNF-α, IL-6, and IL-1β) production in HBHA-treated WT, TLR2−/−, or TLR4−/− DCs. The expression of surface molecules (Fig. 2E) and proinflammatory cytokine secretion (Fig. 2F) were enhanced in WT or TLR2−/− DCs by HBHA. In contrast, these effects were strongly diminished in TLR4−/− DCs indicating that HBHA is an agonist for TLR4 in DCs.
TLR4 signals via the MyD88- and TRIF-dependent pathways (26). To investigate the importance of the MyD88- and TRIF-dependent pathways in HBHA-induced cytokine production by DCs, we compared DC-based cytokine production in WT, MyD88−/− and TRIF-deficient mice. HBHA-induced production of IL-1β, IL-6, and TNF-α was significantly reduced in the absence of MyD88 and TRIF (Fig. 2G). Our results suggest that MyD88 and TRIF are crucial for an optimal HBHA-induced cytokine response. Furthermore, proteinase K- or heat-treated HBHA lost its activity to stimulate IL-1β production in DCs. However, HBHA was resistant to polymyxin B treatment, indicating that LPS contamination was not responsible for the observed effects (Supplementary Fig. 2).
TLR9 signaling is not required for HBHA-induced DC activation
TLR activation and signal transduction such as TLRs1, 2, 4, 5, and 6 are modulated by subcellular compartmentalization of receptors and downstream signaling components (27), and the intracellular localization of nucleic acid-sensing TLRs such as TLRs3, 7, and 9 appears to facilitate self versus nonself discrimination (28). Recent study has suggested that DNA derived from M. tuberculosis induces proinflammatory cytokines via TLR9-dependent pathway in macrophages and DCs (29). Thus, we decided to determine whether TLR9 affected to the HBHA-induced DC maturation. We showed that HBHA did not bind to TLR9−/− DC (Fig. 3A) and TLR9 deficiencies had no effect on the level of surface molecules (Fig. 3B) and proinflammatory cytokines (Fig. 3C). These results provided the evidence that HBHA is an efficient TLR4 agonist.
HBHA enhances DC migration
To investigate whether HBHA affects DC migration, we measured the CCR7 expression in DCs. The CCR7 expression was upregulated in HBHA-treated DCs, similar to the level of LPS-treated DCs (Fig. 4A). Next, we analyzed the migratory capacity of DCs using a transwell migration assay chamber. HBHA increased the migratory capacity of DCs in response to CCL19 in vitro (Fig. 4B).
We also observed an increase in the number of CFSE-positive HBHA-treated DCs in the draining LN compared to that of CFSE-positive HBHA-untreated DCs in vivo (Fig. 4C). The migratory capacity of HBHA was further analyzed by using an in vivo image system. NEO-LIVE-labeled HBHA-untreated DCs were detected in the footpad, but not in the popliteal LN. In contrast, a remarkably strong fluorescence signal was detected in the popliteal LN (arrow) of mice injected with HBHA- or LPS-treated DCs (Fig. 4D). Overall, these results demonstrate that HBHA promotes DC migration in vitro and in vivo.
HBHA induces the activation of CD4+ and CD8+ T cells through TLR4-mediated DC activation
To precisely characterize HBHA activity on the interaction between DCs and T cells, we performed a syngeneic MLR assay using OT-I T-cell receptor (TCR) transgenic CD8+ T cells, which express a TCR specific for the MHC class I-restricted OVA peptide 257–264 Ag (OVA257–264) in DCs (30). HBHA-treated DCs pulsed with OVA257–264 elevated the cluster formation compared to untreated control DCs pulsed with OVA257–264 (Supplementary Fig. 3). Additionally, transgenic CFSE-labeled OVA-specific CD8+ T cells co-cultured with HBHA-treated DCs pulsed with OVA257–264 proliferated to a greater extent than did T cells co-cultured with untreated DCs pulsed with OVA257–264 (Fig. 5A). These results demonstrate that HBHA is a potent immunostimulator for T cells through DC activation. We then investigated the IFN-γ production in CD8+ T cells activated with HBHA-treated DCs. Syngeneic T cells primed with HBHA-treated DCs produced a significantly higher level of IFN-γ than those primed with untreated DCs (P < 0.05–0.01; Fig. 5C, left panel). Because DCs are also capable of inducing the polarization of naïve T cells, we evaluated the ability of HBHA-activated DCs to induce a Th1 phenotype from naïve CD4+ T cells. CD4+ splenic T cells from OT-II TCR transgenic mice were co-cultured with HBHA-treated DCs pulsed with OVA323–339 also proliferated to greater extent than did T cells co-cultured with untreated DCs pulsed with OVA323–339 (Fig. 5B). Furthermore, analysis of culture supernatants showed that IFN-γ secretion increased in response to HBHA (Fig. 5C, right panel). Furthermore, we also measured the proliferation of T cells co-cultured with DCs pulsed with OVA whole protein instead of OVA peptide. Similar to OVA peptide pulsing, HBHA-treated DCs pulsed with OVA whole protein also enhanced the proliferation of CD4+ and CD8+ T cells (Supplementary Fig. 4). These results suggest that HBHA directs T-cell differentiation toward a Th1 phenotype by inducing IL-12 production.
