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Clinical Significance and Therapeutic Potential of the Programmed Death-1 Ligand/Programmed Death-1 Pathway in Human Pancreatic Cancer

Authors' Affiliations: ¹ Department of Surgery, ² Second Department of Internal Medicine, ³ First Department of Internal Medicine, Nara Medical University, Nara, Japan; ⁴ Department of Immunology, Juntendo University School of Medicine; and ⁵ Department of Molecular Immunology, Graduate School, Tokyo Medical and Dental University, Tokyo, Japan

Requests for reprints: Masayuki Sho, Department of Surgery, Nara Medical University, 840 Shijo-cho, Kashihara, Nara 634-8522, Japan. Phone: 81-744-29-8863; Fax: 81-744-24-6866; E-mail: m-sho{at}naramed-u.ac.jp.

	Abstract

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Purpose: The programmed death-1 ligand/programmed death-1 (PD-L/PD-1) pathway has been recently suggested to play a pivotal role in the immune evasion of tumors from host immune system. In this study, we tried to reveal the clinical importance and therapeutic potential of the PD-L/PD-1 pathway in pancreatic cancer, which is one of the most aggressive and intractable malignant tumors.

Experimental Design: We used immunohistochemistry to investigate PD-L expression in 51 patients with pancreatic cancer who underwent surgery and explored the therapeutic efficacy of blocking the PD-L1/PD-1 pathway in murine pancreatic cancer in vivo.

Results: PD-L1–positive patients had a significantly poorer prognosis than the PD-L1–negative patients, whereas there was no significant correlation of tumor PD-L2 expression with patient survival. PD-L1 expression was inversely correlated with tumor-infiltrating T lymphocytes, particularly CD8⁺ T cells. These clinical data have suggested that the PD-L1/PD-1 pathway may be a critical regulator in human pancreatic cancer. Monoclonal antibodies against PD-L1 or PD-1 induced a substantial antitumor effect on murine pancreatic cancer in vivo. PD-L1 blockade promoted CD8⁺ T-cell infiltration into the tumor and induced local immune activation. Furthermore, the combination of anti–PD-L1 monoclonal antibody and gemcitabine exhibited a significant synergistic effect on murine pancreatic cancer and resulted in complete response without overt toxicity.

Conclusion: Our data suggest for the first time that PD-L1 status may be a new predictor of prognosis for patients with pancreatic cancer and provide the rationale for developing a novel therapy of targeting the PD-L/PD-1 pathway against this fatal disease.

Programmed death-1 (PD-1) is an immunoglobulin superfamily member related to CD28 and CTLA-4 (4–6). PD-1 is induced on T cells, B cells, and monocytes on activation. Accumulating evidence indicates that PD-1 plays a crucial role in regulating peripheral tolerance and autoimmunity (4, 7). PD-1 has two ligands: PD-1 ligand 1 (PD-L1; B7-H1) and PD-1 ligand 2 (PD-L2; B7-dendritic cells; refs. 8–12). PD-L1 and PD-L2 are involved in the negative regulation of cellular and humoral immune responses by engaging PD-1 receptor (4). PD-L1 is expressed on resting T cells, B cells, dendritic cells, and macrophages. PD-L1 is also expressed on parenchymal cells, including vascular endothelial cells and pancreatic islet cells (7). In contrast, PD-L2 is inducibly expressed only on dendritic cells and macrophages (4, 8). The distinct expression patterns of PD-L1 and PD-L2 suggest that their relative functions may depend on the tissue microenvironment (4, 7, 10). Recent studies have also shown that the PD-L/PD-1 pathway might play critical roles in tumor immunity (4, 13, 14). PD-L1 on tumors or antigen-presenting cells in tumor environment has been proposed to promote tumor growth and induce apoptosis of tumor-reactive T cells expressing PD-1 (13, 14). More recently, we and others have also shown the potential negative regulatory role for PD-L1 in clinical cancers (15–18). Thus, PD-L1 may play an important role in the immune evasion from host immune system in cancer patients. On the other hand, some studies have suggested that, in contrast to PD-L1, PD-L2 might serve as a costimulator in tumors (19, 20). They have shown that PD-L2 expression led to rapid tumor rejection by enhancing tumor-reactive T-cell priming and effector function (19). PD-L2 also augmented T helper 1 and CTL response in vivo (21). However, analysis of the clinical data on tumor PD-L2 expression has been limited at present (17).

