Figures
Abstract
While treating stage III melanoma patients with autologous therapeutic TIL in an adjuvant setting, we previously reported a significant benefit of treatment on both progression-free survival and overall survival in patients with only one invaded lymph node (early stage III) compared to patients with more than one invaded lymph nodes (advanced stage III). In this context, in order to understand the difference of activity of TIL therapy according to the progression of the illness at stage III, the first objective of the present study was to determine potential differences in the characteristics of TIL populations obtained from an early stage III and a more advanced stage III when tumor burden is more important. The second objective was to determine possible differences in tissue expression level of several molecules involved in interactions between tumor cells and T cells between early and advanced stage III considering that the tumor microenvironment of invaded lymph nodes could become more tolerant with the progression of the disease. A total of 47 samples of melanoma invaded LN from stage IIIb (AJCC 2007) melanoma patients treated with TIL plus IL-2 were included in this study. We confirmed that both PFS and OS were significantly associated to the presence of tumor-reactive T-cells among TIL injected to the patients and that these tumor reactive T cells were more frequently observed at the early stage III. Moreover, while analyzing the expression of 17 markers on 34/47 tumor specimens using immunohistochemistry, we identified that 3 tissue markers involved in interactions between melanoma cells and T cells have a significant difference of expression between early and advanced stage III: MHC class I, adhesion molecule ICAM-1 and the co-stimulation molecule LFA-3 had a significantly weaker expression in melanoma tissue specimens from advanced stage III. In addition, the expression of the alpha chain of the IL-2 receptor (CD25) and the nuclear transcription factor Foxp3 was significantly increased in the melanoma tissue specimens from advanced stage III. Our results suggest differences in the immunological status of the tumor microenvironment between early and advanced stage III, which could explain the difference in clinical response to TIL infusion in an adjuvant setting between early and advanced stage III.
Citation: Knol A-C, Nguyen J-M, Pandolfino M-C, Quéreux G, Brocard A, Peuvrel L, et al. (2012) Tissue Biomarkers in Melanoma Patients Treated with TIL. PLoS ONE 7(12): e48729. https://doi.org/10.1371/journal.pone.0048729
Editor: Lucienne Chatenoud, Université Paris Descartes, France
Received: June 27, 2012; Accepted: September 28, 2012; Published: December 20, 2012
Copyright: © 2012 Knol et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by grants from “la Ligue Nationale contre le cancer”, from “la Société Française de Dermatologie”, from “l'Association Française contre les Myopathies” and from the European Program “Cancer Immunotherapy”. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Metastatic melanoma prognosis remains poor and clinical success is still limited at this stage of the illness even if new treatments appear promising such as therapies targeting the CTLA-4 (cytotoxic T-lymphocyte associated antigen-4) or the mutated form of BRAF. Molecular markers that are able to predict patient prognosis after lymph node resection are therefore of clinical relevance. Independent prognostic factors could thus enable the identification of patients with a high risk of progression and who therefore would most benefit from adjuvant treatment. During the last decade, new insights in cellular and molecular biology have lead to the development of both active (vaccination) and adoptive immunotherapy protocols, the latter based on the transfer of high amounts of autologous expanded tumor infiltrating lymphocytes (TIL) extracted from the tumor tissue to melanoma patients [1]–[2]. The success of this immunotherapeutic approach would thus be directly related to the immunological status of the tumor microenvironment.
In advanced-stage (stage IV, AJCC, American Joint Committee on Cancer) melanoma patients, clinical trials using TIL combined with interleukin-2 (IL-2) have shown a response rate of 35% [3]–[4], and more recently, while using rapidly expanded tumor infiltrating lymphocyte cultures and high-dose IL-2 therapy after lymphodepleting conditioning, authors reported a 51% rate of objective clinical responses [5]. Another group reported that that lymphodepleting chemotherapy followed by transfer of short-term cultured TIL can mediate tumor regression in 50% of metastatic melanoma with manageable toxicity [6]. While treating stage III (AJCC 2007) melanoma patients with autologous therapeutic TIL, our group previously reported that both progression-free survival (PFS) and overall survival (OS) were significantly increased in the group of patients with only one invaded lymph node (early stage III) compared to the group of patients with more than one invaded lymph node (advanced stage III) [7]. With a long-term follow-up of 7 years, we confirmed that both PFS and OS were prolonged in the group of patients with early stage III (p-adjusted 0.0285) [8]. Moreover, while evaluating the presence of tumor-reactive T-cells among infused TIL in this 2 groups, we observed an absence of tumor-reactive TIL in advanced stage III only [9], and that the infusion of tumor-reactive TIL was statistically correlated with a prolonged PFS of early stage III patients [10].
