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Interleukin-27 Signaling Promotes Immunity against Endogenously Arising Murine Tumors

  • Karlo D. T. Natividad,

    Affiliation Immunological Diseases Division, Garvan Institute of Medical Research, Sydney, New South Wales, Australia

  • Simon R. Junankar,

    Affiliation Cancer Division, Garvan Institute of Medical Research, Sydney, New South Wales, Australia

  • Norhanani Mohd Redzwan,

    Affiliation Immunological Diseases Division, Garvan Institute of Medical Research, Sydney, New South Wales, Australia

  • Radhika Nair,

    Affiliation Cancer Division, Garvan Institute of Medical Research, Sydney, New South Wales, Australia

  • Rushika C. Wirasinha,

    Affiliation Immunological Diseases Division, Garvan Institute of Medical Research, Sydney, New South Wales, Australia

  • Cecile King,

    Affiliations Immunological Diseases Division, Garvan Institute of Medical Research, Sydney, New South Wales, Australia, St. Vincent's Clinical School, University of New South Wales, Sydney, New South Wales, Australia

  • Robert Brink,

    Affiliations Immunological Diseases Division, Garvan Institute of Medical Research, Sydney, New South Wales, Australia, St. Vincent's Clinical School, University of New South Wales, Sydney, New South Wales, Australia

  • Alexander Swarbrick,

    Affiliations Cancer Division, Garvan Institute of Medical Research, Sydney, New South Wales, Australia, St. Vincent's Clinical School, University of New South Wales, Sydney, New South Wales, Australia

  • Marcel Batten

    Affiliations Immunological Diseases Division, Garvan Institute of Medical Research, Sydney, New South Wales, Australia, St. Vincent's Clinical School, University of New South Wales, Sydney, New South Wales, Australia

Interleukin-27 Signaling Promotes Immunity against Endogenously Arising Murine Tumors

  • Karlo D. T. Natividad, 
  • Simon R. Junankar, 
  • Norhanani Mohd Redzwan, 
  • Radhika Nair, 
  • Rushika C. Wirasinha, 
  • Cecile King, 
  • Robert Brink, 
  • Alexander Swarbrick, 
  • Marcel Batten


Interleukin-27 (IL-27) is a pleiotropic cytokine but its immunosuppressive effects predominate during many in vivo immunological challenges. Despite this, evidence from tumor cell line transfer models suggested that IL-27 could promote immune responses in the tumor context. However, the role of IL-27 in immunity against tumors that develop in situ and in tumor immunosurveillance remain undefined. In this study, we demonstrate that tumor development and growth are accelerated in IL-27 receptor α (Il27ra)-deficient mice. Enhanced tumor growth in both carcinogen-induced fibrosarcoma and oncogene-driven mammary carcinoma was associated with decreased interferon-γ production by CD4 and CD8 T cells and increased numbers of regulatory T-cells (Treg). This is the first study to show that IL-27 promotes protective immune responses against endogenous tumors, which is critical as the basis for future development of an IL-27 based therapeutic agent.


Tumor immunosurveillance and anti-tumor immune responses are now appreciated to be an important mechanism for protection against the emergence and growth of tumors. The importance of immune mediated protection against cancer is demonstrated by the enhanced rates of tumor initiation and growth in immune compromised patients and mice [1]. However, it is clear that inflammation and antigen specific adaptive immunity can have both pro- and anti-tumorigenic effects [1], [2]. Thus, the type of response elicited is critical in determining the outcomes for tumor growth. In general, a T helper Type 1 (TH1) response, with accompanying IFN-γ production and cytotoxic T and NK cell activation, is associated with effective anti-tumor immune activity while TH2 and TH17 responses are pro-tumorigenic [2]. Regulatory T cells (Treg) actively inhibit anti-tumor responses and high levels of Treg cells in patients correlate with poor prognosis in multiple cancer types [3], [4]. Thus, therapeutics that enhance TH1 responses or inhibit Treg cell activity are actively being sought for cancer treatment.

