- Open Access
C4b-binding protein α-chain enhances antitumor immunity by facilitating the accumulation of tumor-infiltrating lymphocytes in the tumor microenvironment in pancreatic cancer
Journal of Experimental & Clinical Cancer Research volume 40, Article number: 212 (2021)
Recent studies indicate that complement plays pivotal roles in promoting or suppressing cancer progression. We have previously identified C4b-binding protein α-chain (C4BPA) as a serum biomarker for the early detection of pancreatic ductal adenocarcinoma (PDAC). However, its mechanism of action remains unclear. Here, we elucidated the functional roles of C4BPA in PDAC cells and the tumor microenvironment.
We assessed stromal C4BPA, the C4BPA binding partner CD40, and the number of CD8+ tumor-infiltrating lymphocytes in resected human PDAC tissues via immunohistochemical staining. The biological functions of C4BPA were investigated in peripheral blood mononuclear cells (PBMCs) and human PDAC cell lines. Mouse C4BPA (mC4BPA) peptide, which is composed of 30 amino acids from the C-terminus and binds to CD40, was designed for further in vitro and in vivo experiments. In a preclinical experiment, we assessed the efficacy of gemcitabine plus nab-paclitaxel (GnP), dual immune checkpoint blockades (ICBs), and mC4BPA peptide in a mouse orthotopic transplantation model.
Immunohistochemical analysis revealed that high stromal C4BPA and CD40 was associated with favorable PDAC prognosis (P=0.0005). Stromal C4BPA strongly correlated with the number of CD8+ tumor-infiltrating lymphocytes (P=0.001). In in vitro experiments, flow cytometry revealed that recombinant human C4BPA (rhC4BPA) stimulation increased CD4+ and CD8+ T cell numbers in PBMCs. rhC4BPA also promoted the proliferation of CD40-expressing PDAC cells. By contrast, combined treatment with gemcitabine and rhC4BPA increased PDAC cell apoptosis rate. mC4BPA peptide increased the number of murine T lymphocytes in vitro and the number of CD8+ tumor-infiltrating lymphocytes surrounding PDAC tumors in vivo. In a preclinical study, GnP/ICBs/mC4BPA peptide treatment, but not GnP treatment, led to the accumulation of a greater number of CD8+ T cells in the periphery of PDAC tumors and to greater tumor regression than did control treatment.
These findings demonstrate that the combination of GnP therapy with C4BPA inhibits PDAC progression by promoting antitumor T cell accumulation in the tumor microenvironment.
Pancreatic ductal adenocarcinoma (PDAC) is a highly malignant tumor and is unusually resistant to chemotherapy, radiotherapy, and immunotherapy [1, 2]. PDAC exhibits the tumor microenvironment (TME) characterized by an extensive desmoplastic stroma and a cellular infiltrate composed of immunosuppressive leukocyte populations [3, 4]. We have identified a component of the complement, C4b-binding protein α-chain (C4BPA), as a novel serum biomarker for detecting PDAC at an early stage using a comprehensive proteomic approach . However, its mechanism of action remains unclear.
C4BPA is a regulatory component of the classical pathway that is synthesized by liver cells and activated monocytes [6,7,8]. CD40 belongs to the tumor necrosis factor superfamily of receptors and is mainly expressed on antigen-presenting cells (APCs) like B cells, dendritic cells, and macrophages . In malignant tumors, CD40 expression is ubiquitously observed in most B cell malignancies and various solid tumors . CD40 ligand (CD40L) is a binding partner of CD40 and is predominantly expressed on activated CD4+ T cells . The CD40–CD40L interaction between B cells and activated T cells is essential for responses to T cell-dependent antigens, including antitumor T cell activation [12,13,14,15].
As most PDACs exhibit low T cell infiltration and are designated as immunologically “cold”, single-agent immune checkpoint blockade (ICB) therapy is not effective in PDAC patients . To increase responsiveness to checkpoint blockade, there is a need to convert immunologically “cold” to “hot” tumors that have robust T cell infiltration . Agonistic CD40 monoclonal antibodies (αCD40) mimic CD40L in vivo and have been shown to enhance the immunogenicity of cancer vaccines and trigger the regression of highly immunogenic tumors [15, 18,19,20]. αCD40 can reportedly drive T cell responses, reduce tumor rejection in chemotherapy [21,22,23,24,25,26,27], and synergize with ICB [28, 29]. C4BPA directly binds to and activates CD40, and they do not compete for B cell binding because C4BPA and CD40L bind on distinct CD40 sites. Thus, C4BPA mimics CD40L in causing B cell activation .
Herein, we hypothesized that C4BPA exhibits an antitumor T cell response with the accumulation of tumor-infiltrating lymphocytes (TILs) via the C4BPA-CD40 axis in PDAC. In this study, we highlighted the role of C4BPA in the acceleration of T cell antitumor immunogenicity in the TME of PDAC. These data provide novel insight into the immunologic antitumor response in the TME of PDAC and a new platform for multidisciplinary therapeutics.
Human tissue samples
PDAC tissues were obtained from 171 consecutive patients who underwent pancreatectomy at the Department of General Surgery, Chiba University Hospital, Japan from January 2010 to December 2014. All patients were histologically diagnosed with primary invasive PDAC. Whole tissue lysates were extracted from 5 pairs of PDAC and adjacent normal pancreas tissues resected in 2019. The study protocol was approved by the Ethics Committees of Chiba University (protocol #2958) and written informed consent was obtained from each patient before operation.
Human and murine cell lines and culture conditions
The human PDAC cell lines BxPC-3, MIA PaCa-2, PANC-1, Capan-2, AsPC-1, Hs766T, CFPAC-1, and Capan-1 were obtained from the American Type Culture Collection (Manassas, VA, USA). The BxPC-3, MIA PaCa-2, PANC-1, and Hs766T cell lines and all the mouse pancreatic cell lines were cultured in Dulbecco’s modified Eagle medium (DMEM; Sigma-Aldrich, St. Louis, MO, USA) with 10% fetal bovine serum (FBS) and antibiotics (1% penicillin and streptomycin). Capan-2 cells were cultured in McCoy’s 5A Medium (Cytiva, Issaquah, WA, USA) with 10% FBS and antibiotics. AsPC-1 cells were cultured in RPMI-1640 medium (Thermo Fisher Scientific, Waltham, MA, USA) with 10% FBS and antibiotics. CFPAC-1 cells were cultured in Iscove’s modified Dulbecco’s medium (Thermo Fisher Scientific) with 10% FBS and antibiotics. Capan-1 cells were cultured in DMEM with 20% FBS and antibiotics.
