PD1 signal transduction pathways in T cells

PDF |  HTML  |  How to cite  |  Order a Reprint

Oncotarget. 2017; 8:51936-51945. https://doi.org/10.18632/oncotarget.17232

Metrics: PDF 2957 views  |   HTML 3118 views  |   ?  

Hugo Arasanz, Maria Gato-Cañas, Miren Zuazo, Maria Ibañez-Vea, Karine Breckpot, Grazyna Kochan and David Escors _


Hugo Arasanz1,*, Maria Gato-Cañas1,*, Miren Zuazo1,*, Maria Ibañez-Vea1,*, Karine Breckpot3, Grazyna Kochan1 and David Escors1,2

1Immunomodulation Group, Navarrabiomed-Biomedical Research Centre, IdISNA, Pamplona, Spain

2Rayne Institute, Division of Infection and Immunity, University College London, London, United Kindom

3Laboratory of Molecular and Cellular Therapy Department of Biomedical Sciences, Vrije Universiteit Brussel, Brussels, Belgium

*These authors have contributed equally to this work

Correspondence to:

David Escors, email: descorsm@navarra.es

Grazyna Kochan, email: grazyna.kochan@navarra.es

Keywords: PD-L1, PDL1, PD1, B7-H1, cancer

Received: February 28, 2017     Accepted: March 24, 2017     Published: April 19, 2017


The use of immune checkpoint inhibitors for the treatment of cancer is revolutionizing oncology. Amongst these therapeutic agents, antibodies that block PD-L1/PD1 interactions between cancer cells and T cells are demonstrating high efficacies and low toxicities. Despite all the recent advances, very little is yet known on the molecular intracellular signaling pathways regulated by either PD-L1 or PD1. Here we review the current knowledge on PD1-dependent intracellular signaling pathways, and the consequences of disrupting PD1 signal transduction.

PD1 signal transduction pathways in T cells | Arasanz | Oncotarget


Anti-cancer immunotherapies are finally becoming clinically efficacious after many decades of intense research and development. Amongst these, antibody-mediated disruption of programmed death ligand 1 (PD-L1)/programmed death receptor 1 (PD1) interactions is one of the most efficacious with milder adverse effects than chemo- and radiotherapy [1]. However, this therapy is not successful for all patients and the mechanisms underlying anti-PD1 blockade need to be explored. Important breakthroughs are continuously being made such as the identification of mutations in JAK1, JAK2 and β2-microglobulin genes associated to primary and acquired resistance to PD1 blockade therapy [2, 3].

PD1 is a type I transmembrane protein preferentially expressed in immune cells such as T, B and NK cells. PD-L1 is a member of the B7 family of co-stimulatory/co-inhibitory molecules of antigen presentation expressed by a wide range of cell types, including cancer cells. When engaged to its receptor PD-L1, PD1 strongly interferes with T cell receptor (TCR) signal transduction through several poorly understood molecular mechanisms. PD1 is made of an extracellular immunoglobulin-like binding domain, a transmembrane region and a cytoplasmic domain containing an immunoreceptor tyrosine-based inhibitory motif (ITIM) and an immunoreceptor tyrosine-based switch motif (ITSM) [4]. These motifs are implicated in its immunosuppressive effects. Interfering with PD1 signal transduction either by antibody blockade or any other means enhances T cell functions by potentiating signal transduction from the TCR signalosome. Here we review the known molecular pathways by which PD1 exerts its immunosuppressive functions in T cells.


T cell activation and expansion is a complex process regulated by the interaction of several signaling pathways. T cells get activated and expand exponentially after encountering antigenic peptides specific for their cognate TCRs. Antigenic peptides are presented to T cells usually by professional antigen presenting cells (APCs) such as dendritic cells (DCs) through a highly regulated process called antigen presentation (Figure 1A). APCs capture and intracellularly process antigens from pathogens and cancer cells into short antigenic peptides which are loaded into major histocompatibility molecules (peptide-MHC complexes, or pMHC) and then exposed to the surface. There, peptide-MHC complexes bind to the TCR within the immunological synapse (Figure 1A). This recognition entails the initial step of the activation of the TCR signaling cascade (signal 1). However, T cells need at least a second co-stimulatory signal to escape from anergy or apoptosis [5]. A wide range of stimulatory or inhibitory interactions between receptors on the T cell surface and their ligands on the surface of the APC lead to signal 2. Thus this signal 2 will determine the level of T cell activation. Possibly the most important co-stimulatory interaction is provided by CD80 on the APC binding to CD28 on the T cell. There is also a third signal delivered by cytokines which regulates T cell differentiation and effector capacities [6]. Then, other inhibitory interactions take place between the APC and the T cell which modulate the strength and duration of the stimulatory signals.

Antigen presentation and T cell activation through the T cell receptor signalosome.

Figure 1: Antigen presentation and T cell activation through the T cell receptor signalosome. (A) T cells receive from antigen presenting cells (APCs, left of the picture) three signals. APCs present antigenic peptides complexed to MHC molecules (pMHC, as indicated) to T cells through binding to their TCR as shown. This interaction triggers intracellular signaling events (signal 1) as indicated within the T cell on the right. T cells simultaneously receive additional “positive” and “negative” signals through ligand-receptor interactions within the immunological synapse. On top is shown the co-stimulatory interaction driven by CD80-CD28, and below two inhibitory interactions between PD-L1/PD1 and CD80-CTLA4. The integration of these signals delivers a second signal regulating the extent of T cell activation. A third signal is also provided by cytokines (top). (B) Simplified scheme of the TCR signalosome including the αβ TCR chains associated to CD3 molecules as indicated. In this example, only CD3ζ dimers are shown. Signal 1 is initiated through αβ TCR and CD4/CD8 molecules. This signal depends on LCK activation that phosphorylates CD3 and CD28 cytoplasmic domains. ZAP70 then binds to CD3ζ and phosphorylates LAT and p38 as shown. Phosphorylated LAT recruits other enzymes and adaptor molecules as shown which will trigger calcium-dependent and MAPK-dependent pathways. Signal 2 depends on PI3K associated to CD28 when associated to CD80 on the surface of the APC. PI3K generates PIP3 leading to proliferation and survival by regulating AKT-mTOR pathways. CD28 engagement prevents apoptosis and acts synergistically with CD3-dependent signals. In green, adaptor molecules. In red, kinases and phospholipase C.


