Review | Open | Published:
Inflammation and breast cancer. Balancing immune response: crosstalk between adaptive and innate immune cells during breast cancer progression
Breast Cancer Researchvolume 9, Article number: 212 (2007)
Recent insights into the molecular and cellular mechanisms underlying cancer development have revealed that immune cells functionally regulate epithelial cancer development and progression. Moreover, accumulated clinical and experimental data indicate that the outcome of an immune response toward an evolving breast neoplasm is largely determined by the type of immune response elicited. Acute tumor-directed immune responses involving cytolytic T lymphocytes appear to protect against tumor development, whereas immune responses involving chronic activation of humoral immunity, infiltration by Th2 cells, and protumor-polarized innate inflammatory cells result in the promotion of tumor development and disease progression. Herein we review this body of literature and summarize important new findings revealing the paradoxical role of innate and adaptive leukocytes as regulators of breast carcinogenesis.
Breast cancer is the most frequent malignant tumor of women in North America . Standard treatment modalities have improved the overall outlook and quality of life for women with breast cancer; however, the fact that 40% still succumb to disease highlights the need for new therapeutic approaches and identification of new therapeutic targets. While genetic and epigenetic changes in genes that regulate mammary epithelial cell proliferation, survival, polarity and/or differentiation are probable 'initiators' of breast carcinogenesis, several lines of evidence indicate that stromal cell responses in premalignant mammary tissue may 'promote' progression to cancer and/or the metastatic capability of malignant mammary epithelial cells. Cellular components of tumor stroma include (myo)fibroblasts, vascular cells, infiltrating leukocytes and specialized mesenchymal support cells unique to each tissue microenvironment. A growing body of evidence has recently implicated tumor-infiltrating leukocytes as causal players in cancer development [2–8].
The present review focuses on the paradoxical roles of innate and adaptive leukocytes as regulators of breast carcinogenesis, and highlights recent experimental data indicating that therapeutically targeting these diverse immune cell types by either neutralizing and/or bolstering their specific bioactivities may provide a therapeutic advantage to patients with breast cancer.
Leukocytes and carcinoma development
Leukocytes represent a diverse assortment of immune cells composed of both innate (myeloid) and adaptive (lymphoid) lineages. Innate immune cells, including macrophages, granulocytes, mast cells, dendritic cells (DCs), and natural killer (NK) cells, represent the first line of defense against pathogens and foreign agents. When tissue homeostasis is perturbed, tissue-resident macrophages and mast cells locally secrete soluble factors such as cytokines, chemokines, bioactive mediators, and matrix-remodeling proteins that recruit additional leukocytes from the circulation into damaged tissue (that is, inflammation) [3, 9, 10]. Recruited innate immune cells can directly eliminate pathogenic agents in situ. At the same time, DCs take up foreign antigens (including tumor antigens) and migrate to lymphoid organs, where they present their antigens to adaptive immune cells. Upon recognition of foreign antigen presented by DCs or other professional antigen-presenting cells, adaptive immune cells, such as T lymphocytes or B lymphocytes, undergo clonal expansion in order to mount an 'adaptive' response targeted against the foreign agent [11, 12]. Acute activation of innate immunity therefore sets the stage for activation of more sophisticated, antigenically committed, adaptive immune responses. Once foreign agents have been eliminated, inflammation resolves and tissue homeostasis is restored.
The inflammatory responses necessary for enabling an immune reaction may, however, also set the stage for promoting neoplastic disease. As early as 1863, Virchow first postulated that cancer originates at sites of chronic inflammation, in part based on his hypothesis that some classes of irritants causing inflammation also enhance cell proliferation . When tissues are injured or are exposed to chemical irritants, damaged cells are removed by the induction of cell death pathways, while cell proliferation is enhanced to facilitate tissue regeneration in an attempt to re-establish tissue homeostasis. Proliferation and inflammation resolve only after insulting agents are removed or tissue repair is completed. In contrast, when insulting agents persist over time, sustained cycles of cell proliferation and death in environments rich in inflammatory cells and their bioactive products may increase neoplastic risk and foster tumor progression . While sporadic or inherited genetic mutations in critical genes regulating cell cycle, programmed cell death, differentiation and adhesion may represent initiating events in tumorigenesis ('initiation'), chronic inflammation favors selection of additional features in initiated cells that may promote their full malignant transition ('promotion').
