The combination of immunotherapy and chemotherapy is regarded as a promising approach for the treatment of certain types of cancer. However, the underlying mechanisms need to be fully investigated to guide the design of more efficient protocols for cancer chemoimmunotherapy. It is well known that danger-associated molecular patterns (DAMPs) can activate immune cells, including dendritic cells (DCs), via Toll-like receptors (TLRs); however, the role of DAMPs released from chemical drug-treated tumor cells in the activation of the immune response needs to be further elucidated. Here, we found that colorectal cancer (CRC) cells treated with oxaliplatin (OXA) and/or 5-fluorouracil (5-Fu) released high levels of high-mobility group box 1 (HMGB1) and heat shock protein 70 (HSP70). After OXA/5-Fu therapy, the sera of CRC patients also exhibited increased levels of HMGB1 and HSP70, both of which are well-known DAMPs. The supernatants of dying CRC cells treated with OXA/5-Fu promoted mouse and human DC maturation, with upregulation of HLA-DR, CD80 and CD86 expression and enhancement of IL-1β, TNF-α, MIP-1α, MIP-1β, RANTES and IP-10 production. Vaccines composed of DCs pulsed with the supernatants of chemically stressed CRC cells induced a more significant IFN-γ-producing Th1 response both in vitro and in vivo. However, the supernatants of chemically stressed CRC cells failed to induce phenotypic maturation and cytokine production in TLR4-deficient DCs, indicating an essential role of TLR4 in DAMP-induced DC maturation and activation. Furthermore, pulsing with the supernatants of chemically stressed CRC cells did not efficiently induce an IFN-γ-producing Th1 response in TLR4-deficient DCs. Collectively, these results demonstrate that DAMPs released from chemically stressed cancer cells can activate DCs via TLR4 and enhance the induction of an anti-tumor T-cell immune response, delineating a clinically relevant immuno-adjuvant pathway triggered by DAMPs.
Colorectal cancer (CRC) is the third most common cancer and the third leading cause of cancer deaths in developed countries. Oxaliplatin (OXA)- and 5-fluorouracil (5-Fu)-based FOLFOX chemotherapy is the first-line therapeutic regimen in the treatment of patients with advanced CRC.1,2 Chemical drugs mainly kill tumor cells through cytotoxic effects and also kill normal cells at the same time, which causes lymphopenia and suppresses the immune system's function. Immunotherapy is now becoming a promising approach for CRC treatment, and much attention has been paid to the combination of chemotherapy and immunotherapy. Efficiently killing tumor cells with chemical drugs while enhancing induction of the anti-tumor immune response is becoming increasingly important. CRC cells treated with OXA and 5-Fu may release danger-associated molecular patterns (DAMPs), which play important roles in immunogenic tumor cell death. Through experiments performed in vivo and in vitro, DAMPs induced by chemical drugs have been demonstrated to stimulate dendritic cells (DCs) to induce an anti-cancer immune response.3,4,5 However, DAMPs also play a putative role in the promotion of tumor progression by attracting immature myeloid cells and triggering tumor cell proliferation.6,7,8 Thus, how to more efficiently trigger an anti-cancer immune response mediated by DAMPs is worthy of attention.
DCs are characterized by their ability to efficiently present antigens and are uniquely equipped to stimulate T-cell responses. DCs have a strong ability to activate CD8+ cytotoxic T lymphocytes and CD4+ Th1 immunity and therefore play an essential role in the anti-tumor immune response.9,10,11,12,13 DCs in the tumor environment are mainly immature and are ideally equipped to engulf and process dying cells. However, tumor-derived factors maintain DC immaturity, trapping the cells within the tumor and hence impairing effective presentation of ingested antigens to T cells. Moreover, these immature DCs have immunosuppressive rather than immunostimulatory properties.14,15 Therefore, improving the immunogenicity of tumor cells and the efficiency of stimulated DCs in inducing potent anti-tumor immunity is an important way to enhance the efficacy of cancer therapy.