Murine PanIN cells (KC), PDAC cells (KPC: KPC1 and 2), and paired metastasis (KPCLiv: KPC1Liv and KPC2Liv) cell lines were provided by Dr. Sunil Hingorani (University of Washington). In brief, a KC cell line was established from primary PanIN cells from a genetically engineered mouse model (GEMM) of PanIN (KC mouse: Pdx1-cre;LSL-KrasG12D/+) and KPC cell lines were established from primary PDAC of a GEMM of PDAC (KPC mouse: Pdx1-cre;LSL-KrasG12D/+;p53R172H/+). Further, the KPCLiv cell lines were isolated from paired liver metastases arising in KPC mice. PKCY (PKCY1 and 2) cells, derived from Pdx1-cre;LSL-KrasG12D/+;p53fl/+;R26YFP mice (PKCY mice), were provided by Dr. Andrew D. Rhim (The University of Texas MD Anderson Cancer Center).
Immunohistochemical and immunofluorescence staining
Immunostaining was performed following standard protocols. Briefly, paraffin-embedded tissue blocks were cut into sections with a thickness of 4 μm. Antigen-retrieved and protein-blocked slides were incubated with specific antibodies overnight at 4 °C. EnvisionTM+ Kits (Agilent, Santa Clara, CA, USA), VECTASTAIN® Elite® ABC Kit (Vector Laboratories, Inc., Burlingame, CA, USA) or appropriate horseradish peroxidase (HRP)-conjugated secondary antibodies were used for detecting the primary antibodies. The slides were then developed with 0.01% 3,3-diaminobenzidine. Slides were counterstained with hematoxylin and eosin (H&E) and dehydrated in ethanol and xylene. The staining patterns of C4BPA and CD40 in resected human PDAC tissues were scored as follows: low expression, staining intensity of stroma around cancer cells less than the that of islet cells (internal positive control); and high expression, staining intensity of stroma around cancer cells greater than or equal to that of islet cells. The staining patterns of CD8 in resected human PDAC tissues were scored by counting tumor stromal lymphocytes with positive staining in an average of 5 different high-power fields (HPFs) (×400). The staining patterns were classified as above and below the median (range: 2–48, median: 16, average: 17.1). The immunohistochemical staining score was evaluated independently by three investigators. The primary and secondary antibodies are listed in Supplementary Table 3.
CD40 siRNAs (CD40 siRNA1: Cat. #SI00024213, CD40 siRNA2: Cat. #SI00024227) and control siRNA (AllStars negative control siRNA) were purchased from Qiagen (Hilden, Germany). Cells (4.0 × 105) were plated in a 60-mm dish and incubated for 24 h. Cells were then treated with siRNA (5 nM final concentration) in LipofectamineTM RNAiMAX Transfection Reagent (Invitrogen, Carlsbad, CA, USA). Cells were detached and replated for the cell proliferation assay after 24 h of siRNA treatment. Protein was harvested from cells after culturing for 72, 96, 120, and 144 h.
Cell proliferation assay
Human or mouse primary pancreatic cell lines were cultured in 96-well plates and incubated in 5% CO2 at 37 °C. Cell Counting Kit-8 (CCK-8; Dojindo Laboratories, Kumamoto, Japan) was used to assess cell proliferation following the manufacturer’s protocol. The absorbance was measured on a microplate reader at a wavelength of 450 nm. Each experiment was performed independently in quadruplicate for a total of three experiments. P < 0.05 was considered statistically significant (Mann–Whitney–Wilcoxon test) and the error bars represent the standard error of the mean (SEM).
Western blot analysis
Total protein was purified from cultured cells using radioimmunoprecipitation assay (RIPA) buffer (Sigma-Aldrich) and preserved at -80 °C. Twenty micrograms of protein was loaded onto a 5–12.5% XV PANTERA Gel (DRC, Tama, Tokyo, Japan) and transferred onto a polyvinylidene difluoride membrane. The membranes were blocked at room temperature for 60 min in 5% milk in 0.1% Tris-buffered saline with Tween-20 (TBS-T). Membranes were incubated with anti-C4BPA (Abcam, Cambridge, United Kingdom), anti-CD40 (GeneTex, Irvine, CA, USA), and anti-β-actin (Cell Signaling Technology, Danvers, MA, USA) antibodies overnight at 4 °C, washed three times for 5 min each with TBS-T, and incubated with secondary antibodies. The membranes were developed using ImageQuant LAS-4000UV mini Mac (Cytiva) after immersion in the detection reagent. Western blots were quantified by densitometry analysis and normalized to β-actin using ImageJ software. A list of antibodies is shown in the Supplementary Information.
Isolation of human and murine PBMCs and culture conditions
Peripheral blood from healthy volunteers was obtained by phlebotomy in heparinized tubes. PBMCs were isolated by centrifugation on Ficoll-Paque PLUS (Cytiva), according to the manufacturer’s instructions. Cells were washed with phosphate-buffered saline (PBS) and plated in RPMI-1640 medium (Thermo Fisher Scientific) with 10% FBS and antibiotics. PBMC suspensions were aliquoted into plastic tissue culture plates and incubated for 2 h at 37 °C in a 5% CO2 incubator. After transfecting nonadherent cells and washing with PBS, the nonadherent cells (lymphocytes) were cultured for 3 days in RPMI-1640 medium (Thermo Fisher Scientific) with 10% FBS and antibiotics. The cells were supplemented with 0.5% concanavalin A as a T cell mitogen and stimulated with or without recombinant human C4BPA (rhC4BPA) (Abnova, Taipei, Taiwan, 50 ng/mL) or human CD40L (Peprotech, Rocky Hill, NJ, USA, 500 ng/mL). Differentiated CD4+ or CD8+ T cells were washed and analyzed by flow cytometry. For murine PBMCs (mPBMCs), murine peripheral blood was obtained from 12 mice by cardiac puncture. mPBMCs were isolated and cultured in the same manner as human PBMCs (hPBMCs). The culture medium was RPMI-1640 medium with 10% FBS and antibiotics, without concanavalin A, and supplemented with or without mouse C4BPA peptide.
