The TME of PC is characterized by a complex network of cellular and non-cellular elements that create a highly immunosuppressive environment. It is composed of a dense desmoplastic stroma, comprising CAFs, PSCs, extracellular matrix (ECM) and immune suppressive cells[76].

Initially, the notable capacity of CAFs to generate and remodel the ECM plays a pivotal role in immunotherapy resistance in PCs. These cells comprise distinct subtypes, each exerting specific influences on the TME. Firstly, α-smooth muscle actin, + myofibroblasts (myCAFs), which are transforming growth factor (TGF) signaling-dependent, contribute to the synthesis of ECM components[77,78]. On the other hand, inflammatory CAFs, exhibit elevated expression of interleukin (IL)-6, which is related to cancer progression[78,79], while major histocompatibility complex class II (MHC class II) + CAFs are able to present antigens but lack costimulatory molecules, potentially leading to deactivation of CD4⁺ T cells and further immune suppression in the TME (Figure 1)[80,81].

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Figure 1 Simplified scheme of the tumor microenvironment. PSCs: Pancreatic stellate cells; CXCL2: C-X-C chemokine ligand 2; iCAFs: Inflammatory cancer-associated fibroblasts; apCAF: Antigen-presenting cancer-associated fibroblast; ECM: Extracellular matrix; TAM: Tumor-associated macrophage; MHC II: Major histocompatibility complex class II; IL: Interleukin; TGF: Transforming growth factor.

In the context of immunotherapy resistance, myCAFs emerge as a key player in this process, as they lead to the development of a dense, fibrotic stroma around the tumor, which provides a physical barrier that impedes the infiltration of immune cells and, consequently, impairs the effectiveness of immunotherapeutic agents[77,82]. Also, evidence suggests that secreted phosphoprotein 1 (SPP1) derived from CAFs in hepatocellular carcinomas apparently increases resistance to tyrosine kinase inhibitors (TKIs) through the induction of epithelial-to-mesenchymal transition[83,84]. However, as the direct correlation between SPP1 and TKI resistance remains unexplored in PC, further research is required to clarify this issue.

Additionally, the combination of a dense stroma and limited vascularization induces severe hypoxia within the TME, triggering the stabilization of hypoxia-inducible factors 1 and 2 (HIF2)[82]. CAF-specific deletion of HIF2 is associated to increased survival in PC, by reducing the intratumoral recruitment of M2 macrophages; and therapeutic HIF2 inhibition leads to increased response to immune checkpoint blockade[85]. These findings highlight the critical role of hypoxia in shaping the pancreatic TME and influencing immunotherapy resistance.

Finally, PSCs also seem to play a role in desmoplasia, as they become activated in response to signals from PC cells and contribute to the formation of the fibrotic stroma[82]. PSCs are associated with the secretion of immunosuppressive molecules, including C-X-C chemokine ligand (CXCL) 2, IL-6 and galectin-1, sustaining immunosuppression within the TME[86]. These dynamic interactions between PSCs and PC cells sustain underlying mechanisms that promote immunotherapy resistance (Figure 1).

Therefore, therapeutic agents that target the aforementioned components could be a potential next step in overcoming immunotherapy resistance in PCs.

Evidence also suggests that genetic/epigenetic factors may play a role in immunotherapy resistance in PC, even though current literature provides minimal information on the subject. Some studies indicate that mutations in the p53 gene are associated with alterations in the innate immune response, which may underlie tumorigenesis and promote immunotherapeutic resistance in PDACs[87]. In this regard, the Trp53^R172H mutation in PC cells has been identified as a promoter of neutrophil accumulation, potentially contributing to resistance against immunotherapy[88].

Pancreatic ductal adenocarcinoma is typically associated with a low mutation burden, resulting in a paucity of neoantigens and a scarcity of tumor-infiltrating effector T cells[89,90]. This gives rise to an "immunologically cold" TME, which is characterized by a dearth of tumor antigen-specific CD8+ T cells and a limited expression of activation markers such as interferon-gamma (IFN-γ) and granzyme B[91-95]. In turn, CD4+ helper T cells are more abundant within the TME compared to CD8+ T cells, displaying diverse immunological effects, including both anti- and pro-tumor activities across various phenotypes such as effector CD4+ T helper (Th) 1, Th2, Th17, FoxP3+ regulatory Ts (Tregs), and γδ T cells[96]. Nevertheless, the evaluation of antigen-specific CD4+ T cells remains elusive in both animal and human PDAC models[97]. Moreover, These observations imply a deficit or impediment in adaptive T cell immunity, recognized as the primary factor contributing to the concerning resistance against immune checkpoint blockade therapies[81].