In this study, we investigated the clinical significance of PD-L1 and PD-L2 expression in human pancreatic cancer and the therapeutic efficacy of targeting the PD-L/PD-1 pathway toward future clinical application for the treatment of pancreatic cancer.

	Materials and Methods

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Patients. We examined 51 patients with pancreatic cancer who underwent surgery at Department of Surgery, Nara Medical University, between 1996 and 2004. The median age of the patients was 63 years, with a range of 46 to 73 years. Tissues were obtained from the resected specimens and then were rapidly frozen at –80°C for storage until use. For immunohistochemistry, a part of fresh tumor tissue specimen was immediately embedded in optimum cutting temperature compound (Miles, Kankakee, IL), and frozen sections were then cut on the cryostat to thickness of 5 mm. A serial section from each specimen was stained with H&E for histologic evaluation. The median follow-up for all patients was 22 months, with a range of 3 to 91 months. Most of the patients received systemic chemotherapy after surgery. Positive surgical margin was identified in 24 (47.1%) patients and negative in 27 (52.9%).

Animal and cell line. Female C57BL/6 mice (8-12 weeks old) were obtained from CLEA Japan (Tokyo, Japan). All mice were maintained under specific pathogen-free conditions in the animal facility at Nara Medical University. All experiments were conducted under a protocol approved by our institutional review board. A murine pancreatic adenocarcinoma, PAN 02, was obtained from the DCTD Tumor Repository, National Cancer Institute (Frederick, MD). Cells were grown in RPMI 1640 supplemented with 10% heat-inactivated fetal bovine serum. To evaluate the inducible expression of PD-L1 on PAN 02, cells were treated for 72 h with recombinant murine IFN- (10 ng/mL; PharMingen, San Diego, CA). Then, PD-L1 expression was measured by fluorescence-activated cell sorting analysis.

Antibodies. Monoclonal antibodies (mAb) against human PD-L1 (MIH1, mouse immunoglobulin G1) and PD-L2 (MIH18, mouse immunoglobulin G1) were previously described (17). RMP1-14 and MIH6 against mouse PD-1 and PD-L1 (rat immunoglobulin G) were generated as previously described (10). Antihuman CD4 and CD8 T-cell mAbs were purchased from Dako Japan (Kyoto, Japan). Antimouse CD4 and CD8 T-cell mAbs and isotype immunoglobulin were purchased from PharMingen. Gemcitabine was a generous gift of Eli Lilly Japan (Kobe, Japan).

Immunohistochemistry. Immunohistochemical staining was done using Dako Envision system (Dako Japan) as previously described (17). After neutralization of endogenous peroxidase, cryostat sections on glass slides were preincubated with blocking serum and then were incubated overnight with each mAb. After three washes in PBS, the sections were incubated for 1 h with biotinylated antimouse immunoglobulin G, washed thrice with PBS, incubated with avidin-biotinated peroxidase complex for 1 h, and again washed for 10 min with PBS. Reaction products were visualized with 3,3'-diaminobenzidine tetrahydrochloride and the slides were counterstained with hematoxylin.