IL-27 is a heterodimeric cytokine (IL-27p28:Ebi3) expressed by activated antigen presenting cells, which has sequence and structural similarity to IL-6, IL-23 and IL-12 [5]. IL-27 signals through a heterodimeric receptor, consisting of gp130 and IL-27rα, that is expressed by most hematopoietic cells [5], [6]. However, it is the regulation of T helper cell differentiation and function that appears to be the major biological function of IL-27. Analogous to IL-12, IL-27 promotes the differentiation of TH1 cells through activation of STAT1, induction of T-bet and the synthesis of IFN-γ [7], [8]. Meanwhile, it suppresses TH2 and TH17 differentiation [9], [10]. We and others have found that IL-27 can also potently suppress the differentiation of inducible Treg cells [11], [12]. Taken together, these properties of IL-27 suggest it could enhance anti-tumor immunity by both promoting beneficial TH1 responses and suppressing Treg activity.

Consistent with this proposition, a number of reports have suggested that IL-27 can promote anti-tumor cell line immune responses. These studies indicate IL-27 may act via a variety of mechanisms, including increasing IFN-γ production, promoting cytotoxic T cell and/or NK cell activity, inhibiting COX-2 expression or decreasing Treg cell numbers [13], [14]. In each case, however, these studies have relied on transplanted cell line models and most have used forced expression of recombinant IL-27, or its receptor, ectopically in tumor cells lines [13][19]. In other words, previous work has been limited to studying late stage tumor cell expansion and excluded the processes of tumorigenesis and early stage neoplasia where immunosurveillance and immunoediting occur. Tumor cell lines, derived from established tumors, have already escaped host immunity in the originating mouse and have therefore already undergone cancer immunoediting. They are therefore likely to have different immunogenicity compared with tumors that develop in situ. Analysis of the effects of physiological IL-27 signaling on endogenously arising, heterogeneous tumors is required to properly assess the anti-tumor potential of this cytokine.

Here, we test the initiation and growth of carcinogen-induced fibrosarcomas and oncogene-driven mammary carcinomas in Il27ra deficient mice. Our data demonstrate that loss of IL-27 signaling leads to earlier emergence and more rapid growth of tumors. In addition, loss of IL-27 signaling results in reduced production of IFN-γ by CD4+ T cells and enhanced generation of regulatory T cells, effects which can inhibit an effective anti-tumor response. Our data therefore indicate a prominent role for IL-27 signaling in controlling physiologically arising tumors.

Materials and Methods

Ethics Statement

Mouse experimentation was carried out at the Garvan Institute of Medical Research and was handled in accordance with the Garvan Institute of Medical Research and St. Vincent's Hospital Animal Experimentation Ethics Committee, this study was specifically approved by that body (approval number 10/06).


Il27ra/ mice, Il27ra+/+ mice [20] (C57BL/6 background, n>36) and C57BL6 mouse mammary epithelial cell (MMEC) donors were bred and housed in specific pathogen free conditions at the Garvan Institute of Medical Research. Adult mice (8–12 wk old) were used in all experiments.

MCA-induced sarcoma model

Male Il27ra+/+ and Il27ra/ mice were inoculated s.c. in the right hind flank with a single dose of 100 μl of corn oil containing 25 μg or 10 μg of 3-methylcholanthrene (MCA) (Sigma-Aldrich). Mice were examined weekly for tumor development and subcutaneous tumor size were measured using calipers fitted with a vernier scale. Tumor diameter was calculated based on the average of two perpendicular measurements ([L+W]/2). When tumors reach >11 mm in diameter, mice were sacrificed and tumor tissues removed and processed for histological analysis.