At the molecular level, signal one is delivered by kinase-dependent pathways triggered when TCR-CD3 molecules are bound to pMHC complexes in the immunological synapse (Figure 1A). TCR-CD3 and co-receptor (CD4 or CD8) cross-linking results in tyrosine phosphorylation of the TCR-CD3 intracellular domains by LCK and FYN kinases (Figure 1B). LCK also phosphorylates ZAP70 kinase which is then recruited to the CD3ζ chain [7]. ZAP70 starts multiple signaling events through LAT phosphorylation and association to GRB2 and PLCγ1, culminating with activation of the MAPKs ERK and JNK [8] involved in several cellular processes such as proliferation, differentiation, motility, stress response, apoptosis, and survival. PLCγ1 produces diacyl glycerol (DAG) and inositol 1,4,5-triphosphate (IP3) causing release of calcium ions from the ER and inducing NFAT and CREB translocation, which enhances IL2 transcription. Additionally, ZAP70 phosphorylates p38 associated to the scaffold protein DLGH1, resulting in its autophosphorylation at the activation loop by the so-called “alternative p38 activation pathway” which contributes to proliferation and cytokine production [9, 10].

Signal 2 (T cell co-stimulation) is exemplified by CD80-CD28 interactions between APCs and T cells (Figure 1). In this situation, LCK phosphorylates CD28 intracellular domain, providing a docking site for the PI3K complex. PI3K then generates phosphatidylinositol 3,4,5-triphosphate (PIP3), that activates downstream kinases including AKT which enhances proliferation and survival through the mTOR pathway [11], and PKCθ which activates NF-κB and MKK7, required for IL2 production. T cells require AKT and PKCθ activation to acquire full proliferative and effector activities.

Nevertheless, there are other associations between ligands and receptors in APCs and T cells (Figure 1A). Many of these will inhibit T cell activation to modulate their activities and have been extensively reviewed elsewhere [12].


Similarly to CD80-CTLA4, PD-L1/PD1 interactions are antagonists of CD80-CD28 co-stimulation. PD-L1-engaged PD1 strongly counteracts TCR signal transduction and CD28-co-stimulation even at very low PD1 expression levels. As a result, PD1 abrogates cytokine production, causes cell cycle arrest and decreases transcription of the pro-survival factor Bcl-XL [13]. In the direct pathway of TCR inhibition, engaged PD1 terminates ZAP70 and PI3K phosphorylation by recruiting SHP1 and SHP2 phosphatases to its tyrosine phosphorylated ITIM and ITSM motifs [14, 15] (Figure 2A). However, the specific mode of action is still poorly understood. Interestingly, only inactive mutations in the phosphorylatable ITSM tyrosine residues abolish PD1-inhibitory effects, but not in the ITIM motif [13]. SHP1 can also bind both ITIM and ITSM motifs, while SHP2 only binds the ITSM [14]. Nevertheless, whether SHP1 and SHP2 can simultaneously bind the ITSM is yet unknown (Figure 2A). It might be possible that binding of one prevents binding of the other, behaving like a regulatory switch motif similar to the ITSM of CD150 [16] that may regulate PD1 activities. In agreement with this, SHP2 but not SHP1 has been observed associated to PD1 in microclusters within the immunological synapse [17]. All these evidences support SHP2 as the main driver of PD1 inhibitory functions. Unlike SHP2, it is yet unclear whether PD1-bound SHP1 really contributes to PD1 suppressive function [17]. Nevertheless, SHP1 can bind to tyrosine-phosphorylated substrates such as ZAP70 [18]. It is thought that it could follow a pathway similar to termination of “standard” TCR signal transduction upon T cell activation through SHP1 dephosphorylating ZAP70 [18]. Even so, it has to be remarked that direct dephosphorylation of TCR proximal signaling kinases by SHP1 and SHP2 associated to PD1 has not yet been demonstrated [14].

PD1-dependent inhibitory mechanisms.

Figure 2: PD1-dependent inhibitory mechanisms. (A) Direct inhibitory mechanisms over the TCR signalosome are shown. The figure represents PD1-dependent proximal inhibitory mechanisms, which depend on the recruitment of SHP1 and SHP2 phosphatases as shown. These phosphatases inhibit ZAP70 and PI3K activities (blue arrows). Downstream intracellular pathways are also terminated, as exemplified in the figure with ERK and PKCθ. (B) Indirect inhibitory mechanisms over TCR signaling and T cell proliferation are shown through regulation of CK2 expression and activities. On the left, the PI3K-dependent signaling pathway activating CDK2 and inhibiting SMAD3 is shown. Briefly, PIP3 activates AKT leading to production of the ubiquitin ligase SCF that degrades the CDK2 inhibitor Kip1. Activated CDK2 triggers cell cycle progression and inactivates SMAD3 by phosphorylation. These pathways are negatively regulated by the PTEN phosphatase that degrades PIP3. During TCR activation CK2 phosphorylates PTEN with a concomitant decrease in its activities. When PD1 is engaged CK2 expression and activities decrease resulting in active PTEN that eliminates PIP3 shutting off AKT activation. (C) Regulation of TCR surface expression by PD1. PD1 engagement promotes expression of E3 ubiquitin ligases of the CBL family, as shown. As indicated, other ligases may be up-regulated as well. These ubiquitin ligases ubiquitylate TCR chains and PI3K, leading to the removal of TCRs from the T cell surface, possibly by endocytosis. Thus, T cells cannot respond to antigenic stimulation. (D) Metabolic control by PD1. Engaged PD1 alters T cell metabolism from glycolysis to β-oxidation by inhibition of ERK and PI3K-AKT activities. PD1-stimulated T cells would then metabolically resemble long-lived memory T cells.