Historically, leukocytes found in and around developing tumors were thought to represent an attempt by the host to eradicate transformed neoplastic cells. Certain leukocytes, such as cytotoxic T lymphocytes (CTLs) and NK cells, undeniably play a vital function in constraining tumor development , and as such it has been postulated that many more neoplasms arise than those that eventually develop to fully malignant disease. Epidemiologic data support this contention, as evidenced by the increased incidence of viral-associated cancers , including human papillomavirus-related cervical and squamous carcinoma, herpesvirus-8-associated Kaposi's sarcoma and Epstein–Barr virus-related non-Hodgkin's lymphoma in immunocompromised individuals [15–19]. Similar to viral-associated cancers, there are data revealing an increased incidence of carcinogen-associated cancers in immune-compromised populations, including melanoma and lung adenocarcinoma [17, 20]. Where carcinogen exposure and pathogen exposure are not thought to be etiologic factors, however, immune-compromised women exhibit reduced relative risk for common epithelial cancers, including breast adenocarcinoma [17, 20–23]. Together, these epidemiological studies indicate that the overall risk for, and development of, (breast) cancer may, in part, be regulated by the immune status of the individual.
Adaptive immunity and carcinoma development: a role for B lymphocytes
A growing body of literature has emerged demonstrating that leukocytes functionally contribute to the development of most human solid tumors. Leukocytic infiltrates into the neoplastic stroma increase, paralleling breast tumorigenesis (Figures 1 and 2). Profiles of these immune cells vary but, in general, include both lymphoid and myeloid lineages.
B lymphocytes are recognized as contributing to anticancer immune responses via their secretion of antigen-specific immunoglobulins. While it is clear that acute activation of B cells may play a role in eradicating early neoplastic cells, or may participate in spontaneous regression of tumors through classical and well-studied immunoglobulin-mediated mechanisms, recent data also indicate that chronic activation of B cells may paradoxically play a role in potentiating carcinoma development (Figure 3).
B-cell precursors mature within bone marrow, where somatic recombination of immunoglobulin genes results in expression of a diverse array of B-cell receptors. Mature antigen-committed B cells migrate to secondary lymphoid organs (lymph nodes or spleen, predominantly). Upon antigen recognition by B-cell receptors, the B lymphocytes become activated and undergo clonal expansion, resulting in their enhanced capacity to recognize foreign antigens . Acute activation of B-lymphocyte responses (to foreign antigens or tissue damage) can also result in rapid induction of several soluble mediators, including diverse immunoglobulin subtypes, B-cell-derived cytokines such as IL-6 and activation of complement cascades, which together trigger recruitment of innate immune cells from the circulation. In this manner, acutely activated B cells orchestrate phagocytic or cytotoxic destruction of immunoglobulin-complexed antigens (pathogens or damaged cells) by innate immune cells. Such acute B-cell responses are critical for protecting tissues from pathogens and nonself-antigens. Chronic activation of B cells can be deleterious, however, as evidenced by their association with several pathologic disease states (rheumatoid arthritis and other autoimmune diseases) and some cancer types .
During breast carcinogenesis, mature B cells (including naive cells and activated cells) can be found in secondary lymphoid tissues as well as in tumor-associated stroma (Figure 2). As compared with healthy patients without evidence of cancer, the sentinel (draining) lymph nodes of breast cancer patients contain enriched populations of proliferating and affinity matured (IgG+) B lymphocytes . Moreover, data from retrospective studies examining the percentages of B cells present in sentinel and auxiliary lymph nodes of breast cancer patients reveal that their presence and/or maturation (IgG+) correlates with increases in disease stage (stage I versus stage II) and in total tumor burden [27, 28]. Urdiales-Viedma and colleagues utilized immunohistochemical detection of IgA, IgG and IgM in axillary lymph nodes from 50 unselected ductal breast carcinomas, and found that lymph nodes with IgG+ lymphoid follicles and/or metastatic lymph nodes with IgM+ lymphoid cells were statistically related to breast tumors of high histologic grade and more than three lymph node metastases .