Polyoma middle T antigen (PyMT) driven-carcinoma model

PyMT expression was induced in primary MMEC isolated from C57BL6 mice by viral transduction of the pMIG-PyMT-IRES-GFP (pMIG-PyMT) construct as described previously [21], [22]. Infected MMECs (1.5×105 cells in 10 μl PBS) were transplanted into the 4th mammary fat pad of virgin female Il27ra+/+ and Il27ra−/− mice. Tumor development was monitored by in vivo GFP imaging using the IVIS lumina II (Perkin Elmer) and measurement of palpable tumors for 280 days. For tumor transplant experiments, primary tumors were resected and cut into approx 1 mm3 pieces, which were surgically transplanted into the 4th mammary fat pad of recipient female Il27ra+/+ and Il27ra/ mice.

Flow cytometry

Single cell suspensions were made from spleens, tumor draining lymph nodes (TDLN; inguinal LN proximal to the tumor site), NDLN (contra-lateral inguinal LN) by mechanical disruption. Cells were stained for surface protein expression using the following Abs: anti-CD4 (RM4.5, BD), anti-CD8 (53-6.7, BD), anti-CD44 (IM7, eBioscience), anti-CD25 (PC61.5, eBioscience) and intracellularly stained with anti-FoxP3 (FJK-16s, eBioscience). Data for Foxp3+ cells is given as a percentage of CD4+CD25+ T cells. To assay in vitro cytokine production, cells were stimulated with PMA (50 ng/ml) and Ionomycin (500 ng/ml) for 5 hours with protein transport inhibitor (BD GolgiStop). Expression of cytokines was detected by intracellular staining using the following antibodies: anti-IFN-γ (XMG1.2, BD), anti-IL17 (17B7, eBioscience), anti-IL10 (JES5-16E3, Biolegend) and anti-IL4 (11B11, eBioscience), and data are given as a percentage of cytokine producing cells in the CD4+CD44+ gate.


Paraffin embedded tumors were sectioned (5 μm) and stained using purified anti-mouse/rat FoxP3 (FJK-16s, eBioscience) and Biotin-SP conjugated Fab goat anti-rat IgG (Jackson ImmunoResearch). Immunodetection was performed using Vectastain Elite ABC kit (Vector Laboratories) according to the recommendations of the manufacturer. Treg cells were quantified by an observer, blinded to the genotype of the mice, by counting FoxP3+ cells in 5 independent fields of view (100× magnification) for each tumor section.

Statistical Analysis

To determine the significance of differences in time to tumor incidence, a log-rank (Mantel-Cox) test was used. For comparing differences between genotypes at a single point in time, a two-tailed Student's t-test was used. P<0.05 was considered significant.


Loss of IL-27 signaling leads to accelerated development of carcinogen-induced fibrosarcomas

To assess the role of endogenous IL-27 in tumor development, mice with a genetic deletion of the IL-27 receptor alpha chain (Il27ra−/−) were used. These mice display no overt abnormalities and have been used extensively to study the effects of IL-27 on the immune system [9], [20], [23].

Carcinogen-induced tumors allow analysis of spontaneous tumor initiation and growth without the introduction of new cells or genetic material. The 3-Methylcholanthrene (MCA)-induced fibrosarcama model has been used extensively to characterize immune-mediated control of tumor initiation and progression [1]. We therefore examined the effect of IL-27 signaling on MCA-induced fibrosarcoma development by administering MCA to groups of Il27ra+/+ or Il27ra/ mice. After injection of 10 μg MCA, palpable tumors were observed in 70% of Il27ra+/+ controls (n = 10) and 90% of Il27ra/ mice (n = 11) over the course of 20 weeks (Fig. 1 A–C). Tumor development occurred significantly earlier in Il27ra/ mice, with median disease free survival of 11 weeks, compared with 16.5 weeks in Il27ra+/+ mice (Fig. 1A–C). At a higher MCA dosage of 25 μg per mouse, 84% (n = 19) of Il27ra−/− mice developed sarcoma compared to 68% (n = 19) from Il27ra+/+ mice. Again, sarcomas appeared slightly earlier in the Il27ra−/− mice (Fig 1D), although the difference did not reach statistical significance at this dose. Previous studies have also observed that the immune dependent protection is lost at higher doses of MCA [24]. These data show that IL-27 signaling plays a protective role, and point to important effects in the tumor initiation phase after carcinogen exposure.