Engaged PD1 has to be recruited to the immunological synapse to exert its activities. Thus, TCR engagement with pMHC is sufficient to cause SHP2 recruitment to PD1, but no T cell suppressive effects are exerted unless PD1 is simultaneously ligated [13]. This would suggest that PD1-associated phosphatases need the proximity to the TCR signalosome to dephosphorylate signal transduction kinases in analogy to CTLA4 recruiting SHP2 to dephosphorylate CD3ζ [13, 19]. The consequent inhibition of TCR-dependent distal signaling pathways such as ERK are probably the result of direct ZAP70 inhibition (Figure 2A).


PD-L1-engaged PD1 exerts an additional indirect inhibitory control over CD28-costimulation by regulating the expression levels and activities of CK2 and cyclin-dependent kinases (CDKs) (Figure 2B) [20]. In the absence of PD1 engagement, TCR activation increases CK2 expression that inactivates PTEN by phosphorylation. Thus, PTEN cannot dephosphorylate PIP3 produced by PI3K allowing TCR signal transduction to proceed. Interestingly, engaged PD1 reduces CK2 expression and activity with the result of an active PTEN that terminates the PI3K-AKT- PKCθ pathway inhibiting T cell growth and survival [14].

Engaged PD1 arrests lymphocytes at the G0-G1 phase through an indirect pathway which inhibits CDKs (Figure 2B). The resulting inhibition of AKT and ERK either by direct or indirect pathways inhibits transcription of SKP2 (part of SCFskp2 ubiquitin ligase) (Figure 1A and 1B) [21]. SCFskp2 ubiquitin ligase normally tags the CDK2 inhibitor p27Kip1 to proteosomal degradation during T cell activation, driving CDK2-dependent cell division. Thus, PD1 activities cause an accumulation of p27Kip1 that associates with CDK2 inhibiting its kinase activities. CDK2 inhibition also eliminates the SMAD3 inhibiting phosphorylation on Ser213, resulting in the expression of SMAD3-responsive genes including p15INK4B (a potent inhibitor of CDK4 and CDK6), and repressing transcription of the tyrosine phosphatase CDC25A that normally removes inhibitory tyrosine phosphorylations of CDK4, CDK6 and CDK2 causing T cell arrest [22].

PD1 regulation of TCR down-modulation

Down-modulation and degradation of the TCR signalosome is a feature of T cells in cancer patients and animal cancer models, especially in tumor-infiltrating lymphocytes [2325]. The most effective way to prevent T cells from recognizing antigens is to remove TCRs from their surface. Then, T cell function is severely impaired as a direct consequence of down-modulated TCRs and their associated receptors and signaling mediators (signalosome, Figure 1B and 2C). Cancer-associated TCR down-modulation is not caused by low affinity interactions with tumor antigens. This was demonstrated in a C-MYC-dependent OVA-expressing hepatocarcinoma murine model. Prolonged TCR down-modulation was observed in adoptively transferred OVA-specific transgenic CD8 OTI cells which have high affinity TCRs [26]. Thus, other mechanisms must be in place.

PD1 expression is characteristically high in tumor-infiltrating T cells [27, 28]. Thus, PD-L1-engaged PD1 contributes to prolonged TCR down-modulation by up-regulating the expression of E3-ubiquitin ligases CBL-B, c-CBL and ITCH which ultimately causes TCR internalization [29, 30] (Figure 2C). Interfering with PD-L1/PD1 interactions either with blocking antibodies or by gene silencing during antigen presentation to T cells leads to hyperactivated TCRhigh T cells with decreased expression of c-CBL and CBL-b [30].

All the evidence shows that E3 ubiquitin ligases are closely linked to regulation of TCR levels and termination of TCR-dependent signal transduction. CBL-b and c-CBL double-knockout T cells exhibit impaired TCR down-modulation upon T cell activation, causing hyperactivation in the absence of CD28 co-stimulation [31]. CBL-b single knock-out T cells also show impaired TCR down-modulation during physiological immune responses or after antigen recognition, similarly to disruption of PD-L1/PD1 interactions [30, 32]. Mechanistically, CBL-b and ITCH cause K33-polyubiquitination of CD3ζ, impairing its phosphorylation and the subsequent association of ZAP70 [33]. PI3K is also a direct target for CBL-b causing proteolysis-independent PI3K inactivation [34]. Overall, CBL-b negatively regulates CD28 co-stimulation in T cells [35, 36]. Thus, it is highly likely that the strong CD28-counteracting activities of PD1 could be partly caused by E3 ubiquitin ligases. It is worth noting that PD-L1 blockade also inhibits down-modulation of additional T cell activation markers such as ICOS, making PD1-driven receptor down-modulation a major regulatory mechanism of T cell functions [30, 37].

PD1 control of T cell metabolism

It is well known that T cell activation requires a fast energy increase which is achieved by glycolysis-dependent metabolism. Interestingly, engaged PD1 may be fundamental to rapidly shift the metabolic reprogramming of T cells from an effector to a long-lived memory-like phenotype with a shift from increased glycolysis towards fatty acid β-oxidation [38, 39] (Figure 2D). It is thought that this metabolic change might extend the lifespan of PD1high T cells. The exact molecular mechanisms are still unclear, although it could be mediated by PD1-dependent inhibition of PI3K and ERK. Thus, simultaneous inhibition of PI3K/AKT and ERK recapitulated some of PD1-dependent metabolic changes [39]. It is remarkable that PD1-engaged T cells closely resemble long-lived memory T cells from a metabolic point of view, when the current view is that sustained PD1 stimulation leads to T cell exhaustion. The implications of PD1 signaling in T cell differentiation will probably expand the accepted roles of PD1 as an immunosuppressive pathway.


