- Research article
- Open Access
Stromal regulatory T-cells are associated with a favourable prognosis in gastric cancer of the cardia
BMC Gastroenterology volume 9, Article number: 65 (2009)
Recent evidence suggests that CD4+CD25+FoxP3+ regulatory T-cells (Treg) may be responsible for the failure of host anti-tumour immunity by suppressing cytotoxic T- cells. We assessed the prognostic significance of tumour infiltrating lymphocytes (TIL) in intestinal-type gastric cardiac cancer.
Tumour infiltrating lymphocyte (TIL) subsets and tumour infiltrating macrophages (TIM) were investigated in 52 cases using tissue microarrays. The interrelationship between the cell populations (CD3+, CD8+, CD20+, CD68+, GranzymeB+, FoxP3+) in different compartments and NED-survival was investigated (median follow-up time: 61 months).
Intraepithelial infiltration with TIL and TIM including Treg was generally low and not related to NED-survival. However, patients with large numbers of FoxP3+ Treg in the tumour stroma (>125.9 FoxP3+TILs/mm2) had a median survival time of 58 months while those with low FoxP3+ TIL counts (<125.9 FoxP3+TILs/mm2) had a median survival time of 32 months (p = 0.006). Patients with high versus low stromal CD68+/FoxP3+ cell ratios in primary tumour displayed median survivals of 32 and 55 months, respectively (p = 0.008).
Our results suggest that inflammatory processes within the tumour stroma of gastric intestinal-type adenocarcinomas located at the gastric cardia may affect outcome in two ways. Tumour-infiltrating macrophages are likely to promote carcinogenesis while large numbers of Treg are associated with improved outcome probably by inhibiting local inflammatory processes promoting carcinogenesis. Thus, inhibition of Treg may not be a feasible treatment option in gastric adenocarcinoma.
Gastric carcinoma is the third most common gastrointestinal tumour type in developed countries . Similarities in risk-factors for adenocarcinoma of the gastric cardia and the oesophagus  together with the stable incidence of cardiac gastric cancer despite an overall decline of gastric malignancies  suggest that these tumours should be separated from distally located gastric adenocarcinomas .
Escape from immunosurveillance is a fundamental step in cancer development. There is accumulating evidence indicating that CD4+CD25+FoxP3+ regulatory T-cells (Treg) are able to induce tolerance to self-antigens and may also inhibit anti-tumour immune response. Tregs can inhibit effector T-cells, suppress the antigen presenting function and promote the immunosuppressive function of dendritic cells, monocytes and macrophages [5, 6].
The prognostic significance of tumour infiltrating lymphocytes (TIL) in cancer therapy is not fully understood. A beneficial prognostic effect of increased lymphocyte infiltration has been shown for various tumour types. In ovarian carcinoma both intratumoural CD3+ and CD8+ TIL were associated with improved survival [7, 8] while Treg were identified as a significant negative prognostic factor . An inverse effect was observed in anal cancer where low amounts of CD3+ and cytotoxic TIL were prognostically favourable, while Treg presence had no influence on prognosis . A recent investigation of gastric malignancies found no correlation between the number of Treg and patient survival, but emphasized the significance of their distribution pattern .
We investigated the prognostic value of infiltration by various TIL-subgroups and macrophages including Treg in adenocarcinoma of the cardia in both primary tumour and draining lymph nodes.
Between 1993 and 2004, 135 patients with gastric adenocarcinoma of the cardia underwent evaluation and primary surgical treatment at the Erlangen University Hospital. A subgroup of 52 patients was enrolled in the present study according to the following criteria: All patients were required to have invasive gastric adenocarcinoma of the intestinal subtype according to the Laurén classification without distant metastases at presentation. Patients with oesophageal Barrett's adenocarcinoma were excluded. An exclusively surgical treatment regimen with complete resection (R0) was performed. No patient received (neo)adjuvant radiotherapy or chemotherapy. Staging was recorded according to the International Union against Cancer system (UICC 2002). We gathered data concerning recurrence and survival both from our university hospital, the patients' physicians and the respective residents registration office. The minimum follow-up time was 36 months; the mean follow-up time was 71.2 months (median 61.0 months) with a 95% confidence interval of 54.7 to 57.8 months. The use of the tissue sections and the patients' survival data following patient consent was approved by the Friedrich-Alexander University Erlangen-Nuremberg ethics committee.
