Pancreatic cancer is a malignancy with a dismal prognosis. Set to become the second leading cause of cancer-related death worldwide by 2030, little progress has been made in the treatment of pancreatic cancer over the past five decades[1,2]. Surgery remains the only potentially curative option, however, with the majority of patients typically presenting with advance stage disease, most cases are unresectable. Further to this, with approximately 80% of surgery patients relapsing, frequently within two years, pancreatic cancer has solidified itself as one of medicine’s most urgent areas of unmet need[3].

Characterised by its strong desmoplastic reaction, the pancreatic ductal adenocarcinoma (PDAC) tumour microenvironment (TME) plays a crucial role in disease progression[4,5]. Primary tumour sites display extensive fibrosis characterised by overexpression of extracellular matrix proteins (such as laminin, collagen and fibronectin) and activation of fibroblastic cells. Multiple cell types, both cancer and stromal, are present in the pancreatic TME, including; pancreatic stellate cells (PSCs), myeloid-derived suppressor cells (MDSCs), tumour associated macrophages (TAMs) and regulatory T-cells (Tregs), amongst many other cell types[6,7]. The dense fibrosis associated with PDAC (largely orchestrated by PSCs) results in tumour hypoxia, a feature characteristic of PDAC, which is exacerbated by the secretion of anti-angiogenic factors (such as endostatin and angiostatin) by both pancreatic cancer and stellate cells[6,8]. Development of a hypoxic TME has been linked to disease aggressiveness and progression, as well as chemotherapy resistance. Importantly, in addition to developing resistance to chemotherapeutics, the pancreatic TME is highly immunosuppressive, limiting the efficacy of the immune-mediated cancer surveillance[6]. MDSCs release reactive oxygen species (ROS) and reactive nitrogen species which have been shown to inhibit T cell proliferation and migration into the TME. In addition, release of immunosuppressive cytokines including interleukin (IL)-10 and transforming growth factor beta (TGF-β) sustains the development of Tregs which further modulate the TME[9]. Tregs secrete immunosuppressive cytokines such as IL-10 and TGF-β which recruit additional immunosuppressive cells to the TME and stimulate the transition of CD4⁺ T cells to FoxP3⁺ regulatory cells, facilitating immune evasion[6,10]. Through the release of IL-10 and TGF-β, tumour associated macrophages are also able to induce T-cell anergy leading to the development of an immune-privileged microenvironment[11]. Finally, pancreatic cancer cells can downregulate Fas, resulting in resistance to CD8⁺ T cell-induced Fas/FasL apoptosis[6,12]. Key components of the PDAC TME are shown in Figure 1.

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Figure 1 Pancreatic ductal adenocarcinoma tumour microenvironment. Upon activation, pancreatic stellate cells secrete an abundance of extracellular matrix proteins including collagen, fibronectin, laminin, and hyaluronic acid, leading to dense desmoplasia. In addition, fibroblastic cells (CAFs) become active, and immune suppressive cells (myeloid-derived suppressor cells, regulatory T-cells and tumour associated macrophages) are sequestered to the tumour microenvironment (TME). Secretion of anti-angiogenic factors, in addition to dense desmoplasia, results in the development of a hypoxic TME. Cancer stem cells are also observed in pancreatic ductal adenocarcinoma.

Following initial interactions between activating/inhibitory receptors and target cells, the balance of signals received by the NK cell determines its activation status. If activated, NK cells must form an immunological synapse with the target cell. Formation of this synapse enables stable adhesion, polarisation of cytotoxic granules and subsequent lysis of the target cell. This is achieved through binding of the β2 integrin, LFA-1[17]. Consisting of two chains, α_L and β₂, LFA-1 is a heterodimer whose reactivity to its ligands (ICAM family members) can be modified via conformational changes. Specifically, a bent conformation exhibits a low affinity for its ligands, intermediate affinity can be achieved through a closed/extended conformation, whilst an open/extended conformation results in high-affinity binding (Figure 3)[17,19,20].

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Figure 3 Leukocyte function-associated antigen 1 conformation. Leukocyte function-associated antigen 1 (LFA-1) affinity can be altered by its conformation. When bent, LFA-1 exhibits low affinity for its ligand, ICAM1. Intermediate affinity is achieved through a closed/extended conformation, whilst an open/extended conformation results in high affinity binding to ICAM1 and generation of an effective, stable immunological synapse.