In addition to a decrease in the number of tumor-reactive T-cells in several invaded lymph nodes, another hypothesis potentially explaining the difference of clinical results could be the development of in situ tumor escape mechanisms together with the progression of the illness. One of our challenges now is to identify which mechanisms could be involved in the development of this immune-tolerance between early and advanced stages. Melanoma tumor cells are discussed as cells able to induce an immune-tolerance in the tumor microenvironment. Tumor cells themselves may thus induce impairment of melanoma antigen presentation or secretion of immunosuppressive molecules such as IL-10 or TGF-β. Regulatory T-cells (Tregs) present in the tumor might also inhibit anti-tumor immune responses [11]–[12].
In this context, the first objective of the present study was to complete the analysis of TIL characteristics between early and advanced stage III melanoma (number of TIL, phenotype, proportion of tumor-reactive T-cells). The second objective was to determine possible differences in in-situ immunoreactivity of the tumor microenvironment between early and advanced stage III by studying the tissue expression level of several molecules involved in interactions between melanoma cells and T cells (tumor-associated antigens, major histocompatibility complex (MHC) molecules, cytokines, molecules implicated in T cell activation).
Materials and Methods
Melanoma samples
A total of 47 samples of melanoma invaded lymph nodes (LN) from stage IIIb (AJCC 2007) melanoma patients treated with TIL plus IL-2 were included in this study, corresponding to TNM classification T1-4b/N1a or N2a/M0 and T1-4a/N1b or N2b or N2c/M0 (AJCC 2010). Twenty-seven patients had only one invaded node (early stage III melanoma) and 20 patients had more than one invaded node (advanced stage III melanoma). The primary melanomas of these patients were all of the superficial spreading subtype (SSM) and of stage IIb or IIc corresponding to TNM classification T3b or T4a or T4b/N0/M0 (AJCC 2010).
After lymph node resection, one part of the invaded LN was used for producing therapeutic autologous TIL; another part was used for the immunohistochemical analysis and to establish the autologous tumor cell-line. The third part of invaded lymph node was processed for pathologic examination. Metastases were macrometastases. Written informed consent was provided by all patients and the study was approved by the Ethics Committee of Pays de La Loire (France).
TIL production from the invaded LN
The same number of tumor fragments were placed in culture for both groups of patients. TIL were cultured according to a procedure previously described [2], [9]. Briefly, short term cultured TIL were isolated by culturing fragments of stage ΙΙΙ metastatic LN into 12-well tissue culture plates with X-VIVO 15 serum-free medium (BioWhittaker, Walkersville, MD, USA) containing 150 U/mL recombinant interleukin-2 (rIL-2) (Eurocetus, Rueil Malmaison, France) and glutamine (1 mM, BioWhittaker) for 10–14 days. Ex vivo expanded TIL were derived as follows: 1.8×106 short term cultured TIL were plated at 300 viable lymphocytes/well with irradiated feeder cells (allogeneic peripheral blood leukocytes (PBL) and B-EBV cells: Epstein-Barr virus infected B-cells) into U-bottom microplates in 150 µL of rIL-2 medium. PHA-L (phytohemagglutinin-L or leucoagglutinin) (Difco, Detroit, ML, USA) was added on day 0 (1 µg/mL). Ten days later, lymphocytes were recovered from the culture plates, adjusted to 1×106 cells/mL in rIL-2 medium and transferred into culture cell bags for an additional 10 days. The final TIL harvest was obtained by centrifuging, washing and suspending the TIL in 4% human serum albumin (LFB, Les Ulis, France). A second TIL expansion was performed within one month of the first, starting from cryopreserved short-term cultured TIL. Aliquots of TIL suspensions injected in the patients were cryopreserved to study their tumor specificity, which was carried out later once the autologous tumor cell line had been established in culture.