Toll-like receptors (TLRs) play important roles in the initiation of innate and adaptive immune responses. Increasing numbers of DAMPs are being reported as candidate agonists of TLRs, and particularly TLR4, including heat shock proteins (HSPs) (HSP70, HSP90),16,17,18 high-mobility group box 1 (HMGB1)19,20 and uric acid crystals.21 These molecules can bind to TLR4, thereby causing inflammatory responses and providing DCs with danger signals, which can be translated into the promotion of an anti-tumor T-cell response. Supporting these findings, patients with breast cancer who have lost TLR4 function have been shown to relapse more quickly after chemotherapy than patients with normal TLR4 expression.22
Here, to improve the efficacy of DC vaccines in the induction of an anti-tumor immune response, we investigated whether DCs pulsed with DAMPs from dying CRC cells could efficiently induce an anti-tumor T-cell response. We showed that OXA and 5-Fu induced the release of DAMPs from CRC cells and that DAMPs from CRC cells activated DCs to more significantly induce anti-tumor immune responses than did the supernatants of untreated CRC cells. More importantly, we found that TLR4 in DCs was essential for CRC cell-derived DAMPs to activate DCs and induce an anti-tumor immune response. Thus, our data demonstrate that TLR4 is essential for DC activation and anti-tumor T-cell response enhancement by DAMPs from chemically stressed cancer cells, providing a molecular mechanism for the synergy of immunotherapy and chemotherapy in the induction of an anti-tumor effect.
Materials and methods
Sera were obtained from patients with CRC stage III/IV who had received FOLFOX (5-Fu+OXA) chemotherapy at Shanghai Changzheng Hospital (Shanghai, China). All patients gave written informed consent, and the protocol was approved by local institutional review boards. Blood was collected before and after the first chemotherapy treatment (any day among the third to seventh days after the treatment).
Animals and cell lines
Wild-type (WT) C57BL/6 and Balb/c mice, 6–8 weeks of age, were obtained from the Shanghai Laboratory Animal Center of the Chinese Academy of Sciences (Shanghai, China). TLR4-deficient mice (TLR4−/−, C57BL/6 strain) were kindly provided by Dr S Akira (Research Institute for Microbial Diseases, Osaka, Japan).23 All mice were housed in a specific pathogen-free facility during all experiments. The human CRC cell line SW480 (HLA-A2.1+) and the mouse CRC cell line CT-26 were obtained from the American Type Culture Collection (Manassas, VA, USA) and cultured according to the provided instructions.
Preparation of supernatants from chemically stressed cancer cells
SW480 cells and CT-26 cells were cultured in cell culture flasks (1×106/ml) in the presence of 10 mg/ml 5-Fu (Sigma, St Louis, MO, USA) and/or 0.5 mg/ml OXA (Sanofi, Paris, France). Supernatants were collected after 0, 6, 12, 18, 24, 30, 36 and 42 h, and HSP70 and HMGB1 levels were then measured using ELISA kits (Stressgen, Cedar Creek, TX, USA). To remove the chemical drugs, the supernatants collected after 30 h were dialyzed in phosphate-buffered saline at 4 °C for 48 h and concentrated by centrifugation in 10000 MWCO centrifuge tubes at 2000g for 15 min at 4 °C. Untreated sup-CTR describes the supernatants of untreated SW480/CT26 cells (the control group); OXA-sup, the supernatants of SW480/CT26 cells treated with OXA; 5-Fu-sup, the supernatants of SW480/CT26 cells treated with 5-Fu; and OXA+5-Fu-sup, the supernatants of SW480/CT26 cells treated with OXA and 5-Fu.
Generation of DCs
Human peripheral blood monocytes were isolated from healthy volunteers (HLA-A2.1+), and monocyte-derived DCs were prepared as described previously.24 Mouse bone marrow-derived DCs (BMDCs) were prepared as previously described.25
Assays for cytokine and chemokine production
Human DCs and BMDCs were cultured for 5 days and adjusted to a final concentration of 5×105 cells/ml in 24-well plates. Next, 100 µl/ml untreated CTR-sup, OXA-sup, 5-Fu-sup and OXA+5-Fu-sup and 100 ng/ml lipopolysaccharide (LPS) were added to separate wells of the 24-well plates. Supernatants from designated wells were harvested after 24 h for quantification of cytokines, such as IL-6, IL-1β and TNF-α, and of chemokines, including MIP-1α, MIP-1β and RANTES, using ELISA kits (R&D Systems, Minneapolis, MN, USA).
After 5 days of culture, human DCs and BMDCs were stimulated with 100 µl/ml untreated CTR-sup, OXA-sup, 5-Fu-sup or OXA+5-Fu-sup or 100 ng/ml LPS for 24 h. The DCs were then collected; washed with phosphate-buffered saline; and stained with phycoerythrin-conjugated anti-CD40 or anti-CD86 or fluorescein isothiocyanate-conjugated anti-HLA-DR (I-Ab) monoclonal antibody (PharMingen, San Diego, CA, USA) for analysis with a FACSCalibur flow cytometer (Becton Dickinson, Mountain View, CA, USA) and CellQuest software (Becton Dickinson).