Similarly, B cells present in breast tumor-associated stroma may also play a role in disease progression. Several studies have reported that infiltrating B lymphocytes represent the predominant lymphocytic population (in excess of T lymphocytes) in premalignant breast tissue, including hyperplasia and early ductal carcinoma in situ (DCIS) [30, 31] (Figure 2). Approximately 20% of invasive breast cancers contain high numbers of B cells; when present, these cells can comprise up to 60% of the neoplasia-associated lymphocyte population . These observations are not specific to breast cancer – 70% of solid tumors contain elevated populations of B cells . Although the presence of chronically activated B cells in breast cancer patients is clear, how these cells might be effecting disease progression has not been established. In DCIS and invasive carcinoma, tumor-associated B cells are typically found in perivascular locales clustering in aggregates with T cells, forming ectopic follicles [32, 34, 35]. These follicles contain B cells interdigitated around CD21+ follicular DCs, thus identifying them as authentic ectopic follicles. Formation of ectopic follicles containing mature plasma cells indicates that the presence of B cells in neoplastic mammary tissue is the result of chronic activation rather than nonspecific chemoattraction. Extra-nodal B-cell proliferation and ectopic follicle formation have also been described in several autoimmune diseases (rheumatoid arthritis, multiple sclerosis, Sjogren's disease and Graves disease), where they are thought to underlie the disease pathogenesis [36–39].
How might B lymphocytes regulate carcinoma development? A vast literature exists describing the occurrence of (auto)-antibodies in either the serum of cancer patients or in interstitial antibody deposition in tumors . An early presence of autoantibodies (in particular, antinuclear antibodies and smooth muscle antibodies) in serum of cancer patients is well known to correlate with an unfavorable prognosis . Approximately 50% of breast cancer patients contain circulating immunoglobulins that specifically react with tumor-derived antigens – autoantibodies against ErbB2/HER2/neu are present in 20% of patients with ErbB2-positive breast cancer, making it the most common breast cancer 'autoantigen' . Paradoxically, the presence of specific autoantibodies in serum and/or at tumor sites correlates with poor patient survival [40, 41, 43] – perhaps indicating that immunoglobulins resulting from chronic B-cell activation in response to tumor-specific antigens might promote disease progression (Figure 3).
Despite the presence of antitumor antibodies in greater than one-half of all breast cancer patients, there are only few reports of spontaneous tumor regression (presumed to be immunologic) in the absence of therapy [44, 45]. Several factors may influence the efficiency of antitumor antibodies in inducing tumor regression/destruction, including the immunoglobulin concentration, HLA expression, tumor tolerance/immune suppression, and impaired cytotoxic T-cell activity. Whether individuals with progressing tumors harbor a higher antigen load that thus triggers enhanced immunoglobulin production, or whether an increased presence of serum or interstitial immunoglobulins predisposes patients to development of more advanced or recurrent cancers, therefore requires further study. While the answer is not clear, the combined implication of the data is that B lymphocytes do play a role in human carcinoma development, therefore necessitating a mechanistic evaluation of their role and specificity to determine whether they represent tractable targets for anticancer therapy.
Adaptive immunity and carcinoma development: a role for T lymphocytes
Histochemical detection of T lymphocytes in archival human carcinoma tissues has revealed that they also are commonly associated with developing carcinomas (Figure 2); however, the prognostic significance of T-cell infiltrations during breast carcinogenesis is subject to great debate. While B cells appear to represent the predominant lymphocyte during early breast cancer progression , infiltrating T lymphocytes (both CD4+ and CD8+) are more extensive in higher grade DCIS and invasive carcinomas .