Figure 1. Rapid development of MCA-induced fibrosarcoma in Il27ra-deficient mice.

Groups of Il27ra+/+ (filled grey circles) and Il27ra−/− (open black squares) mice were treated with a single dose of 10 µg (A, B & C) or 25 µg (D) of MCA and tumor development was monitored weekly for 20 weeks. Tumors >3 mm in mean diameter and progressively growing were scored positive. (A & B) tumor growth curves of individual Il27ra+/+ (A) and Il27ra−/− (B) mice with sarcoma. (C & D) cumulative incidence (%) in groups of mice injected with 10 μg (C; Il27ra+/+ n = 10, Il27ra −/− n = 11, data are representative of 2 independent experiments) and 25 μg (D; data from 2 experiments are combined to give n = 19 per group) of MCA respectively. The overall tumor incidence is indicated. * p<.05 (Log-rank test).

Loss of IL-27 signaling leads to accelerated development and growth of mammary carcinomas

Breast cancer is the most common cancer in women worldwide, comprising 16% of all female cancers (WHO). We therefore wished to test the effect of IL-27 signaling in a model of mammary carcinoma. A polyoma middle T (PyMT) induced mammary carcinoma model was used, wherein the expression of PyMT oncogene specifically in the mammary gland is achieved by retroviral transduction of primary mouse mammary epithelial cells (MMECs). Mammary neoplasias arise in this model through a process bearing close similarity with human breast cancer initiation [25].

Il27ra+/+ and Il27ra−/− mice were transplanted with primary C57BL6 MMECs transduced with pMIG-PyMT, encoding GFP as a reporter. Since we were interested in the kinetics of tumor initiation, we used the encoded GFP reporter to sensitively detect the emergence of tumors. In line with our observations in the carcinogen-induced model, palpable tumors (Fig. 2A,B) and GFP signal (Fig. 2 C,D and Fig. S1) were detected earlier in Il27ra−/− compared to Il27ra+/+ mice. After 280 days, palpable tumor incidence in both Il27ra+/+ and Il27ra−/− mice reached 55%. Amongst mice that developed tumors, the time to GFP detection was significantly earlier in the Il27ra−/− group (Fig. 2D). Two tumors, both arising late in the study, could not be detected by in vivo imaging. The lateness of detection may reflect that the tumors were deep in the tissue where GFP, having low tissue penetrance, was not detectable.

Figure 2. Accelerated development and growth of PyMT-induced mammary tumors in Il27ra-deficient mice.

(A-D) WT mouse mammary epithelial cells (MMECs), retrovirally transduced with the pMIG-PyMT vector were transplanted to Il27ra+/+ (filled grey circles) and Il27ra−/− (open black squares) hosts (n = 9/group). Tumor development and growth was monitored by in vivo GFP imaging and measurement of palpable tumors using Vernier calipers for 280 days. (A & B) tumor growth, as measured by calipers, of individual Il27ra+/+ mice (A) and Il27ra−/− mice (B) with palpable mammary tumor. (C) cumulative % of mice with a detectable GFP signal in the mammary gland. (D) Average days to tumor detection (GFP) for mice that developed tumors for each genotype. (E) Primary mammary tumors that arose after implantation of pMIG-PyMT transduced tissue were excised and dissected into pieces (∼1 mm3) and surgically transplanted into groups of Il27ra+/+ and Il27ra−/− mice (n = 5/group/time point). Mean tumor diameter (mm) at harvest, 14 and 28 days p.t., is shown. * p<.05 (unpaired t tests). Data presented are from one of three independent studies.