Flow cytometry analysis
One million cells were suspended in 100 μL PBS and incubated with antibodies for 60 min on ice in the dark. The antibodies used were PerCP anti-human CD3, FITC anti-human CD4, PE anti-human CD8, PE anti-mouse CD4, and FITC anti-mouse CD8a (BioLegend, San Diego, CA, USA). After washing with PBS, the cells were resuspended in 500 μL PBS and measured using a CANTO II system (Beckton-Dickinson, Franklin Lakes, NJ, USA). All data were analyzed using FlowJo v10.7.1 software (Ashland, OR, USA).
PANC-1 and Capan-2 cells were analyzed for gemcitabine (Gem) exposure with or without rhC4BPA by Cell Counting Kit-8 and an annexin V FITC/propidium iodide double-staining method. After 24 h of siRNA treatment, the PDAC cells were exposed to rhC4BPA for 72 h and Gem for 24 h. The cells were then used to assess cell proliferation by CCK-8. Furthermore, after exposure to rhC4BPA for 54 h and Gem for 6 h, the PDAC cells were collected and subjected to flow cytometry. By using an Annexin V-FITC Apoptosis Detection Kit (Nacalai Tesque, Kyoto, Japan), the apoptotic cells were identified by flow cytometry. A minimum of 10,000 cells were analyzed. Cells were detached and replated for the cell proliferation assay after 24 h of siRNA treatment.
Orthotopic transplantation model
In the orthotopic transplantation model, 8–10-week-old female C57BL/6JJcl mice (CLEA Japan, Tokyo, Japan) were injected with 2 × 105 PKCY cells suspended in 25 μL DMEM/10% FBS into the subcapsular space of the pancreatic tail under anesthesia. The study protocols were described previously. Mice were euthanized on a predetermined day and the primary pancreatic tumor and the whole liver were removed. To define the baseline tumor volume, the mice were sacrificed 11 days after cell injection and the mean tumor volumes were measured. For histological analysis, the resected pancreas and livers were fixed in 4% paraformaldehyde for 24 h, transferred to 100% ethanol, and embedded in paraffin. Some parts of the specimens were embedded in tissue freezing medium (Tissue Tek O.C.T. compound, Sakura Finetek, Tokyo, Japan), placed in liquid nitrogen, stored at -80 °C, and sectioned (5 μm) using a cryostat (Leica, Wetzlar, Germany). The volume of the primary tumor was measured using a Vernier caliper and calculated using the following formula: π/6 × (L ×W× W), where L is the tumor at its longest, and W is the tumor at its shortest. The primary sites were analyzed by immunohistochemical staining followed by microscopic examination. The numbers of mouse CD8+ and CD4+ cells in 2 different HPFs per sample were quantified manually. The stromal expression of CD11c was assessed and divided into two groups (high and low) based on the intensity and area of expressions in the TME of murine PDAC.
Murine in vivo antibodies and drug preparation
Mice were treated intraperitoneally with αPD-1 (RMP1-14, BioXcell, Lebanon, NH, USA; 200 μg per dose), αCTLA-4 (9H10, BioXcell; 200 μg per dose), and mC4BPA peptides consisting of 30 or 54 amino acids (Toray Research Center, Tokyo, Japan; 50 μg of 30 amino acids or 100 μg of 54 amino acids). Mouse IgG2a (Agilent; 200 μg) was used as an isotope control. All antibodies were endotoxin-free. Pharmaceutical grade Gem (Yakult Pharmaceutical, Tokyo, Japan) and nab-paclitaxel (Taiho Pharmaceutical, Tokyo, Japan) powders were purchased from Chiba University Hospital and resuspended in sterile normal saline at 40 mg/mL and 5 mg/mL, respectively. The drugs were administered by intraperitoneal injection at a dose of 120 mg/kg diluted in PBS.
All statistical analyses were conducted using JMP® Pro, version 13.2.0 (SAS Institute Inc., Cary, NC, USA). Cumulative rates were calculated using the Kaplan-Meier method. The significance of differences in survival rate was analyzed by the log-rank test. Data are expressed as the mean ± standard deviation (SD) or SEM. Survival data were evaluated using univariate and multivariate Cox proportional regression analyses. Statistically significant differences were determined by Welch’s t-test, chi-square test, and Mann–Whitney–Wilcoxon test. P < 0.05 was considered statistically significant in all analyses. The asterisk (*) indicates a significant value. Each experiment was repeated at least three times.
Stromal C4BPA expression was positively correlated with TILs and is associated with a favorable prognosis in PDAC patients
To investigate C4BPA expression and localization in PDAC, immunohistochemical staining of resected human PDAC tissues was performed. C4BPA was not expressed in the PDAC tumor cells but was predominantly expressed in the stroma surrounding the PDAC cells (Fig. 1a). Based on the staining intensity of C4BPA in the stroma, PDAC samples were categorized into two groups, with 75 cases (43.9%) in the high stromal expression group and 97 cases (56.1%) in the low stromal expression group (Fig. 1a). However, there were no significant differences in various clinicopathological parameters between the high and low stromal C4BPA groups (Table 1). Kaplan-Meier analysis indicated that patients with high stromal C4BPA presented significantly longer disease-free survival (DFS) (P=0.0053) and overall survival (OS) than did those with low stromal C4BPA (P=0.0012) (Fig. 1b).