Generation of T-cell response
Human DCs and BMDCs (from WT or TLR4−/− C57BL/6 mice) were cultured for 5 days; harvested; stimulated with 100 µl/ml untreated CTR-sup, OXA-sup, 5-Fu-sup or OXA+5-Fu-sup for 24 h; and then washed twice in serum-free RPMI 1640 medium. In the TLR4-antagonist group, 30 µg/ml HTA125 (HBT, Uden, The Netherlands), an anti-TLR4 monoclonal antibody, was administered before stimulation with untreated CTR-sup, OXA-sup, 5-Fu-sup or OXA+5-Fu-sup.26 Human DCs (2×105) and autologous peripheral blood lymphocytes (2×106) or BMDCs (2×105) and autologous splenocytes (2×106) from WT or TLR4−/− C57BL/6 mice were cocultured in 1 ml RPMI 1640 medium supplemented with 10% fetal calf serum in 24-well plates. The human peripheral blood lymphocytes or mouse splenocytes were restimulated with autologous fresh supernatant-pulsed DCs every 7 day for three times respectively. On the third day after the second stimulation, 20 IU/ml rhIL-2 (Sigma) was added. Half of the medium was removed every 3 days and replaced with fresh medium containing rhIL-2 (20 IU/ml). On the seventh day after the final stimulation, the cells were harvested and prepared for ELISPOT analysis.
Human lymphocytes were re-stimulated with 50 µg/ml SW480 tumor cell lysate antigen (prepared by repeatedly freezing and thawing SW480 cells) for 72 h, as described above, and then collected and used as effector cells. SW480 (1×105) tumor cells, serving as stimulator cells, were cocultured with 2×105 effector cells and seeded into 96-well polyvinylidene difluoride-backed microplates coated with anti-human IFN-γ mAb. After incubation at 37 °C for 24 h, the cells were removed, and the plates were processed following the manufacturer's protocol (R&D Systems).
Splenocytes from WT or TLR4−/− C57BL/6 mice were re-stimulated with 50 µg/ml CT-26 tumor cell lysate antigen for 72 h and then collected and used as effector cells. BMDCs (1×105) pulsed with CT-26 tumor lysate antigen, serving as stimulator cells, were cocultured with 2×105 effector cells and seeded into 96-well polyvinylidene difluoride-backed microplates coated with anti-mouse IFN-γ mAb. After incubation at 37 °C for 24 h, the cells were removed, and the plates were processed following the manufacturer's protocol for the ELISPOT kit (R&D Systems). The resulting spots were counted using an ImmunoSpot Analyzer (Cellular Technology Ltd, Cleveland, OH, USA).
BMDCs generated from Balb/c mice were harvested on the fifth day; plated at a cell concentration of 2×106/ml; pulsed with 100 µl/ml untreated CTR-sup, OXA-sup, 5-Fu-sup or OXA+5-Fu-sup for 24 h; and then washed three times with phosphate-buffered saline. Balb/c mice were subcutaneously immunized three times at an interval of 1 week with supernatant-pulsed BMDCs (1×106 per mouse).
Five days after the final immunization, the C57BL/6 mice were subcutaneously challenged with 2×105 CT-26 tumor cells in the flank area. Tumor growth was monitored by measuring the diameter of the tumor with a caliper every 2 days and was recorded as the average of two perpendicular diameter measurements. The survival time following tumor challenge was also recorded.
Differences in the growth of the CT-26 tumors, as indicated by the tumor diameters within each group, were compared using the Mann-Whitney U test. To compare mouse survival between the treatment groups and the control group, a Kaplan–Meier statistical analysis was performed. All other statistical analyses were based on the Student's t-test. P<0.05 was considered as a statistically significant difference.
DAMPs release from cancer cells induced by chemical drugs
HMGB1 and HSP70 are prototypical DAMPs that are hallmarks of cancer and are released following chemotherapy.3,4,27 The release of HMGB1 and HSP70 was detected in the supernatants of the mouse CRC cell line CT-26 (Figure 1a) and the human CRC cell line SW480 (Figure 1b) after treatment with the chemical drugs OXA and/or 5-Fu. We found that HSP70 and HMGB1 release into the cell supernatants 6 h after treatment with OXA and/or 5-Fu was significantly increased compared with release in the untreated control group (P<0.05). Additionally, the HSP70 and HMGB1 concentrations in the cell supernatants 18, 24 and 30 h after treatment with the combination of OXA and 5-Fu were even higher than following treatment with OXA or 5-Fu alone (Figure 1a and b).
