Lack of effector T-cell infiltration in PDAC has been hypothesized to be a product of poor tumor immunogenicity stemming, in part, from lower frequency of neoantigens.26 Attempts to directly interrogate the immunogenicity of PDAC have employed sophisticated techniques involving patient tissue and the genetically engineered KPC mouse model (LSL-Kras ^G12D/+ ;LSL-Trp53 ^R172H/+ ;Pdx-1-Cre), which recapitulates much of the microenvironment in human PDAC.27 28 Impressive efforts have employed novel methods to isolate and sequence neoplastic cells within pancreatic tumors while excluding stromal regions which may have confounded past studies.29 30 These reports indicate a complex and highly diverse mutational landscape in PDAC that challenges previous work.29 Certainly, recent clinical data from the ‘Know your Tumor’ initiative demonstrated that choice of personalized, targeted therapy based on genomic features can improve outcomes in PDAC.31 While PDAC is capable of appropriate antigen stimulation of T cells, these studies indicate release or presentation of antigen may be inhibited or obscured in cases with poor T-cell response.

Perhaps the most unique aspect of pancreatic cancer is the overwhelming stroma which shapes the TME. The abundant stroma associated with PDAC has been long hypothesized to physically restrain T-cell and therapeutic drugs or antibodies due to the collagen, fibronectin and other extracellular matrix (ECM) components secreted by fibroblasts and cancer cells.32 However, research by two separate groups demonstrated no significant relationship between thickness of the desmoplasia, fibrotic content in the TME or presence of cancer-associated fibroblasts with the exclusion of infiltrating T cells from neoplastic lesions.8 33 While the stroma represents a barrier for T-cell infiltration into PDAC, these studies indicate this exclusion may occur through mechanisms more complicated than only a physical barrier. Indeed, research dissecting individual components of PDAC stroma and associated mechanisms reveals complex immunosuppressive mechanisms involving cancer-associated fibroblasts, T-regulatory cells (Tregs), tumor-associated macrophages (TAMs) and dendritic cells, each of which affect T-cell infiltration into tumors (figure 1).

The fibroblast components of PDAC tumors are riddled by heterogeneity and plasticity. Previous research defined distinct populations of fibroblasts within PDAC possessing inflammatory or myofibroblastic properties termed inflammatory cancer associated fibroblasts (iCAFs) and myofibroblastic cancer associated fibroblasts (myCAFs), respectively.34 These cells have potential to modulate tumor growth and stromal composition and may alter immune responses to PDAC by contact-dependent and independent properties.34 The inflammatory iCAF subsets are characterized by production of soluble factors, such as interleukin (IL)-6, leukemia inhibitory factor and IL-11, with immune modulatory potential.34 35 myCAFs assume a more traditional activated fibroblast phenotype, secreting ECM components such as collagen and fibronectin.34–36 Work by Ohlund et al elucidated a dynamic interplay between tumor cell-derived interleukin-1-alpha (IL-1α) and transforming growth factor beta (TGFβ) within the stroma that significantly influences cancer associated fibroblast (CAF) fate.35 IL-1α from cancer cells polarized directly adjacent CAFs to a myCAF phenotype; however, IL-1α signaling can be disrupted by the presence of TGFβ in more distant stromal regions, promoting the inflammatory profile seen in iCAFs.35 Of note, TGFβ activation in the stroma has been linked to infiltration and activity of non-degranulated mast cells, which associate with CAFs, and whose infiltration has been linked with worse overall survival in tissue from previously untreated patients with resectable PDAC.37–40

Cross-species sequencing of pancreatic tumors in mice and humans has also revealed the existence of another interesting CAF population with the ability to present antigen.36 These antigen-presenting CAFs express both CD74 and major histocompatability complex-II (MHC-II), indicating a propensity to present antigen to CD4⁺ T cells in vivo, potentially resulting in increased activation of CD4⁺ T cells.36 The plasticity of these CAF populations and this ‘Jekyll and Hyde’ influence on the immune system present a complicated case for targeting the stroma to mediate immune activation in PDAC. Indeed, past challenges with pharmacological agents targeting stromal pathways such as sonic hedgehog have rightfully tempered enthusiasm for launching into clinical trials without rigorous data.41 Furthermore, two key reports have demonstrated that in vivo depletion of fibroblasts in murine models resulted in aggressive progression toward metastatic disease and that degree of stroma was inversely related to clinical outcome.42 43 Despite these data, tumors that arose in mice lacking α-SMA⁺ fibroblasts were exquisitely sensitive to immunotherapy, again implying the stroma restrains immune response to PDAC tumors. Taken together, these data indicate consideration of individual CAF subsets is likely necessary in designing approaches to treat PDAC.42–44