To test the capacity of HBHA to induce the interaction between DCs and T cells via TLR4, we performed a syngenic MLR assay using OT-I and OT-II TCR transgenic CD4+ and CD8+ T cells. HBHA-treated DCs derived from WT, TLR2−/−, and TLR4−/− mice pulsed with OVA257–264 or OVA323–339 and then co-cultured with transgenic CFSE-labeled OVA-specific CD8+ and CD4+ T cells. The proliferation of OT-I (Fig. 5D) and OT-II (Fig. 5E) cells were enhanced in HBHA- or LPS-treated WT and TLR2−/− DCs pulsed with OVA peptide, whereas there effects were diminished in HBHA- or LPS-treated TLR4−/− DCs pulsed with OVA peptide indicating that HBHA induce T-cell proliferation through TLR4-mediated DC activation.
HBHA enhances the antitumor efficacy
To show the therapeutic antitumor potential of HBHA, we used a murine tumor model in which EL4 or OVA-expressing E.G7 cells were implanted. On day 35 days following E.G7 tumor implantation, injection of DCs pulsed with OVA257–264 significantly suppressed the E.G7 tumor growth (mean size, 5630.8 [97.3] mm3) compared to tumors in mice receiving PBS (mean size, 19,202.8 [277.4] mm3) or DCs alone (mean size, 16,949.4 [208.2] mm3; P < 0.01). Meanwhile, injection of OVA-pulsed DCs did not affect the EL4 tumor growth (Data not shown). Interestingly, E.G7 tumors in mice that received HBHA-treated DCs pulsed with OVA257–264 were significantly smaller (mean size, 2,925.7 [60.1] mm3) than that in mice received DCs pulsed with OVA (Fig. 6A). Notably, only 20% of mice injected with OVA-pulsed DCs survived beyond 60 days following E.G7 tumor implantation as compared to over 50% survival of mice injected with HBHA-treated OVA-pulsed DCs. In contrast, all mice in the PBS and HBHA-untreated DCs-injected groups had a median survival of 34 days with no long-term survivors (Fig. 6B).
To test the engagement of TLR4 in the retardation of tumor growth by immunization with HBHA-treated DCs pulsed with OVA, E.G7 cells implanted mice were immunized with DCs pulsed with OVA257–264 (DC-OVA), HBHA-treated WT DCs pulsed with OVA257–264 [HBHA-DC(WT)-OVA], HBHA-treated TLR2−/− DCs pulsed with OVA257–264 [HBHA-DC(TLR2 KO)-OVA], or HBHA-treated TLR4−/− DCs pulsed with OVA257–264 [HBHA-DC(TLR4 KO)-OVA]. Although injection of HBHA-DC(WT)-OVA (mean size, 6,869.3 [753.4] mm3) and HBHA-DC(TLR2 KO)-OVA (mean size, 8,178.8 [664.7] mm3) significantly suppressed the E.G7 tumor growth compared to tumors in mice receiving DC-OVA (mean size, 18,256.7 [803.3] mm3), injection of HBHA-DC(TLR4 KO)-OVA (mean size, 16,115.9 [971.0] mm3) did not suppressed the E.G7 tumor growth (Fig. 6C). In addition, the survival rate was also significantly decreased in HBHA-DC(TLR4 KO)-OVA compared to mice receiving HBHA-DC(WT)-OVA (P < 0.001; Fig. 6D).