DAMPs in sera from cancer patients induced by chemotherapy
Next, we investigated changes in the expression of HMGB1 and HSP70 in the sera of 11 patients with advanced CRC who had received FOLFOX chemotherapy (5-Fu+OXA). We found that the serological concentrations of HSP70 and HMGB1 in the patients who had received chemotherapy increased markedly after chemotherapy (Figure 1c). The results indicated that chemotherapy can increase DAMPs release in cancer patients.
Supernatants from chemically stressed human cancer cells induce maturation of human DCs in TLR4-dependent manner
DAMPs are shown to be candidate TLR4 agonists and to promote the maturation and activation of DCs.4,18,19 To investigate the role of TLR4 in mediating DC maturation by supernatants from chemical drug-treated SW480 cells, we observed the phenotypic changes in DCs stimulated with supernatants from chemically stressed SW480 cells. We found that stimulation with OXA-sup, 5-Fu-sup or OXA+5-Fu-sup induced upregulation of HLA-DR, CD80 and CD86 expression on human DCs compared with stimulation with untreated sup-CTR. Stimulation with OXA+5-Fu-sup particularly induced greater phenotypic changes than did stimulation with OXA-sup or 5-Fu-sup alone. When we used the mAb HTA125, a TLR4 antagonist, to block the interaction of TLR4 with DAMPs in the supernatants of SW480 cells treated with chemical drugs, the upregulation of HLA-DR, CD80 and CD86 expression on DCs was reversed (Figure 2a), indicating that TLR4 on the DCs mediated the enhancing effect.
Next, we investigated whether TLR4 was essential for the induction of pro-inflammatory cytokine and chemokine secretion by DCs stimulated with supernatants from chemically stressed SW480 cells. We found an increase in pro-inflammatory cytokine and chemokine secretion by DCs stimulated with OXA-sup, 5-Fu-sup or OXA+5-Fu-sup, especially when stimulated with OXA+5-Fu-sup (P<0.05), but not DCs blocked with the TLR4 antagonist (Figure 2b). These results indicated that TLR4 was the crucial receptor mediating the DC maturation induced by DAMPs from SW480 cells treated with chemical drugs.
Supernatants from chemically stressed mouse cancer cells induce maturation of mouse DCs in TLR4-dependent manner
Next, we prepared DCs from WT and TLR4−/− C57BL/6 mice and observed the phenotypic changes in these DCs when stimulated with supernatants from chemically stressed CT-26 cells. We found that stimulation with OXA-sup, 5-Fu-sup or OXA+5-Fu-sup induced upregulation of I-ab, CD80 and CD86 expression on WT DCs, but not TLR4−/− DCs (Figure 3a). The production of pro-inflammatory cytokines (IL-1β, TNF-α and IL-6) and chemokines (MIP-1α, MIP-1β, RANTES and IP-10) was significantly increased among WT mouse DCs stimulated with OXA+5-Fu-sup. However, there was no significant increase in the production of these cytokines and chemokines by TLR4−/− DCs stimulated with OXA+5-Fu-sup (Figure 3b).
Taken together, the results suggest that the supernatants of CRC cells treated with chemical drugs induced DC phenotypic maturation and production of chemokines and pro-inflammatory cytokines via TLR4, indicating that TLR4 was one of the functional receptors mediating DC activation by the supernatants of the chemically stressed CRC cells.
DCs pulsed with supernatants from chemically stressed cancer cells induce Th1 response in vitro in TLR4-dependent manner
To assess whether TLR4 played an important role in the in vitro induction of a Th1 response by the DCs pulsed with DAMPs, we incubated peripheral blood lymphocytes from health donors and autologous DCs pulsed with the supernatants of chemically stressed SW480 cells in vitro. Alternatively, we incubated splenocytes from WT or TLR4−/− C57BL/6 mice and syngeneic DCs pulsed with the supernatants of chemically stressed CT-26 cells. As shown in Figure 4, the number of IFN-γ-producing cells induced by the DCs pulsed with OXA-sup, 5-Fu-sup or OXA+5-Fu-sup was significantly higher than the number in the untreated sup-CTR group (P<0.01). However, the number of IFN-γ-producing cells was decreased by the TLR4 antagonist HTA125 (Figure 4a), and an increase in the number of IFN-γ-producing cells was not observed in the TLR4−/− mice immunized with syngeneic DCs pulsed with supernatants from chemical drug-treated CT-26 cells (Figure 4b). These results further indicated that TLR4 functioned as the receptor by which DAMPs activated the DCs. The data suggested that the DCs were activated by the DAMP-containing supernatants of chemically stressed CRC cells via TLR4 and then triggered the Th1 response more potently.