More recently, checkpoint-mediated interactions between CAFs and pancreatic cancer cells (PCCs) have been implicated as a mechanism by which T cells are trapped and killed or inactivated in the PDAC stroma.45 PDAC-associated CAFs display higher expression of programmed death ligand 1 (PD-L1) and programmed death ligand 2 than normal fibroblasts, with the latter more highly expressed. In vitro experiments demonstrate the ability of CAFs to upregulate programmed cell death protein 1 (PD-1), cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), and T-cell immunoglobulin and mucin domain-containing protein 3 on both CD4⁺ and CD8⁺ T cells, as well as lymphocyte-activation gene 3 on CD4⁺ T cells. This phenotypical shift eventually leads to decreased T-cell proliferation. Alternatively, fibroblast populations in the TME of PDAC can control immunity through contact-independent mechanisms such as secretion of cytokines and chemokines. In addition to secretory factors discussed previously, other investigations indicate a role for fibroblast-derived CXCL12 in facilitating T-cell exclusion in PDAC.46 Feig et al found CXCL12 from fibroblasts was responsible for excluding T cells in PDAC and mediating failure of both αPD-L1 and αCTLA-4 therapy.46 These data have led to clinical trials blocking the receptor for CXCL12 (CXCR4) with the Food and Drug Administration-approved drug plerixafor (NCT02179970). These results highlight the numerous complementary aspects of the PDAC stroma that drive T -cell exclusion from PDAC.

Interestingly, immunosuppressive Tregs and B cells with regulatory properties can localize to stromal areas of PDAC, rather than within foci of adenocarcinoma.9 47–50 These Tregs are most often characterized as CD4-positive, with high expression of the IL-2 receptor CD25 and the transcription factor Forkhead Box P3 (FOXP3). Definitive histological detection of these cells in tissue is challenging, and often their characterization omits CD25 for technical simplicity.51 52 Like effector CD4⁺ or CD8⁺ T cells, Tregs preferentially localize to stroma, rather than tumor foci in PDAC, but can be found in uninvolved and tumor compartments in equal proportion.9 53 However, the central location for the inhibitory action of these cells may be in peritumoral lymph nodes associated with PDAC. Indeed this is where the majority of Tregs in tumor-bearing mice are found.53 This research also revealed CTLA4/CD80 interactions between Tregs and dendritic cells (DCs) as essential molecular mediators of CD4 T-cell exclusion, but the specifics of how CD4 T cells are actually excluded as a result of these interactions are only now becoming clear. A novel observation by Jang et al describes prolonged interactions between Tregs and DCs in PDAC, demonstrating the ability for Tregs to outcompete CD8⁺ T cells and limit CD8⁺ T-cell interactions with DCs54 (figure 2). In this manner, Tregs limit T-cell priming in the periphery and significantly diminish cytotoxic T-cell responses to PDAC.53 54

Naturally occurring Tregs express the transcription factor FOXP351 55–57; however, CD4⁺ Tregs without canonical FOXP3 expression can also repress immune responses.58 59 In fact, a CD4⁺ Treg subset positive for IL-10 and IL-17 and negative for FOXP3 was identified in murine PDAC models.60 These FOXP3⁻ Tregs promote tumor progression and have a similar phenotype to type I regulatory (Tr1) cells that develop from mature antigen-stimulated CD4⁺ T cells.60 61 Tr1 cells, identified over 30 years ago in patients, characteristically secrete large amounts of IL-10 and can negatively impact antigen-presenting myeloid cells.62 63 While natural Tregs traditionally develop in the thymus from naïve cells, Tr1 cells can be altered and differentiated in the TME of both mouse and human hosts, identified by their expression of CD49 and LAG3.60 61 64 A recent study by Barilla et al describes the influence of specialized DC subsets in skewing of CD4⁺ T cells to this Tr1 phenotype and the protumorigenic effect of this interaction60 (figure 2). Additionally, CD4⁺ T cells exposed to a suppressive DC subset from the PDAC TME shifted to a Th17 phenotype, including a population of Th17-like cells expressing FOXP3.60 Thus, DC subsets have the capacity to induce multiple regulatory T-cell subsets which suppress immune responses.60 The expansion of these cells from antigen-experienced CD4⁺ T cells also diminishes potential helper cells within the PDAC TME. Interestingly, DCs isolated from pancreata or spleens of naïve mice or from spleens of PDAC tumor-bearing mice do not have the same abilities, indicating PDAC exerts a unique influence over DCs in the TME.60 These data highlight the complex interactions mediating the presence of effector T-cell populations within the TME.