Evaluation of immunostaining. Immunohistochemistry for PD-L was evaluated as previously described (17). All of the immunostained sections were examined under low power (4x objective) to identify regions containing low-staining tumor cells. In case of multiple areas with low intensity, five randomly selected areas were scored, and in sections where all of the staining appeared intense, one field was selected at random. The proportion of tumor cells showing high and low staining in each selected field was determined by counting individual tumor cells at high magnification. At least 200 tumor cells were scored per x400 field. Because most prognostic factors are usually considered as dichotomized, discontinuous variables, a cutoff point was selected to give the optimal separation between low risk and high risk of the overall survival as previously described by others and us (17, 22, 23). Then, we selected 10% as cutoff point based on preliminary analysis and recent report on PD-L1 expression in human cancer (16). Specimens with a 10% PD-L–positive tumor cells were classified as positive. Immunohistochemistry for CD4⁺ and CD8⁺ T cells was evaluated. An average number of >50 accumulating CD4⁺ and CD8⁺ tumor-infiltrating T lymphocytes (TIL) per field at x200 magnification were scored. We used the mean number of infiltrating cells as a cutoff point to divide all tumors into groups as having either positive or negative infiltration by TILs in tumor tissue. Fifty-one cases were classified as having positive (150) levels of T-cell infiltration in tumor tissue and the remainder as having negative (<150) infiltration. Tumor samples were examined and classified by two observers who had no knowledge of the patients' clinical status and outcome.

Extraction of total RNAs and real-time reverse-transcriptase PCR analysis. Total RNA was isolated using the guanidine isothiocyanate method (RNeasy Protect Mini Kit, Qiagen, Tokyo, Japan) and was transcribed to cDNA using cDNA synthesis kit (Pharmacia, Piscataway, NJ) according to the manufacturer's protocol. A human tonsil tissue was used as the positive control for PD-L. Real-time quantitative PCR analysis was done by using ABI Prism 7700 sequence detector system (PE Applied Biosystems, Foster City, CA). All primer/probe sets were purchased from PE Applied Biosystems. PCR was carried out with the TaqMan Universal PCR Master Mix (PE Applied Biosystems) using 1 µL of cDNA in a 20-µL final reaction volume. The PCR thermal cycle conditions were as follows: initial step at 95°C for 10 min, followed by 40 cycles of 95°C for 15 s and 60°C for 1 min. The expression level of the housekeeping gene ß₂-microglobulin was measured as an internal reference with a standard curve to determine the integrity of template RNA for all of the specimens. The ratio of mRNA level of each gene was calculated as follows: (absolute copy number of each gene) / (absolute copy number of ß₂-microglobulin).

Animal experimental protocol. Cells (1 x 10⁶ PAN 02) were s.c. inoculated on one side of the ventral surface in the lower flank region of syngeneic C57BL/6 mice. Treatment was started 10 days later when a small palpable lump was evident, ranging from 3 to 4 mm in diameter. Some mice were injected i.p. with 0.3 mg of each mAb thrice per week. Control mice received control immunoglobulin G. Gemcitabine was given i.p. at a dose of 60 µg/g every third day. The dose was elected based on our preliminary experiments as well as previous reports in murine tumor models. Tumor size was determined by caliper measurements. At 4 weeks after tumor establishment, mice were sacrificed and tumors were taken for further analysis.

Statistical analysis. The overall cancer-specific survival time was calculated from the date of surgery to the date of death from pancreatic cancer. The significance of the difference between PD-L expression and several clinical and pathologic variables was assessed by the ² test or Mann-Whitney U test. The Kaplan-Meier method was used to estimate the probability of survival, and significance was assessed by the log-rank test. Multivariate analysis was done using the Cox regression model to study four factors (PD-L1 status, tumor status, nodal status, and metastatic status). We use the term of tumor status as T factor, nodal status as N factor, and metastatic status as M factor in tumor-node-metastasis classification, respectively. Some data in murine model were analyzed using Student's t test to determine significant differences between two different groups. P < 0.05 was considered as statistically significant.

	Results

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PD-L expression in human pancreatic cancer. Of the 51 tumors evaluated in this study, 20 (39.2%) were positive for PD-L1 expression at protein level and 31 (60.8%) were negative, whereas PD-L2 was positive in 14 (27.5%) and negative in 37 (72.5%). PD-L1 and PD-L2 were expressed mainly in the plasma membrane and cytoplasm of cancer cells (Fig. 1 ). In addition, PD-L1 and PD-L2 expression was also found in some infiltrating lymphocytes as well as stromal cells in pancreatic cancer tissue.

View larger version (131K): [in this window] [in a new window]   Fig. 1. Immunohistochemical staining of human pancreatic cancer tissue for PD-L1 and PD-L2. Representative case of PD-L1–positive (A) and PD-L2–positive (C) tumor. B and D, negative controls stained with mouse immunoglobulin G. Original magnification, x400.