Due to the heterogeneity of mammary carcinoma appearance in this model (between 67 and 258 days p.t.), comparison of the immune phenotypes between the experimental groups could not be achieved at a common time point. We therefore tested the growth of established primary mammary carcinomas upon direct transfer to naive Il27ra+/+ and Il27ra−/− hosts. Mice were sacrificed at days 14 and 28 days post-transplant (p.t.). Tumors implanted into Il27ra−/− grew significantly more rapidly compared to WT mice, with 4-fold and 3.15-fold larger tumors on average observed in Il27ra−/− mice at 14 and 28 days, respectively (Fig. 2E). This data show that IL-27 signaling plays an important role in protection against tumor growth in this mammary carcinoma model, as well as during carcinogen-induced tumorigenesis. Since IL-27 receptor is expressed predominantly on leukocytes and since IL-27 signaling is intact on the WT MMEC tumor tissue, enhanced tumor growth in Il27ra−/− mice can be attributed to reduced effectiveness of the anti-tumor immune response. The early tumor induction observed in Il27ra−/− mice in both cancer models suggests that IL-27 signals play an important role in immunosurveillance during neoplasia. Accelerated growth of established tumor tissue in the mammary tumor transplant model (Fig. 2E) suggests that IL-27 signals can contribute to anti-tumor responses during carcinoma growth, as well as influencing tumor initiation.

Reduced IFN-γ production in tumor bearing Il27ra/ mice

In order to compare the immune responses occurring in Il27ra+/+ and Il27ra/ animals, it is necessary to choose a common time point. The rapid emergence of MCA-induced tumors in Il27ra/ mice, and subsequent euthanasia, meant that a suitable time point could not be found using a 10 µg dose of MCA. We therefore examined the immune phenotype of mice injected with 25 µg MCA at 14 weeks post-induction, a time at which the majority of mice injected had developed palpable sarcomas (Fig. 1D). To overcome the kinetic heterogeneity of primary PyMT driven mammary carcinoma development (Fig. 2 A–B), transplantation of primary tumor into recipient mice (Fig. 2E) was used for analysis of the immune phenotype.

To examine the immunological effects of the loss of IL-27 signaling during the anti-tumor response, we isolated TDLN, NDLN and spleens from tumor bearing Il27ra+/+ and Il27ra−/− mice. A panel of immune cell subset markers was assessed by flow cytometry. No significant differences were observed in the total percentages or cell numbers of naïve, effector or central memory CD4 or CD8 T cells (based on CD62L and CD44 expression; NK cells (NK1.1+TCRβ); NKT cells (CD1d-tetramer+TCRβ+), CD11c+, CD11b+ or GR1+ granulocytes, nor myeloid suppressor cells (CD11b+ GR1+)(d.n.s.).

Cytokine production by T cells from Il27ra+/+ and Il27ra−/− tumor bearing mice was assessed by flow cytometry. Since the tumor antigens are not known in these spontaneously arising tumors, PMA and Ionomycin were used to polyclonally restimulate previously activated T cells. IFN-γ production was found to be significantly reduced in the CD4+CD44+ T cell compartment in Il27ra−/− compared to Il27ra+/+ mice in both the fibrosarcoma (Fig. 3A, B) and mammary carcinoma models (Fig. 3C). The caveat of polyclonal restimunation is that non-specific antigen experienced cells were also activated. However, increased percentages of total CD44+ T cells observed in the TDLN compared with NDLN (d.n.s) suggest that tumor specific responses were occurring. This data are in line with previous reports that IL-27 can promote TH1 responses and that IFN-γ levels are reduced in Il27ra−/− mice during certain immunological challenges [26][29]. Decreased percentages of IFN-γ producing cells were also observed in the CD8+ compartment of Il27ra−/− mice, although the magnitude of this reduction was diminished compared with the CD4 compartment (Fig. 3 D,E).

Figure 3. Reduced IFN-γ production by activated CD4+ T cells in tumor bearing Il27ra-deficient mice.