Establishment of melanoma cell lines
Melanoma cell lines were established as previously described [13]–[14] and were successfully established for the 47 tumor samples.
Briefly, fresh LNs with metastasis were minced into small tumor pieces (approximately 1–2 mm3) with scissors and biopsy punch. The resultant fragment suspension was centrifuged and then pieces were inoculated (at a rate of 2 or 3 per well) in a 24-wells plate (NUNC) and 1.5 ml per well of RPMI (Roswell Park Memorial Institute) medium supplemented with 10% fetal calf serum (FCS) was added. Plates were placed at 37°C in a humidified incubator with 5% CO2 and observed under a light microscope every week and sub-cultured if necessary. The presence of tumor cells within established melanoma cell lines was assessed using both polymerase chain reaction (PCR) and flow cytometry based on the intracellular expression of tumor associated antigens (gp100, Melan-A/MART-1, tyrosinase, NY-ESO-1 and MAGE).
Antibodies and flow cytometric analysis
The following antibodies were used: PE anti-CD2 (clone S5.2), PE anti-CD56 (clone MY31), PE anti-CD25 (clone 2A3), all from BD Pharmingen, Le Pont de Claix, France. We also used PC5 anti-CD3 (clone UCHT1), PE anti-CD8 (clone B9.11), APC anti-CD4 (clone 13B8.2), APC anti CD19 (clone J3-119), PC7 anti-CD45 (clone J.33), PE anti-CD16 (clone 3G8), all from Beckman Coulter, Marseille, France. Lymphocytes were gated according to their forward and size scatter characteristics, and FACSCanto analysis was performed using the BDFACS Diva software (BD Biosciences, San Jose, CA, USA).
Cytokine production assay for evaluating the proportion of tumor-specific TIL
The fraction of tumor-reactive TIL was determined from the measurement of the fraction of interferon-gamma (IFN-γ)-secreting T cells among TIL stimulated by the autologous melanoma cell line, as described previously [9]. Briefly, about 1×105 lymphocytes were stimulated by 3×105 autologous melanoma cells in 200 µL of X-VIVO 15 medium in the presence of brefeldin A, 10 µg/ml (Sigma, St Louis MO, USA) in round-bottom 96-well plates. The cultures were incubated for 6 h at 37°C in 5% CO2 humidified atmosphere. Then cells were stained for surface markers with fluorochrome-labeled monoclonal antibodies (anti-human CD4 APC, anti-human CD8 FITC, BD Biosciences, France). For intracytoplasmic cytokine staining, cells were then fixed 10 min at room temperature in a solution of phosphate-buffered saline (PBS) 4% paraformaldehyde (Sigma), washed and stored at 4°C until labeling. Fixed stimulated lymphocytes were stained for cytokine production using the method described by Jung et al. [15]. Anti-IFN-γ specific antibody was purchased from BD Biosciences, France and diluted in PBS containing 0.1% bovine serum albumin (BSA) and 0.1% saponin (Sigma). After staining, cells were resuspended in PBS and 105 events were analyzed on a FACScalibur flow cytometer using the BDFACS Cell Quest Pro software (BD Biosciences, San Jose, CA, USA). T cell responses were considered significant when the mean fluorescence labeling of TIL stimulated by the autologous tumor cell line exceeded, by at least half a log, the mean fluorescence of the background responses of non-stimulated TIL and/or of TIL stimulated by an HLA-mismatched melanoma line. A value of 0.3% was considered as the significance threshold.