Next, as CD40 is the C4BPA receptor known to be expressed in various immunocompetent cells, we examined its expression pattern in the PDAC tissues. CD40 expression was observed in almost all PDAC cells and was observed in various quantities in the stroma of PDAC (Fig. 1c). Similar to C4BPA, stromal CD40 expression was divided into two groups based on the CD40 staining score in the PDAC stroma (high stromal CD40, n=89 [52.0%]; low stromal CD40, n=82 [48.0%]) (Fig. 1d, Supplementary Table 1). According to Kaplan-Meier analysis, the high stromal CD40 group also presented better prognosis than did the low stromal CD40 group (P=0.042) (Supplementary Fig. 1a). Notably, even though stromal CD40 expression was not correlated with stromal C4BPA expression in PDAC tissues (Fig. 1d), patients with both high stromal C4BPA and CD40 demonstrated a favorable outcome in PDAC (P=0.0005) (Fig. 1e).
One of the most crucial reactions of the host immune response against tumor cells is the accumulation of CD8+ T cells (CD8+ cells), which are considered TILs and enhance antitumor immunity. The number of CD8+ cells at the invasive front of the tumor was analyzed in resected human PDAC tissues by immunohistochemical staining (Fig. 1f, Supplementary Table 2). According to Kaplan-Meier analysis, the high CD8+ group showed better prognosis than that of the low CD8+ group (P=0.0013) (Supplementary Fig. 1b). Interestingly, stromal C4BPA expression strongly correlated with the number of CD8+ cells in primary PDAC (P=0.001) (Fig. 1g). Notably, Kaplan–Meier analysis showed that patients with high stromal C4BPA and CD8+ had a significantly longer OS than did those with lower expression (P=0.0005) (Fig. 1h). Additionally, according to Cox proportional hazard models, lymph node metastasis and low stromal C4BPA expression were independent factors in poor prognosis of patients with PDAC via multivariate analysis (Table 2). These data suggest that stromal C4BPA expression is positively correlated with TILs and that high stromal C4BPA is associated with a favorable prognosis in PDAC patients.
C4BPA is coexpressed with CD8+ T cells in the stroma surrounding PDAC cells
To validate the localization of C4BPA, CD40, and TILs in PDAC tissues, immunofluorescence staining was performed in resected PDAC tissues. Quadruple staining indicated that C4BPA, CD40, and CD8+ are coexpressed in the stroma surrounding PDAC cells (Fig. 1i–m). Taken together, these data suggest that the activation of the C4BPA-CD40 axis may facilitate an antitumor response via CD8+ T cell accumulation in the TME of PDAC. Cancer-associated fibroblasts (CAFs) are pathologically activated fibroblasts that are abundant in the stroma of PDAC. CAFs are a highly secretory cell population that plays key roles in constructing the TME and modulating its functions during tumor progression. We investigated whether C4BPA was coexpressed in CAFs expressing α-smooth muscle actin (α-SMA). Immunofluorescence staining indicated that C4BPA did not merge with α-SMA in the stroma of PDAC (Supplementary Fig. 1c). This result suggests that C4BPA is not secreted by CAFs in the TME of PDAC.
C4BPA stimulation increases the number of both CD4+ and CD8+ T cells in PBMCs
Previous reports have described that C4BPA directly binds to CD40 on dendritic cells, B cells, and macrophages, resulting in CD4+ and CD8+ T cell activation [30,31,32,33]. To confirm the effect of C4BPA on CD4+ and CD8+ T cell proliferation, PBMCs including dendritic cells, B cells, T cells, and macrophages were analyzed using flow cytometry (Fig. 2a). PBMCs were stimulated with concanavalin A and rhC4BPA or human CD40L, which was used as positive control. The number of both CD4+ and CD8+ T cells was significantly increased in the rhC4BPA group compared with that in the control and CD40L groups (Fig. 2b, c). These results indicated that C4BPA stimulation activates CD4+ and CD8+ T cell proliferation in PBMCs in vitro.
C4BPA promotes cancer cell proliferation in CD40-expressing PDAC cells
In the immunohistochemical analysis, CD40 was observed not only in stromal immunocompetent cells, but also in tumor cells of PDAC tissues. We hypothesized that C4BPA may also affect the tumor cell itself in PDAC. To clarify this hypothesis, we first confirmed C4BPA and CD40 protein expression in human PDAC cell lines. C4BPA was not expressed in human PDAC cell lines of primary and metastatic lesions or in the supernatant of cultured cells (Fig. 3a, Supplementary Fig 2a). In contrast, CD40 protein showed various amounts of expression in human PDAC cell lines (Fig. 3a). To validate the presence of C4BPA in the TME of PDAC, we extracted proteins from frozen human resected PDAC tissues. C4BPA was expressed in both PDAC lesions and adjacent normal pancreatic tissues (Fig. 3b). These data firmly support that C4BPA is expressed not in tumor cells, but in the TME of PDAC. Among all the human primary PDAC cell lines, PANC-1 and Capan-2, which are cells that highly express CD40, were used for further experiments.
To explore the relationship between CD40 and epithelial plasticity in PDAC cells, endogenous CD40 expression was suppressed by two CD40 specific siRNAs (Fig. 3c). The effect of CD40 knockdown was maintained until 6 days after the siRNA transfection (Supplementary Fig. 2b). CD40 knockdown did not affect the expressions of various representative epithelial or mesenchymal markers in PANC-1 or Capan-2 cells (Fig. 3c). This finding suggests that intrinsic CD40 expression is not involved in epithelial plasticity in PDAC cells. Next, to assess the in vitro effects of C4BPA on tumor cell proliferation that are exerted via CD40, we examined PDAC cell proliferation with CD40 knockdown. CD40 knockdown cells were obtained using CD40 siRNAs with or without rhC4BPA stimulation. The proliferation assays demonstrated that CD40 knockdown significantly decreased cell proliferation in PANC-1 and Capan-2 cells (Fig. 3d). Interestingly, rhC4BPA promoted cell proliferation in all cell lines that highly express CD40, whereas it did not alter the proliferation of CD40 knockdown cells. Additionally, rhC4BPA significantly increased cell proliferation in the high CD40 expression cell line CFPAC-1, while it did not increase proliferation in the low CD40 expression cell line MIA PaCa-2 (Supplementary Fig. 2c, d). These data revealed that C4BPA stimulation increases cell proliferation ability in CD40-expressing PDAC cells.
