Claire Galand1,2,3† Sabrina Donnou1,2,3† Thierry Jo Molina3,4 Wolf Herman Fridman1,2,3 Sylvain Fisson1,2,5,6,7 Catherine Sautès-Fridman1,2,3*- 1 INSERM, UMRS872, Centre de Recherche des Cordeliers, Paris, France
- 2 Université Pierre et Marie Curie-Paris 6, UMRS 872, Paris, France
- 3 Université Paris Descartes, UMRS 872, Paris, France
- 4 Service d’Anatomie Pathologique, Hôtel Dieu, Assistance Publique Hôpitaux de Paris, Paris, France
- 5 Genethon, Evry, France
- 6 INSERM, U951, Evry, France
- 7 Université d’Evry Val d’Essone, UMRS 951, Evry, France
Diffuse large B-cell lymphomas (DLBCLs) are heterogeneous diseases growing either in nodal or extranodal locations including the central nervous system. One key issue is to decipher the prognostic value of immune cells infiltrating these tumors as DLBCLs developing in sanctuaries are more aggressive than nodal DLCBLs. Here, we summarize available data from the literature regarding the prognostic values of the different immune cell types found in these two types of human primary tumors (i.e., nodal vs brain). In nodal DLBCLs, memory T-cells and dendritic cells (DCs) densities are of good prognostic value whereas the influence of regulatory T-cells (Tregs) is less clear, in accordance with other types of cancers. Data for primary central nervous system lymphomas are very sparse for these cell types. By contrast, CD8+ cytotoxic T-cells seem to be of poor prognosis in either location. Their presence is linked to a loss of MHC expression providing a possible immune escape mechanism for these tumors. Clearly, tumor-associated macrophages are not associated to a significant prognostic value even in the brain where they highly infiltrate the tumor. Animal models indicate some specific features of lymphoma developing in sanctuaries by comparison to splenic location, with a higher infiltration of Tregs and less DCs, most likely reflecting the immunosuppressive context of these organs. All these informations illustrate the high impact of the immune system on patient outcome, encourage the pursuit of the immune environment’s analysis and of immunotherapeutic approaches.
Introduction
Around one third of all adult lymphomas are diffuse large B-cell lymphomas (DLBCL), the most common form of non-Hodgkin lymphoma (NHL) in Western countries. The primary location of this cancer is intranodal for 2/3 of patients and extranodal for the remaining 1/3 (Groves et al., 2000). Nonetheless, although the overall incidence of DLBCL (8/105 individuals in 2006) has been increasing slightly, at a rate of about 1% per year (Flowers et al., 2010), the incidence of extranodal B-cell lymphoma is rising faster, at about 3–6.9% per year (Chiu and Weisenburger, 2003). In particular, the incidence of primary central nervous system lymphoma (PCNSL) has climbed by 224% in 20 years and this cannot be solely attributed to HIV progression (Chan, 2003). The aggressiveness of DLBCL differs strongly according to tumor location. Overall survival (OS) rates in patients with DLCBL in immune sanctuaries, such as the CNS and testis (5-year OS: 30 and 48%, respectively; Shibamoto et al., 2008; Zucca, 2008), are substantially lower than those in other types of extranodal DLCBL (5-year OS: 63–91%) and in all DLBCL sites (5-year OS: 54%; Schaffel et al., 2007). DLBCL is currently treated by chemotherapy (cyclophosphamide, doxorubicin, vincristine, and prednisone, CHOP) now combined with immunotherapy (Rituximab). PCNSL is usually treated with chemotherapy and methotrexate (Shibamoto et al., 2008).
The aggressiveness of DLBCL also depends on the tumor’s molecular signature. Three DLCBL subtypes have been described by gene expression profiling: germinal center B-cell like (GCB), activated B-cell like (ABC or post-GCB) and PBML (primary B-cell mediastinal lymphoma; Alizadeh et al., 2000; Rosenwald et al., 2003). Survival of patients with the GCB subtype (5-year OS: 76%) is significantly higher than that of those with the ABC subtype (5-year OS: 16%) among patients treated with chemotherapy (Rosenwald et al., 2003) or R-CHOP (Jais et al., 2008; Lenz et al., 2008). PCNSLs belong mostly to the ABC subtype (Gurbuxani et al., 2009). One study reports that the molecular signature of extranodal DLCBL is characterized by a lower rate of genetic alterations targeting 18q (92% for nodal vs 53% for extranodal DLBCL; Lopez-Guillermo et al., 2005). Moreover, PCNSL and testis lymphomas are also characterized by numerous alterations in MHC gene expression that can impair the cellular immune response (Jordanova et al., 2003).