Tissue microarray and immunohistochemistry
474 core biopsies from primary tumour, uninvolved draining lymph nodes and, if applicable, metastatic nodes were processed into tissue microarrays (TMA) (Figure 1). As guide for microarray sampling, representative areas on standard H.E.-stained sections were marked by an experienced GI-pathologist (A.D.). A manual tissue arrayer (MTA-1, Beecher Instruments, Inc., Sun Prairie, WI, USA) was used for TMA construction. From each marked region three 1.0 mm cores were collected resulting in a total of six samples from the primary tumour site, three samples from uninvolved lymph nodes and three samples from metastatic lymph nodes, respectively. Among patients with positive lymph nodes, sufficient metastatic tissue for further processing was available in 22 of 28 cases. The samples punched off from the donor blocks were arrayed in a recipient paraffin block. TMA slides were stained as described before  using CD3, CD8, CD20, CD68, anti-Granzyme B antibodies (all from Dako, Hamburg, Germany), and a polyclonal anti-FoxP3 reagent (Abcam, Cambridge, United Kingdom).
Quantification of TIL
Evaluation of the immunostained microarrays was performed using a standard light microscope at a magnification of ×200, a CCD-camera and a semi-automatic image processing software (Biomas, Erlangen, Germany). Labelled lymphocytes and macrophages were counted. In each image surface areas of the epithelial and the stromal compartments were calculated and glandular luminal areas were subtracted. Thus, it was possible to assess separately intraepithelial and stromal lymphocyte and macrophage infiltration both in the primary tumour site and lymphatic metastatic tissue (Figure 1). For each case and immune cell subset six images with most abundant infiltration were acquired both of intraepithelial and stromal compartments (mean total area per case determined for CD3: 0.466 mm2, mean epithelial surface area per case: 0.241 mm2, mean stromal surface area per case: 0.225 mm2). In stromal tissue, only areas adjacent to tumour infiltration were selected. In uninvolved lymph-nodes, two images were acquired per core adding to a total of six images per case.
Clinical variables evaluated were age, gender, UICC stage, T category and N category. Overall survival was defined as the period from surgery until death or end of follow-up. No-evidence-of-disease (NED) survival was evaluated as the period from surgery until evidence of recurrence (tumour recurrence, nodal recurrence or distant metastases). A univariate regression analysis of NED-survival was performed using Cox's proportional hazards model (SPSS, Chicago, IL, USA). For a multivariate analysis of NED-survival we adopted only variables being of significant impact in univariate analysis. Survival was analyzed by the Kaplan-Meier method . The log-rank test  was used to compare survival curves between subgroups of patients. Median values of TIL/TIM-infiltration were used as cut-off.
The patients' clinical and histological characteristics are depicted in Tables 1 and Tables 2. Overall survival and NED-survival rates of the study group were 53.7% and 63.7% at 5 years, respectively. Twelve patients died of unrelated diseases. Median overall survival and NED-survival time for all patients were 50 months (range, 46.4 - 70.8 months) and 41.5 months (range, 43.1 - 68.3 months), respectively.
Distribution pattern of lymphocytes in gastric adenocarcinoma
Due to the clear border between the stromal and epithelial compartment in intestinal-type carcinomas, we evaluated the two compartments separately. A pronounced difference in TIL/TIM- infiltration between these stromal compartments was detected both at primary tumour site and in lymph node metastasis (Table 3).
All TIL subsets and macrophages were found predominantly in stroma adjacent to epithelial tumour cell clusters while they occurred only infrequently between epithelial cells within the tumour cell nests (Figures 1 and 2).
The proportion of Tregs of total T cell counts was larger in areas of tumour infiltration (tumour stroma, affected lymph nodes) than in the control lymph nodes (Table 3).
Prognostic significance of tumour infiltrating lymphocytes (TIL) and tumour infiltrating macrophages (TIM)
FoxP3+ TIL infiltration of the tumour stroma at the primary site was of pronounced prognostic significance: patients with high stromal FoxP3+ TIL counts (>125.9 FoxP+ TIL/mm2) had a median survival time of 58 months while those with low FoxP3+ counts (<125.9 FoxP3+ TIL/mm2) had a median survival time of 32 months (hazard ratio = 0.23; C.I. 0.08 - 0.72; p = 0.006; Figure 3C and Table 3). Considering the epithelial compartment of the primary tumour site only, none of the TIL subsets or macrophages had significant prognostic impact on NED-survival.