The extent of T-cell infiltration into invasive breast carcinomas has been reported to range from 1% to 45% of the total cellular mass . In rapidly proliferating tumors, the presence of T lymphocytes (by histopathological determination) at tumor sites is a good prognostic indicator when compared with nonimmunogenic tumors, and correlates with auxillary lymph node negativity, a smaller tumor diameter, a lower histological grade and recurrence-free survival  – therefore supporting an overall role for T cells in immune surveillance. The exact composition of T lymphocyte infiltration varies greatly, however, and may profoundly affect disease progression and overall patient survival.
During breast carcinogenesis, the presence of metastatic mammary epithelial cells in sentinel lymph nodes draining the primary tumor represents the strongest prognostic indicator for disease progression and overall patient outcome [49–51]. While it is unclear whether the presence of CD8+ CTLs alone provides any prognostic information, the presence of high percentages of CD4+ T-helper cells at primary tumor sites positively correlates with disease progression, including metastatic spread to sentinel lymph nodes and increased primary tumor size [47, 52]. Perhaps more significant is the ratio of CD4+ to CD8+ cells, where primary tumors with ratios greater than one correlate with lymph node metastasis and reduced patient survival [47, 52]. Similar results have been reported for colorectal carcinoma , renal carcinoma, esophageal carcinoma, and small-cell lung carcinoma .
Why are CD8+ CTL-mediated responses not more effective in eradicating or minimizing cancer occurrence and how might CD4+ T cells be involved in enhancing breast cancer progression? One plausible mechanism may have to do with the 'polarity' of the CD4+ T-helper-cell response at primary tumor sites and/or their distant metastases (Figure 3). CD4+ T-helper cells are activated in response to soluble factors and can be classified generally into two categories as either Th1 cells or Th2 cells (Figure 4) . Following an activating stimulus, CD4+ T-helper cells that are Th1-polarized secrete IFNγ, transforming growth factor beta, TNFα and IL-2 . These cytokines collaborate with the cytotoxic/cell killing functions of CD8+ T cells  and can induce upregulation of antigen processing (in the proteasome), can induce expression of MHC class I and II molecules, and can induce other antigen display cofactors in neoplastic cells. Th1 CD4+ T-helper cells also enhance antitumor immune responses by secretion of INFγ, which in turn induces activation of macrophage cytotoxic activity . In contrast Th2-polarized CD4+ T-helper cells express IL-4, IL-5, IL-6, IL-10 and IL-13, which induce T-cell anergy and loss of T-cell-mediated cytotoxicity while also enhancing humoral immunity (B-cell function) . Taken together, Th1 responses are thought to be beneficial toward antitumor immunity [60–63] whereas Th2 responses may downregulate cell-mediated antitumor immunity [63–67] and enhance protumor humoral responses [68, 69].
Role for regulatory T lymphocytes
In addition to T-helper-cell polarity, developing neoplasms can escape CD8+ T-cell cytotoxicity by promoting expansion of regulatory T cells (Treg). Treg cells normally function to protect tissue from autoimmune disease by suppressing self-reactive cells. Typically characterized by expression of CD4, CD25 and FOXP3, Treg cells can account for approximately 5–10% of all T lymphocytes in healthy tissues.
In breast cancers the percentage of Treg cells, as assessed by FOXP3 positivity, increases in parallel with the disease stage, from normal to DCIS and from DCIS to invasive carcinoma . In patients with invasive carcinoma the presence of high numbers of FOXP3+ T cells predicts worse relapse-free survival and decreased overall patient survival , and may indicate that the presence of Treg cells promotes tumor progression by inhibiting immunosuppression. The mechanisms underlying immunosuppression are not clear; however, CD4+CD25highFOXP3+ Treg cells retain the ability to actively inhibit CD4+CD25- T cells, CD8+ T cells, DCs, NK cells, and B cells in a cell-to-cell contact and dose-dependent manner [71–75]. The mechanisms by which developing tumors might stimulate proliferation and differentiation of Treg lymphocytes are still not well known, but production of prostaglandin E2 by tumor cells and of CCL22 by tumor-associated macrophages may act as chemotactic and differentiation agents for Treg cells [76–79].