The density of immune cells in the microenvironment of primary non-lymphoid tumors, especially T and dendritic cells (DCs), has been associated with good prognosis in many solid cancers. Galon et al. (2006) demonstrated that a high density of CD3+ cells is positively correlated with better survival of patients with colorectal cancer. More recently they showed the involvement of memory CD8+ and CD4+ cells in this phenomenon (Pages et al., 2009). Studies of antigen-presenting cells (APCs) have also demonstrated a strong association between a high density of mature DCs and survival in patients with non-small-cell lung cancer (Dieu-Nosjean et al., 2008). Cellular organization is also very important as has been shown notably with the importance of tertiary lymphoid structures in non-lymphoid organs (Halle et al., 2009; Fridman et al., 2012). As a consequence, it could be conceivable that anti-tumor immune response is more efficient in nodal tumors, but it does not seem to be as simple at least in the DLBCL context (Kim et al., 2011). Regarding PCNSL, it often develops in immune compromised patients, suggesting a role of the immune system but the implications in terms of immune infiltrate are currently unknown.
There is ample evidence that immune cells infiltrate DLBCLs, either in nodal or extranodal locations. One key issue is to decipher the prognostic value of immune cells infiltrating nodal DLBCLs. The strikingly lower survival rates of patients with DLBCL developing in sanctuaries compared with those patients with nodal DLCBL, suggests that an immunosuppressive environment might harness tumor aggressiveness. We will first review the data available from the literature about the prognostic values of the different types of immune cells found in these two types of primary tumors in humans. Thereafter, we will discuss how available animal models have helped to address some of these questions.
Immune Infiltrate
T-cells
Lippman et al. (1990) showed that tumor-infiltrating T-cells are associated with a good prognosis for patients with DLCBL, and more specifically that the number of tumor-infiltrating lymphocytes (TILs) was associated with relapse-free survival (see Table 1). That study however, did not distinguish between the major subtypes of T-cells. Since then, numerous studies have attempted to determine the relation between each type of immune subpopulation and patient’ survival.
Table 1. Comparison of the prognostic value of the immune environment between nodal (DLBCL) and central nervous system (PCNSL) diffuse large B-cell lymphomas.
CD4+ T-cells are essentially linked to a favorable prognosis
Infiltrating CD4+ T-cells accounting for more than 20% of cells in a biopsy specimen have been positively correlated with better OS for 98 patients with DLBCL (Ansell et al., 2001). The number of CD4+ T-cells related to the total number of activated T-cells (CD3+ HLA-DR+ cells) suggests that most of infiltrating T-cells were activated. The role of CD4+ T-cells is crucial in the anti-tumor immune response. They indeed recognize the antigenic peptide presented by APCs and then shape the immune response by differentiating into Th1, Th2, Th17, or Treg cells. They are necessary for full activation of CD8+ effector T-cells and therefore crucial for tumor elimination.
Several authors have described Foxp3+ regulatory T-cells (Tregs) in the microenvironment of nodal B-cell lymphomas (Riemersma et al., 2005; Yang et al., 2006; Lee et al., 2008). The prognostic value of these intratumoral Tregs vary according to the author, the sample preparation and the DLBCL classification (Table 1). Hasselblom et al. (2007) reported that Foxp3 expression had no influence on the OS of 195 patients while in a study of 96 patients, Lee et al. (2008) found that the prognostic value of high percentages of Foxp3-positive Tregs for OS was good. A third study highlighted the difference in prognosis between the GCB subtype and non-GCB DLBCLs (Tzankov et al., 2008). A higher density of Tregs was associated with a good outcome in GCB DLBCL (32/55 patients) and with a poor outcome in non-GCB DLBCL (28/70 patients). The ability of these cells to kill lymphoma B-cells depending on the specific genetic characteristics of the tumor cells, might explain this poor prognosis (Zhao et al., 2006).
