Worldwide, lung cancer is the most frequently diagnosed malignancy and the leading cause of cancer death (1). This is largely due to over 50% of non-small cell lung cancer (NSCLC) patients presenting with disease that has metastasized to distant organs, where life expectancy under chemotherapy has generally not exceeded 12 to 18 months (2). In this group, systemic treatment is the mainstay and has undergone a series of paradigm shifts where options have evolved from chemotherapy to targeted molecular agents to the most recent immunotherapy strategies (3).
Approximately two-thirds of the lung tumor microenvironment (TME) immune cells are composed of T and B cells (4). The effects of lung cancer infiltrating T cells have been extensively studied. As a result, the most successful immune-oncology approaches in lung cancer consist of antibodies that block inhibitory receptors (“checkpoints”) that are upregulated on T cells infiltrating the tumor, thereby enhancing the patient’s T cells to act against the tumor cells (5,6). However, while preliminary findings of these T cell-targeted inhibitors have been promising, a significant proportion of patients with NSCLC do not achieve sustained disease control. This indicates the need to understand other immune cells in the TME in order to develop alternative therapeutic approaches (7).
Recent evidence suggests a critical role exists for B cells in lung cancer where studies indicate that proliferating B cells are observed in 35% of lung cancer (8), and where they are present at all stages of lung cancer development with variations across clinical stages and histological subtypes (9,10). However, relative to T cells, knowledge of B cell biology in lung cancer remains less well developed. The purpose of this review is to provide a comprehensive overview of the phenotypic diversity and roles of B cells in lung cancer, and to offer insight into potential mechanisms by which they may be utilized as an integral component of immunotherapeutic strategies and as biomarkers of treatment responsiveness. We present the following article in accordance with the Narrative Review reporting checklist (available at http://dx.doi.org/10.21037/tlcr-20-788).
A literature search was conducted through PubMed and cross references, from inception to April 2020, to identify publications describing the nature and function of B cells in lung cancer. Search strategies were developed using subject headings and text words based on two terms: “B cells” and “lung cancer”.
B cells develop in the bone marrow to give rise to diverse effector cells
B cells are the central players of humoral immunity through their capacity for immunoglobulin (antibody) production (11). Generation of antibodies is the end result of a complex and highly regulated process of B cell development and signalling that involves many subpopulations that can be defined by anatomical location, cell morphology, specific cell surface markers and immunoglobulin heavy (H) chain and light (L) chain gene loci arrangements.
In the first instance, B cells originate in the bone marrow from common lymphoid progenitor cells. With the acquisition of specific cell surface markers, they develop sequentially into early pro-B cells, late pro-B cells, large pre-B cells, small pre-B cells, before migrating to the spleen as immature B cells. As immature transitional (T1) B cells then exit the bone marrow and migrate to the spleen, they transition to a T2 B cell subtype. T2 cells further differentiate into follicular (FO) B cells, the most abundant and are found in the B cell areas of lymph nodes, Peyer’s patches and spleen; and marginal zone (MZ) B cells, which reside in the marginal sinus of the spleen (11).
B cells not only differ in their geographic location, but in their mode of activation through T cell-independent or T cell-dependent pathways (12). Polysaccharide or lipid antigens can stimulate MZ B cells directly, independent of T cells, to become short-lived plasma cells that produce low affinity (mostly non class-switched IgM) antibodies. Conversely, T cell-dependent responses are associated with protein antigens that are processed and presented to cognate FO T helper cells through MHC class II molecules, which in turn via CD40 engagement, IL-21 and IL-4 production, directly modulate the outcomes of the immune response.
Activation of naïve B cells occurs following encounter with their cognate antigen, which specifically binds to the B cell receptor (BCR). Once activated, MZ B cells may initiate an extrafollicular response and differentiate into plasmablasts that produce antibodies that are generally weak affinity and short-lived (13). Alternatively, activated FO B cells may enter a lymphoid follicle and initiate a germinal center (GC) response. GC are highly organised, transient tissue structures formed in secondary lymphoid tissue during the course of the immune response. The exquisitely coordinated movement of lymphocytes in these structures is directed by antigen-specific recognition, activation, and chemokines to bring into close contact antigen-specific B and T cells that define adaptive immunity and memory. Here, activated B cells may undergo somatic hypermutation and affinity maturation selection, where mutations caused by the enzyme activation-induced cytidine deaminase (AID) are randomly introduced into variable regions of the BCR to further diversify the immunological repertoire and those with increased affinity for antigen preferentially selected for clonal expansion (14). B cells may also undergo AID-induced immunoglobulin class switching where their BCR isotype is switched from IgM to downstream isotypes IgG, IgA or IgE to alter effector functions (15,16). The specific class of switching and differentiation into antibody-secreting cells is directly influenced by the T cell derived cytokine signals (17).