Accordingly, PDAC appears to utilize two primary strategies to circumvent anti-tumor immune responses: (1) intrinsic T-cell receptor (TCR)-mediated exhaustion; and (2) extrinsic TME-driven immunosuppression[81,98]. Indeed, CD8+ T cells targeting tumor-specific antigens can trigger cell death. Nonetheless, in cases where the tumor persists and these cells face continual antigen exposure, sustained TCR activation leads to their differentiation into exhausted T (Tex) cells[99-101]. Tex cells express cell surface inhibitory receptors such as PD-1, MUC-3/T-cell immunoglobulin, and T-cell activation gene[94,102-105]. Upon interaction with their specific ligands expressed on cells within the TME, Tex cells undergo a progressive decline in effector function, differentiation state, and proliferative capacity[81]. Notably, these cells not only experience a reduction in functionality, such as decreased tumor necrosis factor (TNF)-α and IFN-γ expression, but also demonstrate a gradual increase in IL-10 expression within the TME[106]. These alterations thus contribute to the establishment of a local immunosuppressive milieu (Figure 2).

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Figure 2 Intrinsic and extrinsic mechanisms of T cell-associated immunosuppression. MDSCs: Myeloid-derived suppressor cells; TME: Tumor microenvironment; TCR: Intrinsic T-cell receptor; TAM: Tumor-associated macrophage; IRs: Inhibitory receptors; TIM-3: Mucin-3/T-cell immunoglobulin; LAG-3: T-cell activation gene; TGF: Transforming growth factor; PD-1: Programmed cell death-1; IL: Interleukin; TNF-α: Tumor necrosis factor-α; IFN-γ: Interferon-gamma.

On the other hand, extrinsic factors encompass elements in the TME that hinder T cell function[107]. The oncogenic activation of KRAS in pancreatic cells initiates PanIN at the outset of cancer development, which triggers an immunosuppressive milieu orchestrated by tumor-associated macrophages (TAMs), myeloid-derived suppressor cells (MDSCs), and Treg and Breg cells, compounded by inhibitory cytokines and metabolic limitations[108-110].

In this scenario, macrophages represent the predominant leukocyte population identified within PDAC[111]. Studies have unveiled the origin of TAMs in PDAC from two primary sources: (1) Bone marrow-derived inflammatory monocytes; and (2) embryonic-derived tissue-resident macrophages[112,113]. These cells typically exhibit an immunosuppressive phenotype, which is characterized by the expression of immune checkpoints, inhibitory ligands, and the secretion of immunoregulatory cytokines such as IL-10[114-116].

Concurrently, the recruitment of bone marrow-derived myeloid cells toward PDAC involves a complex process orchestrated by granulocyte-macrophage (GM) colony-stimulating factor (CSF), granulocyte-CSF (G-CSF), IL-3, vascular endothelial growth factor, and the orchestrated interplay between the CXCL12/C-X-C chemokine receptor 4 (CXCR4) or C-C chemokine ligand 2/C-C chemokine receptor 2 signaling cascades[111,117,118]. Ultimately, tumor cell production of GM-CSF and G-CSF and tumor cell production of IL-1β fosters the proliferation of immature myeloid cells and drives their acquisition of a suppressive phenotype (MDSCs)[119-121].

Additionally, stromal-associated fibroblasts are known to produce CXCL13, which serves as a recruitment signal for IL-35-producing regulatory B cells within the TME[122]. This phenomenon further exacerbates PDAC immune evasion by harnessing IL-35-mediated inhibition, effectively suppressing T cell proliferation[123].

Collectively, TAMs, MDSCs, and Bregs exhibit a robust capacity to suppress the proliferation in both CD4+ and CD8+ T cells[124]. They also generate elevated levels of immunosuppressive cytokines, such as IL-10, IL-27, and TGF-β[106,122,124]. This coordinated activity facilitates the recruitment of regulatory Foxp3+CD4+ Tregs, which may also impede the antitumor immunity of CD8+ T cells at local intratumoral sites[125,126]. In summary, these factors collectively reduce T cell infiltration, impair their function, or promote their exhaustion within the TME, contributing to resistance against immunotherapy interventions (Figure 2).