HBHA increases CTL activity in tumor-bearing mice via TLR4 signaling
To further investigate the mechanism of tumor protection after HBHA-treated DC vaccination, we first sought to determine whether a humoral antitumor immune response was induced. Serum from E.G7 tumor implanted mice was collected at day 7 after final immunization with PBS, untreated DCs (iDC), DCs pulsed with OVA257–264 (DC-OVA), or HBHA-treated DCs pulsed with OVA257–264 (HBHA-DC-OVA) and assessed for IgG2a production. The level of IgG2a was increased in tumor-bearing mice received with DC-OVA, whereas that was significantly (P < 0.001) enhanced in tumor-bearing mice received with HBHA-DC-OVA (Supplementary Fig. 5).
Next, to examine the in vivo cytolytic function of the memory T cells, mice were immunized with PBS, untreated DCs (iDC), DCs pulsed with OVA257–264 (DC-OVA), or HBHA-treated DCs pulsed with OVA257–264 (HBHA-DC-OVA) at days 1 and 7. At 7 days after the last immunization, the mice were injected with a mixture of syngeneic splenocytes pulsed with OVA257–264 (CFSEhi) or without OVA257–264 (CFSElow), and the elimination of OVA-pulsed splenocytes (CFSEhi) was examined by flow cytometry.
In addition, a significantly high level of target cell lysis was observed in mice received HBHA-DC-OVA (79.3 [0.68]%) compared to those received PBS (0 [0.05]%), iDC (0.43 [0.15]%), or DC-OVA (49 [2.05]%; Fig. 7A). These results suggested that HBHA could be an important element in a cancer vaccine against OVA positive thymoma tumor by inducing killing activity to target cells.
To assess whether the lymphocytes induced by the HBHA-treated DCs pulsed with OVA257–264 is able to produce the essential cytokine, we observed significantly higher levels of IFN-γ and IL-2 secretion when splenocytes from mice injected with HBHA-treated DCs pulsed OVA257–264 (HBHA-DC-OVA) were restimulated with OVA257–264, compared to those of splenocytes from mice injected with DCs pulsed with OVA257–264 (DC-OVA; P < 0.001; Fig. 7B).
To test the engagement of TLR4 in the induction of CTL activity by immunization with HBHA-treated DCs pulsed with OVA, mice were immunized with PBS, untreated DCs (iDC), DCs pulsed with OVA257–264 (DC-OVA), HBHA-treated WT DCs pulsed with OVA257–264 [HBHA-DC(WT)-OVA)], HBHA-treated TLR2−/− DCs pulsed with OVA257–264 [HBHA-DC(TLR2 KO)-OVA)], or HBHA-treated TLR4−/− DCs pulsed with OVA257–264 [HBHA-DC(TLR4 KO)-OVA)]. Target cell lysis in mice received HBHA-DC(TLR4 KO)-OVA was significantly suppressed compared to mice received HBHA-DC(WT)-OVA (Fig. 7C). This data suggest that HBHA can modulate the CTL activity via TLR4-dependent pathway.
To further delineate the mechanism by which OVA-specific DC vaccination resulted in improved tumor retardation, we analyzed surface expression of CD62L and CD44, both of which have been implicated in cell migration to the site of Ag deposition (31), on CD8+ T cells in spleen. Using flow cytometry, we identified naive (CD62LhighCD44low) and effector/memory cells (CD62LlowCD44high). By day 7 after final immunization with HBHA-treated DCs-pulsed with OVA, CD8+ T cells in spleen showed significantly downregulated CD62L and upregulated CD44 expression when immunized with DCs pulsed with OVA (Fig. 7D).
The immune system can recognize many tumor Ags however, the ability of tumors to evade the immune system suggests that host defense mechanism cannot effectively prevent some tumors. In an attempt to boost the antitumor immunity, we focused on a DC-based antitumor immunotherapy using HBHA as an adjuvant.
DCs are the most potent APCs and versatile regulators of T lymphocyte responses (32, 33). Immature DCs capture Ags, process them into peptides, and present on the cell surface in association with MHC class I or II to prime CD8+ CTLs or CD4+ Th1 cells, respectively (32, 33). Immunization with ex vivo tumor Ag-loaded DCs is a promising tool for eliciting efficient antitumor immunity (34). This approach has been successfully used to vaccinate mice and to activate CTL responses in preclinical human trials (35–38).