The immune response is highly complex, and many factors can influence the outcome of immunotherapies. In addition, response patterns of PD-L1/PD1 blockade therapy are strikingly different from those of chemotherapy or targeted therapies. Targeted therapies cause fast tumor remissions but with prompt acquisition of resistance (Figure 3). In contrast, patients who respond to PD-L1/PD1 blockade show significant and durable responses, although a delay of even months can be observed. From a clinical point of view there is a strong need to identify biomarkers that can predict the outcome of PD-L1/PD1 blockade. It is naturally assumed that PD-L1 expression in cancer cells would correlate with therapeutic outcome. However, the results from clinical trials differ on the usefulness of PD-L1 expression as a biomarker, as patients with PD-L1-positive and PD-L1-negative tumors may benefit from the treatment [1].

Immunotherapies and targeted therapies display distinct patterns of response.

Figure 3: Immunotherapies and targeted therapies display distinct patterns of response. The graph displays a model of responses for immunotherapies and targeted therapies such as kinase inhibitors. The percentage of survival is plotted over time after the initial treatment. While targeted therapies exhibit fast anti-tumor effects, tumors acquire resistance to treatments. This is exemplified as a sudden drop of survival as indicated within the dotted square on the right. In contrast, immunotherapies show a significant group of patients that are intrinsically resistant to therapy, evidenced as an initial sudden drop in survival as indicated within the dotted square on the left. Then, long-term survivors are found with durable responses. So far, there are not effective biomarkers discriminating patients that could benefit from immunotherapies from those with intrinsic resistance.

To explain the apparent contradictions observed in clinical trials we have first to consider that PD-L1/PD1 functions are context-specific. The regulatory functions of this interaction take place in at least three stages: (i) During antigen presentation to T cells [30]; (ii) in peripheral tissues to maintain tolerance [40, 41], and (iii) at the inflammation site to dampen excessive autoreactive damage [4, 40]. Thus, systemic disruption of PD-L1/PD1 interactions in cancer patients will unleash several events contributing to therapeutic efficacy but also to side effects:

Hyperactivation of naïve T cells undergoing antigen presentation

Systemic PD-L1/PD1 blockade very likely affects naïve T cells undergoing antigen presentation by professional APCs in lymphoid organs, as PD-L1 is normally highly expressed by professional APCs such as DCs [30, 40, 42]. PD-L1 expression is strongly up-regulated following DC maturation probably as a regulatory negative feedback mechanism. However, PD-L1/PD1 interactions play a critical role in physiological T cell activation during antigen presentation. Engaged PD1 in T cells during antigen presentation by DCs causes prolonged ligand-induced TCR down-modulation, which is followed by exponential clonal expansion rather than permanent T cell inactivation [30]. TCR surface expression is recovered within two weeks when a significant number of antigen-specific T cells have accumulated, ready to exert cytotoxic activities over target cells [43]. Disruption of PD-L1/PD1 interactions at this stage leads to hyperactivated TCRhigh effector T cells which mediate an early immune attack [43, 44]. The resulting expansion of activated T cells from the pool of naïve T cells may enhance the anti-tumor response. Some evidence in preclinical models has been recently published which suggests that this could in fact be the case [45]. Moreover, interference of PD-L1/PD1 interactions during antigen presentation by DCs also favors that T cells do not lose their capacities to simultaneously express more than one cytokine (such as TNF-α, IL2, IFN-γ and MIP-1β) [42], in agreement with the capacities of PD-L1/PD1 blockade to revert (or prevent) T cell exhaustion [46].

Recovery of T cell functions of cancer-specific memory T cells

Tumors are infiltrated with an array of immune cells which includes memory PD1+ T cells. These T cells are antigen-experienced but they have been inactivated by the tumor [47]. Reactivation of these experienced memory T cells might be the cause of the efficacy of PD-L1/PD1 blockade in patients with PD-L1-positive tumors [48]. These intra-tumor T cells usually lack expression of the TCR signalosome, and PD-L1/PD1 blockade may contribute to the recovery of TCR surface expression and signal transduction. The reactivation of this pool of antigen-experienced T cells seems to be the driver of the efficacy of PD-L1/PD1 blockade in human therapy [49]. In fact, T cell infiltration can be used as a predicting factor. Tumor infiltration with PD1high CTLA4high exhausted CD8 T cells can be an accurate predictor of response to anti-PD1 therapy in melanoma [50, 51].

Polyclonal expansion of T cells in peripheral tissue

PD-L1/PD1 interactions in peripheral tissues between many cell types and T cells ensure that circulating T cells do not react with autoantigens. This is also reinforced by the decreased expression of surface TCR in activated T cells during the clonal expansion phase [30, 43]. However, systemic disruption of PD-L1/PD1 may have a significant impact on antigen recognition in peripheral tissue. In fact, it has been shown that local PD-L1 silencing in peripheral tissue expands polyclonal CD8 T cells [41] suggesting that systemic administration of PD-L1/PD1 blocking antibodies may expand a polyclonal pool of T cells following antigen recognition in peripheral tissues. The nature of these T cells has not been elucidated yet, but these reactivated T cells may be behind of some of the autoreactive adverse events associated to treatments with immune checkpoint inhibitors [52, 53]. Nevertheless, these T cells may also contain a significant pool of tumor antigen-specific cells that can be recruited to the tumor environment.

Direct effects over cancer cells

The current conventional view states that direct disruption of PD-L1/PD1 interactions between cancer and T cells is behind the therapeutic efficacy of blocking antibodies. However, PD-L1/PD1 interactions may also take place between melanoma cells in the absence of T cells [54]. This suggests that a minor population of melanoma cells may express some PD1 on their surface. Elimination of PD1 expression in murine mouse melanoma models and also in human xenografts inhibited cancer cell growth. Antibody-mediated disruption of this interaction directly delayed tumor growth without the need of enhanced T cell anti-tumor activities. The same result was achieved by either PD1 silencing or PD-L1 silencing in tumor cells [41, 54]. Thus, intercellular PD-L1/PD1 interactions transmit survival signals to cancer cells and promote in vivo tumor growth Therefore, disruption of PD-L1/PD1 interactions between cancer cells will delay tumor growth while anti-cancer T cells become activated [41].