B lymphocytes, or B cells, can have immunosuppressive activity in several tumor types.47–50 B cells can associate with CD8⁺ T cells in both murine PDAC models and pancreatic intraepithelial neoplasias (PanIN) of patients.48 50 Several studies have uncovered B-cell phenotypes in PDAC, and targeting these cells improves immune responses in PDAC.48–50 Emerging reports highlight a role for B-cell-derived IL-35, as well as B-cell control of macrophage polarization to a tumor-promoting phenotype. While separate studies have alternatively defined tumor-promoting B-cell subsets, it should be noted that growth of orthotopic pancreatic tumors in B-cell-deficient mice (μMT) was severely diminished.50 Further, depletion of B cells in mice with PanIN significantly inhibited progression.48 Several pathways such as IL-35 secretion, dynamic fluctuation of hypoxia-inducible factor 1-alpha and Bruton tyrosine kinase activation are potential targets for inhibiting B cells in PDAC48–50 (figure 2). Balancing these immune suppressive properties of B cells in PDAC are other strong data demonstrating B cells can cluster in tertiary lymphoid tissues (TLTs). Further, B-cell clustering is significantly correlated with improved T-cell activity in murine models65 and more favorable outcomes for patients with PDAC.66 67 While TLTs have recently emerged as an interesting feature of potent antitumor responses,68 their presence and make-up in PDAC tissues is quite understudied. Indeed, the role of B cells and TLT in PDAC progression deserves further exploration.

Macrophages represent a sizeable proportion of cells in the PDAC TME and have complex characteristics. Available evidence suggests these cells are either derived from circulating monocytes, or established in the organ during embryonic development.69 Through a set of elegant preclinical experiments, the role of these two macrophage lineages in the PDAC TME has been elucidated. These studies revealed embryonically derived, TAMs promote fibrosis and tumor growth, while monocyte-derived TAMs directly influence immune suppression.69 Embryonically-derived TAMs are distinguished by expression of colony-stimulating factor one receptor (CSF1R) in mice and CXCR4 in humans, and expand during tumor development.69 In contrast to established roles for these TAM subsets, dynamic imaging microscopy showed prolonged interactions between TAMs and CD8⁺ T cells in murine pancreatic tumors.69 These interactions were localized to dense stromal regions of tumors, whereby T cells were trapped and prevented from infiltrating tumors.69 These data indicate a dual role for embryonically derived TAMs in promoting fibrosis and tumor growth and also preventing the infiltration of cytotoxic T cells into tumors.

In comparison, monocyte-derived TAMs express high levels of MHC-II and are more adept at sampling and presenting antigen. Monocyte-derived TAMs in circulation can infiltrate into pancreatic tumors or tumor-draining lymph nodes, by virtue of interactions with chemokine receptor 2 (CCR2).24 70–73 A recent study characterizing extratumoral Ly6C^low F4/80⁺ macrophages (monocytic phenotype markers) demonstrates these cells act outside of tumors to drive CD4⁺ T-cell-specific exclusion from PDAC.74 Clodronate depletion of macrophages from mice with spontaneously arising PDAC increased infiltration of CD4⁺ T cells into tumors.74 As with studies of Tregs, the effects of macrophages on CD4⁺ T-cell exclusion are localized to extratumoral locations, as clodronate had no effect on macrophages in the TME.74

Taken together, the available data indicate investigation should extend to regions outside of tumor tissue, to consider how local and distal mechanisms influence immune suppression in PDAC. In addition to T-cell exclusion, there are numerous immune interactions in PDAC mediating suppression of T-cell activation, which we highlight in figure 2.