In this study, we identified the novel properties of HBHA that HBHA can induce DC maturation via TLR4 activation. Importantly, HBHA improved the efficacy of the DC-based antitumor immunotherapy in mice by acting as an adjuvant. The evidence for these novel characteristics of HBHA includes: (1) increased expression of surface molecules and proinflammatory cytokines in HBHA-treated DCs; (2) reduced HBHA-induced DC activation in TLR4−/− DCs but not in TLR2−/− DCs; (3) increased migratory capacity of HBHA-treated DCs; and (4) significantly elevated OVA-specific CTL activity and suppression of tumor growth.
We showed that the interaction of HBHA with DCs inhibits the endocytic ability of DCs and induces the increased expression of surface molecules. Furthermore, HBHA-treated DCs enhanced primary syngeneic T-cell proliferation more efficiently than untreated DCs. HBHA-treated DCs also triggered the secretion of IL-1β, IL-6, IL-12p70, and TNF-α. Because IL-12 is essential for Th1 polarization (39) HBHA might promote Th1 immune responses. Furthermore, HBHA-treated DCs triggered the IFN-γ production in CD4+ and CD8+ T cells, which is another feature of Th1 responses. These findings indicate that the antitumor effect of HBHA-treated DCs is closely related to the increased production of IFN-γ.
In addition, to investigate the adjuvant activity of HBHA, we administered the model adjuvant OVA alone or in combination with HBHA. It is well documented that the type of IgG subclass reflects the pattern of immune responses in mice: IgG2a for Th1 and IgG1 for Th2 (40). OVA alone significantly enhanced IgG1 responses (Supplementary Fig. 6). Interestingly, however, HBHA dramatically augmented IgG2a (Th1-associated) but not IgG1 (Th2-associated) responses to OVA. Thus, HBHA is a potent adjuvant triggering Th1-mediated humoral immune responses.
In addition, HBHA induced the CCR7 expression, which is critical for the migration of DCs from the periphery to T-cell–rich regions of secondary lymphoid organs (41, 42). Importantly, HBHA enhanced the migration of DCs toward CCL19 in vitro and resulted in the draining of LNs in vivo. HBHA has multiple effects on DC function, indicating that it can be an effective adjuvant for DC-based antitumor immunotherapies.
TLRs are expressed by many immune cells and play a key role in innate and adaptive immune responses (43). TLR4 agonists have important immunoregulatory applications, such as adjuvants for vaccines in antitumor therapies (44). Moreover, adjuvant studies for cancer treatment have recently been focused on TLR4 agonist because the signal through these receptors are mediated by either MyD88- and TRIF-dependent pathway and appear to be especially powerful immunopotentiators (45). Although LPS, the most studied and well-characterized TLR4 agonist, showed highly effective adjuvancity in both experimental and clinical setting (46), it is not suitable for clinical use due to its toxicity in humans. Thus, novel TLR4 agonists will be extremely beneficial as vaccine adjuvants in antitumor therapy.
Some M. tuberculosis proteins have a significant immunostimulatory potential. Both TLR2 and TLR4 mediate M. tuberculosis-induced intracellular signaling in APCs (47). Furthermore, several molecules from M. tuberculosis have now been identified as TLR2 agonists and are known to induce APC activation (48, 49). However, TLR4 agonists have not yet been identified. We showed that HBHA directly binds TLR4 and activates TLR4-mediated MyD88 and TRIF signaling, leading to the expression of surface molecules and proinflammatory cytokines' production by DCs (Fig. 2).
On the basis of the results described herein, we suggest that HBHA could be used for DC-based antitumor immunotherapies. It is obvious that immunotherapy using HBHA for tumor treatment has not yet been explored in detail including safety issue. However, because of its ability to stimulate DCs, which then further activate T cells that are able to lyse tumor cells and suppress tumor growth, we propose HBHA as a novel and potent adjuvant with potential applications in antitumor immunotherapy.
Disclosure of Potential Conflicts of Interest
No potential conflicts of interest were disclosed.
This study was supported by a grant of the Korea Healthcare Technology R&D Project, Ministry for Health Welfare & Family Affairs, Republic of Korea (A091047) and by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MEST; 2010–0008728).
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.
We thank Dr. Clifton E. Barry III and Dr. Yong-Soo Bae for critical reading of the manuscript and discussions.
Note: Supplementary data for this article are available at Cancer Research Online (http://cancerres.aacrjournals.org/).
- Received September 23, 2010.
- Revision received February 8, 2011.
- Accepted February 19, 2011.
- ©2011 American Association for Cancer Research.