PD-L1/PD1 antibody blockade has yielded encouraging results for the treatment of a wide range of cancer types. The exact molecular and cellular mechanisms behind its potent anti-cancer activities are still poorly understood. PD1 engagement by PD-L1 leads to rapid termination of TCR intracellular signaling and inhibition of T cell proliferation through direct and indirect mechanisms. Most of the evidence points to SHP-2 recruitment as the main driver of all these mechanisms. However, it has to be mentioned that many experimental evidences so far come from immortal Jurkat T cells. Therefore, it cannot be ruled out that PD1 employs other yet unknown pathways to disrupt TCR signaling cascades and alter T cell metabolism.

A key issue with PD-L1/PD1 blockade therapy is the identification of predictive markers of response. Recently, inactivating mutations in the interferon signal transduction pathway and in class I antigen presentation have been shown to correlate with both primary and adaptive resistance to anti-PD1 therapy treatment [2, 3]. Therefore, there is a frantic need to identify alternative targets susceptible of therapeutic intervention that could minimize cancer cell escape. The tumor environment is a complex system in which many cell types cooperate to protect it, including myeloid-derived suppressor cells, tumor-infiltrating macrophages, regulatory T cells and other cell types of the tumor stroma [5558]. Many of these cell types utilize the PD-L1/PD1 signaling axis to suppress anti-tumor immune responses. Therefore, the understanding of the mechanisms behind PD1-dependent cell suppression will surely uncover a number of novel targets susceptible of therapeutic intervention.

During the last years, therapies targeting main regulatory components of the immune synapse have been developed and are progressively displacing chemotherapy in different clinical contexts [1, 51, 59, 60]. Preliminary results from the simultaneous blockade of PD1 and CTLA4 in metastatic melanoma were also published, and now this combination is being tested in many different neoplasms [61, 62]. The better understanding of the signaling pathways underlying the immune response has revealed potential targets that might improve the efficacy of the current treatments. Many new drugs are now under evaluation, both potentiating co-stimulatory molecules such as 4-1BB, OX40, CD27, CD40, GITR, or blocking immunosuppressive proteins including LAG-3 or VISTA [6365]. Their efficacy in combination with PDL1/PD1 blockade and CTLA4-targeted therapies will surely be reported in the near future.


The authors declare no conflicts of interest.


MGC is funded by a Government of Navarre PhD fellowship (BMED 033-2014); MZ is funded by a Gobierno de Navarra Project grant (GN 33/14) and a “Precipita” crowdfunding project grant from Fundación Española para la Ciencia y la Tecnología (FECYT). MIV is funded by a Sara Borrel post-doctoral fellowship. DE is funded by a “Miguel Servet” Fellowship (CP12/03114) from the Instituto de Salud Carlos III (ISCIII), Spain. GK is funded by a “Proyecto Tractor ProCel” from the Government of Navarre. The authors gratefully acknowledge the “Sandra Ibarra” Foundation, the “Navarrese Association against Breast Cancer” (SARAY), “Caixa Foundation” and ISCIII (FIS. PI14/00579 project grant) for their financial support.


1. Gato-Cañas M, Arasanz H, Blanco-Luquin I, Glaría E, Arteta-Sanchez V, Kochan G, Escors D. Novel immunotherapies for the treatment of melanoma. Immunotherapy. 2016; 8:613–32.

2. Shin DS, Zaretsky JM, Escuin-Ordinas H, Garcia-Diaz A, Hu-Lieskovan S, Kalbasi A, Grasso CS, Hugo W, Sandoval S, Torrejon DY, Palaskas N, Rodriguez GA, Parisi G, et al. Primary Resistance to PD-1 Blockade Mediated by JAK1/2 Mutations. Cancer Discov. 2017; 7:188–201.

3. Zaretsky JM, Garcia-Diaz A, Shin DS, Escuin-Ordinas H, Hugo W, Hu-Lieskovan S, Torrejon DY, Abril-Rodriguez G, Sandoval S, Barthly L, Saco J, Homet Moreno B, Mezzadra R, et al. Mutations Associated with Acquired Resistance to PD-1 Blockade in Melanoma. N Engl J Med. 2016; 375:819–29.

4. Sharpe AH, Wherry EJ, Ahmed R, Freeman GJ. The function of programmed cell death 1 and its ligands in regulating autoimmunity and infection. Nat Immunol. 2007; 8:239–45.

5. Curtsinger JM, Johnson CM, Mescher MF. CD8 T cell clonal expansion and development of effector function require prolonged exposure to antigen, costimulation, and signal 3 cytokine. J Immunol. 2003; 171:5165–71.

6. Curtsinger JM, Lins DC, Mescher MF. Signal 3 determines tolerance versus full activation of naive CD8 T cells: dissociating proliferation and development of effector function. J Exp Med. 2003; 197:1141–51.

7. Chan AC, Iwashima M, Turck CW, Weiss A. ZAP-70: a 70 kd protein-tyrosine kinase that associates with the TCR zeta chain. Cell. 1992; 71:649–62.

8. Sieh M, Batzer A, Schlessinger J, Weiss A. GRB2 and phospholipase C-gamma 1 associate with a 36- to 38-kilodalton phosphotyrosine protein after T-cell receptor stimulation. Mol Cell Biol. 1994; 14:4435–42.

9. Round JL, Humphries LA, Tomassian T, Mittelstadt P, Zhang M, Miceli MC. Scaffold protein Dlgh1 coordinates alternative p38 kinase activation, directing T cell receptor signals toward NFAT but not NF-kappaB transcription factors. Nat Immunol. 2007; 8:154–61.

10. Salvador JM, Mittelstadt PR, Guszczynski T, Copeland TD, Yamaguchi H, Appella E, Fornace AJ Jr, Ashwell JD. Alternative p38 activation pathway mediated by T cell receptor-proximal tyrosine kinases. Nat Immunol. 2005; 6:390–95.