Over the past decade, there has been significant interest in the pancreatic TME, particularly in its capacity to influence therapy response. The focus has shifted towards recognizing the TME as a key factor and obstacle affecting the effectiveness of immunotherapy in pancreatic ductal adenocarcinoma[127].

Numerous promising therapies targeting various mechanisms are currently undergoing preclinical and clinical development. These approaches encompass novel strategies to enhance T-cell responses, modify myeloid and stromal compartments, and attract new immune cells to the TME of PDAC[128].

From this perspective, targeting the tumor stroma holds potential advantages in the treatment of PC. The matricellular protein Secreted Protein Acidic and Rich in Cysteine (SPARC), produced by CAFs, has the ability to bind albumin[127]. This led to the hypothesis that SPARC could enhance the accumulation of nab-paclitaxel within the PC microenvironment, thereby augmenting its anti-tumor efficacy[129]. In a phase III study combining albumin-bound paclitaxel (nab-paclitaxel) with gemcitabine, the results indicated an increased intracellular concentration of gemcitabine, possibly attributed to the disruption of the tumor stroma and the reduction of CAFs[129].

Despite the promising outcomes mentioned earlier, efforts to target the tumor stroma have yielded contradictory consequences. Matrix metalloproteinases, a family of proteolytic enzymes essential for maintaining tissue homeostasis, play a crucial role in cancer invasion when expressed abnormally[130]. However, attempts to target matrix metalloproteinases using marimastat and tanomastat did not show any discernible benefits when combined with gemcitabine[131,132].

Furthermore, follow-up studies have indicated that depleting the stroma may, in fact, promote tumor growth, highlighting the intricate and multifaceted role that stroma plays in tumor biology. This underscores the complexity of the interactions within the TME and suggests that a nuanced approach is needed when considering stroma-targeted therapies in cancer treatment[133].

In preclinical mouse models of PC, the depletion of stroma by inhibiting the Hedgehog cellular signaling pathway has been demonstrated to enhance the delivery of gemcitabine to tumors[134]. This intervention resulted in improved survival and reduced metastasis by increasing the intracellular concentration of gemcitabine. The Hedgehog pathway's involvement in the formation of desmoplasia highlights its role in impairing drug delivery in the context of PC[134]. Despite the conflicting results of tumor response to stroma-depleting therapies, the TME plays a significant role in tumor biology and in modulating the immune recognition of PC.

Another therapeutic avenue under investigation involves targeting hyaluronic acid, which is abundant in PCs and contributes to angiogenesis and chemoresistance[135]. In a phase II study involving untreated, metastatic PC patients, the targeting of hyaluronic acid using pegvorhyaluronidase alfa, a pegylated formulation of recombinant hyaluronidase, in combination with nab-paclitaxel/gemcitabine resulted in a significant improvement in progression-free survival and OS[136].

Still in this scenario of trying to manipulate the microenvironment, it is known that the TME in PC represents a formidable therapeutic challenge when using traditional immunotherapies. Nevertheless, there is a shift towards utilizing combination approaches to reprogram the TME, aiming to unlock the potential benefits of immunotherapy. Early results from these endeavors are showing promise in the pursuit of more effective treatments for PC.

As aforementioned, targeting immunosuppressive cells within the TME enhances the likelihood of efficacy in immunotherapy treatments. One primary target is CSF1 receptor (CSF1-R), located on TAMs. The binding of CSF1 to CSF1-R facilitates TAM proliferation and extended survival, promoting tumor growth, resistance to treatments, and metastasis[137]. Inhibition of CSF1-R results in fewer TAMs, leading to a heightened immune response, increased tumor regression, and improved survival[138].

Looking at another relevant pathway for manipulation, it is notable that pancreatic ductal adenocarcinoma tumors show infiltration of M2 macrophages, which have an immunosuppressive function. This phenotype is characterized by the expression of CD206, CSF-1R, and IL-10, along with reduced expression of MHC class II[81]. The CSF-1 pathway plays a crucial role in the differentiation and survival of M2 macrophages. Inhibiting the CSF-1 pathway has been demonstrated to redirect TAMs toward the M1 phenotype, leading to distinct remodeling of the TME[139-141].