More efficient induction of anti-tumor effect in vivo by immunization with DCs pulsed with supernatants from chemically stressed cancer cells
Induction of the in vivo anti-tumor immune response by DAMPs was assessed in a murine model with CT-26 tumor challenge. Balb/c mice were subcutaneously immunized three times at an interval of 1 week with BMDCs that had been stimulated with the supernatants of chemically stressed CT-26 cells. On the seventh day after the last immunization, the mice were subcutaneously challenged with CT-26 cells, and the tumor size of the mice was measured every 2 days. Tumor growth was significantly suppressed in the OXA+5-Fu-sup group compared with the control group (P<0.05) (Figure 5a), and the survival time was markedly prolonged in the OXA+5-Fu-sup group compared with the untreated sup-CTR group (P<0.05) (Figure 5b). These data demonstrated that immunization of mice with DCs that had been pulsed with the DAMP-containing supernatants of chemically stressed CRC cells more efficiently induced an anti-tumor immune response.
It has recently been shown that DAMPs are released from dying cells treated with certain chemical drugs, such as OXA, cyclophosphamide and doxorubicin.4,5,28,29 In our study, we found that the release of HSP70 and HMGB1 into CRC cell supernatants was significantly increased after OXA and/or 5-Fu treatment. Additionally, HSP70 and HMGB1 concentrations in the supernatants of cells treated with the combination of OXA and 5-Fu were even higher than after treatment with OXA or 5-Fu alone. Indeed, our data showed that the combination of OXA and 5-Fu treatment significantly increased DAMPs release, suggesting that the combination chemotherapy FOLFOX directly triggers more CRC cell death while more efficiently stimulating endogenous immune responses against the tumor. Timing is critical for effective anti-tumor immunotherapy. It has been reported that sequential events are associated with chemically stressed tumor cells. When tumor cells are treated with doxorubicin, intracellular calreticulin rapidly translocates to the cell surface (within 1 h). At 12 h after drug treatment, molecular chaperones, such as HSP70, may appear on the tumor cell surface. Finally, at 18 h, the release of HMGB1 from dying tumor cells can be observed.30,31 In contrast to the results for doxorubicin, our data showed that the levels of HSP70 and HMGB1 peaked at 30 h after exposure to OXA and 5-Fu and gradually decreased afterward. Thus, we evaluated the anti-tumor effect of adjuvant immunotherapy induced by a DC vaccine, including protocols for maturing DCs pulsed with 30-h supernatants. Consistent results were also collected from human patients, showing that the serum concentrations of HSP70 and HMGB1 in patients receiving FOLFOX chemotherapy increased markedly following chemotherapy.
DAMPs appear to play an alternate paradoxical role during tumor formation. It has been reported that DAMPs recognition can favor tumor progression by attracting immature myeloid cells and triggering the proliferation, migration and sprouting of endothelial cells in tumor beds.6,7,8 Moreover, in CRC, HMGB1 expression is increased at metastatic sites compared with primary tumor sites in non-metastatic patients.32 In addition to the putative role of HMGB1 in the promotion of tumor progression, certain preclinical and clinical data have revealed that HMGB1 seems to induce the functional maturation of DCs and to trigger protective anti-cancer T cell responses.4,5,16,20 The question of how DCs decode DAMPs needs to be further investigated. Recent studies have highlighted that after treatment with chemotherapeutic drugs, apoptotic tumor cells can release microparticles, which may contain DAMPs that stimulate DCs and can be used to effectively kill tumor cells.33,34 Therefore, when appropriate antigenic transfer to DCs occurs, the acute release of DAMPs may help to elicit immune responses in cancer-bearing patients. Maturation and activation of DCs is required for DC migration to T-cell regions within the lymph node.9,10,11
In this study, we found that DAMPs from CRC cells treated with OXA and 5-Fu promoted mouse and human DC maturation in vitro, activating the DCs to produce pro-inflammatory cytokines, such as IL-1β and TNF-α, whose autocrine or paracrine secretion can stimulate DC maturation.9,14,16 Moreover, in our study, increased MIP-1α, MIP-1β, RANTES and IP-10 secretion by DCs stimulated with DAMPs was also observed. These chemokines have been shown to play important roles in the immune response due to their involvement in the inflammatory response and their capacity to chemoattract leukocytes. Our previous studies have shown that chemokine gene transfer can enhance DC-mediated and T cell-dependent anti-tumor immunity and thus represents a potent anti-tumor immunotherapeutic approach.35,36,37 Therefore, increased chemokine secretion by DAMP-stimulated DCs is expected to exert strong chemoattractant effects on DCs and T cells, resulting in improved protective immunity and an enhanced T-cell response.