Combining C4BPA with Gem cancelled proliferative status by facilitating chemosensitivity in PDAC cells
The classical chemotherapeutic agent Gem was designed to impair the proliferative capacity of cancer cells by inhibiting DNA synthesis. Cancer cells with hyperproliferative capacity possibly show vulnerability to chemotherapy before acquiring chemoresistance. We examined whether C4BPA stimulation induces more sensitivity to increase the efficacy of Gem in PDAC cells. Despite an increase in cell proliferation due to C4BPA stimulation, the cytotoxic efficacy of low-dose Gem was increased, offsetting the increase in cell proliferation by C4BPA in PANC-1 and Capan-2 cells (Supplementary Fig. 3). Apoptosis is one of the major mechanisms for programmed cell death. Therefore, we next assessed whether apoptotic cell death is a canonical mechanism for increasing cytotoxicity by combining Gem and rhC4BPA. C4BPA stimulation significantly increased the number of early apoptotic cells, as demonstrated by annexin V/PI staining in PANC-1 and Capan-2 cells (Fig. 4a, b). These results suggest that C4BPA increases Gem sensitivity by driving apoptotic cell death, functioning as a chemosensitizing agent in CD40-expressing PDAC cells.
Mouse C4BPA peptide increases murine CD4+ and CD8+ T cell proliferation
C4BP consists of seven α-chain subunits and one β-chain. Structurally, heptameric C4BPA oligomerizes at the C-terminus, which contains intermolecular disulfide bridges to form the core complex . A recent report described that the C-terminus of C4BPA mediates its interaction with CD40 . Furthermore, the C-terminus domain of the alpha chain of mouse C4BP (mC4BPA) can act as an adjuvant to enhance the immune response in mice . Considering that the C-terminal C4BPA binds to CD40, we designed two mC4BPA peptides composed of 30 amino acids (mC4BPA peptide) (Fig. 5a) and 54 amino acids (named as mC4BPA peptide ) from the C-terminus of mC4BPA (Supplementary Fig 4a). To conduct functional analyses in vitro, we assessed whether mC4BPA peptide activates cellular proliferation in murine cells as well as in human cells. We initially examined mC4BPA expression in murine pancreatic neoplastic cells. Similar to human PDAC cell lines, mC4BPA expression was not observed in all murine cells (Supplementary Fig. 4b). Consistent with the results observed in humans, flow cytometry revealed that the mC4BPA peptide successfully facilitated proliferation in both mCD4+ and mCD8+ T cells (Fig. 5b–d). Additionally, mouse PDAC cells also significantly increased cell proliferation 4 days after stimulation with mC4BPA peptide (Fig. 5e). The results of these experiments using mC4BPA peptide  were similar to those observed by stimulation with the mC4BPA peptide composed of 30 amino acids (Supplementary Fig 4c–e). These results revealed that the mC4BPA peptide increases the number of T lymphocytes in mice in vitro. Thus, we selected the mC4BPA peptide composed of 30 amino acids for further in vivo experiments.
Mouse C4BPA peptide induces CD8+ T cell accumulation around PDAC tumors in an orthotopic transplantation model
Based on the in vitro findings, we conducted orthotopic transplantation of PDAC cells to assess the increase and recruitment of T lymphocytes in an in vivo experiment. After randomization at 7 days after cancer cell injection, experimental mice were treated with mC4BPA peptide twice by intraperitoneal injection (Fig. 6a). Compared to the control group, the tumor volume and the body weight showed no difference in the mC4BPA peptide group at 14 days after cell injection (Fig. 6b, Supplementary Fig 5a). Importantly, the number of CD8+ cells and CD4+ cells surrounding the PDAC tumor in the mC4BPA group were significantly higher than those in the control group (CD8+, P=0.044) (Fig. 6c, d), (CD4+, P=0.033) (Fig. 6e, f). Furthermore, the stromal expression of CD11c which is a typical mouse dendritic cell marker, was divided into two groups based on the staining intensity in the mouse PDAC stroma, the rate of high stromal CD11c (70%) was higher in the mC4BPA group compared with the control group (40%) (Supplementary Fig 5b–c). These findings implicated that mC4BPA acts on dendritic cells and fosters the accumulation of CD8+ T cells, resulting in the induction of antitumor immunogenicity in the TME of the PDAC tumor.
C4BPA is recruited to the surrounding PDAC with TILs, showing T cell antitumor immunogenicity in in vivo models
Considering the increase of cytotoxic effects induced by combining Gem with C4BPA, we conducted a preclinical trial to confirm the efficacy of Gem plus nab-paclitaxel (GnP), dual immune checkpoint blockades [ICBs; agonistic programmed cell death-1 (αPD-1) and agonistic cytotoxic T-lymphocyte-associated antigen-4 (αCTLA-4)], and mC4BPA peptide in the orthotopic transplantation model. To visualize the capture and localization of the extrinsic mC4BPA peptide in the TME of the PDAC tumor, we conjugated carboxylic acid 5 (Cy5) at the N-terminus of the mC4BPA peptide (Fig. 7a). After randomization, experimental mice were treated with standard chemotherapy, GnP, dual ICBs, and mC4BPA peptide (Fig. 7b, Supplementary Fig 6a). Immunofluorescence staining revealed that mC4BPA was abundantly expressed (Fig. 7c, d) and coexpressed with CD8+ T cells (Fig. 7e, f) in the stroma surrounding YFP-positive cancer cells. Notably, intraperitoneally injected mC4BPA peptides conjugated with Cy5 were observed in the periphery of PDAC lesions (Fig. 7g, h). Among these three experimental groups, the numbers of CD8+ cells in the GnP/ICBs/mC4BPA groups were greater than those in the control group (P=0.042) (Fig. 7i). Additionally, the numbers of CD4+ cells in the GnP/ICBs/mC4BPA group were significantly higher than those in the control group (P=0.048) (Supplementary Fig. 6b), and the rate of high stromal CD11c in the GnP/ICBs/mC4BPA group was the highest among the three groups (Supplementary Fig. 6c). These data suggest that mC4BPA facilitates the arrangement of anti-tumor immunogenicity and is accumulated to recruit cytotoxic CD8+ T cells and into the surrounding PDAC cells. Finally, we assessed and compared the antitumor efficacy of these experimental groups. Based on a comparison with the mean tumor volume (defined as the baseline) in mice that were sacrificed at 11 days after cancer cell injection, the antitumor effects of GnP/ICBs/mC4BPA peptide treatment group were evident by observing the induction of a greater number of tumor regressions among the three groups (Fig. 7j, Supplementary Fig. 6d). These results suggest that combination with classical chemotherapy, ICBs, and the mC4BPA peptide treatment impairs PDAC tumor volume in a mouse model of orthotopic transplantation.