Acquired immunity and carcinoma development
It is well established that chronic infiltration of tissue by some innate immune cell types (for example, immature monocytes, macrophages, mast cells or neutrophils) contributes to epithelial cancer development [3, 8, 80]. Many studies have reported that inflammatory leukocytes promote cancer development due to their enormous plasticity and their capacity to produce a myriad of cytokines, chemokines, metalloserine and metallocysteine proteases, reactive oxygen species, histamine and other bioactive mediators [3, 8, 80]. Several physiological processes necessary for tumor development, such as enhanced cell survival, tissue remodeling, angiogenesis and suppression of antitumor adaptive immune responses, are thus regulated by leukocytic infiltrates in neoplastic environments. This regulation is exemplified by positive correlations between numbers of innate immune cells (macrophages, mast cells and neutrophils) infiltrating human tumors with the number of blood vessels [81, 82], and by experimental findings in mouse models where attenuating innate immune cell infiltration of premalignant tissue reduces angiogenesis and limits tumor development [83–90].
The earliest reports revealing a potential tumor-enhancing effect of adaptive immunity found that passive transfer of tumor-specific antibodies enhanced in vivo outgrowth of transplanted tumor cells or chemically induced tumors [91–93]. More recently, the availability of de novo carcinogenesis mouse models for the study organ specific cancer development has allowed experimentalist to revisit these analysis. Their experiments have revealed that the tumor enhancing roles of humoral immunity are more involved in innate immune cell responses, as opposed to direct regulation of neoplastic cell survival. For example, active immunization of mice harboring a mutant ras oncogene resulted in activation of humoral immune responses and enhanced papilloma formation upon chemical promotion [94, 95].
Studies by Barbera-Guillem and colleagues reported that 'antitumor' humoral immune responses potentate in vivo growth and invasion of injected murine and human tumor cell lines via recruitment and activation of protumor granulocytes and macrophages [94, 96, 97]. Once in the neoplastic microenvironment, deposited immunoglobulin may mediate recruitment of innate immune cells via activation of complement cascades or engagement with Fc receptors expressed on resident or recruited innate immune cells that trigger various cellular responses, including phagocytosis, antigen presentation, secretion of proinflammatory mediators and antibody-dependent cytotoxicity [98, 99]. During breast cancer development, immunoglobulin deposition in neoplastic stroma is known to increase the bioavailability of vascular endothelial growth factor (VEGF) by binding to Fc receptors on tumor-associated macrophages, thus triggering release of VEGF into the interstitium . Moreover, the presence of endocytosed immunoglobulin in macrophages in breast carcinoma tissues corresponds with local extracellular VEGF protein levels and local angiogenic vascular buds .
The significance of tumor-associated macrophages has been experimentally addressed in a mouse model of mammary carcinogenesis; that is, mouse mammary tumor virus–polyomavirus middle T antigen transgenic mice . In this model of mammary carcinogenesis, infiltration of macrophages into premalignant mammary tissue is associated with tumor progression . Failure to recruit macrophages into neoplastic tissue does not alter the hallmarks of premalignancy, but instead significantly delays development of invasive carcinomas and results in reduced pulmonary metastases . Metastatic potential is restored by transgenic expression of colony-stimulating factor (CSF)-1 in the mammary epithelium of CSF-1-deficient/polyomavirus middle T antigen mice . Macrophage stimulation of mammary tumor progression is at least in part due to their ability to enhance angiogenesis via regulating VEGF levels and bioavailability . These experimental data combined with the positive correlation between CSF-1 levels, macrophage recruitment and poor prognosis in human cancers  support the notion that macrophages and/or their products play a major role in facilitating late-stage metastatic progression of tumors . Other cells of myeloid lineage have also been reported to contribute to tumor development – NK cells can play a role in protection against experimental tumor growth, in part by producing mediators with antiangiogenic properties [103, 104]. These studies have together induced a paradigm shift regarding the role of immune cells during malignant progression. Whereas the historical viewpoint suggested that host immunity is protective with regards to cancer, it is now clear that certain subsets of chronically activated innate immune cells promote growth and/or facilitate survival of neoplastic cells.