It is strongly recommended that vaccination strategies aiming to induce immunity against cancer include a means to stimulate the maturation of the targeted DCs. However, tumor-derived factors maintain DC immaturity, trap these cells within the tumor and hence, impair the effective presentation of ingested antigens to T cells.38 The presence of HSPs from dying tumor cells promotes the formation of tumor antigen–HSP complexes, which are processed by DCs for T-cell cross-priming more efficiently than tumor antigens alone.9,11 In the current study, the release of HSP70 and HMGB1 into the cell supernatants was significantly increased after OXA and/or 5-Fu treatment. HSP70 could have chaperoned tumor antigen generated by dying cells, triggering tumor-specific T-cell responses and anti-tumor effects via cross-presentation by DCs. We also found that a vaccine generated by pulsing DCs with the supernatants of chemically stressed CRC cells induced a polarizing IFN-γ-producing Th1 response in vitro. Induction of a Th1 response could be a vital mechanism underlying anti-tumor immunotherapy. We have previously reported that gene modification of Th1 cytokines (e.g., IL-18 and IFN-γ) can efficiently induce a T cell response to treat immunological disorders, including cancer and chronic infection.12,13,39 Moreover, a CEA576–669-HSP70L1 fusion protein promotes the secretion of Th1 cytokines (such as IL-12 and IFN-γ) and stimulates an anti-tumor cytotoxic T lymphocyte response to a DC vaccine.40 Thus, certain types of chemotherapy can kill tumor cells through efficient cytotoxic effects while enhancing the induction of an anti-tumor immune response.
An increasing number of endogenous proteins are being reported as stimulating TLRs (in particular, TLR2 and TLR4), such as HMGB119,20 and HSPs, including HSP60, HSP70, endoplasmin and HSPB8.9,11,41,42 In this study, we found phenotypic maturation and significantly increased cytokine secretion among WT DCs, but not TLR4−/− DCs, after stimulation with the supernatants of chemically stressed CT-26 cells. Similarly, the supernatants of chemically stressed SW480 cells failed to promote the maturation and activation of human DCs when the mAb HTA125 was used to block TLR4 function in DCs. HMGB1 and HSP70 bind promiscuously to multiple proteins and are reported to bind to the receptor for advanced glycosylation endproducts,43,44 TLR241,42 and TLR4,16,19,20 all of which can be presented on the surfaces of DCs. Our data suggest that the effect of the supernatants of dying CRC cells on DCs is mainly TLR4 mediated. Therefore, our current study indicated that TLR4 on DCs is one of the most important members of the TLR family to target in order to enhance the anti-tumor immune response.
The activation of TLRs by their cognate ligands leads to inflammatory cytokine production and upregulation of costimulatory signals and MHC molecules among DCs, thereby linking innate recognition to adaptive T- and B-cell immune responses, as well as to memory responses after the immune system encounters any pathogen. Interestingly, TLR4 appears to be required for efficient DC-mediated induction of a T-cell response. Our studies have proven that DCs pulsed with the supernatants of chemically stressed CRC cells induce an IFN-γ-producing T cell response in a TLR4-dependent manner. Thus, during chemotherapy, DAMPs, which are released from chemically stressed tumor cells, can activate the TLR4 signaling pathway and induce anti-tumor T-cell immunity against tumor cells, delineating a clinically relevant immuno-adjuvant pathway triggered by DAMPs.
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This work was supported by grants from the National Natural Science Foundation of China (81273332, 81101657 and 81123006) and the National High Technology Research, Development Program of China (2012AA020902).
All authors declare no conflict of interest.
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