In this study, we demonstrate that C4BPA promotes CD8+ cell proliferation, resulting in the recruitment of TILs into the TME of PDAC by activating CD40 and enhancing T cell-mediated antitumor immunity in PDAC. Furthermore, C4BPA increases the chemosensitivity of Gem by inducing apoptotic programmed cancer cell death (Fig. 8). High stromal C4BPA and CD40 expression is associated with good clinical outcomes in patients with PDAC after surgery. To our knowledge, this is the first study to show that the C4BPA-CD40 axis fosters the activation of CD8+ TILs to facilitate the antitumor effect, resulting in better prognosis in solid tumors.
The TME is thought to greatly influence cancer growth and spread, thus impacting the clinical outcome of cancer patients. The majority of PDAC displays low T cell immunogenic features with poor TILs in the TME, indicating an “immuno-escape” mechanism for evading the host immune response . Imbalanced complement activation in the TME blocks the release of immunocompetent cytokines by the antitumor CD8+ T cell responses. The roles of complement factors in cancer progression vary across cancer types, as they can promote or suppress tumor growth depending on the context . Recent evidence suggests that components of the complement cascade function in cancer cell proliferation or survival. A previous study has provided evidence that local complement activation of C3a and C5a in the TME results in an immunosuppressive response to melanoma by inhibiting CD8+ TIL function .
C4BP is primarily known as a circulating soluble inhibitor of the classical complement pathways; it physiologically regulates inflammation caused by bacterial infections . Contrary to the cancer-promoting functions of complement in tumors, we demonstrate that C4BPA mediates the recruitment of CD8+ TILs, presenting cancer-suppressive functions in the TME of PDAC. In this study, we demonstrated that C4BPA increases the cell proliferation ability of CD4+ and CD8+ T cells and PDAC cells in CD40-expressing PDAC cells. This finding suggests that C4BPA stimulation shows “a double-edged sword” effect for PDAC treatment; however, C4BPA stimulation increases Gem chemosensitivity, offsetting the increase of cell proliferation by inducing apoptosis in PDAC cells.
The loss of APCs surrounding the cancer cells in the stroma is one of the critical mechanisms that allow cancer cells to evade CD8+ T cell infiltration in PDAC. The ‘licensing’ of APC, in particular dendritic cells, results in up-regulation of membrane co-stimulatory molecules and the production of pro-inflammatory cytokines . In that case, CD40 is closely involved in the functional maturation of APC and consequently the activation of antigen-specific T cells . Recent evidence suggests that CD40 is a robust target for chemoimmunotherapy in PDAC. In mice, there is overwhelming evidence that CD40 activation enables a vaccination effect and the concomitant expansion of antigen-specific CD8+ T cells, which is dependent on CD40-expressing dendritic cells . Indeed, our in vivo study implicated that C4BPA stimulation increases dendritic cells in the stroma of PDAC. Agonistic CD40 antibody (αCD40) has been developed as an immunotherapeutic agonist to activate T cell priming in PDAC . Although tumor regressions were observed with agonistic αCD40 alone in a clinical trial of patients with metastatic PDAC, durable tumor regressions were not observed in the PDAC patients, with similar results obtained in mice [44, 45]. Mechanistically, the combination of αCD40/ICBs primed durable T cell responses, resulting in tumor regression and immunological memory . Similarly, the present study demonstrates that the combination of GnP and ICBs/mC4BPA peptide treatment facilitates tumor regression in an orthotopic transplantation model of PDAC. Taken together, these reports suggest that mC4BPA peptides contribute to enhancing T cell antitumor immunity in a manner similar to that of αCD40 and could be an attractive model for treating PDAC in the future.
The limitations of this study are that CD40-expressing immunocompetent cells in which C4BPA directly activates CD8+ T cells, such as dendritic cells or B cells, were not assessed in the PBMC experiments. Long-term survival analysis was not conducted in the in vivo GEMM using combination chemotherapy and immunomodulatory therapy (ICBs/mC4BPA peptide). Further studies are warranted to determine the antitumor effect of C4BPA and the impact of immunomodulatory therapy.
We demonstrate that the C4BPA-CD40 axis induces the activation of CD8+ TILs to exert an antitumor effect. Moreover, this axis can be targeted to improve the prognosis of PDAC patients. This study provides novel insight into complement-based combination therapy to further enhance T cell immunogenicity, presenting the possibility of its clinical application as a PDAC treatment strategy.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
α-Smooth muscle actin;
C4b-binding protein α-chain
Dulbecco’s Modified Eagle Medium
Fetal bovine serum
Hematoxylin and eosin
Human peripheral blood mononuclear cells
Immune checkpoint blockade
Mouse C4b-binding protein α-chain
Murine peripheral blood mononuclear cells
Peripheral blood mononuclear cells
Pancreatic ductal adenocarcinoma
Recombinant human C4b-binding protein α-chain
Standard error of the mean
Siegel RL, Miller KD, Jemal A. Cancer statistics, 2020. CA Cancer J Clin. 2020;70:7–30.
Ryan DP, Hong TS, Bardeesy N. Pancreatic adenocarcinoma. N Engl J Med. 2014;371:1039–49.