View larger version (11K): [in this window] [in a new window]   Fig. 2. A, overall survival of 51 patients with pancreatic cancer in relation to tumor PD-L1 status. PD-L1–positive patients had a poorer prognosis than the PD-L1–negative patients (P = 0.016). B, overall survival of 51 patients with pancreatic cancer in relation to tumor PD-L2 status. There was no significant difference in prognosis between PD-L2–positive and PD-L2–negative patients (P = 0.297).

View larger version (20K): [in this window] [in a new window]   Fig. 3. Therapeutic efficacy of PD-L1/PD-1 blockade in murine pancreatic cancer. A, expression of PD-L1 on murine pancreatic cancer cells, PAN 02. IFN- stimulation for 3 d in vitro induced its high expression (>95%) as estimated by flow cytometric analysis. Dashed line, negative control; thin line, naïve PAN 02; bold line, PAN 02 stimulated with IFN-. B, PD-L1 or PD-1 blockade induced significant antitumor effect and inhibited tumor growth. Mice were treated with anti–PD-L1 or anti–PD-1 mAb at a dose of 0.3 mg thrice per week for 4 wk. Tumor size at 4 wk after tumor establishment: anti–PD-L1 mAb, 6.3 ± 1.0 mm, n = 5; anti–PD-1 mAb, 6.0 ± 0.8 mm, n = 5; P = 0.0087 and P = 0.0025, respectively, compared with controls (9.0 ± 0.4 mm, n = 10). Points, mean maximal tumor size; bars, SE. C, immunohistochemical staining of CD8+ T cells in tumor tissue at 4 wk after tumor establishment. Representative pictures of three mice for each treatment. PD-L1 blockade induced massive CD8+ T-cell infiltration (magnification: top right, x100; bottom right, x400) compared with controls (top left, x100; bottom left, x400). D, induction of local immune activation by PD-L1 blockade. The expressions of IFN-, granzyme B, and perforin were significantly higher in tumors treated with anti–PD-L1 mAb than in controls (P = 0.030, P = 0.015, and P = 0.012, respectively). Points, mean of real-time PCR data from three individual mice for each group; bars, SE.

View larger version (14K): [in this window] [in a new window]   Fig. 4. Combination of PD-L1 blockade and gemcitabine. A, gemcitabine and delayed PD-L1 blockade significantly inhibited tumor growth of pancreatic cancer. Gemcitabine was given i.p. on days 1, 4, 7, 10, and 13 at a dose of 60 µg/g. Anti–PD-L1 mAb was given at a dose of 0.3 mg on days 15, 17, 19, 22, 24, and 26. Tumor size at 4 wk after tumor establishment: gemcitabine + anti–PD-L1 mAb, 5.8 ± 0.2 mm; P = 0.0077, versus gemcitabine alone, 6.8 ± 0.2 mm; P < 0.0001, versus anti–PD-L1 mAb alone, 9.0 ± 0.3 mm. B, gemcitabine and simultaneous PD-L1 blockade had a synergistic antitumor effect and resulted in complete response in treated mice. Anti–PD-L1 mAb was given at a dose of 0.3 mg for thrice per week for 4 wk. Tumor size at 4 wk after tumor establishment: gemcitabine + anti–PD-L1 mAb, 1.2 ± 0.2 mm; P < 0.0001, versus gemcitabine alone, 6.8 ± 0.2 mm; P = 0.001, versus anti–PD-L1 mAb alone, 6.2 ± 1.0 mm. Points, mean tumor size of five mice; bars, SE.