Among the CD4+ effector T-cells, Th17 lymphocytes have also been characterized in the DLBCL microenvironment. Th17 cells are present in very small numbers in this cancer compared with other non-Hodgkin B-cell lymphomas (B-NHLs), such as small lymphocytic lymphoma (Yang et al., 2009). The B-NHL microenvironment has even fewer Th17 cells than the peripheral blood. B-NHLs can indeed induce the suppression of effector T-cell polarization, i.e. Th17, by promoting Treg polarization.
CD4+ T-cells infiltrate tumor-bearing brains in PCNSL (Bashir et al., 1996) as they do in DLBCL of the testis (Riemersma et al., 2005). Very little information is available about CD4+ cells in these rare tumors.
CD8+ T-cells are associated with a poor outcome
CD8+ TILs are present in the DLBCL microenvironment. Their presence is positively linked to the loss of major histocompatibility complex (MHC) class I and II molecules from the tumor cell surface (List et al., 1993). The loss of MHC, described as a mechanism of immune escape, has been shown to be a feature of DLBCL aggressiveness (Riemersma et al., 2005). This loss of MHC class I molecules could be explained by the phenomenon of tumor editing, where CD8+ T-cells eliminate all MHC class I bearing tumor cells thereby favoring the emergence of new clones of tumor cells. Hasselblom et al. (2007) showed that a high number of activated TIA-1+ cytotoxic T-cells was correlated with poorer survival among patients (143 patients in a cohort of 195 patients). The percentage of CD3-positive lymphocytes with granzyme B expression was found to be an indicator of unfavorable prognosis in 70 patients with primary nodal DLBCL (Muris et al., 2004; Table 1). These data demonstrate that CD8+ cytotoxic T-cells infiltrate is a marker of poor prognosis. The relationship between the down regulation of MHC class I molecules and percentage of cytotoxic T-cells suggest possible immune–escape mechanisms in nodal DLBCL.
In the brain, an initial study of six patients reported the almost total absence of CD8+ cells in PCNSL biopsies (Bashir et al., 1996). In a more recent work, CNS lymphomas contained high densities of cytotoxic T-cells expressing granzyme B, more than in nodal DLCBLs (Riemersma et al., 2005). The authors noted that the loss of MHC class I is more common in CNS than in nodal lymphomas, and is correlated to the number of cytotoxic T-cells. It is therefore conceivable that the loss of MHC class I is the consequence of a strong selective pressure from the T-cells in PCNSL.
Antigen-Presenting Cells
Dendritic cells favor the host anti-tumor response
Data about the density of DCs and patients survival in DLBCL are sparse (reviewed in Table 1). Monti et al. (2005), molecularly profiled DLBCLs and described three subgroups, including one called the “host-response” subgroup, which was characterized by abundant immune infiltrate. The infiltrating cells included DCs that expressed both GILT (gamma interferon induced lysosomal thiol reductase) and S100 molecules and did not express either CD1a or CD123. This phenotype is characteristic of interdigitating DCs, present in secondary lymphoid organs, but not of migrating DCs, which could be recruited at the tumor site. It is indeed noteworthy that DCs are already present in lymphoid organs and are therefore ideally located to induce an anti-tumor response contrary to the extranodal tumors. The number of interdigitating DCs was highly correlated with that of infiltrating T-cells, but this study did not determine their prognostic values.
Chang et al. (2007) analyzed DCs and T-cells in DLBCL tissues by immunohistochemistry in 48 cases of DLBCL, including nodal and extranodal types. DCs were not always detected and were sparse in most cases. In 20% of the tumors however, S100+ DCs adopted a characteristic peritumoral localization that was associated with significantly better OS. The authors also found that the density of peritumoral CD45RO+ T-cells, which colocalized with S100+ DCs was correlated with a favorable prognostic value.