Clark CE, Beatty GL, Vonderheide RH. Immunosurveillance of pancreatic adenocarcinoma: insights from genetically engineered mouse models of cancer. Cancer Lett. 2009;279:1–7.
Feig C, Gopinathan A, Neesse A, Chan DS, Cook N, Tuveson DA. The pancreas cancer microenvironment. Clin Cancer Res. 2012;18:4266–76.
Sogawa K, Takano S, Iida F, Satoh M, Tsuchida S, Kawashima Y, et al. Identification of a novel serum biomarker for pancreatic cancer, C4b-binding protein a-chain (C4BPA) by quantitative proteomic analysis using tandem mass tags. Br J Cancer. 2016;115:949–56.
Kusada-Funakoshi M, Sasaki J, Takada Y, Soji T, Arakawa K. Evidence that C4b-binding protein (proline-rich protein) is synthesized by hepatocytes. Biochem Med Metab Biol. 1991;45:350–4.
Lappin DF, Whaley K. Interferon-induced transcriptional and post-transcriptional modulation of factor H and C4 binding-protein synthesis in human monocytes. Biochem J. 1990;271:767–72.
Blom AM, Villoutreix BO, Dahlback B. Complement inhibitor C4b-binding protein - friend or foe in the innate immune system? Mol Immunol. 2004;40:1333–46.
Banchereau J, Dubois B, Fayette J, Burdin N, Brière F, Miossec P, et al. Functional CD40 antigen on B cells, dendritic cells and fibroblasts. Adv Exp Med Biol. 1995;378:79–83.
Vonderheide RH. Prospect of targeting the CD40 pathway for cancer therapy. Clin Cancer Res. 2007;13:1083–8.
Lederman S, Yellin MJ, Krichevsky A, Belko J, Lee JJ, Chess L. Identification of a novel surface protein on activated CD4+ T cells that induces contact-dependent B cell differentiation (help). J Exp Med. 1992;175:1091–101.
Croft M, Siegel RM. Beyond TNF: TNF superfamily cytokines as targets for the treatment of rheumatic diseases. Nat Rev Rheumatol. 2017;13:217–33.
Foy TM, Durie FH, Noelle RJ. The expansive role of CD40 and its ligand, gp39, in immunity. Semin Immunol. 1994;6:259–66.
Splawski JB, Lipsky PE. CD40-mediated regulation of human B-cell responses. Res Immunol. 1994;145:226–34.
Sotomayor EM, Borrello I, Tubb E, Rattis FM, Bien H, Lu Z, et al. Conversion of tumor-specific CD4+ T-cell tolerance to T-cell priming through in vivo ligation of CD40. Nat Med. 1999;5:780–7.
Brahmer JR, Tykodi SS, Chow LQ, Hwu WJ, Topalian SL, Hwu P, et al. Safety and activity of anti-PD-L1 antibody in patients with advanced cancer. N Engl J Med. 2012;366:2455–65.
Sharma P, Allison JP. The future of immune checkpoint therapy. Science. 2015;348:56–61.
Diehl L, den Boer AT, Schoenberger SP, van der Voort EI, Schumacher TN, Melief CJ, et al. CD40 activation in vivo overcomes peptide-induced peripheral cytotoxic T-lymphocyte tolerance and augments anti-tumor vaccine efficacy. Nat Med. 1999;5:774–9.
French RR, Chan HT, Tutt AL, Glennie MJ. CD40 antibody evokes a cytotoxic T-cell response that eradicates lymphoma and bypasses T-cell help. Nat Med. 1999;5:548–53.
van Mierlo GJ, den Boer AT, Medema JP, van der Voort EI, Fransen MF, Offringa R, et al. CD40 stimulation leads to effective therapy of CD40(-) tumors through induction of strong systemic cytotoxic T lymphocyte immunity. Proc Natl Acad Sci U S A. 2002;99:5561–6.
Cho HI, Celis E. Optimized peptide vaccines eliciting extensive CD8 T-cell responses with therapeutic antitumor effects. Cancer Res. 2009;69:9012–9.
Ahonen CL, Wasiuk A, Fuse S, Turk MJ, Ernstoff MS, Suriawinataet AA, et al. Enhanced efficacy and reduced toxicity of multifactorial adjuvants compared with unitary adjuvants as cancer vaccines. Blood. 2008;111:3116–25.
Nowak AK, Robinson BW, Lake RA. Synergy between chemotherapy and immunotherapy in the treatment of established murine solid tumors. Cancer Res. 2003;63:4490–6.
Honeychurch J, Glennie MJ, Johnson PW, Illidge TM. Anti-CD40 monoclonal antibody therapy in combination with irradiation results in a CD8 T-cell-dependent immunity to B-cell lymphoma. Blood. 2003;102:1449–57.
Byrne KT, Vonderheide RH. CD40 stimulation obviates innate sensors and drives T cell immunity in cancer. Cell Rep. 2016;15:2719–32.
Rech AJ, Dada H, Kotzin JJ, Henao-Mejia J, Minn AJ, Twyman-Saint Victor C, et al. Radiotherapy and CD40 activation separately augment immunity to checkpoint blockade in cancer. Cancer Res. 2018;78:4282–91.
Carpenter EL, Mick R, Rüter J, Vonderheide RH. Activation of human B cells by the agonist CD40 antibody CP-870,893 and augmentation with simultaneous toll-like receptor 9 stimulation. J Transl Med. 2019;7:93.
Winograd R, Byrne KT, Evans RA, Odorizzi PM, Meyer AR, Bajor DL, et al. Induction of T-cell immunity overcomes complete resistance to PD-1 and CTLA-4 blockade and improves survival in pancreatic carcinoma. Cancer Immunol Res. 2015;3:399–411.
Li J, Byrne KT, Yan F, Yamazoe T, Chen Z, Baslan T, et al. Tumor cell-intrinsic factors underlie heterogeneity of immune cell infiltration and response to immunotherapy. Immunity. 2018;49:178–93.
Brodeur SR, Angelini F, Bacharier LB, Blom AM, Mizoguchi E, Fujiwara H, et al. C4b-binding protein (C4BP) activates B cells through the CD40 receptor. Immunity. 2003;18:837–48.