(A, B, D, F–H) Fibrosarcomas were induced in Il27ra+/+ (grey bars) and Il27ra−/− (black bars) by injecting 25 µg of MCA s.c.. 14 wk after tumor induction, lymphocytes from spleen, tumor draining LN (TDLN; inguinal) and non tumor draining LN (NDLN; contralateral inguinal) of tumor bearing mice were harvested (n = 6 per genotype). (C, E) PyMT-driven mammary carcinoma cells were transplanted into Il27ra+/+ (grey bars) and Il27ra−/− (black bars) mice. 32 days after tumor transplantation, lymphocytes from spleen, TDLN and NDLN of tumor bearing mice were harvested (n = 3 per genotype). Cells were re-stimulated with PMA and ionomycin for 5 hours in the presence of a protein transport inhibitor then IFNγ, IL-4, IL-10 and IL-17 production was determined by flow cytometry. (A) Representative cytometry plots illustrating IFNγ versus CD44 expression. (B-H) The percentage of cytokine (as indicated) producing cells in the CD4+ CD44hi gate (B, C, F-H) or the CD8+ CD44hi gate (D, E) is shown. Error bars indicate SEM. * p<.05, ** p<.01, *** p<.001 (unpaired t tests). Each dataset is representative of two independent studies.

IL-27 has also been shown to enhance IL-10 production and negatively regulate IL-4 and IL-17 [5], [10], however, subtle effects of Il27ra genotype were observed for these cytokines in the tumor models. The TH2 associated cytokine IL-4 was found to be produced by a significantly higher proportion of Il27ra−/− CD4+ T cells in the TDLN, and numbers of splenic IL-10 producing cells were significantly reduced, when MCA-induced fibrosarcoma bearing mice were analyzed (Fig. 3 F,G), while IL-17 producing CD4+ T cells remained unchanged (Fig 3H). Thus the major difference in cytokine expression appears to be in the IFN-γ production by the CD4+ T helper subset.

Increased Treg cells in tumor tissue and lymphoid organs of Il27ra/ mice

Treg cells are CD4+ T cells that actively suppress the function of effector T cells, and are usually defined based on expression of the transcription factor Foxp3. In the MCA fibrosarcoma model, Treg cells have been demonstrated to suppress the anti-tumor response, allowing accelerated tumor growth [30], [31]. We have recently shown that Il27ra−/− CD4+ T cells show a greater propensity to differentiate into Treg cells after activation [11]. We therefore investigated Treg cells in tumor bearing mice.

Immunohistochemical analysis of FoxP3+ cells within MCA tumor tissues revealed an average 2-fold increased Treg numbers in Il27ra−/− compared to Il27ra+/+ mice (Fig. 4 A,B). In addition, significantly increased Treg cell percentages were observed in TDLN (day 28; Fig. 4C) and in the spleen (Fig. 4D) of Il27ra−/− mice with PyMT tumor transplants, compared to Il27ra+/+ controls. The lack of an observed difference in Treg numbers in the non-draining LN (Fig. 4E), distant from the immune activation site, as well as the observation that Treg percentages are not altered in unchallenged or mock-transplanted Il27ra−/− mice ([11] and d.n.s.) suggest that changes in Treg percentage are in direct response to the tumor challenge. These data indicate that Treg numbers are controlled by IL-27 signaling in tumor tissues and peripheral lymphoid organs during anti-tumor immune responses. This finding is consistent with the observed increase in tumor growth and with our previous work showing that Il27ra−/− T cells more readily differentiate into Treg [11].

Figure 4. Increased percentage of Treg cells in Il27ra-deficient mice.