The central nervous system (CNS) is naturally devoid of DCs. Some of these cells can be found in meninges, the choroid plexus, or circumventricular organs, but very few if any of these cells can be detected in healthy brain parenchyma. DCs are known to infiltrate CNS tumors such as gliomas (Morimura et al., 1990; Parney et al., 2009) or even such ocular tumors as uveal melanomas (Polak et al., 2007). Almost no study has assessed the presence of DCs in PCNSL. Interestingly however, the integrin alpha X (or CD11c) gene is reported to be expressed at significantly lower levels in PCNSL compared with nodal DLBCL (Rubenstein et al., 2006).
All these studies strongly suggest that DCs have significant value as favorable prognostic factors in DLBCLs. However, the great heterogeneity of this cell type makes it difficult to draw a clear conclusion. Further research on the specific subpopulations present and involved in the anti-tumor response would be both interesting and useful.
Macrophages play ambiguous roles and lack discriminative markers
Tumor-associated macrophages have been highlighted as key players in the tumor microenvironment in mouse models (Mantovani et al., 2011; Allavena and Mantovani, 2012). They may contribute to tumor growth via different mechanisms such as angiogenesis promotion. But macrophages can also be considered as potential APCs as they can upregulate costimulatory molecules and restimulate locally infiltrating T-cells. These cells therefore play ambiguous role.
Several studies have detected CD68+ cells, characteristic of macrophages in DLBCL. For example, DLBCLs contain substantially greater CD68+ CD14+ cell populations than other B lymphomas. Interestingly, the in vitro conversion of these cells into a DC-type population suggests CD14+ cells might be DC precursors (Marmey et al., 2006). Hasselblom et al. (2008) showed that the density of CD68+ cells had no prognostic value in 176 patients with DLBCL. Another study assessed the absolute number of peripheral blood monocytes at diagnosis and reported that an elevated monocyte count was associated with a significantly poorer OS and that this finding combined with a low absolute lymphocyte count, identified a group of patients at high risk (Wilcox et al., 2011). The poor prognosis associated with high monocyte numbers may be explained by the observation that these cells are able to favor lymphoma cells survival and proliferation at least in vitro (Mueller et al., 2007).
Macrophages have been the subject of several investigations in PCNSLs. It is clear that these cells strongly invade all kinds of brain tumors, including B-cell lymphomas at least in part because the tumor cells secrete MCP-1, a macrophage chemoattractant (Kitai et al., 2007). Recent studies have demonstrated that some tumor-associated macrophages, have the alternative (or M2) phenotype, one that suggests a mainly pro-tumorigenic function (Kadoch et al., 2009). These results were confirmed by Komohara et al. (2011) who showed that most PCNSLs contained CD68+ CD204+ and/or CD163+ M2 macrophages and that these macrophages were correlated with high activation of the Stat3 transcription factor known to be involved in tumor escape. Interestingly none of these markers had any prognostic significance in a series of 43 patients (Table 1).
Follicular Dendritic Cells
Follicular dendritic cells (FDC) meshworks are another finding of interest. Usually, these cells reflect the global architecture of the lymph node and are associated with follicular lymphomas. However, two studies noted their presence in about 25% of the DLBCL cases analyzed, including both GCB and non-GCB subtypes and nodal and extranodal localizations. In the first study, which included 66 patients, the presence of CD21+ FDC was associated with a better treatment response rate but not with a better survival (van Imhoff et al., 2006). A larger cohort of 414 cases of DLBCLs confirmed the positive effect of FDCs, showing that the presence of CD23+ FDCs was an independent prognostic factor associated with better outcome (Bernd et al., 2009). It is not yet clear either if these meshworks represent remnants of the organ architecture or if lymphoma cells interact closely with FDCs.