Immunohistochemistry on tumor LN
Immunohistochemistry (IHC) was performed using the streptavidin/peroxidase technique as previously described [16]. Deep-frozen sections were incubated for 30 minutes at room temperature with the primary antibody. 17 different monoclonal antibodies were used to explore the expression of tumor-associated antigens: anti-gp100 (clone HMB45, 8 µg/ml, Dako, Trappes, France), anti-Melan-A (clone A103, 8 µg/ml, Dako, Trappes, France), anti-tyrosinase (clone T311, 4 µg/ml, Novocastra); adhesion molecules: anti-ICAM-1 (CD54, clone 84H10, 5 µg/ml, Beckman Coulter), anti-LFA-3 (CD58, clone BRIC5, 10 µg/ml, AbSerotec); immunosuppressive cytokines: anti-IL-10 (clone B-S10, 2 µg/ml, Diaclone), anti-TGF-β (clone TB21, 2 µg/ml, AbSerotec); MHC molecules: anti-MHC class I (clone G46-2.6, 5 µg/ml, Becton Dickinson), anti-MHC class II (clone TU39, 5 µg/ml, Becton Dickinson); and T-cell associated molecules: anti-CD4 (clone MT310, 2.5 µg/ml, Dako), anti-CD25 (clone ACT1, 2 µg/ml, Dako), anti-Foxp3 (clone 236A/E7, 5 µg/ml, ebioscience, San Diego, California, USA), anti-PD-1 (clone J105, 5 µg/ml, ebioscience), anti-CD80 (clone MAB104, 5 µg/ml, Beckman Coulter), anti-CD86 (5 µg/ml, Lifespan), anti-PD-L1 (clone MIH1, 5 µg/ml, ebioscience), anti-PD-L2 (clone MIH18, 5 µg/ml, ebioscience). Negative controls were done using a mouse monoclonal immunoglobulin-G1 (IgG1) isotype control or a monoclonal immunoglobulin-G2a (IgG2a) isotype control (DakoCytomation). Slides were read with a Leica microscope (magnification×25). In each immunostained serial section, the entire tumour area was evaluated. Each score was evaluated on a five-point scale: an absence of expression, weak (1–25% of positive cells), moderate (26–50%), intermediate (51–75%) and strong expression (>75%) was represented respectively by levels 0, 1, 2, 3 and 4. Photographs were taken using a digital SLR Nikon D70S camera. To avoid the subjectivity of the reading, all the slides were read by two independent examiners in a blinded reading.
Statistical analysis
Statistical analysis was performed using Wilcoxon test and t test to compare results from the group of patients with more than one invaded LN to results from the group with only one invaded LN. Correlation between the number of invaded LN and each parameter was assessed using Spearman correlation test.
Overall survival (OS) was defined as the time elapsed from the date of surgery to the date of death from any cause. Progression-free survival (PFS) was defined as the time elapsed from the date of surgery to the date of the first event. Survival curves were estimated using the Kaplan-Meier method. The Cox proportional hazard model was used for assessment of the predictive value of continuous parameters. R statistical software was used and statistical significance was set at p<0.05. No correction for multiple testing was applied in this exploratory study.
Results
A total of 47 samples of melanoma invaded LN from stage IIIb (AJCC 2007) were included in this study. Mean age of the 47 patients from which melanoma samples were obtained was 55.1±11.3 years (median: 53; min.-max.: 34–75); sex ratio was 27 males for 20 females. For the 47 stage IIIb melanoma patients, median event-free survival was 26.2 months and median survival was 37.5 months.
PFS was confirmed significantly associated to the number of invaded nodes, being worse in the group of more than one invaded nodes (p = 0.00289). OS was also confirmed significantly associated to the number of invaded nodes, being worse in the group of more than one invaded nodes (p = 0.00496). The median survival duration without death or relapse was 5.25 months for the group of more than one invaded LN (advanced stage III) and 157.02 months for the group with only one invaded LN (early stage III).
TIL obtained from the invaded LN
The 47 samples of melanoma invaded LN were used for producing therapeutic autologous TIL.
Amount of TIL produced between early and advanced stage III melanoma lymph nodes Patients with advanced stage III melanoma received significantly more therapeutic TIL (t test, p = 0.000585; Wilcoxon, p = 0.000539) (early stage III, 1st expansion, mean 4.89×109 TIL, 2nd expansion, mean 4.5×109 TIL; advanced stage III, 1st expansion, mean 7.95×109 TIL, 2nd expansion, mean 10.22×109 TIL). This result was confirmed using Spearman correlation test (p = 0.000319).
Phenotype of TIL
There was no significant difference in the phenotype of expanded TIL infused to the patients between the two groups, regarding CD2-positive cells, CD3-positive cells, CD3/CD4 double positive cells, CD3/CD8 double positive cells or CD3/CD25 double positive cells (Table 1).