ICI, specifically targeting CTLA-4 or the PD-1/programmed death ligand 1 (PD-L1) axis, has gained traction due to success in several oncological settings. Unfortunately, these drugs have shown little promise as single agents for patients with PDAC.2 75 Equipped with new and emerging knowledge of immune suppression in PDAC, many groups are pursuing combinatorial approaches to alleviate immune suppression and enhance ICI in PDAC. These include neutralization of growth factors or cytokines, inhibition of chaperone proteins and kinases, simultaneous blockade of multiple immune checkpoints and a host of others. Many strategies have emanated from encouraging preclinical results into first in human clinical trials in the setting of PDAC (table 1). It is worth noting that the effects of radiation and chemotherapy, which are commonly incorporated into combination therapeutic strategies (table 1), have not been fully characterized with respect to their immune influence. Recent studies addressing the effects of radiation have revealed this approach to control local tumor growth but with detrimental effects on antitumor immunity within the TME. Results from these studies indicate an influx in suppressive macrophages, Tregs and increases in inducible Nitic Oxide Synthase (iNOS) release by cancer-associated fibroblasts that together result in poor T-cell activity and sparse infiltration of pancreatic tumor tissues.76–78 In contrast, chemotherapy is hypothesized to increase T-cell priming, which we discuss further briefly, and data from our group and others indeed suggest immune changes elicited by chemotherapy are significant.76 79 Thus, considering how immunotherapy approaches can be strategically combined with radiation or chemotherapy will be key in moving forward.

The complicated cytokine and chemokine milieu of PDAC contributes to immune suppression in various ways. However, certain soluble factors are consistently upregulated by multiple cell subsets in PDAC. IL-6 represents one prominent cytokine consistently present within the PDAC TME. Although this cytokine can be derived from multiple cellular sources, it is transcribed in abundance by human pancreatic stellate cells and drives expansion of myeloid-derived suppressor cells (MDSC) in vitro80 (figure 3). The influence of IL-6 on myeloid cells has also been demonstrated in metastatic PDAC, where IL-6 signaling through serum amyloid A1 and A2 promotes myeloid cell recruitment and a prometastatic niche in the liver.81 IL-6 can also polarize T-cell responses away from Th1 immunity, characteristic of effective antitumor responses, and regulate balance of Th17 or T regs in a context-dependent manner82–84(figure 3). Using murine PDAC models, in vivo blockade of IL-6 enhanced efficacy of anti-PD-L1 antibodies in a CD8⁺ T-cell-dependent manner.85 The combination of blocking IL-6 and PD-L1 has since been extended to models of brain, colon, non-small cell lung cancer and others.86–88 These preclinical data provide rationale for an ongoing early phase clinical trial at our institution that encompasses a robust series of correlative studies on immune and stromal biomarkers in paired biopsies (NCT04191421). Exciting studies testing IL-6R blockade in combination with chemotherapy (NCT02767557) and immunotherapy/radiotherapy combinations (NCT04258150) have also recently opened at other institutions for patients with metastatic PDAC.

Another potent mediator of tumor progression in PDAC is TGFβ, which is present in the stroma of pancreatic tumors.89 90 While TGFβ has a powerful influence on malignant cells, this cytokine also influences T-cell function and differentiation (figure 3). With respect to CD4⁺ T cells, TGFβ regulates expansion of cells with Th17 or regulatory phenotypes, depending on the presence of IL-6.91 TGFβ also influences the phenotype of CD4⁺ T ells by inhibiting expression of the transcription factors GATA binding protein 3, T-box protein expressed in T cells and subsequent signaling to prevent activation of inflammatory CD4⁺ T cells.92–94 More recently, evidence has emerged demonstrating TGFβ signaling in CD8⁺ T cells inhibits both trafficking into tumors and activation of CD8⁺ T cells.95 While dual blockade of TGFβ and PD-1 led to tumor regression in preclinical studies, activation of T cells both in the tumor and in the periphery demonstrates the ability of this combination to overcome broad immune suppression in these models.96 Currently, a TGFβ ligand trap (M7824) is in clinical trials alongside standard of care gemcitabine for patients with untreated PDAC (NCT03451773).

Investigation of tumor-associated myeloid populations has revealed important mechanisms of suppressed T-cell immunity in PDAC and new targets for therapy. Recently, colony-stimulating factor 1 (CSF1) and its receptor, colony-stimulating factor 1 receptor (CSF1R) have garnered attention in PDAC. The source of CSF1 is likely PCCs themselves, with CSF1R expression localized to the immediately adjacent stroma.97 Initial mouse studies blocking CSF1/CSF1R interactions revealed a significant impact on myeloid populations, reducing M-MDSCs and MHC-II expressing macrophages that can directly inhibit T-cell activity in PDAC97 (figure 3). Subsequent studies using dual blockade of CSF1R and PD-1 or CTLA-4 profoundly increased both CD4 and CD8 infiltration of tumors and resulted in tumor regression, including complete regression in about 30 percent of mice.97 This strategy has now led to a national phase Ia/b clinical trial (NCT02526017) incorporating αPD-1 blockade and cabiralizumab, an antibody against CSF1R.