From a molecular perspective, it is important to analyze that CXCL12, a chemokine produced by CAFs, is frequently expressed at elevated levels in the PDAC TME. This creates a network of dense stroma, which, in turn, hinders the migration of immune cells and the recognition of cancer cell antigens. The elevated levels of CXCL12 in the PDAC TME play a role in creating an immunosuppressive environment, thereby diminishing the effectiveness of immune responses directed at cancer cells[142]. In preclinical studies, interrupting the interaction between CXCL12 and its receptor, CXCR4, enhanced the impact of ICIs in models of PDAC[142,143].

Also in this scenario, pancreatic tumor cells, fibroblasts, and other stromal cells release TGF-β, a cytokine that contributes to the creation of an immunosuppressive structure in the TME[144]. Using the small molecule inhibitor galunisertib to target TGF-β, combined with gemcitabine as the initial treatment for PDAC, resulted in only a marginal improvement in median mOS compared to gemcitabine alone and did not achieve statistical significance[145]. Following this, galunisertib was evaluated in conjunction with durvalumab in a cohort of 32 patients with advanced PDAC and demonstrated restricted effectiveness, yielding only one partial response[146]. Novel approaches, such as exploring a bifunctional fusion comprising a monoclonal antibody targeting TGF-β along with other ICIs, are currently being investigated[147].

Therefore, the combination of treatment strategies aimed at stimulating the immune response and overcoming barriers in the TME represent a promising avenue for improving the treatment of patients with PC.

The genetic mutation background of PC is well known, being found in CDKN2A, MLH1, BRCA2, ATM, KRAS and BRCA1. The most prevalent change of an oncogene in PC cells is the mutation of KRAS. Other than that, some tumor suppressor pathways are genetically inactivated, such as INK4a/ARF (p16), TP53, DPC4/Smad4[148-153].

Thus, the key principles of gene therapy are to induce immune effects that combat tumors with different signaling pathways, delivering genetic material to cells, focusing on the resolution of a disorder[154]. An effective gene therapy regimen is dependent upon the following factors: Efficient delivery of the gene, therapy specifically targeted at the tumor, and careful selection of optimal targets[155].

Against this backdrop, there are many possibilities that surround gene-therapy on PC cells. Gene editing and gene transfer can be utilized as a therapeutic intervention, employing an array of vectors and molecular tools, including interference RNA and genome editing techniques, which have shown promise in bridging preclinical cancer research and clinical trials[156,157].

In addition, various strategies have been applied to eliminate tumor cells based on known genetic alterations. Gene transfer strategies with TP53 have been utilized to treat multiple cancers[158]. However, attempts to restore TP53 expression during tumor growth have yielded disappointing results, indicating the limited efficacy of gene transfer in vitro[158].

Still in the scenario of genetic manipulation, suicide gene therapy is a major topic of discussion, based on the transfer of a suicide gene with a strong neighboring antitumor effect that can compensate the weakness of gene expression within the tumor[155]. The classic suicide gene strategy is the herpes simplex virus thymidine kinase gene (HSV-TK gene)[159]. This therapy is capable of causing toxicity and cell death, through metabolites and inhibition of DNA synthesis[159,160], It also elicits a robust immune response targeting tumor cells by releasing tumor antigens, resulting in a reaction against additional tumor cells by the body[159-161]. HSV-TK delivery via adenovirus and retrovirus have shown great anti-tumor efficiency in pancreatic cells both in vitro and in vivo[160,162].

Other examples of suicide/prodrug gene system that has been also tested, with success, in PC models is the cytochrome P450/isofosfamide system, was developed through in vitro and in vivo proof of concept to conduct phase I and II trials in patients with PC, the treatment has shown significant success in improving survival rates[158,163-165].

Other than that, miRNA is another potent point for therapeutic approach. Several studies have shown that miRNAs play important roles in the development of pancreatic tumors and also in the process of resistance to various therapies, including immunotherapy[166-168]. Loss of miRNA expression may result in significant dysfunctionality and promote carcinogenesis, owing to their crucial role in modulating apoptosis, cell cycle, and differentiation[158].