Cytokine production assay for evaluating the proportion of tumor-reactive TIL
The same 47 samples of melanoma invaded LN from which TIL were obtained, were used to evaluate the proportion of T cells reactive to the autologous melanoma cell line among TIL infused to the patients (Table 2, Figures 1 and 2).
PFS (A) and OS (B) curves for 47 patients from metastatic melanoma based on the presence of tumor-reactive TIL: cases were divided into two groups, presence of tumor-reactive TIL and absence of tumor-reactive TIL.
Black bars indicate relapse-free patients. * Indicates patients with only one melanoma-metastatic lymph node (early stage III patients).
In the global population, we first observed that both PFS and OS were associated to the presence of tumor-reactive T-cells (Figure 1A and 1B): the duration of survival without death or without death or relapse, was increased by the injection of melanoma-reactive TIL (PFS: p = 0.00289; OS: p = 0.00279). The median survival duration without death or relapse was 31.4 months for patients that received tumor-reactive T-cells and 5.2 months for patients that did not receive tumor-reactive T-cells. Moreover, the presence of tumor-reactive TIL in the cellular expansion, was significantly associated to the stage of the illness number of invaded LN: 27/27 early stage III patients received melanoma-reactive TIL whereas 10/20 advanced stage III patients received melanoma-reactive TIL (t test, p = 0.000401; Wilcoxon, p = 0.000401): this result was confirmed using Spearman correlation test (p = 0.000401).
In addition, early stage III patients received significantly more specific TIL (1st expansion: 6.89+/−7.87%, mean 0.37×109, 2nd expansion: 5.76+/−5.74%, mean 0.27×109) than advanced stage III patients (1st expansion: 1.17+/−1.47%, mean 0.11×109, 2nd expansion: 0.99+/−1.29%, mean 0.13×109) (1st expansion: t test, p = 0.004027; Wilcoxon, p = 0.000934, 2nd expansion: t test, p = 0.000734; Wilcoxon, p = 0.000811) (Table 2, Figure 2). These results were confirmed using Spearman correlation test (1st expansion: p = 0.000401, 2nd expansion: p = 0.001414).
Immunohistochemistry on tumor LN
A total of 34/47 tissue specimens of tumor invaded LNs from stage IIIb (AJCC) melanoma patients were available for protein expression using immunohistochemistry (21 early stage III and 13 advanced stage III). While analyzing a total of 17 markers, we found that the expression of 5 of them was significantly different between early stage III specimens and advanced stage III specimens.
The expression of MHC class I molecules was significantly decreased in LN samples from advanced stage III patients (Figures 3A and 3B) (early stage III, mean expression: 2.8; advanced stage III, mean expression: 1.2; t test, p = 0.00002; Wilcoxon, p = 0.000132): this result was confirmed using Spearman correlation test (p = 0.0000342).
(A) and (B): MHC class I expression, (C) and (D): ICAM-1 expression, (E) and (F): Foxp3 expression (magnification×25). (A), (C) and (E) are specimens from the group with only one invaded LN whereas (B), (D) and (F) are specimens from the group with more than one invaded LN.
The expression of intercellular adhesion molecule-1 ICAM-1 (CD54) and co-stimulation molecule lymphocyte function-associated antigen 3 LFA-3 (CD58) was also significantly decreased in LN samples from advanced stage III patients (Figures 3C and 3D) (CD54: early stage III, mean expression: 2; advanced stage III, mean expression: 1.2; t test, p = 0.03715; Wilcoxon, p = 0.04918; CD58: early stage III, mean expression: 1.4; advanced stage III, mean expression: 0.3; t test, p = 0.0057; Wilcoxon, p = 0.00727): these results were confirmed using Spearman correlation test for CD58 only (p = 0.008).