In multivariate analysis including stromal FoxP3+ TIL, UICC-stage and nodal status, stromal Treg count was the only independent significant variable with impact on NED-survival (Table 4).
The ratio of stromal CD8+ and FoxP3+ cells was not associated with significant differences in survival. However, the stromal CD68+/FoxP3+ cell ratio was of prognostic significance (Table 4). In survival analysis, patients with a high stromal CD68+/FoxP3+ cell ratio (> 2.9) at the primary tumour site had a median survival of 32 months while those with a lower CD68+/FoxP3+ cell ratio (< 2.9) had a median survival of 55 months (p = 0.008) (graph not shown). Considering the uninvolved regional lymph nodes alone, higher numbers of Granzyme B+ cells were linked to a beneficial outcome (hazard ratio = 0.35; C.I. = 0.12 - 0.99; p = 0.05).
Correlation between TIL/TIM and clinical factors
Early disease (UICC stage I) was associated with significantly better NED-survival rates compared to advanced disease (UICC II-IV) (hazard ratio = 3.72; C.I. = 1.07 - 12.08; p = 0.04). An increasing stromal FoxP3+ TIL infiltration was inversely correlated with UICC-stage (Pearson's correlation coefficient, r = -0.40; p = 0.001), number of lymph node metastases (r = -0.36; p = 0.009) and N category in general (r = -0.36; p = 0.023). For other cell types, no such correlation could be found.
Tregs inhibit the function of effector cells [5, 6]. Consequently, an inhibitory effect of Treg on anti-tumour immunity has been predicted. In agreement with this hypothesis, large numbers of tumour-infiltrating Treg were shown to be associated with poor outcome in ovarian carcinomas . However, studies of other tumours have produced conflicting results. Thus, no prognostic effect of Treg was observed in a study of anal carcinomas . In certain lymphomas, tumour-infiltrating Treg were associated with favourable prognosis . A recent study of FoxP3+ Treg in colorectal cancer also showed high Treg numbers to be associated with improved survival .
Studies on gastric carcinomas have also yielded conflicting results. Kono et al. found a higher percentage of Treg among PBMCs in patients with advanced gastric carcinoma. Higher numbers of Treg in PBMCs had an adverse effect on outcome, and numbers of Treg declined to normal values following curative resection . Mizukami et al. found no effect of Treg counts on survival but showed that a diffuse dissemination of Treg was associated with poor survival while accumulation of Treg in the peritumoural region correlated with a more favourable outcome. But the former distribution pattern was associated with diffuse gastric cancers while the latter was predominantly found in intestinal type carcinomas . Kawaida et al. found that tumour draining lymph nodes showed an increased prevalence of CD4+CD25+ TIL as compared to control mesenteric nodes. However, no specific correlation between survival and intensity of Treg infiltration could be demonstrated . These previous studies have analyzed TIL numbers in different compartments ranging from primary tumour to PBMC, thus making comparison of results difficult.
For these reasons, we have decided to focus on a morphologically homogeneous group of intestinal-type adenocarcinomas located at the gastric cardia. We have assessed the numbers of tumour-infiltrating immune cells in different tumour-related compartments in relation to outcome parameters. We show firstly that the presence of various TIL subsets including Treg, cytotoxic T-cells as well as tumour-infiltrating macrophages within the epithelial compartment had no significant influence on survival rates. This is in contrast to our previous analysis of anal carcinomas . This may be attributable to the differing growth patterns of the two tumour entities with anal carcinomas growing in a more solid fashion with less stromal support as compared to gastric adenocarcinoma. We identified only two parameters which were of prognostic significance. High numbers of Treg in the tumour stroma at the primary site were associated with improved prognosis while this was not the case for other tumour-related compartments. Furthermore, high numbers of macrophages in combination with low numbers of Treg in the tumour stroma indicated poor outcome. Moreover, we show that the number of Tregs as a proportion of total T-cells is higher in both in tumour stroma and in affected lymph nodes as compared to uninvolved lymph nodes. This enrichment of Tregs suggests that these cell are actively recruited to the tumour site and points to a role for Tregs in inhibiting local immune reactions by direct cell-to-cell contact .