Thus, the methods for modulating intracellular miRNA levels primarily consist of miRNA replacement therapy and anti-miRNA oligonucleotides. In miRNA replacement therapy, oligonucleotide mimics are used to increase miRNA levels, while in anti-miRNA oligonucleotides, miRNA silencing is induced[169,170]. However, some barriers still exist when thinking in miRNA therapy such as low in vivo stability, improper biodistribution, insufficient cell specificity, disruption and saturation of endogenous RNA machinery, as some examples[171].

In this scenario, several miRNAs that are upregulated or downregulated in PC have demonstrated their contribution to tumor cell growth by targeting specific molecules[172-174]. An elevation in circulating miRNAs, such as miR-21, miR-25, miR-155 and miR-196, demonstrated a strong correlation with chemotherapy resistance among PC patients[175,176]. In this sense, an experimental study showed that targeting the oncogenic miRNA21 could suppress tumor growth in PC in vitro and in vivo[177]. However, no miRNA therapeutics have been tested clinically for PC treatment[178].

From another perspective of genetic manipulation, oncolytic virotherapy is one of the most promising anti-cancer therapies using agents with high antitumor potency and strong oncolytic effect[154,179]. Natural pathogens have either been selected or designed to specifically infect and destroy cancer cells, being engineered in a way that enables the production of cytokines, antigens, or suicide genes[158]. Oncolytic adenoviruses have been considered highly eligible vehicles for delivery of therapeutic genes to treat cancer due to their tumor-restricted replication capabilities[158,180], and because of them being non-pathogenic and with a high selectivity and cytotoxicity to cancer cells[181].

With this in mind, it is important to point out that a known viral vector is the HSV type designed with an efficient blockade of experimental tumor growth, used alone or in combination with gemcitabine[182]. A study with a HSV that showed an promising anti-cancer activity was Myb34.5, which has been assessed preclinically in PC models, being used inducing apoptosis and inhibition of pancreatic tumor growth[183]. Other studies are being conducted, dealing with possible viruses that can be used on a therapeutic concept, such as the oncolytic parvovirus H-1, in some clinical trials[184,185].

Numerous genetic alterations that directly contribute to pancreatic tumorigenesis have been identified or are being actively studied; because of it, novel therapies for PC patients by targeting specific genes are a promising future, associated with a lot of new trials searching novel possibilities[154,156,158]. This approach to personalized medicine can be utilized for patients with PC, providing appropriate treatment that is tailored to their individual needs.

The mechanisms of resistance to immunotherapy present in PC are rooted in an intense interaction between molecules and cells of the TME and cells of the immune system, with this impact being particularly focused on the activity of T cells, leading to a reduction in the tumor activity of these cells[186]. Thus, novel approaches to treating immunotherapy-resistant PC involve manipulating the activity of T cells and immune system cells that directly interact with these anti-tumor cells[187].

One of the primary immunotherapy strategies used in oncology is to block the immune checkpoint, but resistance to existing methods has prompted the need to employ immunomodulators, such as PD1-IL2v[188,189]. PD1-IL2v is a bispecific antibody molecule that binds to PD-1 on CD8+ T cells and incorporates a modified IL-2 molecule in its structure[189]. This modification stimulates the cytotoxic activity of CD8+ T cells without binding to CD25 present on Treg cells, consequently avoiding the activation of these regulatory cells[189]. Thus, the study conducted by Tichet et al[189] in mice was based on the combination of anti-PD-L1 with the immunomodulator PD1-IL2v and achieved promising results, including tumor regression, improved efficiency of anti-tumor T cells, increased infiltration of CD8+ T cells into the TME, modulation of TAMs, and demonstrated a positive response for cancers resistant to immunotherapy[189].

From another perspective, Siglec-15 was detailed by Wang et al[190] in 2019, demonstrating that it can be expressed in cancer cells and TAMs, with increased expression in macrophages leading to the inhibition of anti-tumor T cell proliferation[190]. Consequently, Siglec-15 has become a new target for therapy based on blocking the immune checkpoint, despite the absence of published studies to comprehend all its functions in PC[190,191]. Sun et al[191] describe Siglec-15 as a potential therapeutic target for cancer based on ongoing clinical studies[191]. Therefore, as analyzed by Chen et al[192], Siglec-15-based therapy may offer a promising solution for PC patients resistant to anti-PD-1 treatment[192]. It can be utilized alone or in conjunction with other immune checkpoint blockade techniques, resulting in increased infiltration of CD8+ T cells into the TME[192].