On the contrary, the expression of the alpha chain of the IL-2 receptor (CD25) and of the nuclear transcription factor forkhead/winged helix transcription factor 3 (Foxp3) was significantly increased in LN samples from advanced stage III patients (Figures 3E and 3F) (CD25: early stage III, mean expression: 0.7; advanced stage III, mean expression: 1.2; t test, p = 0.0335; Wilcoxon, p = 0.04299; Foxp3: early stage III, mean expression: 0.2; advanced stage III, mean expression: 0.8; t test, p = 0.001626; Wilcoxon, p = 0.003021). These results were confirmed using Spearman correlation test (CD25, p = 0.02968; Foxp3, p = 0.000486).
The expression of the remaining 12 markers (gp100, Melan-A, tyrosinase, MHC class II, CD4, interleukin-10 (IL-10), transforming growth factor β (TGF-β), programmed cell death 1 (PD-1), programmed cell death ligands 1 and 2 (PD-L1 and PD-L2), CD80 and CD86) was not significantly different between the two groups.
Discussion
In the present study, regarding the treatment, that consists to infuse ex-vivo expanded TIL to autologous melanoma patients, we first confirm our previously reported observation showing that both PFS and OS of patients treated with TIL were correlated with the presence of tumor-reactive T-cells among TIL infused to the patients [9]–[10].
In addition, we report here that despite patients in advanced stage III received a significantly higher amount of total TIL than patients in early stage III; early stage III patients received significantly more tumor-reactive TIL than advanced stage III patients.
Our results suggest that the pattern of infiltrating T lymphocytes in melanoma metastasis (from which TIL populations are obtained) in early stage III is different from that of advanced stage III. The earlier stages of the illness would thus be associated with a greater number of tumor-reactive T-cells that might explain that we obtain more specific T cells with a higher efficacy against melanoma cells within TIL expansions.
Melanoma patients usually display a spontaneous T cell response against their tumor, thanks to the presence of tumor-reactive T lymphocytes. However, at some point, the responder T cells become ineffective, probably because of a local immunosuppressive process occurring at the tumor sites [17]. Numerous immunomodulatory mechanisms have been described that either render tumor cells less sensitive to immune attack (resistance) or inhibit anti-tumor immune responses (immunosuppression). Considering that anti-tumor T cells are clearly capable of rallying to the tumor site, the spontaneous anti-tumoral T cell response must become ineffective either because the tumor cells have become insensitive to the effector cells or because the effector cells themselves have become unable to be stimulated by the antigen or to exert their function, a state referred as anergy by Boon et al [17]. Anergy may possibly be caused by tumor cells themselves, anergyzing directly the potential responder T cells, or by the generation of regulatory T cells.
In the present study, we then identified 5 tissue markers associated with a different level of in situ expression between early and advanced stage III which could potentially explain the difference of clinical response to the adoptive transfer of TIL between these two groups. The expression of MHC class I molecule, adhesion molecule ICAM-1 (CD54) and co-stimulation molecule LFA-3 (CD58) was significantly decreased in LN tumor samples from advanced stage III. In addition, the expression of the alpha chain of the IL-2 receptor (CD25) and the nuclear transcription factor Foxp3 which are notably expressed by Treg cells, was significantly increased in LN tissue from the group of advanced stage III.
The most common cause of resistance to immune cells is decreased antigenicity owing to MHC class I molecule down regulation or loss, which frequently occurs in human tumors [18]. In a previous work, we already reported a loss of expression for MHC class I molecule for 6 out of the 38 LN tissue specimens analyzed, all of these 6 samples coming from patients with more than one invaded LN [19], despite no statistical significance probably related to low number of patients. Recently, Yuan et al reported low to no expression of MHC class I and II molecules by all of the metastatic tumor samples of one patient pre vaccinated with gp100 and tyrosinase peptides and treated with anti-CTLA-4 Ipilimumab [20]. The absence or weak immune response against tyrosinase or gp100 was consistent with the recurrence of disease in that patient. Therefore, authors suggest that tumor escape from immune surveillance could be the consequence of the lack of expression of MHC class I and II molecules by the tumor tissue that would prevent effective antigen presentation to T cells. While studying 15 metastases from 2 vaccinated patients with melanoma [21], Carretero et al observed a differential activation of genes involved in inflammatory processes between regressing and progressing lesions obtained after immunotherapy and detected upregulation of genes related to antigen presentation in regressing lesions, particularly HLA expression [22]. Finally, authors propose that progressing lesions are not recognized by immune cells due to irreversible alterations in MHC class I molecules.