In contrast to T cells, NK cells do not require inside-out signals (such as chemokines and T cell receptor activation) to stimulate LFA-1 binding and can signal autonomously[15,21]. Following integrin activation, a signalling network is employed to facilitate the convergence of cytotoxic granules to the microtubule organising centre (MTOC) which is subsequently polarised towards the target cell, allowing degranulation (Figure 4)[21-26]. Actin remodelling is also carried out at the immunological synapse in response to NK cell activation, facilitating docking of the cytolytic granules[27]. Integrin-linked kinase, paxillin, Pyk2 and RhoGEF7 signalling cascades are employed for the polarisation of MTOC, with Cdc42, CLIP-170, Par6 and APC components of this signalling cascade being key for granule polarisation[21,28]. During this process, the mitochondria and Golgi complex have also been shown to polarise towards the immunological synapse[29,30]. Following polarisation of the cytotoxic granules, the pore-forming protein, perforin, and the serine proteases, granzymes, are exocytosed leading to target cell death via perforin induced necrosis, or granzyme stimulated caspase-dependent apoptosis[28,31,32]. Non-granule dependent cytotoxic mechanisms include the binding of death ligands such as TNF-related apoptosis-inducing ligand and FasL to their receptor on target cells result in extrinsic apoptosis via caspase-8 activation[33] and release of IFN-γ[13,34,35].

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Figure 4 Cytotoxic granule convergence and microtubule organising centre polarisation. A: Following receptor stimulation leading to natural killer (NK) cell activation, leukocyte function-associated antigen 1 engages with its ligand ICAM1 on the malignant cell, forming a stable immunological synapse; B: F-actin accumulates and polymerises at the immune synapse, forming a filamentous mesh which modulates the release of cytolytic granules. Tubulin microtubules then form from the microtubule organising centre (MTOC); C and D: Cytotoxic granules converge on the microtubules (C) and are polarised towards the MTOC where they converge (D); E: This granule movement is dependent on dynein/dynactin motor function. Dynamic rearrangement of the microtubules facilitates polarisation of MTOC towards the immunological synapse; F and G: This polarisation is stimulated via Integrin-linked kinase, paxillin, Pyk2 and RhoGEF7 signalling. Following polarisation to the immunological synapse, a subsection of cytotoxic granules fuse with the plasma membrane (F) (a process largely regulated by Munc 13-4 and Rab27a) and undergo degranulation via either complete or incomplete fusion (G); H: Cytotoxic granules which do not degranulate are recycled and are hypothesised to remain converged at the MTOC to facilitate serial NK cell killing. Granules which undergo incomplete fusion are rapidly recycled through clathrin mediated endocytosis of granule membrane proteins, further facilitating serial killing; I: Finally, the malignant cell undergoes perforin induced necrosis or granule dependent apoptosis. NK cells detach from the malignant cell and move on to the next target.

Initially identified as a result of their ‘natural’ cytotoxicity towards both syngeneic and allogeneic tumour cells, NK cells have widely demonstrated potent anti-tumoral cytotoxicity[36-38]. However, they are highly heterogeneous both between cancer types and intra-tumourally[36]. Moreover, the variable functional status of NK cells is seen to greatly impact their anti-tumoral efficacy[36]. Upregulation of the inhibitory receptor NKG2A has been associated with NK cell exhaustion and poorer prognosis in patients with liver cancer[39], whilst PD-1 engagement of NK cells has been shown to block the polarisation of lytic granules and impair outside-in integrin signalling[40]. Increased expression of PD-1 on NK cells has also been associated with poorer overall survival in patients with hepatocellular carcinoma[41]. Conversely, high proportions of functionally active NK cells result in favourable outcomes in many cancer types[42]. Retrospective flow cytometric assessment of peripheral blood samples from metastatic prostate cancer patients (Gleason scores between 6-9) followed by univariate Cox regression analysis demonstrated a significant correlation between expression of the activating receptors NKp46 and NKp30, and longer overall survival[42]. Similarly, immunostaining of tissue samples from 98 patients with gastric cancer (stage 1-4) combined with multivariate analysis revealed a positive correlation between NKG2D expression in tumour infiltrating lymphocytes and prolonged OS (hazard ratio 0.34)[43]. With the propensity to exhibit potent anti-tumoral activity, NK cell-based immunotherapy research has flourished in the past few years[36].