Another growing immunotherapy technique in cancer treatment is ACT, based on the ex vivo manipulation of T cells to expand their anti-tumor activity[193]. After manipulation, these cells are reinserted into the individual to exert more potent anti-tumor effects[193]. Despite the various factors contributing to resistance to immunotherapy in PC, impacting the efficiency of ACT for this type of cancer, the primary obstacle remains the immunosuppressive and challenging-to-access TME, hindering the infiltration of immune cells[72]. In this regard, Rataj et al[194] demonstrated a promising approach to overcoming resistance by developing a fusion protein with the extracellular domain of the PD-1 receptor fused to the intracellular T-cell activation domain of CD28[194]. This fusion protein was implanted into CD4+ T cells using the ACT technique. When these modified cells were introduced into the TME, the PD-1 domain interacted with its ligand PD-L1[194]. However, instead of inducing immunosuppression, the activated CD28 protein coupled to PD-1 resulted in increased antitumor activity of CD4+ T cells through enhanced cytokine secretion and stimulation of the cytotoxic activity of CD8+ T cells[194].

Still from the perspective of manipulating the extrinsic and intrinsic mechanisms associated with T cells, even more recent studies have concentrated on the use of nanomedicines to overcome resistance to immunotherapy[195]. In this context, Jung et al[196] conducted a study in humanized mice employing an siRNA nanoparticle targeting PD-L1 as the therapeutic approach[196]. The study yielded promising results, leading to an increase in CD8+ T cells in the TME as a result of the blockade of PD-L1 induction caused by the nanoparticle absorbed by cells in the TME[196].

When analyzing molecular pathways, it is known that the use of cytokines as immunomodulators is an immunotherapeutic strategy employed in cancer treatment, but it has not yielded promising responses when used alone in PC, primarily due to immune resistance mechanisms[197]. Many therapies utilizing cytokines with immunosuppressive activity are employed as adjuvants to other immunotherapy models[197]. Nonetheless, more targeted studies investigating the action of specific cytokines may lead to new strategies for addressing immunotherapy-resistant PC.

With this in mind, Huang et al[198] conducted a study with the aim of inhibiting the immunosuppressive activity resulting from the action of IFN-γ, a pivotal cytokine in the process of resistance to immunotherapy[198]. According to this analysis, the action of gamma interferon leads to the production of proteins such as indoleamine 2, 3-dioxygenase 1 and CD274, which possess immunosuppressive properties and are included in the category of therapies based on inhibiting the immune checkpoint[198]. The study utilized dinaciclib to block the expression of these proteins induced by IFN-γ in murine models and achieved promising results in curtailing the immunosuppressive activity of IFN-γ, reducing cancer immune invasion, and blocking the expression of immune checkpoint[198].

In a similar vein, Tsukamoto et al[199] demonstrated in a study involving 235 patients that TNF-α overexpression is directly associated with increased PD-L1 expression in TME cells, leading to immunosuppression through the neutralization of cytotoxic T cells[199]. Consequently, anti-TNF-α may also exhibit promising efficacy in addressing resistance to existing immunotherapy in PC by impacting the PD-L1 receptor, which is immunosuppressive and also a target of immune checkpoint blockade[199]. Nevertheless, additional clinical trials aimed at analyzing the impact of anti-TNF-α on PD-L1 expression are still necessary.

The mechanisms of resistance to immunotherapy in the treatment of PC have brought a new challenge for medicine: To identify therapeutic combinations that help overcome resistance, thus increasing the efficiency of immunotherapy and improving the patient's prognosis[200].

From this perspective, Mehla et al[201] utilized a murine monoclonal antibody (mAb-AR20.5), which modulates the TME by binding to MUC1, in conjunction with PolyICLC (a vaccine adjuvant) and anti-PD-L1 in their murine models for the treatment of PC[201]. The combined therapy induced superior anti-tumor activity, leading to the rejection of tumor cells expressing MUC1 and heightened cytotoxic activity of CD8+ T cells[201]. This resulted in immune modulation and promising tumor control for PC through the use of an TME modulator, an immune checkpoint blocker and a vaccine adjuvant[201].