A key role of GC B cells is the differentiation into memory B cells, which can circulate or reside in secondary lymphoid organs as quiescent cells for decades (18) poised to respond rapidly to subsequent exposure. Alternatively, they may terminally differentiate into long-lived plasma cells, which preferentially migrate to the bone marrow and are capable of secreting large amounts of high affinity antibody upon subsequent encounters (19).
B cells are critical for antigen presentation, antibody production, and immune homeostasis
B cells are capable of directly internalizing antigen via the BCR, with subsequent presentation and activation of T cells in the context of MHC class II molecules. B cells and dendritic cells provide a further co-stimulatory signal for expansion of effector T cell populations via cross-linking of CD40 with CD40 ligand on CD4+ T cells, which in turn induces additional second co-stimulatory signals of CD86 and CD80 expression on the B cell surface (11).
Specific recognition and binding of a foreign antigen to the BCR also results in a downstream signaling cascade mediated by membrane bound protein tyrosine kinases, including spleen tyrosine kinase (STK), Bruton tyrosine kinase (BTK), and PI3K. Together, these processes activate NF-κB signaling and other key processes essential for B cell proliferation and differentiation into antigen-specific memory B cells and antibody secreting plasma cells.
B cells also play a role in immune regulation via secretion of anti-inflammatory cytokines, which can affect T cells, dendritic cells, lymphoid tissue reorganization and neogenesis. These so-called regulatory B cells (Bregs) have been poorly characterized, but have been shown to inhibit T cell-mediated immunity through production of inhibitory cytokines such as IL-10, IL-35 and transforming growth factor beta (TGF-β) (20,21).
B cells represent an important proportion of infiltrating cells in solid cancers
Tumor-infiltrating lymphocytes (TILs) are now known to play a significant role in tumor progression. While the effects of T cells have been extensively studied, the function of B cells in this context remains poorly defined. However, there is evidence that B cells have been found to represent a critical component of infiltrating immune cells in a variety of solid tumors, including breast cancer and melanoma where they comprise almost half of the total infiltrating lymphocyte population (11,12).
In breast cancer, multiple studies report that CD20+ B cells are associated with favorable outcomes, particularly in specific breast cancer subtypes, such as the highly proliferative basal-like and HER2+ tumors (22). However, there is simultaneous evidence suggesting that tumor-infiltrating B cells may be linked with worse prognosis, particularly in breast ductal carcinoma in situ, which is a microinvasive form of breast cancer, suggesting that CD20+ B cells may play a tumor-promoting role in early-stage disease (22).
In melanoma, several studies have reported improved outcomes in tumors that have a high CD20+ B cell density, specifically, better overall survival and lower likelihood of metastasis (23). However, the converse is also apparent in the context where accumulation of CD138+ terminally differentiated (long-lived) plasma cells is associated with poor prognosis in cutaneous melanoma (23). Furthermore, the immunoglobulin isotype appears to have relevance where elevated IgG4+ plasma cells were predictive of disease progression (23).
Movement of B cells and other immune cells in response to tumor, or indeed any immunological threat, is a carefully regulated process, balanced by coordinated expression of chemokine and chemokine receptors expression to ensure appropriate migration and positioning of immune cells in tissues. Expression of chemokines and chemokine receptors mediate anti-tumor immunity by directing the migration of B cells and other leukocytes to the tumor site. The outcome of this migratory response is context-specific, as it may involve trafficking of leukocytes that have tumor-promoting or anti-tumor activities.