Michel NA, Zirlik A, Wolf D. CD40L and its receptors in atherothrombosis-An update. Front Cardiovasc Med. 2017;4:40.
Schoenberger SP, Toes RE, van der Voort EI, Offringa R, Melief CJ. T-cell help for cytotoxic T lymphocytes is mediated by CD40-CD40L interactions. Nature. 1998;393:480–3.
Lefrançois L, Altman JD, Williams K, Olson S. Soluble antigen and CD40 triggering are sufficient to induce primary and memory cytotoxic T cells. J Immunol. 2000;164:725–32.
Hofmeyer T, Schmelz S, Degiacomi MT, Dal Peraro M, Daneschdar M, Scrima A, et al. Arranged sevenfold: structural insights into the C-terminal oligomerization domain of human C4b-binding protein. J Mol Biol. 2013;425:1302–17.
Draper SJ, Moore AC, Goodman AL, Long CA, Holder AA, Gilbert SC, et al. Effective induction of high-titer antibodies by viral vector vaccines. Nat Med. 2008;14:819–21.
Ithier MC, Parobchak N, Yadava S, Cheng J, Wang B, Rosen T. Fetal lung C4BPA induces p100 processing in human placenta. Sci Rep. 2019;9:5519.
Karamitopoulou E. Tumour microenvironment of pancreatic cancer: immune landscape is dictated by molecular and histopathological features. Br J Cancer. 2019;121:5–14.
Shimazaki R, Takano S, Satoh M, Takada M, Miyahara Y, Sasaki K, et al. Complement factor B regulates cellular senescence and is associated with poor prognosis in pancreatic cancer. Cell Oncol (Dordr). 2021. https://doi.org/10.1007/s13402-021-00614-z.
Wang Y, Sun SN, Liu Q, Yu YY, Guo J, Wang K, et al. Autocrine complement inhibits IL10-dependent T-cell-mediated antitumor immunity to promote tumor progression. Cancer Discov. 2016;6:1022–35.
Ermert D, Blom AM. C4b-binding protein: The good, the bad and the deadly. Novel functions of an old friend. Immunol Lett. 2016;169:82–92.
Caux C, Massacrier C, Vanbervliet B, Dubois B, Van Kooten C, Durand I, et al. Activation of human dendritic cells through CD40 cross-linking. J Exp Med. 1994;180:1263–72.
Ma DY, Clark EA. The role of CD40 and CD154/CD40L in dendritic cells. Semin Immunol. 2009;21:265–72.
Vonderheide RH, Glennie MJ. Agonistic CD40 antibodies and cancer therapy. Clin Cancer Res. 2013;19:1035–43.
Beatty GL, Chiorean EG, Fishman MP, Saboury B, Teitelbaum UR, Sun W, et al. CD40 agonists alter tumor stroma and show efficacy against pancreatic carcinoma in mice and humans. Science. 2011;331:1612–6.
Beatty GL, Torigian DA, Chiorean EG, Saboury B, Brothers A, Alavi A, et al. A phase I study of an agonist CD40 monoclonal antibody (CP-870,893) in combination with gemcitabine in patients with advanced pancreatic ductal adenocarcinoma. Clin Cancer Res. 2013;19:6286–95.
Morrison AH, Diamond MS, Hay CA, Byrne KT, Vonderheide RH. Sufficiency of CD40 activation and immune checkpoint blockade for T cell priming and tumor immunity. Proc Natl Acad Sci U S A. 2020;117:8022–31.
The authors thank Dr. Reiri Shimazaki (Department of General Surgery, Chiba University, Japan) and Dr. Kazuyuki Sogawa (Department of Biochemistry, School of Life and Environmental Science, Azabu University, Japan) for their technical support in experiments. We also appreciate the technical support from Prof. Atsushi Kaneda and Dr. Genki Usui (Department of Molecular Oncology, Chiba University, Japan). We express our gratitude to the Animal Facility of Biomedical Research Center (Chiba University, Japan).
This study was supported by the Grant-in-Aid for Scientific Research (KAKENHI): “KIBAN” B: 19H03725 (ShT, MO), “KIBAN” C: 20K09073 (KS, ShT, MO), and “KIBAN” C: 19K09113 (MO, ShT, SK). This study was also supported by Japanese Foundation for Multidisciplinary Treatment of Cancer (ShT).
Ethics approval and consent to participate
The study protocol (protocol #2958) was approved by the ethics committees of Chiba University and written informed consent was obtained from each patient before surgery.
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The authors declare no conflicts of interest.
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Additional file 1: Supplementary Table 1.
Characteristics of PDAC patients in IHC analysis for stromal CD40 expression. Supplementary Table 2. Characteristics of PDAC patients in IHC analysis for stromal CD40 expression. Supplementary Table 3. List of primary and secondary antibodies.
Additional file 2: Supplementary information.
Supplementary Fig. 1. Clinical outcomes of patients with PDAC based on immunohistochemical analysis of CD40 and CD8 expression in resected human PDAC tissues. Supplementary Fig. 2. Recombinant human C4BPA stimulation increases proliferation in CD40 expressing PDAC cells. Supplementary Fig. 3. The cytotoxic efficacy in the combination of gemcitabine with C4BPA stimulation in human PDAC cells. Supplementary Fig. 4. mouse C4BPA expression and its peptide functions in mouse PDAC cells. Supplementary Fig. 5. Comparisons of mouse body weight and CD11c expression in the stroma of mPDAC tumors between mC4BPA peptide group and control group. Supplementary Fig. 6. Various parameters of the preclinical study.
Additional file 3.
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Sasaki, K., Takano, S., Tomizawa, S. et al. C4b-binding protein α-chain enhances antitumor immunity by facilitating the accumulation of tumor-infiltrating lymphocytes in the tumor microenvironment in pancreatic cancer. J Exp Clin Cancer Res 40, 212 (2021). https://doi.org/10.1186/s13046-021-02019-0
- pancreatic cancer
- T cell antitumor immunogenicity