11. Boise LH, Minn AJ, Noel PJ, June CH, Accavitti MA, Lindsten T, Thompson CB. CD28 costimulation can promote T cell survival by enhancing the expression of Bcl-XL. Immunity. 1995; 3:87–98.

12. Chen L, Flies DB. Molecular mechanisms of T cell co-stimulation and co-inhibition. Nat Rev Immunol. 2013; 13:227–42.

13. Chemnitz JM, Parry RV, Nichols KE, June CH, Riley JL. SHP-1 and SHP-2 associate with immunoreceptor tyrosine-based switch motif of programmed death 1 upon primary human T cell stimulation, but only receptor ligation prevents T cell activation. J Immunol. 2004; 173:945–54.

14. Sheppard KA, Fitz LJ, Lee JM, Benander C, George JA, Wooters J, Qiu Y, Jussif JM, Carter LL, Wood CR, Chaudhary D. PD-1 inhibits T-cell receptor induced phosphorylation of the ZAP70/CD3zeta signalosome and downstream signaling to PKCtheta. FEBS Lett. 2004; 574:37–41.

15. Hui E, Cheung J, Zhu J, Su X, Taylor MJ, Wallweber HA, Sasmal DK, Huang J, Kim JM, Mellman I, Vale RD. T cell costimulatory receptor CD28 is a primary target for PD-1-mediated inhibition. Science. 2017; 355:1428–33.

16. Shlapatska LM, Mikhalap SV, Berdova AG, Zelensky OM, Yun TJ, Nichols KE, Clark EA, Sidorenko SP. CD150 association with either the SH2-containing inositol phosphatase or the SH2-containing protein tyrosine phosphatase is regulated by the adaptor protein SH2D1A. J Immunol. 2001; 166:5480–87.

17. Yokosuka T, Takamatsu M, Kobayashi-Imanishi W, Hashimoto-Tane A, Azuma M, Saito T. Programmed cell death 1 forms negative costimulatory microclusters that directly inhibit T cell receptor signaling by recruiting phosphatase SHP2. J Exp Med. 2012; 209:1201–17.

18. Plas DR, Johnson R, Pingel JT, Matthews RJ, Dalton M, Roy G, Chan AC, Thomas ML. Direct regulation of ZAP-70 by SHP-1 in T cell antigen receptor signaling. Science. 1996; 272:1173–76.

19. Lee KM, Chuang E, Griffin M, Khattri R, Hong DK, Zhang W, Straus D, Samelson LE, Thompson CB, Bluestone JA. Molecular basis of T cell inactivation by CTLA-4. Science. 1998; 282:2263–66.

20. Patsoukis N, Li L, Sari D, Petkova V, Boussiotis VA. PD-1 increases PTEN phosphatase activity while decreasing PTEN protein stability by inhibiting casein kinase 2. Mol Cell Biol. 2013; 33:3091–98.

21. Patsoukis N, Brown J, Petkova V, Liu F, Li L, Boussiotis VA. Selective effects of PD-1 on Akt and Ras pathways regulate molecular components of the cell cycle and inhibit T cell proliferation. Sci Signal. 2012; 5:ra46.

22. Patsoukis N, Sari D, Boussiotis VA. PD-1 inhibits T cell proliferation by upregulating p27 and p15 and suppressing Cdc25A. Cell Cycle. 2012; 11:4305–09.

23. Mizoguchi H, O’Shea JJ, Longo DL, Loeffler CM, McVicar DW, Ochoa AC. Alterations in signal transduction molecules in T lymphocytes from tumor-bearing mice. Science. 1992; 258:1795–98.

24. Finke JH, Zea AH, Stanley J, Longo DL, Mizoguchi H, Tubbs RR, Wiltrout RH, O’Shea JJ, Kudoh S, Klein E, Bukowski RM, Ochoa AC. Loss of T-cell receptor zeta chain and p56lck in T-cells infiltrating human renal cell carcinoma. Cancer Res. 1993; 53:5613–16.

25. Massaia M, Attisano C, Beggiato E, Bianchi A, Pileri A. Correlation between disease activity and T-cell CD3 zeta chain expression in a B-cell lymphoma. Br J Haematol. 1994; 88:886–88.

26. Ney JT, Schmidt T, Kurts C, Zhou Q, Eckert D, Felsher DW, Schorle H, Knolle P, Tüting T, Barchet W, Büttner R, Limmer A, Gütgemann I. Autochthonous liver tumors induce systemic T cell tolerance associated with T cell receptor down-modulation. Hepatology. 2009; 49:471–81.

27. Chou JP, Effros RB. T cell replicative senescence in human aging. Curr Pharm Des. 2013; 19:1680–98.

28. Crespo J, Sun H, Welling TH, Tian Z, Zou W. T cell anergy, exhaustion, senescence, and stemness in the tumor microenvironment. Curr Opin Immunol. 2013; 25:214–21.

29. Nurieva R, Thomas S, Nguyen T, Martin-Orozco N, Wang Y, Kaja MK, Yu XZ, Dong C. T-cell tolerance or function is determined by combinatorial costimulatory signals. EMBO J. 2006; 25:2623–33.

30. Karwacz K, Bricogne C, MacDonald D, Arce F, Bennett CL, Collins M, Escors D. PD-L1 co-stimulation contributes to ligand-induced T cell receptor down-modulation on CD8+ T cells. EMBO Mol Med. 2011; 3:581–92.

31. Naramura M, Jang IK, Kole H, Huang F, Haines D, Gu H. c-Cbl and Cbl-b regulate T cell responsiveness by promoting ligand-induced TCR down-modulation. Nat Immunol. 2002; 3:1192–99.

32. Shamim M, Nanjappa SG, Singh A, Plisch EH, LeBlanc SE, Walent J, Svaren J, Seroogy C, Suresh M. Cbl-b regulates antigen-induced TCR down-regulation and IFN-gamma production by effector CD8 T cells without affecting functional avidity. J Immunol. 2007; 179:7233–43.