A number of chemokine/chemokine receptor antagonists are currently in clinical trials, either alone, or for example, in combination with immune checkpoint inhibitor (ICI) pembrolizumab in advanced solid tumors or metastatic melanoma (24). Chemokine-mediated regulation of immune cell recruitment into tumor sites as well as was recently reviewed, as well as review of emerging evidence that support the direct targeting of chemokines/chemokine receptors as a strategy to disrupt tumor promoting microenvironment towards anti-tumor immunity including potentially inhibiting expression of CCR4 to deplete regulatory T cells in lung cancer (24,25).
To address the conflicting findings regarding the effect of B cells on tumor growth, a recent systematic review of 69 studies was conducted across 19 human cancers to address the prognostic significance of tumor-infiltrating B cells (26). The majority of studies reported positive or neutral prognostic effects, with only a minority reporting a negative effect. Furthermore, in studies that assessed the effects of B and T cells, the prognostic effects of both lymphocyte subsets were largely concordant, suggesting that B cells may work in concert with T cells to exert anti-tumor functions.
B cells play dual roles in lung cancer
In lung cancer, tumor infiltrating B cells have similarly been observed, with their phenotype differing according to clinical stage and histological subtype (17,27,28). Within the tumor, B cells can interact with T cells in tertiary lymphoid structures (TLS), which are GCs forming as ectopic foci of B cells, mature dendritic cells and T cells in cancer tissue (17,29,30). In this context, B cells are associated with dual roles in both anti- and pro-tumor immunity (11). As such, the balance between various B cell subtypes affects the net B cell impact upon tumor immunity (Table 1, Figure 1).
B cells and anti-tumor immunity
A number of studies have found CD20+ B cell infiltration to be associated with favorable prognosis in NSCLC (8,17,27,28). For example, in a comparative study of 196 patients with early-stage untreated NSCLC and advanced stage NSCLC treated with neoadjuvant chemotherapy, increased B cells were associated with prolonged disease-free survival (17).
The favorable clinical outcomes of tumor-infiltrating B cells have been best documented in the adenocarcinoma subgroup of lung cancer where analysis of RNA sequencing data from The Cancer Genome Atlas (TCGA) database that revealed that high levels of expression of B cell and plasma cell signature genes correlated with increased overall survival in lung adenocarcinoma (36). Furthermore, concurrent analysis of programmed death ligand 1 (PD-L1), which is the primary target of current immunomodulatory agents, has identified a significant and positive correlation with B cell levels. This suggests that B cell infiltration may represent a crucial factor in clinical efficacy of anti-PD-L1 therapies in lung adenocarcinoma patients (37). The prognostic relevance of B cells is less well documented in lung squamous cell carcinoma with only a single study demonstrating a correlation between CD20+ B cells and improved disease-specific survival exclusively in squamous cell carcinoma (27). As such, the mechanisms of B cell control of tumors are poorly defined and may differ among lung cancer histological subgroups due to differences in composition and behavior of the B cell subsets that comprise the infiltrate.
B cells that specifically express CD19, CD20, and CD11c can act as antigen presenting cells (APCs) (38,39). In NSCLC models, infiltrating B cells have been shown to present antigen to CD4+ T cells, resulting in robust T cell effector responses. In this setting, two subpopulations of B cells were identified: activated (CD19+CD20+CD69+CD27+CD21+) or exhausted (CD19+CD20+CD69+CD27–CD21–). While activated B cell APCs could induce Th1 differentiation with anti-tumorigenic roles (e.g., IFNγ-producing CD4+ T cells), exhausted B cell APCs led to generation of a regulatory T cell phenotype (Foxp3+CD4+) with pro-tumorigenic functions (38,40).
Tumor-associated antigens, such as LAGE-1, TP53, and NY-ESO-1, can trigger B cell-mediated antibody production (17). This has been demonstrated in an in vitro NSCLC model, where tumor antigen-specific B cell responses are evidenced by the production of tumor-specific antibody and the oligoclonality of TIL B cells in the TLS (40). Furthermore, B cells cultured from TLS have been shown to produce tumor-specific IgG and IgA, which are associated with favorable outcomes (17,41). In turn, tumor-specific antibodies support killing of tumors through a range of pathways. In a study of murine models of large cell lung carcinoma, Mizukami et al. demonstrated that injection of tumor-specific antibodies resulted in complement cascade with tumor cell lysis (42). Furthermore, Carmi et al. showed that antibodies produced by B cells at the early stage of lung tumor development served to activate dendritic cells, which subsequently triggered a cytotoxic T cell response to control tumor growth (43). Lastly, B cell derived antibodies may play a role in triggering tumor cell phagocytosis by macrophages and granulocytes (11).