NK cell number has been found to convey prognostic significance. Through flow cytometric analysis of PBMCs from resectable PDAC patients (stage Ib-III) both pre- and post-surgery, Hoshikawa et al[44] demonstrated a positive correlation between the percentage of NK cells in peripheral blood and recurrence-free survival, with patients who exhibited high NK levels expressing later disease recurrence. Moreover, univariate and multivariate analysis using the Cox proportional hazard regression model demonstrated NK cell frequency to be the only favourable prognostic factor for recurrence-free survival. Additional factors tested included tumour stage, N status, radicality, age and gender. Importantly, no additional circulating mononuclear cells were included in this analysis. NK cell infiltrate within the TME (assessed by gene expression profile) was also found to be associated with later disease recurrence, however, this was not statistically significant[44]. Assessment of a larger cohort of patients would improve the power of this assessment and may provide further insight into the role of tumour infiltrating NK cells in PDAC.

Finally, gene set enrichment analysis revealed that patients with enriched type I and II IFN signatures within tumour tissues had later disease recurrence. Type I and II IFNs are closely associated with NK cell function. Type I IFNs induce NK cell activation both directly, through binding to type I IFN receptor, or indirectly, through stimulating dendritic cell release of IL-15, whilst type II IFNs (namely IFN-γ) are produced by activated NK cells[45,46]. Moreover, IFNs can induce CXCL10 release, leading to the further recruitment of NK cells to the tumour tissue[44]. Thus, enriched IFN signatures were also concluded to be a positive prognostic biomarker in PDAC[44].

Yang et al[47] also suggest prognostic implication of NK cells in PDAC. High densities of NK cells in peripheral blood samples (analysed by flow cytometry) were found to correlate with poor overall survival in patients with advanced PDAC (stage III/IV) when accompanied by a high neutrophil: lymphocyte ratio (obtained from routine hospital data). NK cell number (HR 1.45), as well as patient age (HR 1.34), neutrophil to lymphocyte ratio (HR 1.48) and absence of metastasis (HR 0.72) were found to be independent prognostic markers following univariate and multivariate Cox regression analysis. It is perhaps prudent to note that subsequent ELISAs to measure release of IFN-γ and TNF-α from NK cells as well as serum IL-2 Levels, a known activator of NK cells, demonstrated lower levels of all three markers in patients with high NK cell densities, although only IFN-γ reached significance. These results suggest a distinct subtype of NK cells with impaired function in PDAC patients and thus prognostic significance may rely not just on NK cell numbers, but on functional subtypes[47]. The results obtained within this study focus solely on peripheral blood circulating NK cells. Further work to classify functional NK cell subtypes within PDAC tumour tissue would provide more conclusive insights into the prognostic significance of these effector cells in PDAC.

NK cells have demonstrated potent anti-tumoral efficacy in murine models of PDAC. Using a transgenic mouse model in which oncogenic transposons for KrasG12V and myristoylated Akt2 were introduced into p53fl/fl mice via intra-pancreatic injection and electroporation, along with plasmids for Cre recombinase and sleeping beauty transposase, Brooks et al[48] demonstrated that neo-adjuvant PD-1 blockade plus adjuvant CD96 inhibition in combination with gemcitabine prevented relapse and facilitated long term remission following resection surgery. To further investigate the role of immune cells in neo-adjuvant and adjuvant treatment of PDAC, mice were injected (intraperitoneal) with anti-CD8 and anti-NK.1.1 depletion antibodies. Pre-operatively, depletion of both CD8⁺ T cells and NK cells significantly reduced survival when compared to the control. Furthermore, adjuvant NK but not CD8⁺ depletion was found to impair survival and resulted in an increase in local disease recurrence. In vitro luciferase cytotoxicity assays confirmed NK cell cytolytic efficacy against tumour derived cancer cells, a finding consistent with the results obtained for depletion experiments. Thus, targeting both T and NK cells through immune checkpoint inhibition may confer long term survival benefits in metastatic cases of PDAC[48]. Similarly, in a Kras^LSL-G12D p53^LSL-R172H Pdx1-Cre (KPC) model of PDAC, NK cell-based adoptive transfer immunotherapy was found to significantly delay tumour growth[49]. In addition, immunostaining of KPC tumours at end time-points revealed significantly elevated areas of necrosis in mice treated with adoptive transfer of NK cells compared to control mice, demonstrating the cytotoxic efficacy of NK cell treatment, a finding replicated through in vitro flow cytometry cytotoxicity assays[49].