33. Huang H, Jeon MS, Liao L, Yang C, Elly C, Yates JR 3rd, Liu YC. K33-linked polyubiquitination of T cell receptor-zeta regulates proteolysis-independent T cell signaling. Immunity. 2010; 33:60–70.

34. Fang D, Liu YC. Proteolysis-independent regulation of PI3K by Cbl-b-mediated ubiquitination in T cells. Nat Immunol. 2001; 2:870–75.

35. Bachmaier K, Krawczyk C, Kozieradzki I, Kong YY, Sasaki T, Oliveira-dos-Santos A, Mariathasan S, Bouchard D, Wakeham A, Itie A, Le J, Ohashi PS, Sarosi I, et al. Negative regulation of lymphocyte activation and autoimmunity by the molecular adaptor Cbl-b. Nature. 2000; 403:211–16.

36. Chiang YJ, Kole HK, Brown K, Naramura M, Fukuhara S, Hu RJ, Jang IK, Gutkind JS, Shevach E, Gu H. Cbl-b regulates the CD28 dependence of T-cell activation. Nature. 2000; 403:216–20.

37. Karunarathne DS, Horne-Debets JM, Huang JX, Faleiro R, Leow CY, Amante F, Watkins TS, Miles JJ, Dwyer PJ, Stacey KJ, Yarski M, Poh CM, Lee JS, et al. Programmed Death-1 Ligand 2-Mediated Regulation of the PD-L1 to PD-1 Axis Is Essential for Establishing CD4(+) T Cell Immunity. Immunity. 2016; 45:333–45.

38. Rathmell JC, Vander Heiden MG, Harris MH, Frauwirth KA, Thompson CB. In the absence of extrinsic signals, nutrient utilization by lymphocytes is insufficient to maintain either cell size or viability. Mol Cell. 2000; 6:683–92.

39. Patsoukis N, Bardhan K, Chatterjee P, Sari D, Liu B, Bell LN, Karoly ED, Freeman GJ, Petkova V, Seth P, Li L, Boussiotis VA. PD-1 alters T-cell metabolic reprogramming by inhibiting glycolysis and promoting lipolysis and fatty acid oxidation. Nat Commun. 2015; 6:6692.

40. Latchman YE, Liang SC, Wu Y, Chernova T, Sobel RA, Klemm M, Kuchroo VK, Freeman GJ, Sharpe AH. PD-L1-deficient mice show that PD-L1 on T cells, antigen-presenting cells, and host tissues negatively regulates T cells. Proc Natl Acad Sci USA. 2004; 101:10691–96.

41. Liechtenstein T, Perez-Janices N, Blanco-Luquin I, Goyvaerts C, Schwarze J, Dufait I, Lanna A, Ridder M, Guerrero-Setas D, Breckpot K, Escors D. Anti-melanoma vaccines engineered to simultaneously modulate cytokine priming and silence PD-L1 characterized using ex vivo myeloid-derived suppressor cells as a readout of therapeutic efficacy. OncoImmunology. 2014; 3:e945378.

42. Pen JJ, Keersmaecker BD, Heirman C, Corthals J, Liechtenstein T, Escors D, Thielemans K, Breckpot K. Interference with PD-L1/PD-1 co-stimulation during antigen presentation enhances the multifunctionality of antigen-specific T cells. Gene Ther. 2014; 21:262–71.

43. Karwacz K, Arce F, Bricogne C, Kochan G, Escors D. PD-L1 co-stimulation, ligand-induced TCR down-modulation and anti-tumor immunotherapy. OncoImmunology. 2012; 1:86–88.

44. Bricogne C, Laranga R, Padella A, Dufait I, Liechtenstein T, Breckpot K, Kochan G, Escors D. Critical Mass Hypothesis of T-Cell Responses and its Application for the Treatment of T-Cell Lymphoma. In: Harvey WK, Jacobs RM, editors. Hodgkin’s and T-cell lymphoma: Diagnosis, Treatment Options and Prognosis. Nova Publishers; 2012.

45. Homet Moreno B, Zaretsky JM, Garcia-Diaz A, Tsoi J, Parisi G, Robert L, Meeth K, Ndoye A, Bosenberg M, Weeraratna AT, Graeber TG, Comin-Anduix B, Hu-Lieskovan S, Ribas A. Response to Programmed Cell Death-1 Blockade in a Murine Melanoma Syngeneic Model Requires Costimulation, CD4, and CD8 T Cells. Cancer Immunol Res. 2016; 4:845–57.

46. Sakuishi K, Apetoh L, Sullivan JM, Blazar BR, Kuchroo VK, Anderson AC. Targeting Tim-3 and PD-1 pathways to reverse T cell exhaustion and restore anti-tumor immunity. J Exp Med. 2010; 207:2187–94.

47. Tumeh PC, Harview CL, Yearley JH, Shintaku IP, Taylor EJ, Robert L, Chmielowski B, Spasic M, Henry G, Ciobanu V, West AN, Carmona M, Kivork C, et al. PD-1 blockade induces responses by inhibiting adaptive immune resistance. Nature. 2014; 515:568–71.

48. Ribas A, Shin DS, Zaretsky J, Frederiksen J, Cornish A, Avramis E, Seja E, Kivork C, Siebert J, Kaplan-Lefko P, Wang X, Chmielowski B, Glaspy JA, et al. PD-1 Blockade Expands Intratumoral Memory T Cells. Cancer Immunol Res. 2016; 4:194–203.

49. Kamphorst AO, Wieland A, Nasti T, Yang S, Zhang R, Barber DL, Konieczny BT, Daugherty CZ, Koenig L, Yu K, Sica GL, Sharpe AH, Freeman GJ, et al. Rescue of exhausted CD8 T cells by PD-1-targeted therapies is CD28-dependent. Science. 2017; 355:1423–27.