An important determinant of whether antibodies have anti-tumor effects is the antibody isotype generated. In cancer, the human IgG1 antibody isotype is of primary importance where it can bind to the constant fragment γ receptor (FcγR) and trigger antibody-dependent cellular cytotoxicity (ADCC), antibody-mediated phagocytosis, and complement-dependent cytotoxicity (44). Furthermore, FcγR expressed on dendritic cells and macrophages may capture IgG-bound tumor antigens and present these to T cells. In addition, effector and memory B cells expressing IgG may also execute direct anti-tumor functions through production of granzyme B, tumor necrosis factor-related apoptosis-inducing ligand (TRAIL), and IFNγ. Support for these findings has been illustrated by using human RNA sequencing datasets from TCGA, where a high proportion of IgG1 isotype has been positively correlated with mutation burden in lung adenocarcinoma, thereby linking driver mutations and B cell response (45).
B cells and pro-tumor immunity
The beneficial impact of B cells on NSCLC outcomes has not been universally demonstrated (10,46,47). More specifically, pro-tumor activity has been linked a specific immunosuppressive B cell subset known as IL-10 producing Bregs. These cells were initially defined by their ability to maintain immune tolerance and restore homeostasis following inflammation. Recent accumulating evidence supports a role for B cells in modulating the immune response to malignancy (48-50).
B cell mediated immune suppression with resultant tumor growth is thought to occur through a variety of mechanisms (20,21,51,52). Production of suppressive cytokines such as IL-10, TGF-β, and IL-35 is well-documented where IL-10 is capable of inhibiting the T cell mediated anti-tumor response, and TGF-β facilitates conversion of naïve CD4+ T cells into Foxp3+ T regulatory cells (Tregs) that act to attenuate the anti-tumor immunity. In addition, Bregs may cause suppression of T cells and Natural Killer (NK) cells, with subsequent expansion of Tregs and myeloid-derived suppression cells (MDSCs). Furthermore, Bregs can promote the upregulation of negative immune checkpoint molecules such as PD-1 and PD-L1 that inhibit anti-tumor immunity. Lastly, STAT 3 signaling by Bregs have a role in mediating vascular endothelial growth factor (VEGF) and promoting tumor growth and metastasis via generation of Treg cells and angiogenesis (53,54).
Breg infiltration has been observed in a range of solid tumor malignancies, including NSCLC, where significantly higher frequencies of peripheral Bregs (CD19+CD24hiCD27+) and CD19+IL-10+ B cells have been observed compared with healthy controls (55).
However, characterization of Bregs in the context of malignancy has been challenging for a number of reasons. While similar B cell subpopulations have been shown to migrate to the tumor site, the signals that polarize B cells to a Breg phenotype are unclear (56). Furthermore, despite increasing literature describing subsets of B cells that exhibit regulatory properties, the precise phenotype and characteristic cell surface markers of Bregs in lung cancer are poorly understood (57). For example, while Bregs have conventionally been defined as CD5+CD24hiCD27+CD38hi (31), immature B cell populations have yielded Bregs characterized as CD19+CD24+CD27+IL-10+ and CD19+CD24hiCD27intCD44highCD138+IL-10+. To add to the complexity, animal models have been used to explore the profile and mechanisms of Bregs in promoting carcinogenesis, however their applicability to human disease has been limited by phenotypic and functional diversity of Bregs (58). As a result of these challenges, there are very few published studies that discuss the role of Bregs in human lung cancer (Table 2). There is a need to sub-stratify B cells into distinct developmental subsets as well as functionally in regulatory-, anti-, and pro-tumor functions.
The balance between anti- and pro-tumor activities of B cells is likely to be influenced by the TME
Tumor cells themselves can produce factors, cytokines or metabolites which directly impact the function of B cells. Additionally, tumor cells can secrete extracellular vesicles carrying mRNAs or proteins which can activate Breg populations (11).