As Table 1 shows, these results, taken together, highlight the strong relation between patient outcome and the composition of the immune infiltrate in DLBCLs. Thus, as for solid tumors, the prognostic value of the density of overall T-cells, of CD45RO+ memory T-cells and of DCs is good. The prognostic value of Tregs, on the other hand, depends on the genetic characterization of the tumor. In contrast with most types of solid tumors, however, the density of CD8+ T-cells is associated with a poor prognosis. In nodal DLBCL and PCNSL, high densities of CD8+ T-cells are correlated with the loss of MHC class I and II molecules and tumor aggressiveness. Indeed, the frequent loss or down regulation of MHC class I molecules occurs in many solid cancers (Campoli and Ferrone, 2008). Hence this inverse effect of CD8+ T-cells on patient outcome might reflect the peculiar situation of B-cell lymphomas, which are able to present antigen to MHC class II-restricted cells and activate CD4+ T-cells, therefore allowing T-cell’s help and the CD8+ cytotoxic immune response. This might lead to a high selective pressure on tumor cells and favor escape of MHC negative tumor variants. The following concomitant loss of MHC class I and II molecules may then have a strong negative impact on the anti-tumor immune response. Interestingly, CD68+ macrophages have no prognostic value in DLBCLs, either nodal or extranodal. Studies investigating markers specific to other macrophage subtypes are needed to draw definitive conclusions. All these results are summarized in Figure 1.
Figure 1. Comparison of the presence and prognostic value of different immune cells in human biopsies and mouse models of B-cell lymphomas. Colors refer to prognosis when human data are concerned and to pro- versus anti-tumor functions for murine data. APCs, antigen-presenting cells; CTLs, cytotoxic T lymphocytes; hu, human; mu, murine.
Mouse Models
Murine models are particularly well-suited to study the tumor microenvironment of DLBCL. Implantation of the A20 cell line in syngeneic mice produces one of the models used most often (Donnou et al., 2012). The analysis of immune infiltrate in the brain is justified by the fact that immune deficient animals die prematurely from brain B-cell lymphomas compared to their wild-type counterparts (Donnou et al., 2011), showing the existence of a spontaneous anti-tumor response. Moreover, an efficient anti-tumor response can be induced in PCNSL but this has been very poorly investigated until now. It has nevertheless been shown in a murine model of nude mice that celecoxib was able to induce a prolonged survival time (Wang et al., 2006), or in a syngeneic murine model that rituximab was able to induce tumor rejection in some animals (Mineo et al., 2008). But no study assessed the anti-tumor immune response associated with tumor rejection.
T-cells
Using a model of subcutaneous large B-cell lymphoma, Grille et al. (2010) showed that CD4+-cells represented most of the T-cell infiltrate (10% Th1, 5% Th2, and 15% Tregs). We developed three models more relevant to human locations, specifically to tumor-bearing spleen, brain, and eye. Our analysis of T-cell infiltrate showed that it was composed mainly of CD4+ T-cells (Touitou et al., 2007; Donnou et al., 2011), consistent with the findings of Grille and colleagues. We also showed that Treg account for a very high proportion of the CD4+ T-cells (25%) in intrasplenic lymphoma. This proportion is significantly higher in sanctuaries: 40% in the lymphoma-bearing brain (Donnou et al., 2011) and 47% in lymphoma-bearing eyes (unpublished data). All three localizations had a Th1 and Th17 signature, but we failed to detect a Th2 profile in the PIOL microenvironment (Touitou et al., 2007). These data confirm that the privileged status of the eye is higher than that of the brain. We also demonstrated the anti-tumor activity of Th17 cells in PIOL. Th17 lymphocytes in this microenvironment produce IL-17 and IL-21. IL-21 can directly inhibit the proliferation of tumor cells (A20IIA-GFP) although IL-17 cannot (Galand et al., 2011).
The role of CTLs in lymphoma control has been highlighted by the study of Juszczynski et al. (2008). Perforin is produced by NK cells and CTLs and mice knock out for perforin develop spontaneous lymphomas more often than WT mice (incidence rate increases). These results show that NK and/or CTLs might play a role in preventing or abating lymphoma development (Smyth et al., 2000). Murine models are indeed particularly useful to dissect the anti-tumor immune response. As underlined here, deficient animals allow determining subpopulation functions. And it is conceivable to study T-cell repertoire at different times during the immune response as well as MHC expression on tumor cells to determine if tumor editing is taking place.