Xenograft models of PDAC have also been used to demonstrate the efficacy of ex vivo expansion of NK cells. NOD scid gamma (NSG) mice injected subcutaneously with MiaPaca2 cells demonstrated a significant reduction in tumour growth when treated with adoptive transfer of ex vivo expanded NK cells (versus control group)[50]. This finding demonstrated both successful trafficking of NK cells to the tumour site and tumour control following intravenous injection, suggesting that NK cells may prove an effective systemic treatment in xenograft models of PDAC[50]. It is prudent to note that the nature of this model requires the mice included within the study to be immuno-compromised, and this must be taken into consideration when reviewing the data presented. Employing additional models would add further validity to the therapeutic impact of ex vivo expanded NK cells in murine models of PDAC[50].

Notorious for their resistance to typical anti-proliferative/cytotoxic therapies, cancer stem cells are an important subpopulation involved in cancer progression, metastasis and recurrence. Despite their notoriety, CSCs are preferentially targeted by NK cells in both the autologous and allogeneic setting; an effect which was found to be NKG2D dependent[51]. Metastatic, intra-pancreatic and subcutaneous models of PDAC were established in NSG mice using the PANC-1 cancer cell line. Mice treated with adoptively transferred NK cells were found to have substantial reductions in tumour volume when compared to untreated mice. Flow cytometric analysis also demonstrated a significant reduction in CSC populations in mice treated with adoptive NK cell transfer (denoted by aldehyde and CD24 expression). Moreover, immunostaining revealed co-localisation of NK cells and CSCs within tumour tissues. Ames et al[51] conclude that NK cells possess the ability to identify and preferentially target CSCs in solid tumours. As such, further work investigating the impact of systemic adoptive transfer of NK cells on CSC populations may yield exciting new therapeutic insights into the treatment of this dismal prognosis disease.

Pancreatic tumour cells have developed several methods of NK-cell immune evasion. Murine models of pancreatic cancer specifically designed to express MYC at the Rosa26 Locus, either with or without the Lsl-Kras^G12D allele, were used to determine the role of MYC in pancreatic tumour progression. MYC expression was found to drive pancreatic cancer development and accelerate disease progression in precursor lesions initiated by KRAS. Moreover, bulk RNA sequencing of end stage tumours revealed reduced expression of T-cell, B-cell and NK cell markers in tumour tissue, suggesting that immune cell infiltration may be regulated by MYC. GeneGo analysis revealed that allelic activation of both KRAS and MYC resulted in significant downregulation of type I IFN, an effect that was found to be dependent on repressional binding of MYC-interacting zinc finger protein, MIZ1. Deletion of MIZ1 resulted in restoration of NK and B cell infiltration into tumour tissues, an effect ablated upon antibody dependent blockade of type I IFN[52]. Similarly, the oncoprotein Sloan-Kettering Institute has been shown to inhibit SMAD association with the acetyltransferases CBP and p300, which are key regulators of inducible expression of NKG2D ligands on cancer cells, and facilitate repression of gene transcription via histone deacetylases. This results in downregulation of NKG2D ligands on tumoral cells, reducing NKG2D dependent cytotoxicity and facilitating immune evasion[53]. In addition, tumoral cells are seen to exhibit intricate crosstalk with NK effector cells and have been shown to induce functional deregulation[54]. Co-culture with the pancreatic cancer cell line MiaPaca2 was found to induce NK cell anergy via fibrinogen-like protein 2 and was characterised through decreased expression of DNAM-1, IFN-γ and CD107a and increased expression of PD-1[55]. Importantly, when co-cultured, anergic NK cells were seen to induce anergy in naïve NK cells, reducing IFN-γ and CD107a expression[55]. Further work investigating the reversal of NK cell anergy, both tumour-dependent and bystander anergy may lead to novel therapeutic insights, and provide a baseline from which to further challenge PDAC immune evasion.