50. Daud AI, Loo K, Pauli ML, Sanchez-Rodriguez R, Sandoval PM, Taravati K, Tsai K, Nosrati A, Nardo L, Alvarado MD, Algazi AP, Pampaloni MH, Lobach IV, et al. Tumor immune profiling predicts response to anti-PD-1 therapy in human melanoma. J Clin Invest. 2016; 126:3447–52.

51. Hodi FS, Hwu WJ, Kefford R, Weber JS, Daud A, Hamid O, Patnaik A, Ribas A, Robert C, Gangadhar TC, Joshua AM, Hersey P, Dronca R, et al. Evaluation of Immune-Related Response Criteria and RECIST v1.1 in Patients With Advanced Melanoma Treated With Pembrolizumab. J Clin Oncol. 2016; 34:1510–17.

52. Brahmer JR, Tykodi SS, Chow LQ, Hwu WJ, Topalian SL, Hwu P, Drake CG, Camacho LH, Kauh J, Odunsi K, Pitot HC, Hamid O, Bhatia S, et al. Safety and activity of anti-PD-L1 antibody in patients with advanced cancer. N Engl J Med. 2012; 366:2455–65.

53. Topalian SL, Hodi FS, Brahmer JR, Gettinger SN, Smith DC, McDermott DF, Powderly JD, Carvajal RD, Sosman JA, Atkins MB, Leming PD, Spigel DR, Antonia SJ, et al. Safety, activity, and immune correlates of anti-PD-1 antibody in cancer. N Engl J Med. 2012; 366:2443–54.

54. Kleffel S, Posch C, Barthel SR, Mueller H, Schlapbach C, Guenova E, Elco CP, Lee N, Juneja VR, Zhan Q, Lian CG, Thomi R, Hoetzenecker W, et al. Melanoma Cell-Intrinsic PD-1 Receptor Functions Promote Tumor Growth. Cell. 2015; 162:1242–56.

55. Dufait I, Schwarze JK, Liechtenstein T, Leonard W, Jiang H, Escors D, De Ridder M, Breckpot K, De Ridder M, Breckpot K. Ex vivo generation of myeloid-derived suppressor cells that model the tumor immunosuppressive environment in colorectal cancer. Oncotarget. 2015; 6:12369–82. https://doi.org/10.18632/oncotarget.3682.

56. Liechtenstein T, Perez-Janices N, Gato M, Caliendo F, Kochan G, Blanco-Luquin I, Van der Jeught K, Arce F, Guerrero-Setas D, Fernandez-Irigoyen J, Santamaria E, Breckpot K, Escors D. A highly efficient tumor-infiltrating MDSC differentiation system for discovery of anti-neoplastic targets, which circumvents the need for tumor establishment in mice. Oncotarget. 2014; 5:7843–57. https://doi.org/10.18632/oncotarget.2279.

57. Gato-Cañas M, Martinez de Morentin X, Blanco-Luquin I, Fernandez-Irigoyen J, Zudaire I, Liechtenstein T, Arasanz H, Lozano T, Casares N, Chaikuad A, Knapp S, Guerrero-Setas D, Escors D, et al. A core of kinase-regulated interactomes defines the neoplastic MDSC lineage. Oncotarget. 2015; 6:27160–75. https://doi.org/10.18632/oncotarget.4746.

58. Simpson TR, Li F, Montalvo-Ortiz W, Sepulveda MA, Bergerhoff K, Arce F, Roddie C, Henry JY, Yagita H, Wolchok JD, Peggs KS, Ravetch JV, Allison JP, Quezada SA. Fc-dependent depletion of tumor-infiltrating regulatory T cells co-defines the efficacy of anti-CTLA-4 therapy against melanoma. J Exp Med. 2013; 210:1695–710.

59. Robert C, Long GV, Brady B, Dutriaux C, Maio M, Mortier L, Hassel JC, Rutkowski P, McNeil C, Kalinka-Warzocha E, Savage KJ, Hernberg MM, Lebbé C, et al. Nivolumab in previously untreated melanoma without BRAF mutation. N Engl J Med. 2015; 372:320–30.

60. Borghaei H, Paz-Ares L, Horn L, Spigel DR, Steins M, Ready NE, Chow LQ, Vokes EE, Felip E, Holgado E, Barlesi F, Kohlhäufl M, Arrieta O, et al. Nivolumab versus Docetaxel in Advanced Nonsquamous Non-Small-Cell Lung Cancer. N Engl J Med. 2015; 373:1627–39.

61. Larkin J, Chiarion-Sileni V, Gonzalez R, Grob JJ, Cowey CL, Lao CD, Schadendorf D, Dummer R, Smylie M, Rutkowski P, Ferrucci PF, Hill A, Wagstaff J, et al. Combined Nivolumab and Ipilimumab or Monotherapy in Untreated Melanoma. N Engl J Med. 2015; 373:23–34.

62. Postow MA, Chesney J, Pavlick AC, Robert C, Grossmann K, McDermott D, Linette GP, Meyer N, Giguere JK, Agarwala SS, Shaheen M, Ernstoff MS, Minor D, et al. Nivolumab and ipilimumab versus ipilimumab in untreated melanoma. N Engl J Med. 2015; 372:2006–17.

63. Youlin K, Li Z, Xiaodong W, Xiuheng L, Hengchen Z. Combination immunotherapy with 4-1BBL and CTLA-4 blockade for the treatment of prostate cancer. Clinical & developmental immunology. 2012; 2012:439235.

64. Wang L, Rubinstein R, Lines JL, Wasiuk A, Ahonen C, Guo Y, Lu LF, Gondek D, Wang Y, Fava RA, Fiser A, Almo S, Noelle RJ. VISTA, a novel mouse Ig superfamily ligand that negatively regulates T cell responses. J Exp Med. 2011; 208:577–92.

65. Melero I, Hervas-Stubbs S, Glennie M, Pardoll DM, Chen L. Immunostimulatory monoclonal antibodies for cancer therapy. Nature reviews. 2007; 7:95-106. https://doi.org/10.1038/nrc2051.

Creative Commons License All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 3.0 License.
PII: 17232