(A & B) tumors induced by injection of 25 µg of MCA into Il27ra+/+ and Il27ra−/− were harvested at 14 weeks post-induction and 5 µm sections analyzed by immunohistochemistry to detect FoxP3+ cells. (A) Representative photographs (magnification = 100×) of tumor sections stained with FoxP3 (brown). (B) The average Foxp3+ cells per field of view, over 5 fields of view per mouse, is indicated (n = 7 per group). Bars indicate the average of 7/8 mice per genotype. (C-E) 14 or 28 days after PyMT tumor transplant (as indicated), lymphocytes from Il27ra+/+ (filled grey circles) and Il27ra−/− (open black squares) host spleen, TDLN and NDLN were harvested. Single cell preparations were stained with antibodies against CD4, CD25 and Foxp3 for flow cytometry. The percentage of FoxP3+CD25+ cells in the CD4+ compartment is shown for (C) TDLN, (D) spleen and (E) non-tumor draining lymph node. n = 5 per group *p<.05, **p<.01, ***p<.001 (unpaired t test).


Our data demonstrate that IL-27 signaling enhances the anti-tumor immune response during in vivo development and growth of two diverse tumor types. MCA-induced fibrosarcoma and PyMT-driven mammary carcinoma development are accelerated in Il27ra-deficient mice and are accompanied by reduced IFN-γ production and increased percentages (and numbers) of Treg cells.

The importance of investigating the role of cytokines in a physiological context is illustrated in the case of IL-27 family member IL-23. Strategies testing rIL-23 overexpression in tumor cells resulted in enhanced anti-tumor responses and inhibited cancer progression, analogous to IL-12 and IL-27 [17]. However, studies involving carcinogen-induced tumors (TPA-induced skin papillomas) or syngenic tumor transplants into IL-23 deficient mice clearly showed that they were resistant to tumor development, leading to the current consensus, that IL-23 is in fact pro-tumorigenic [32], [33]. Moreover, studying tumors that arise in situ is necessary to understand the process of immunosurveillance. Established tumor derived cell lines have already escaped host immunity and are therefore likely to have pre-altered immunogenicity. Thus, analysis on the role of physiological IL-27 signaling on endogenously arising tumors is paramount to properly assess the anti-tumor potential of this cytokine.

The MCA-induced fibrosarcoma model has been used extensively to characterize immune-mediated control of tumor initiation and progression [1]. Many immune mediators have been demonstrated to influence tumor development and progression in this model. IL-27 protein family members IL-12 and IL-23 have been shown to have important, although opposing, effects on tumor development in this model [33], [34]. It is known that loss of TH1 associated signals, such as IFN-γ, IFN receptors, STAT-1, and IL-12p40, lead to increased susceptibility to MCA induced fibrosarcomas. Recently, Treg cells have been shown to have a deleterious effect on the response to these tumors, with Treg depletion resulting in reduced tumor development and even eradication of some established tumors [30], [31]. Thus, the loss of IFN-γ production and the increased development of Treg cells in Il27ra deficient mice fits well with rapid tumor development observed. NK, NKT and CD8+ T cells are also known to be important participants in immune mediated protection against MCA induced tumorigenesis [1], however, we did not observe significant changes in these populations in tumor bearing Il27ra−/− mice.

The immunological control of tumorigenesis in PyMT-driven mammary carcinomas is less well defined. However, modulation of cytokine and chemokine expression in PyMT transgenic mice has been shown to alter tumor growth, suggesting that host immune responses are important in determining disease outcome in this model [35], [36]. The accelerated development and growth of PyMT driven mammary carcinomas in Il27ra−/− mice confirms the immunological contribution in this model and recapitulate the data from the MCA fibrosarcomas, wherein tumor bearing Il27ra−/− mice have reduced IFN-γ and increased Treg cells.

Together, these two models provide strong evidence for an important role for IL-27 signals in promoting anti-tumor immunity against de novo tumors. The early tumor induction observed in Il27ra−/− mice in both cancer models suggests that IL-27 signals play an important role in immunosurveillance during neoplasia. Our observation of accelerated growth of established primary mammary carcinomas, as well as a previous report that tumor cell lines grow more rapidly in Il27ra−/− mice [37], show that IL-27 mediated enhancement of the immune response also limits late stage tumor growth.