MHC class-I chain-related molecules A/B (MICA/B) are crucial ligands for the activating receptor NKG2D. Several studies have demonstrated immune evasion as a result of MICA/B shedding by tumour cells. Duan et al[56] demonstrated that high glucose levels, which are widely correlated with pancreatic cancer, could facilitate immune evasion. Specifically, in vitro assays demonstrated a decrease in NK cell induced lysis of pancreatic cancer cell lines (demonstrated by lactate dehydrogenase release assays) when cultured in high glucose conditions. Moreover, western blot and quantitative real-time polymerase chain reaction (PCR) analysis revealed that this decrease in function was a result of reduced expression of MICA/B in cancer cell lines at both the protein and mRNA level. Mechanistically, high glucose was found to inhibit AMP-activated protein kinase signalling, leading to upregulation of the polycomb group protein (PcG) Bmi1, and subsequent promotion of GATA2 expression. This augmentation inhibited expression of MICA/B on pancreatic cancer cells and led to their immune evasion[56]. Similar shedding of the NKG2D ligand has been observed in response to hypoxia. High levels of HIF1α have been correlated with decreased expression of MICA/B on pancreatic tumour cells and also with increased internalisation of the activating receptor NKG2D, suggesting a dual role for the hypoxic TME in NK cell dysfunction[57]. Specifically, immune-histochemical analysis of PDAC patient tumour tissues revealed a significant correlation between MICA surface expression and high HIF1α. Moreover, immune-fluorescent staining of NK cells isolated from patient PBMCs demonstrated clear internalisation of the activating NKG2D receptors as well as MICA/B[57].

Receptor expression is found to be largely augmented in pancreatic cancer patients. Flow cytometric analysis of participant blood samples revealed that expression of the activating receptors DNAM-1 (CD226) and CD96 were significantly reduced in pancreatic cancer patients (stage I-IV) when compared to healthy controls. This downregulation was suggested to lead to NK cell dysfunction and tumour evasion.[58] Downregulation of NKG2D in pancreatic cancer patients has also been correlated to reduced cytotoxicity of the effector cells. In vitro blockade of NKG2D using neutralising antibodies was found to significantly decrease killing of MiaPaca2, BxPC3 and Capan2 cell lines by IL-15 stimulated NK cells[59]. This finding highlights the functional importance of NKG2D expression on NK cell function and may prove to be a crucial marker of NK cell efficacy against malignancy.

Additionally, flow cytometric analysis of cell surface markers following in vitro co-cultures of NK cells derived from healthy PBMCs and pancreatic cancer cell lines revealed downregulation of the NK activating receptors NKG2D, NKp30, NKp46 and DNAM-1. ELISA analysis suggested that this dysfunction was induced as a result of matrix metalloproteinase 9 (MMP9) and Indoleamine 2,3 dioxygenase (IDO) signalling cascades.[60] In addition to downregulation of activating receptors, exposure to MMP9 and IDO also led to decreased TNF-α and IFN-γ production by NK cells, an effect that was reversed upon blockade of MMP9 and IDO using tissue inhibitor of metalloproteinases 1 and 1-Methyl-DL-tryptopan, respectively[60]. This finding was replicated in a comprehensive study of surface receptor expression and cytotoxic granule positive cells in pancreatic (stage II and IV), gastric (stage 0-IV) and colorectal cancer (stage I-IV) patients. Using flow cytometry, Peng et al[61] identified significant downregulation of the activating receptors NKG2D, NKp30, NKp46 and DNAM-1 on NK cells identified in peripheral blood samples from pancreatic cancer patients when compared to healthy controls, whilst expression of the inhibitory receptor KIR3DL1 was significantly upregulated. Moreover, the percentage of perforin positive circulating NK cells was found to be significantly reduced in pancreatic cancer patients. Taken together, these alterations evidence the dysfunction of NK cells observed in malignancy.

Impairment in degranulation was also identified by Jun et al[62]. In an in vitro flow cytometry-based degranulation assay, PBMCs derived from malignant patients, non-malignant patients or healthy controls were mixed with target cells before staining with CD107a. NK cells derived from pancreatic cancer patients showed significantly impaired degranulation when compared to non-malignant and/or healthy control samples. Despite demonstrating impaired cytotoxic capabilities, no significant difference in NK cell IFN-γ production was observed between cancer patients and healthy controls. Importantly, multivariate analysis revealed that tumour-induced NK cell dysfunction correlated with disease stage, suggesting progressive impairment of NK cells with advanced-stage disease. Thus, as previously suggested, NK functional status may prove an attractive prognostic marker in PDAC.