Blockade of the chemokine CCR2 has elicited similar, even redundant mechanisms of response to that of CSF1R blockade.70 CCR2 has been identified as a crucial mediator of macrophage migration and infiltration into various tumor types.24 72 73 While CCR2 inhibitors only modestly impact tumor growth, an impressive antitumor response was mounted in mice treated simultaneously with gemcitabine and CCR2 inhibitor (CCR2i).70 Following these promising studies, a clinical trial at Washington University (NCT01413022) and a multicenter trial (NCT02345408) treated advanced/metastatic patients with PDAC with the combination of fluorouracil, leucovorin, irinotecan, and oxaliplatin (FOLFIRINOX) and one of two distinct CCR2i.^{10 98} Both clinical trials elicited excitement with objective responses and prolonged overall survival compared with published results of FOLFIRINOX alone.10 98 Correlative studies from these trials revealed decreases in MDSCs, and increased CD4⁺ and CD8⁺ T-cell infiltration in tumor tissue, consistent with data reported in murine models71 (figure 3).

FAK inhibitors are being explored as a therapeutic option with similar mechanisms of action to CCR2i and CSF1Ri. Interest in FAK has been evident for some time, as the multifunctional protein has been studied for its role in invasion, migration, cell survival and proliferation.99–103 Emerging research has exposed a novel role for FAK in mediating immunosuppression.104 105 Infiltrating myeloid cells, specifically tumor-associated macrophages and neutrophils, depend on FAK to penetrate tumors with dense ECM.106 107 In line with these data, increased FAK activation in human PDAC samples correlates with decreased infiltration of CD8⁺ lymphocytes, increased neutrophils and CD15⁺ granulocytes104 (figure 3). These data indicate a correlation between increased FAK activation and cells with an immunosuppressive phenotype in human PDAC tissues. Indeed, FAK inhibition in murine models of PDAC successfully inverted this balance of cytotoxic lymphocytes and suppressive myeloid cells to favor regression of pancreatic tumors104 (figure 3). The combination of FAK inhibition with chemotherapy and PD-1 blockade improved survival in mice bearing spontaneous PDAC.104 These preclinical results culminated in a phase I clinical trial of gemcitabine, the PD-1 blocking antibody pembrolizumab, and the FAK inhibitor defactinib.108 Stable disease was observed in just over 50% of the patients in this trial, with no dose limiting toxicities reported in the dose expansion phase.108 This trial is now enrolling patients in a phase II expansion cohort (NCT03727880).

HSP90 is a chaperone protein at the crux of pathways associated with many hallmarks of cancer. These include assisting the folding of proteins such as BRAF, EGFR, fusion proteins like Bcr-Abl and other factors dysregulated in cancer.109–113 Immune-associated client proteins of HSP90 such as STAT3, STAT5, and C/EBPε are also of interest, given their involvement in expansion of myeloid cells with suppressive functions.114–118 Thus, HSP90 represents a target with a centralized role in many pathways regulating tumor progression while also contributing to a protumorigenic microenvironment. HSP90 inhibitors may also be leveraged for immune modulation.119–122 Preclinical studies demonstrate XL888, an HSP90 inhibitor, can elicit efficacy in murine PDAC models when combined with PD-1 blockade and can enhance tumorous infiltration of both CD4⁺ and CD8⁺ cells123 (figure 3). It is possible the improved response results from the impact of XL888 on the TME of these tumors. Specially, XL888 can limit activation and inflammatory cytokine secretion from pancreatic tumor-associated fibroblasts (figure 3). These preclinical studies complement an ongoing investigator-initiated phase Ib/II clinical trial (NCT03095781) of XL888 and pembrolizumab (anti-PD-1).