APCs Highly Infiltrate B Lymphoma Models
We used these models to compare the immune response developing in the eye, brain and spleen after injection of tumor cells in these sites (Touitou et al., 2007; Donnou et al., 2011). CD11b+ macrophagic/microglial cells were detected in high numbers in all three locations, consistent with human studies and confirmed as well after subcutaneous (Palmieri et al., 2010) and intravenous (Serafini et al., 2008) injections of tumor cells. The antigen-presenting capacity of these CD11b+ cells was not assessed in either study. Many CD11b+ macrophagic cells, have been shown to be immunosuppressive in the form of either M2-type macrophages in a PCNSL model (Kadoch et al., 2009) or myeloid suppressor cells in an intravenous model (Serafini et al., 2008). The murine model allowed the authors to show that these myeloid suppressor cells act by inducing tumor antigen specific regulatory T-cells (Tregs).
CD11c+ DCs have also been detected in the brain and the spleen of PCNSL and intrasplenic lymphoma-bearing mice (Donnou et al., 2011). They were located mainly in the tumor mass, and their number increased with tumor growth. This study showed that there were at least two subpopulations of DCs, those that do and do not express CD11b. It is not yet known whether these cells have pro- or anti-tumor functions. Our inability to detect any DCs in the PIOL model suggests that this site could be even more immune-privileged than the brain (Touitou et al., 2007). Palmieri et al. (2010) also worked with the A20 model implanted subcutaneously. Their analysis of the tumor microenvironment was clearly consistent with the studies cited above, showing large numbers of tumor-infiltrating CD11c+ cells. None of these studies, however, looked at DC subpopulations. These models might therefore be very useful to study the DCs associated with the anti-tumor response and to determine what impairs DC recruitment/differentiation in PIOLs.
In conclusion, these models have made it possible to demonstrate the strong impact that DLBCL location has on the quality and quantity of T-cell infiltrate. The proportions of Tregs in this infiltrate are higher in the ocular and CNS locations and DCs are undetectable in the ocular location. These differences most likely reflect the immunosuppressive context of the immune sanctuaries. As underlined in Figure 1, data regarding the presence of immune subpopulations in human and mouse are alike, but their functions mostly remain unknown justifying more research to now decipher their function and potential applications in new therapeutic strategies.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
Grant support: Our work was supported by the Institut National du Cancer (Grants RC013-C06N631-2005 and C06N748-2006), the Institut National de la Santé et de la Recherche Médicale, the University Pierre and Marie Curie, the University Paris-Descartes and the Association pour la Recherche contre le Cancer. Sabrina Donnou was recipient of a grant from the Institut National du Cancer.
Abbreviations
APC, antigen-presenting cell; CNS, central nervous system; CTL, cytotoxic T-lymphocyte; DLBCL, diffuse large B-cell lymphoma; MHC, major histocompatibility complex; NHL, Non-Hodgkin lymphomas; OS, overall survival; PCL, primary cerebral lymphoma; PCNSL, primary central nervous system lymphoma; PIOL, primary intraocular lymphoma; TIL, tumor-infiltrating lymphocytes.
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Keywords: tumor localization, immune microenvironment, DLBCL, CNS, T lymphocytes, APC
Citation: Galand C, Donnou S, Molina TJ, Fridman WH, Fisson S and Sautès-Fridman C (2012) Influence of tumor location on the composition of immune infiltrate and its impact on patient survival. Lessons from DCBCL and animal models. Front. Immun. 3:98. doi: 10.3389/fimmu.2012.00098
Received: 16 February 2012; Paper pending published: 01 March 2012;
Accepted: 14 April 2012; Published online: 04 May 2012.
Edited by:
Jean-Pierre Abastado, Singapore Immunology Network, SingaporeReviewed by:
Alessandra Nardin, Singapore Immunology Network, SingaporeNadege Bercovici, CNRS, France
Copyright: © 2012 Galand, Donnou, Molina, Fridman, Fisson and Sautès-Fridman. This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
*Correspondence: Catherine Sautès-Fridman, INSERM, UMRS872, Immune Microenvironment and Tumor, Centre de Recherche des Cordeliers, 15 rue de l’Ecole de Médecine, Paris F-75006, France. e-mail: catherine.fridman@crc.jussieu.fr
†Claire Galand and Sabrina Donnou have contributed equally to this work.