NK cell-stromal cell interactions have been shown to result in significant cellular dysfunction and exclusion of NK cells from tumour tissues, suggesting that NK cells can be educated by the TME[47,63]. As crucial players in the development of the pre-metastatic niche, extracellular vesicles are key to the progression of PDAC and contain large numbers of immune regulatory factors including TGF-β, nectin-2 and PVR. Flow cytometric analysis following in vitro co-culture of NK cells and extracellular vesicles demonstrated downregulation of multiple NK cell receptors and cytokines, specifically, IFN-γ, TNFα, CD107a and NKG2D, resulting in gross cytotoxic impairment (demonstrated through tumour sphere cytotoxicity assays) and NK cell dysfunction. This impairment was further associated with the activation of the TGF-β- Smad3/4 signalling pathway[64]. It should also be noted that NK cell dysfunction is heavily regulated by the soluble factors and cytokines secreted by both tumoural and stromal cells, with TGF-β, IDO, MMPs and interleukins proving largely responsible for this impairment (Figure 5)[50,60,65-67].

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Figure 5 Natural killer cell dysfunction caused by tumoral and stromal cells in pancreatic ductal adenocarcinoma. Natural killer (NK) cell interactions with multiple stromal and tumour cells significantly impacts the cytotoxic efficacy of NK cells in pancreatic ductal adenocarcinoma. Transforming growth factor -β, interleukin (IL)-10, IL-6, IL-23 and IL-1β release significantly dampens NK cell cytotoxicity and function, and inhibits intratumoural proliferation of NK cells. NK cell mediated cytokine release is also inhibited within the immunosuppressive tumour microenvironment. Finally, chemokine release may also sequester NK cells in the panstromal compartment, preventing engagement with tumour cells.

NK cell interaction with suppressive immunoregulatory cells has a significant impact on cytotoxic effector function. Both MDSCs and TAMs produce IL-23, IL-6, IL10 and TGF-β which results in the downregulation of IFN-γ, perforin and IL-12 production by NK cells, decreasing cytotoxicity and NK cell proliferation within the TME[65]. TAMs also inhibit NK cell function through cell-cell interactions. M2 macrophages express PDL-1 which binds to PD-1 expressed on NK cells. This checkpoint protein prevents NK cell engagement and induces downregulation of the activating receptors NKG2D, natural cytotoxicity receptors and DNAM1, leading to reduced cytotoxicity[67]. Immunosuppressive Tregs release IL-10 and TGF-β into the TME. This cytokine release decreases NK cell cytotoxicity through the downregulation of activating receptors and decreased production of anti-tumour cytokines such as IFN-γ[65].

Moreover, MDSCs have also been shown to augment FcR mediate NK cell functions. Adoptive transfer of MDSC in a Panc02-EGFR⁺ murine model of pancreatic cancer significantly inhibited the efficacy of monoclonal antibody therapy, with mice receiving Cetuximab + MDSCs expressing significantly larger tumour volumes than did mice treated with Cetuximab + splenocytes. Furthermore, NK cells co-cultured with tumour derived (melanoma) MDSCs were found to express significantly reduced phospho-ERK than did though cultured alone (as measured by flow cytometry). Thus, it was concluded that MDSCs inhibit FcR mediated signal transduction, resulting in impaired cytokine production, ADCC dysfunction and reduced anti-tumour activity. An effect that was found to be, at least in part, in response to MDSC nitric oxide production[68].

Likewise, tumour-associated neutrophils have been shown to impair NK cell function through the release of arginase and ROS[67]. In vitro co-culture assays using PBMCs derived from healthy donors demonstrated that activated granulocytes (stimulated with Phorbol 12-myristate 13-acetate) produced ROS including hydrogen peroxide, which was found to be cytotoxic to CD56^dim CD16⁺ NK cells, but not CD56^brightCD16^- subsets, suggesting that interactions with stromal cells may result in differential effects on cytotoxic effector subset[69].