On the face of it, these findings are unexpected and contrast previous studies of ovarian carcinoma [7–9, 19]. Nevertheless, our findings parallel recent studies of Treg in colorectal cancer . It is important to keep in mind that Treg exert their function via a direct membrane contact mechanism . This might explain the observation that a larger proportion of T cells are regulatory T cells both in the tumor stroma and the affected lymph nodes as compared to the control lymph nodes.
Chronic inflammation, either related to H. pylori infection or to autoimmune gastritis, is considered the major risk factor for the development of gastric cancer of intestinal type. This is probably also true for gastric adenocarcinoma located at the cardia . Development of chronic H. pylori gastritis and progression to gastric atrophy and preneoplastic lesions has been shown to be associated with the development of a Th1-predominant local immune reaction in mouse experiments . Thus, the presence of large numbers of local Treg may well help to dampen these local inflammatory responses. This notion is also supported by the observation that gastric Treg can suppress H. pylori-induced T cell proliferation and IFN-gamma production . It is speculated that Treg may inhibit local effector T-cells contributing to gastric carcinogenesis. A possible mechanism may be that the effect of Treg is mediated via a down-regulation of harmful proinflammatory cytokines known to promote malignancy [23–25]. The notion that Treg may exert an inhibitory effect on gastric cancer development is also in keeping with our observation that Treg are particularly prevalent in earlier stages of gastric carcinogenesis since any effect of these cells is likely to be greatest at this time point. Nonetheless, further functional studies will be necessary to elucidate the exact role of Treg in gastric cancer. Moreover, there is the emerging concept that not all FoxP3 positive cells might be natural Tregs with stable FoxP3 expression. Natural Treg cells might be detected by analyzing the Treg-cell specific demethylated region (TSDR) in tissue specimen .
We also find that a higher number of Granzyme B positive T cells in uninvolved lymph nodes is associated with a better outcome. Granzyme B is a key cytolytic mediator secreted by activated cytotoxic T cells. A large systemic number of activated cytotoxic T cells as represented by large numbers in uninvolved lymph nodes may be an indicator of an efficient systemic host anti-tumor immunity .
Moreover, we show that large numbers of tumour-associated macrophages in conjunction with small numbers of Treg are associated with poor prognosis. This is in agreement with a previous study . It is now well accepted that tumour-associated macrophages promote tumour development for example through stimulating angiogenesis or modulating the plasticity of extracellular matrix . Moreover, it has been shown recently that activated macrophages may activate Wnt signalling in gastric cancer epithelial cells via TNF-alpha thus contributing to tumour development .
Our results suggest that inflammatory processes within the tumour stroma of intestinal-type adenocarcinoma of the gastric cardia may affect outcome in two ways. Tumour-infiltrating macrophages are likely to promote carcinogenesis as has been reported previously for various tumour models. By contrast, Treg may down-modulate local inflammatory processes which promote carcinogenesis. Thus, inhibition of Treg may not be a feasible treatment option in gastric adenocarcinoma.
Brown LM, Devesa SS: Epidemiologic trends in esophageal and gastric cancer in the United States. Surg Oncol Clin N Am. 2002, 11 (2): 235-256. 10.1016/S1055-3207(02)00002-9.
Crane SJ, Locke GR, Harmsen WS, Diehl NN, Zinsmeister AR, Melton LJ, Romero Y, Talley NJ: Subsite-specific risk factors for esophageal and gastric adenocarcinoma. Am J Gastroenterol. 2007, 102 (8): 1596-1602. 10.1111/j.1572-0241.2007.01234.x.
Crane SJ, Locke G, Harmsen WS, Diehl NN, Zinsmeister AR, Melton L, Romero Y, Talley NJ: The changing incidence of oesophageal and gastric adenocarcinoma by anatomic sub-site. Aliment Pharmacol Ther. 2007, 25 (4): 447-453.
McColl KE: Cancer of the gastric cardia. Best Pract Res Clin Gastroenterol. 2006, 20 (4): 687-696. 10.1016/j.bpg.2006.03.005.