	Discussion

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In this study, we first investigated the tumor PD-L expression in human pancreatic cancer. Then we confirmed both PD-L1 and PD-L2 expression in several pancreatic cancer tissues and found that tumor PD-L1 but not PD-L2 expression significantly correlated with postoperative prognosis. We also found that PD-L1 expression was inversely correlated with TILs, particularly CD8⁺ T cells. Furthermore, the subgroup analysis has indicated the significance of PD-L1 in early stage including N₀ and M₀ status, suggesting that PD-L1 might play more important role in tumor progression rather than in tumor metastasis of pancreatic cancer. Our in vivo study in murine pancreatic cancer model may further support that PD-L1 is a critical regulator in tumor growth of pancreatic cancer. In our previous study, in contrast to pancreatic cancer, both PD-L1 and PD-L2 status had a significant effect in advanced stage of esophageal cancer with positive lymph node and distant metastasis (17). Such differences between pancreatic and esophageal cancer may depend on tumor biology and malignancy of each cancer. Taken together with other recent studies, this study might further corroborate that tumor-associated PD-L expression plays a critical role in human cancers (15–18).

Next, using a murine pancreatic cancer model, we investigated the therapeutic efficacy of blocking the PD-L1/PD-1 pathway in pancreatic cancer toward future clinical application. Then, we found several important data in this model. First, both anti–PD-1 and anti–PD-L1 mAbs had a significant antitumor effect on the inhibition of tumor growth, suggesting that the PD-L1/PD-1 pathway is critical for growth of pancreatic cancer. Our data corroborate several previous studies and strengthen the therapeutic potential of targeting the PD-L1/PD-1 pathway for the treatment of cancer patients (13, 24–27). Second, we confirmed that PD-L1 blockade promoted tumor-reactive CD8⁺ T-cell infiltration into the established tumor, thereby resulting in local immune activation as evidenced by the up-regulation of several potent effectors including IFN-, granzyme B, and perforin. However, further studies may be required to clarify the therapeutic effect of PD-L1/PD-1 blockade on the metastasis of pancreatic cancer using other cancer metastasis models because metastasis and metastatic relapse are the most frequent causes of cancer-related death in pancreatic cancer (1, 3, 28). Third, more importantly, data indicated that the combination of gemcitabine with PD-L1 blockade exerted a synergistic antitumor effect on pancreatic cancer. Chemotherapy and immunotherapy have usually been regarded as unrelated or potentially antagonistic forms of therapy (29). This is because most chemotherapies kill target cells by apoptosis and similarly induce cell death of activated T cells by recognizing tumor antigen. In addition, lymphopenia is a common side effect of many anticancer drugs, and this has been assumed to be detrimental to sufficient antitumor immune response. Our data showed that the delayed PD-L1 blockade following preceding gemcitabine treatment significantly augmented antitumor efficacy. Furthermore, the combination of gemcitabine with simultaneous blockade of PD-L1 has exerted a significant synergistic effect on pancreatic cancer and induced complete response without overt toxicity. Gemcitabine is currently the standard chemotherapeutic agent for pancreatic cancer because several clinical trials have proved the some favorable effect on patient survival (1, 30). However, the effect of gemcitabine alone is limited and most patients develop resistance to the therapy. Therefore, gemcitabine in combination with other approaches is currently under investigation (26, 30). Thus, our data may be clinically important and support future application of PD-L1/PD-1 blockade for the treatment of pancreatic cancer.

In conclusion, we have shown for the first time that PD-L1 is a novel prognostic marker for human pancreatic cancer. Furthermore, our data have indicated that targeting PD-L1/PD-1, especially in combination with standard chemotherapy, exhibited significant therapeutic efficacy. Little change in pancreatic cancer mortality for decades has created an urgent demand for the development of new strategies directed toward novel targets. Our data may provide the rationale of developing a novel immunotherapy targeting the PD-L1/PD-1 pathway for this fatal malignant disease.

	Footnotes

 
Grant support: Grants-in-Aid 16591343 for Scientific Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan; Research Grant from Pancreas Research Foundation of Japan; Research Grant from Foundation for Promotion of Cancer Research in Japan; and Research Grant from Daiwa Securities Health Foundation (M. Sho).

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.

Received 11/17/06; revised 12/17/06; accepted 12/28/06.

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This Article Abstract Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Nomi, T. Articles by Nakajima, Y. Search for Related Content PubMed PubMed Citation Articles by Nomi, T. Articles by Nakajima, Y.