In addition to providing a survival advantage to evolving neoplastic cells through their release of protumor mediators, is there evidence that recruited innate immune cells regulate any antitumor bioactivities of T cells present in premalignant/malignant mammary tissue? Neoplastic microenvironments favor polarized chronic protumorigenic inflammatory states, as opposed to those representing acute antitumor immune responses [8, 105]. Clinical data indicate that the 'immune status' of healthy individuals is distinct as compared with those harboring malignant tumors, where T lymphocytes in the later population are found to be functionally impaired . A subset of innate immune cells (for example, myeloid suppressor CD11b+Gr-1+ cells) accumulate in the peripheral blood of cancer patients [107, 108], as well as in tumors and lymphoid organs [105, 108, 109]. Myeloid suppressor cells are known to induce T-lymphocyte dysfunction by direct cell–cell contact and by production of immunosuppressive mediators, and thus actively inhibit antitumor adaptive immunity [108, 109]. Myeloid suppressor cells can also directly promote tumor growth by contributing to tumor-associated angiogenesis . In addition, malignant lesions attract regulatory T cells that can suppress effector functions of CTLs . Immune states such as these disable tumor-killing CD8+ CTL responses and enable states of immune privilege that foster escape from antitumor immunity while simultaneously exploiting activated innate immune cells that enhance cancer development. The degree to which similar mechanisms are at play during breast carcinogenesis is currently being investigated.
Cytokines derived from activated humoral immunity and/or Th2 T lymphocytes also actively regulate chemoattraction and polarization of tumor-associated leukocytes, especially macrophages. Chronically activated B cells (typically in germinal centers or in ectopic follicles) can produce granulocyte–macrophage-CSF, TNFα, IL-6, and IL-10 . These cytokines, in combination with Th2 cytokines such as IL-4, IL-13, and IL-10, are potent effectors of innate immune cell polarization. Protumor M2 polarization in macrophages is induced by the Th2/humoral cytokines IL-4 and IL-10, while simultaneously repressing antitumor M1 macrophage polarization . Granulocyte–macrophage-CSF, IL-6 and IL-10 secreted by activated B cells suppress macrophage cytotoxic activity , while IL-10 inhibits both antigen presentation by macrophages as well as monocyte differentiation into DC lineages . Taken together, factors derived from chronically activated lymphocytes sculpt innate immune cell responses towards tumor tolerance and promotion of disease progression.
During the past decade, insights have been gained regarding mechanisms underlying the dynamic interplay between immune cells and tumor progression. The accumulated data indicate that the outcome of an immune response toward a tumor is largely determined by the type of immune response elicited (Figure 3). A tumor-directed immune response involving cytolytic CD8+ T cells, Th1 cells and NK cells appears to protect against tumor development and progression. If, on the other hand, the immune response involves B cells and activation of humoral immunity, and/or a Th2 polarized response the probable outcome is promotion of tumor development and progression. This balance between a protective cytotoxic response and a harmful humoral or Th2 response can be regulated systemically by the general immune status of the individual, as well as locally by myeloid suppressor cells and Treg cells, and thus offers clinicians attractive targets for anticancer immune-based therapies.
This article is part of a review series on Inflammation and breast cancer, edited by Mina J Bissell and Jeffrey W Pollard.
Other articles in the series can be found online at http://breast-cancer-research.com/articles/review-series.asp?series=bcr_Inflammation
cytotoxic T lymphocyte
ductal carcinoma in situ
- Th cells:
tumor necrosis factor
- Treg cells:
regulatory T cells
vascular endothelial growth factor.
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The authors would like to acknowledge all the scientists who made contributions to the areas of research reviewed here that were not cited due to space constraints. The authors acknowledge support from a Postdoctoral Training Grant NCI T32 CA09043 (DDN), and grants from the National Institutes of Health, Sandler Program in Basic Sciences, the National Technology Center for Networks and Pathways, and a Department of Defense Era of Hope Scholar Award (LMC).
The authors declare that they have no competing interests.