Given the immunologically cold state of pancreatic tumors, licensing of antigen-presenting cells (APCs) to prime and activate T-cell responses is an area of growing attention. On recognition of antigen on APCs, interaction between CD40 ligand on T cells and CD40 receptor on APCs mediates priming of T cells, described as the transition of T cells to a ‘licensed’ state.124–126 This allows for efficient and potent activation of both CD4⁺ and CD8⁺ T cells. The development of CD40 agonists to boost this response was therefore identified as an auspicious therapeutic approach. This strategy was tested in a multicenter phase I dose escalation trial with patients receiving the combination of CD40 agonist and gemcitabine demonstrating improved OS and progression free survival(PFS) versus gemcitabine alone.127 Notably, this trial enrolled patients with newly diagnosed, resectable PDAC rather than advanced disease. Priming T-cell responses requires sufficient antigen presentation by APCs; therefore, patients were treated with gemcitabine with CD40 agonist delivered several days after the first dose of gemcitabine.127 This approach was used with the hypothesis that chemotherapy would elicit some tumor cell killing to provide APCs in the lymphoid organs with antigen released from dying tumors. These studies raise a particularly important question as to the timing of combination therapy.

Similar results were observed in KPC mice treated with gemcitabine and the CD40 agonist FGK45.127 In an interesting mechanistic twist, murine studies in KPC mice revealed macrophages, rather than T cells, as indispensable for FGK45-induced tumor regression, as this CD40 agonist converted the cytokine profile and activity of macrophages to elicit stromal degradation and lysis of pancreatic tumor cells127 (figure 3). The ability of CD40 agonists to stimulate stromal modulation and reorganization via macrophage activity suggests other therapeutic modalities could be enhanced without the immunosuppressive stroma characteristic of pancreatic tumors. In melanoma, αCD40 agonists have been combined with CTLA-4 blockade to significantly enhance both T-cell priming and activation with survival benefits for patients (NCT01103635).128 Employing a similar strategy, a Phase Ia/b clinical trial (NCT03214250) of gemcitabine plus nab-paclitaxel, the CD40 agonist APX005M, and nivolumab (αPD-1) demonstrated safety and tolerability with promising antitumor activity. Based on encouraging initial data, this combination has proceeded to phase II dose escalation.

Very recent advances in technology and understanding of T-cell biology have catalyzed development of vaccine and cellular therapies such as autologous cell transfer and chimeric antigen receptor-expressing T cells (CAR-Ts). There are a number of active clinical trials using vaccine therapies in PDAC with novel strategic targets. These trials include vaccines directing immune responses to tumor-expressed human guanylyl cyclase C and mutated KRAS (NCT04111172 and NCT04117087, respectively), as well as several personalized peptide-based vaccines (NCT03794128 and NCT02600949). The granulocyte-macrophage colony-stimulating factor-based vaccine GVAX is being tested in clinical trials in combination with ICI for PDAC (table 1). Another unique vaccine therapy uses patient-derived, mature DCs, which are directed against mutant KRAS by pulsation with mutant KRAS peptides (NCT03592888). These cells are then used for autologous transfer back into patients to elicit adaptive immune responses.

Adoptive cell therapies have had success in multiple cancer types and are under development for PDAC. These approaches include administration of TIL products and autologous approaches involving T-cell receptor (TCR) or chimeric antigen receptor T cell therapy. While TIL expansion from PDAC tumors can be challenging, CAR-T or TCR-based therapy is governed by identification of appropriate antigens toward which immune responses should be directed.129–132 While several tumor-associated antigens continually emerge as targets in pancreatic cancer, the investigation and identification of viable TCR or CAR-T targets is ongoing. Current clinical trials using CAR-T therapy are targeting a variety of antigens, including carcinoembryonic antigen, mesothelin, CD133, CD70, human epidermal growth factor receptor 2, epithelial cell adhesion molecule and many others, which we have previously reviewed.133 Additionally, prostate stem-cell antigen (PSCA) targeting CAR-T therapy is currently in clinical trials (NCT02744287) and has shown promising interim results. The broad heterogeneity of antigen presentation by cells within solid tumors makes CAR-T design extremely challenging. An innovative approach by Marker Therapeutics is testing a T-cell product directed against up to five tumor-associated antigens simultaneously, which is currently in phase I/II clinical trials (NCT03192462). Additionally, with the discovery of T-cell subsets with high potency against tumors, the field of cellular therapy for PDAC is rapidly expanding. Further, these cellular therapies will encompass significant advances in innovation, such as cytokine, antibody or chemokine receptor engineering that may be advantageous for notoriously hard-to-treat diseases such as PDAC.134