This study is the first to show that physiological IL-27 signaling plays a protective role in immunity against autochthonous tumors. Our results are in agreement with a previous study that showed more rapid growth of B16F10 cell tumors in Il27ra−/− mice, compared with WT controls [37]. Our data also concur with studies that used IL-27-transduced cancer cell lines, including colon carcinoma [16], TBJ neuroblastoma [14], [38] and B16F10 melanoma [17], [18], [37], [39], which showed that induced IL-27 expression, from tumor tissue itself, enhanced the protective immune response.

Effective anti-tumor immune responses are associated with a TH1 response and ergo, high IFN-γ levels. Anti-tumor effects of IFN-γ include induction of anti-angiogenic factors IP-10 and MIG, upregulation of MHC class I on tumor cells, sensitization of tumor cells to apoptosis and enhancing CTL and NKT cell activity [2], [40]. IL-27 can clearly promote TH1 activity in vitro through the phosphorylation of STAT-1, and upregulation of T-bet and IL-12Rβ2 [41], [42]. However, whether or not IL-27 is required for IFN-γ production by CD4+ T cells in vivo has been controversial. IL-27 signals were required for IFN-γ production during DSS colitis, while loss of Il27ra resulted in a transient defect in IFN-γ production in some models infectious models, for example, Leishmania major [29]. Other infectious challenges, such as Mycobacterium tuberculosis, Toxoplasma gondii and Leishmania donovani elicited strong TH1 responses in Il27ra/ mice (reviewed in [5]). Thus, the necessity for IL-27 appears to be context dependent. Our data suggest that IL-27 signals are indispensable for IFN-γ production by CD4+ T cells in tumor immunity.

The moderate reduction in IFN-γ production by CD8+ cells in Il27ra/ mice in tumor models is in contrast with infectious models, where a strong requirement for IL-27R signaling and T-bet induction was observed [43]. These data suggest that other T-bet inducing cytokines may be able to compensate in CD8+ T cells for the loss of IL-27 signals in tumor models.

Our observation of increased Treg cells in Il27ra/ mice is also in line with the known function of IL-27. We have recently reported that IL-27 suppresses the development of inducible Foxp3+ Treg cells in vivo [11] and IL-27 is known to antagonize TGFβ driven Treg differentiation in vitro [12], [44]. We and others have also previously reported reduced IL-10 [45][48], increased IL-17 [23], [49] and increased IL-4 [26] in Il27ra/ mice. While the observed changes in these cytokines in tumor bearing mice were consistent with previous reports, the magnitude of the changes was small compared with IFN-γ and was not significant across all the tissues examined, suggesting minor roles in the IL-27 mechanism of action during the anti-tumor response.

In summary, these data demonstrate the physiological importance of IL-27 signals during immunosurveillance and anti-tumor responses in mouse models of cancer. Together with a recent report that reduced serum IL-27 level is a risk factor for esophageal cancer [50], our data support the concept that IL-27 signaling agonists could be beneficial in immunotherapy for the treatment of cancer.

Supporting Information

Figure S1.

Representative in vivo GFP imaging using the IVIS lumina II to detect pMIG-PyMT (GFP) vector transduced cell expansion. 3/9 from the Il27ra-/- mice showing positive signal compared to 1/9 from the Il27ra+/+ mice 88 days post-transplant.



We thank Dr. Nico Ghilardi from Genentech Inc. USA for Il27ra deficient mice, Dr. Nicola Armstrong for statistical consulting, Andrea McFarland and Nicola Foreman for assistance with animal monitoring and Australian BioResource for animal husbandry.

Author Contributions

Conceived and designed the experiments: MB AS RB CK RN. Performed the experiments: KDTN SRJ NMR RCW MB. Analyzed the data: KDTN SRJ MB AS. Contributed reagents/materials/analysis tools: AS RN SRJ. Wrote the paper: KDTN MB AS SRJ RN RB.


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