In the same context, it is pertinent to examine the promising aspect of using TME modulators alongside immune checkpoint inhibitors, as demonstrated by Rana et al[202]. They conducted a preclinical study with murine models, employing an inhibitor of the TGF-β receptor, responsible for TME progression, and an immune checkpoint blocker (anti-PD-L1/anti-CTLA-4)[202]. The study resulted in the inhibition of tumor growth, enhanced CD8+ T cell infiltration, and increased the population of M1 macrophages in the TME[202]. Additionally, Cappellesso et al[203] adopted a similar approach by analyzing the single-cell RNA of individuals with PC and identifying solute carrier family 4 member 4 (SLC4A4), primarily responsible for maintaining the acidity of the TME and, consequently, tumor progression[203]. This led to the association of an SLC4A4 inhibitor with ICI, such as anti-PD-1/anti-CTLA-4, in studies with mice, resulting in improved survival and overcoming resistance mechanisms that impact treatment alone[203]. Finally, Datta et al[204] employed mitogen-activated protein kinase/extracellular signal-regulated kinase and signal transducer and activator of transcription 3 inhibitors, crucial components of existing resistance mechanisms in the TME, in conjunction with anti-PD-1 in mice[204]. This approach yielded promising responses in terms of enhanced survival and increased anti-tumor response, driven by the greater recruitment of cytotoxic T cells in the TME[204]. These preclinical studies underscore the significant clinical potential of combining TME modelers with immune checkpoint blockers, opening up new possibilities for innovative therapies in the treatment of resistant PC.

In the context of resistance mediated by immunosuppressive molecules, Zhang et al[205] demonstrated the involvement of IL-17 in the process of triggering the inactivation of CD8+ T cells and shaping the TME[205]. Subsequent to this analysis, a study in murine models was established utilizing a triple combination of anti-IL17/IL17R/PD-1 antibodies[205]. This approach resulted in a reduction in tumor size based on increased sensitization of the TME to the action of ICI, a fact corroborated when replacing anti-PD-1 with anti-CTLA-4 in the combination[205]. Similarly, Nelson et al[206] devised a triple combination involving natural killer T cells, a recombinant oncolytic virus designed to express the cytokine IL-15, and anti-PD-1[206]. The study's triple therapy tested in mice exhibited promising results, including prolonged tumor regression and complete elimination of the tumor in 20% of the mice[206].

Another compelling approach was demonstrated by Saung and Zheng[207] using a cancer vaccine (GVAX) in conjunction with anti-PD-1, anti-CSF-1R, and the chemotherapy drug gemcitabine in murine models[207]. The combination yielded enhanced survival of the mice, along with more efficient infiltration of anti-tumor cells and a reduction in myeloid cells[207]. Table 1 summarizes all the pre-clinical studies reported and their respective findings.

The realm of combined immunotherapy to overcome resistant PC has expanded in recent years, and clinical trials are already underway to tackle this significant challenge. Thus, Bockorny et al[208] conducted a phase IIa study to assess the efficacy of the combination of a CXCR4 blocker, BL-8040 (motixafortide), and pembrolizumab (anti-PD-1) for the treatment of 37 patients[208]. They achieved a disease control rate of 34.5% and an increase in OS of 7.5 months, attributed to greater infiltration of anti-tumor CD8+ T cells and a reduction in immunosuppressive cells such as MDSCs and T regs[208]. Similarly, Overman et al[209] used a Bruton's TKI combined with anti-PD-1 in a randomized phase II clinical trial with 40 patients[209]. Although the combination was tolerated and showed limited clinical activity, with a disease control rate of only 21.1%, blood analysis revealed a reduction in MDSCs[209]. Consequently, these clinical trials reveal a relevant potential, paving the way for new studies aimed at manipulating the TME in combination with ICI and other treatment models, seeking improved results for the treatment of patients with PC.

Finally, it is important to analyze the clinical studies carried out with a combination of different PC vaccine models. From this perspective, Le et al[210] employed a combination of the GVAX vaccine and CRS-207 (live attenuated mesothelin-expressing Listeria monocytogenes) in a clinical trial with 90 patients[210]. They observed prolonged survival in these patients treated with this vaccine combination, with little toxicity in the therapeutic process[210]. Similarly, Nair et al[211] used the same immunotherapy combination in a phase IIa clinical trial with 38 patients[211]. They found that patients with higher CD8+ T expression achieved a longer OS under this therapeutic regimen[211]. Table 2 summarizes all the clinical studies reported and their respective findings.