Mahnke K, Bedke T, Enk AH: Regulatory conversation between antigen presenting cells and regulatory T cells enhance immune suppression. Cell Immunol. 2007, 250 (1-2): 1-13. 10.1016/j.cellimm.2008.01.004.
Schabowsky RH, Madireddi S, Sharma R, Yolcu ES, Shirwan H: Targeting CD4+CD25+FoxP3+ regulatory T-cells for the augmentation of cancer immunotherapy. Curr Opin Investig Drugs. 2007, 8 (12): 1002-1008.
Sato E, Olson SH, Ahn J, Bundy B, Nishikawa H, Qian F, Jungbluth AA, Frosina D, Gnjatic S, Ambrosone C, et al: Intraepithelial CD8+ tumor-infiltrating lymphocytes and a high CD8+/regulatory T cell ratio are associated with favorable prognosis in ovarian cancer. Proc Natl Acad Sci USA. 2005, 102 (51): 18538-18543. 10.1073/pnas.0509182102.
Zhang L, Conejo-Garcia JR, Katsaros D, Gimotty PA, Massobrio M, Regnani G, Makrigiannakis A, Gray H, Schlienger K, Liebman MN, et al: Intratumoral T cells, recurrence, and survival in epithelial ovarian cancer. N Engl J Med. 2003, 348 (3): 203-213. 10.1056/NEJMoa020177.
Curiel TJ, Coukos G, Zou L, Alvarez X, Cheng P, Mottram P, Evdemon-Hogan M, Conejo-Garcia JR, Zhang L, Burow M, et al: Specific recruitment of regulatory T cells in ovarian carcinoma fosters immune privilege and predicts reduced survival. Nat Med. 2004, 10 (9): 942-949. 10.1038/nm1093.
Grabenbauer GG, Lahmer G, Distel L, Niedobitek G: Tumor-infiltrating cytotoxic T cells but not regulatory T cells predict outcome in anal squamous cell carcinoma. Clin Cancer Res. 2006, 12 (11 Pt 1): 3355-3360. 10.1158/1078-0432.CCR-05-2434.
Mizukami Y, Kono K, Kawaguchi Y, Akaike H, Kamimura K, Sugai H, Fujii H: Localisation pattern of Foxp3+ regulatory T cells is associated with clinical behaviour in gastric cancer. Br J Cancer. 2008, 98 (1): 148-153. 10.1038/sj.bjc.6604149.
Kaplan EL, Meier P: Non parametric estimation from incomplete observations. J Am Stat Assoc. 1958, 53: 457-481. 10.2307/2281868.
Bland JM, Altman DG: The logrank test. Bmj. 2004, 328 (7447): 1073-10.1136/bmj.328.7447.1073.
Tzankov A, Meier C, Hirschmann P, Went P, Pileri SA, Dirnhofer S: Correlation of high numbers of intratumoral FOXP3+ regulatory T cells with improved survival in germinal center-like diffuse large B-cell lymphoma, follicular lymphoma and classical Hodgkin's lymphoma. Haematologica. 2008, 93 (2): 193-200. 10.3324/haematol.11702.
Salama P, Phillips M, Grieu F, Morris M, Zeps N, Joseph D, Platell C, Iacopetta B: Tumor-infiltrating FOXP3+ T regulatory cells show strong prognostic significance in colorectal cancer. J Clin Oncol. 2009, 27 (2): 186-192. 10.1200/JCO.2008.18.7229.
Kono K, Kawaida H, Takahashi A, Sugai H, Mimura K, Miyagawa N, Omata H, Fujii H: CD4(+)CD25high regulatory T cells increase with tumor stage in patients with gastric and esophageal cancers. Cancer Immunol Immunother. 2006, 55 (9): 1064-1071. 10.1007/s00262-005-0092-8.
Kawaida H, Kono K, Takahashi A, Sugai H, Mimura K, Miyagawa N, Omata H, Ooi A, Fujii H: Distribution of CD4+CD25high regulatory T-cells in tumor-draining lymph nodes in patients with gastric cancer. J Surg Res. 2005, 124 (1): 151-157. 10.1016/j.jss.2004.10.004.
Shevach EM: Regulatory T cells in autoimmmunity*. Annu Rev Immunol. 2000, 18: 423-449. 10.1146/annurev.immunol.18.1.423.