Tumour-associated macrophages and cancer-associated fibroblasts have also been shown to produce growth arrest-specific gene 6 (Gas6) in the pancreatic TME. As a negative regulator of the immune system, the Gas6-AXL pathway is seen to prevent NK cell activation. Orthotopic syngeneic models of pancreatic cancer in which tumour cells derived from KPC mice were transduced with zsGreen/Luciferase and orthotopically injected into the pancreas of immune-compromised mice were used to investigate the role of Gas6 in NK cell activation and pancreatic cancer development. Pharmacological blockade of Gas6 signalling using neutralising antibodies was found to inhibit pancreatic cancer metastasis. Moreover, immunohistochemical analysis of NK cell infiltrates revealed a significant increase in the number of NKp46⁺ NK cells in lung metastasis in mice treated with anti-Gas6 therapy when compared to the control. This finding was also observed in the tumour draining lymph nodes; however no significant difference was observed in NK cell infiltration in primary tumour sites between treatment groups[70]. As such, Gas6 blockade may prove a promising new therapeutic target for the treatment of metastatic lesions in pancreatic cancer.

NK cells have been shown to be excluded from tumour tissue as a result of NK-stromal cell interactions. Through ex vivo immunostaining and Ariol image analysis of tissue micro-arrays, Ene-Obong et al[4] demonstrated that infiltrates of CD56⁺ natural killer cells were significantly lower in the juxtatumoural compartment of PDAC tissues (stage I-III) when compared to panstroma. This finding suggests PSCs sequester NK cells in the panstromal compartment of the TME, preventing NK induced cancer cell death. Similarly, Lim et al[50] demonstrated that NK cell frequencies in malignant tissue from PDAC patients (stage I-IV) were as low as < 0.5% (as assessed by flow cytometry). This low infiltration was attributed to reduced expression of the CXCR2 receptor on NK cells which resulted in poor chemotaxis into tumour tissues.

Known orchestrators of the TME, pancreatic stellate cells are crucial regulators of immune cell infiltrates in pancreatic cancer and have been shown to promote tumour progression through the development of an immunosuppressive environment[5,71-73]. In an orthotopic mouse model of pancreatic cancer in which either Panc02 cells alone or in combination with activated PSCs were injected into the pancreas of C57BL/6 mice, Li et al[74] report a significant reduction in the number of NK cells in tumour tissue in mice co-transplanted with PSCs when compared to mice injected with Panc02 cells alone. This finding is consistent with ex vivo analysis of human PDAC samples[4]. Further work is needed to demonstrate the mechanistic link between PSCs and NK cell tumoural exclusion.

In a recent study, Francescone et al[75] demonstrated dynamic crosstalk between PDAC cancer cells, CAFs and immune cells. Specifically, in in vitro co-culture assays CAFs were found to ectopically express the neural presynaptic protein NetrinG1 (NG1) whilst its binding partner, NGL1 was identified on PDAC cells. This interaction was found to convey protection on cancer cells from NK cell-driven elimination,a fact quantified through CRISPR/Cas9 NG1 knockout which resulted in decreased expression of the immunosuppressive cytokines TGF-β, IL-8 and IL-6, and restored NK cell anti-tumour activation. This finding was reproduced in murine orthotopic models of PDAC in which NGL1 was knocked out of syngeneic mouse cells. This work provides a potential novel target in PDAC in which the immunosuppressive nature of PDAC induce by CAF cells can be reverted.

Finally, in vitro and xenograft models of PDAC in NOD SCID mice demonstrated that stromal TGF-β signalling stimulates CAF cells to secrete IL-6, which in turn suppresses NK cell function as assessed through NK cell killing assays. Concomitantly, stromal TGF-β limits NK cell function itself[76]. In vivo TGFβ blockade using the anti-mouse TGFβR2 mAb, 2G8, was found to reduce tumour progression, an effect that was reversed upon NK cell depletion[76]. Furthermore, a conditional KRAS (G12D) model of pancreatic cancer combined with a high-fat calorie diet demonstrated that stromal adipocytes produce IL-6, reducing NK cell function through IL-6 mediated downregulation of IFN-γ production. Thus, it has been suggested that adipocytes and PSCs may provide tumour sanctuaries within the TME through the immunosuppression of NK cells[77,78].

Taken together these findings demonstrate the complex interactions between NK cells and the PDAC microenvironment. Despite their cytotoxic efficacy against malignancy, the dysfunction induced by stromal cells greatly augments the natural anti-tumoral activity of NK cells. As such, a deeper understanding of these interactions is crucial to fully unlock the potential of NK cells in the treatment of PDAC.