Regarding ICAM-1 and LFA-3, a weaker or absence of expression of these 2 molecules could contribute to a dysfunctional anti-tumor immune response in advanced melanoma, as suggested by the present results where tissue specimens from advanced stage III displayed weaker levels of ICAM-1 and LFA-3 expression. To our knowledge, the predictive value of ICAM-1 or LFA-3 associated with immunotherapy has never been previously investigated in human melanoma.
Although recent studies have questioned whether all Tregs are Foxp3+ or all Foxp3+ T cells are regulatory, Foxp3 remains the most specific marker of Tregs to date. Our group already recently reported that quantitation of Foxp3 expression using quantitative PCR appears as an independent prognostic factor for PFS in stage III melanoma patients with invaded lymph nodes [23]. We thus detected a significant reduced PFS in tissue specimens from patients with Foxp3high expression compared with tissue specimens from patients with Foxp3low expression. Thus, regulatory T cell populations represent a proportion of infiltrating cells and offer a potential for tumor-associated immune dysfunction. In a similar manner than our results, Hamid et al reported recently significant associations between clinical activity and high baseline expression of two immune-related genes, Foxp3 and indoleamine 2,3-dioxygenase (IDO) in advanced melanoma patients treated with anti-CTLA-4 Ipilimumab [24]. They also observed significant associations between clinical activity of Ipilimumab and increase in TIL between baseline and 3 weeks after beginning of treatment. Authors suggest thus that infiltrating lymphocytes may have anti-tumor activity and that changes in the immune microenvironment of the tumor may slow disease progression. In a pilot study on 15 patients treated with anti-CTLA-4 Tremelimumab, clinical response was also associated with increased tumor infiltration by CD8+ TIL and a variable association with CD4+ TIL [25]. In that study, the presence of Foxp3+ cells was variably associated with positive response. In the present work, we did not observe any difference in the expression of IL-10 or TGF-β between tissue specimens from early and advanced stage III patients. In a similar manner, no difference in the expression level of tumor-associated antigens was noted between the 2 groups. Moreover, we did not observe any difference in the expression of 5 additional markers that are relevant for the interaction of lymphocyte and tumor cells (PD-1, CD80, CD86, PD-L1 and PD-L2). These latest results suggest that there is no difference in the expression of some co-stimulatory and co-inhibitory molecules of the B7 family between early and advanced stage III, at least using an immunohistochemical analysis.
These results are consistent with the development of a growing immunosuppressive tumor microenvironment related to the tumor burden in melanoma. This immunosuppressive state would notably be induced by a decrease in the expression of molecules involved in interactions between tumor cells and T cells.
In this context, gene expression profiling in melanoma metastases has recently identified at least 2 broad subsets of tumors characterized by expression of immunomodulatory genes and specific subsets of immune effector cells [26]. While carrying out an open phase II trial of immunization with the recombinant MAGE-A3 protein in 72 patients with stage III–IV metastatic melanoma, a predictive gene signature (GS) that was associated with a significant improvement in the median OS was identified: 16.2 months in the GS(−) versus 28 months in the GS(+) population [27]. In particular, patients who responded clinically showed evidence of a high expression of immune-related cell markers.
In conclusion, in the present work, we report that in early stage III melanoma, a higher proportion of tumor-reactive T-cells among TIL infused to the patients is associated with an increase of both PFS and OS. We then identified 5 biomarkers that could play an important role in the efficacy of TIL infusion to melanoma patients. Therefore, the pattern of the host tumor microenvironment may emerge as a general predictor of possible clinical benefit in particular for treatment using TIL infusion.
Acknowledgments
The authors thank S.Peltier for her precious technical assistance and also wish to thank the laboratory of immunology from CHU de Nantes for realizing the phenotype of TIL populations. We thank N. Labarrière for critical reading of the manuscript.
Author Contributions
Conceived and designed the experiments: ACK MCP BD. Performed the experiments: ACK MCP. Analyzed the data: ACK JMN MCP BD. Contributed reagents/materials/analysis tools: GQ AB LP MSJ SS AK. Wrote the paper: ACK BD.
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