Zhang ZF, Karpeh MS, Lauwers GY, Marrero AM, Pollack D, Cordon-Cardo C, Begg C: Risk factors and p53 nuclear overexpression in early stage intestinal-type adenocarcinoma of the stomach. Cancer Detect Prev. 1995, 19 (2): 156-164.
Egi Y, Ito M, Tanaka S, Imagawa S, Takata S, Yoshihara M, Haruma K, Chayama K: Role of Helicobacter pylori infection and chronic inflammation in gastric cancer in the cardia. Jpn J Clin Oncol. 2007, 37 (5): 365-369. 10.1093/jjco/hym029.
Fox JG, Wang TC: Inflammation, atrophy, and gastric cancer. J Clin Invest. 2007, 117 (1): 60-69. 10.1172/JCI30111.
Enarsson K, Lundgren A, Kindlund B, Hermansson M, Roncador G, Banham AH, Lundin BS, Quiding-Jarbrink M: Function and recruitment of mucosal regulatory T cells in human chronic Helicobacter pylori infection and gastric adenocarcinoma. Clin Immunol. 2006, 121 (3): 358-368. 10.1016/j.clim.2006.07.002.
Erdman SE, Sohn JJ, Rao VP, Nambiar PR, Ge Z, Fox JG, Schauer DB: CD4+CD25+ regulatory lymphocytes induce regression of intestinal tumors in ApcMin/+ mice. Cancer Res. 2005, 65 (10): 3998-4004. 10.1158/0008-5472.CAN-04-3104.
Balkwill F, Coussens LM: Cancer: an inflammatory link. Nature. 2004, 431 (7007): 405-406. 10.1038/431405a.
Mantovani A: Cancer: inflammation by remote control. Nature. 2005, 435 (7043): 752-753. 10.1038/435752a.
Huehn J, Polansky JK, Hamann A: Epigenetic control of FOXP3 expression: the key to a stable regulatory T-cell lineage?. Nat Rev Immunol. 2009, 9 (2): 83-89. 10.1038/nri2474.
Quesnel B: Tumor dormancy and immunoescape. APMIS. 2008, 116 (7-8): 685-694. 10.1111/j.1600-0463.2008.01163.x.
Ishigami S, Natsugoe S, Tokuda K, Nakajo A, Okumura H, Matsumoto M, Miyazono F, Hokita S, Aikou T: Tumor-associated macrophage (TAM) infiltration in gastric cancer. Anticancer Res. 2003, 23 (5A): 4079-4083.
Guruvayoorappan C: Tumor versus tumor-associated macrophages: how hot is the link?. Integr Cancer Ther. 2008, 7 (2): 90-95. 10.1177/1534735408319060.
Oguma K, Oshima H, Aoki M, Uchio R, Naka K, Nakamura S, Hirao A, Saya H, Taketo MM, Oshima M: Activated macrophages promote Wnt signalling through tumour necrosis factor-alpha in gastric tumour cells. EMBO J. 2008, 27 (12): 1671-1681. 10.1038/emboj.2008.105.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-230X/9/65/prepub
This study was supported by the Interdisciplinary Center for Clinical Research (IZKF), University Hospitals of Erlangen, Project D4 (to Gerhard G Grabenbauer, Gerald Niedobitek, Luitpold V Distel). We thank Kunigunda Herbig and Christa Winkelmann for excellent technical assistance.
The authors declare that they have no competing interests.
MH: conception and design, analysis and interpretation of data, drafting of manuscript. AD: analysis and interpretation of data. WH: conception and design. GGG: conception and design, revision of manuscript. GN: conception and design, revision of manuscript. LVD: conception and design, interpretation of data, drafting of manuscript. All authors read and approved the final manuscript.
Gerald Niedobitek and Luitpold V Distel contributed equally to this work.
About this article
Cite this article
Haas, M., Dimmler, A., Hohenberger, W. et al. Stromal regulatory T-cells are associated with a favourable prognosis in gastric cancer of the cardia. BMC Gastroenterol 9, 65 (2009). https://doi.org/10.1186/1471-230X-9-65
- Gastric Cancer
- Gastric Adenocarcinoma
- Tumour Infiltrate Lymphocyte
- Primary Tumour Site
- Gastric Cardia