Immune cells in the TME have been shown to also influence B cell migration, activation and differentiation. Anti-tumor activities may be reinforced though B cells and T cells. The former can produce CXCL13 and lymphotoxin via TLR4 signaling, which are factors required for the formation of lymphoid follicles and can support the formation of TLS, which in turn can generate the anti-tumor effects of CD8+ T cells (62,63). T cells expressing IL-17 may enhance the anti-tumor effects of B cells by inducing B cell migration and increasing FAS/FASL-dependent direct tumor cell killing by B cells (11). Pro-tumor activities may be promoted by other cells of the TME, such as regulatory T cells and MDSCs, by activating Bregs, decreasing antibody production, and killing anti-tumor B cells that have APC capabilities (11).
Given the role of B cells in inflammation homeostasis, factors such as tissue hypoxia are also likely to affect the balance between anti- and pro-B cell functions. Hypoxia is a hallmark of cancer where tumor cell proliferation causes vascular disorganization, with increased oxygen consumption and decreased oxygen supply. This condition results in production of hypoxia-inducible factors (HIFs) that facilitate adaptation of cells to the environment. HIFs can impact a broad range of cellular processes in immune cells, which are postulated to impact tumor growth. However, the role of these mechanisms on B cells in cancer remains poorly understood.
Role of B cells in lung cancer treatment: current approaches and future potential
With multi-faceted functions in tumor development, therapies that target B cells may offer opportunities to further personalize the approach to lung cancer management (Figure 1).
Therapies activating B cells
Several strategies have been explored to harness the anti-tumor potential of B cells. Antigen-specific immunotherapeutic “vaccines” have been designed to induce a B cell humoral response. Antibodies produced by responding B cells may deliver therapeutic effects by direct target of tumor antigens (e.g., anti-CD20 in B cell related lymphoma/leukemia, anti-HER2 in breast cancer) or via immunomodulatory effects (e.g., anti-CTLA4, anti-PD-1/PDL-1, anti-LAG). They have the capacity to activate ADCC, phagocytosis, and complement-dependent cytotoxicity (64). In a randomized placebo-controlled phase 3 trial, the immunotherapeutic targeting the tumor antigen MAGE-A3 was assessed in NSCLC (65). While this mono-valent agent did not increase disease-free survival, there remains tantalizing potential for multi-valent vaccines against personalized B cell antigens, akin to the model of the chimeric antigen receptor T cell (CART) therapy.
Targeted approaches for enhancing conventional B cells through transfer of stimulated B cell ligands has been shown to inhibit tumor growth and lung metastasis. For example, direct CD40:CD40L engagement induces the expression of a range of co-stimulatory molecules and cytokines that both activate B cells as well as naïve and memory T cells. The potential of these CD40-activated B cells has been tested in pre-clinical models of melanoma, lymphoma, breast tumor metastasis, and sarcoma (66). In another study, injection of activated B cells pre-stimulated with CpG DNA, a Toll-like receptor 9 (TLR9) ligand, has been similarly used in a model of lung metastasis to induce regression of disease (67).
Therapies depleting or inhibiting B cells
As some B cell populations, particularly the Breg phenotype, are associated with tumor progression, agents to deplete or inhibit B cells may have therapeutic value. B cell depletion via anti-CD20 monoclonal antibody, Rituximab, is widely used for B-cell malignancies, but has also demonstrated anti-tumor activity in small series of patients with other cancers such as melanoma, colorectal carcinoma, and cutaneous T cell lymphoma (68-70). However, conflicting results have been reported in other studies with tumor growth observed after anti-CD20 therapy (71,72). This is likely, in part due to the non-specific activity of B-cell depleting antibodies which do not distinguish between effector and regulator B cell subsets (73) and do not effectively target CD20 low-expressing plasma cell subsets.
Therefore, specific inhibition of Bregs may be an effective strategy to influence the immunosuppressive TME without negatively impacting other B cell subpopulations that have beneficial anti-tumor properties. Bodogai et al. demonstrated that, in tumor-bearing mice, CXCR5+ Bregs can be depleted in vivo by injecting CXCL13 (CXCR5 ligand) that has been coupled to CpG-ODN, and that the remaining B cells retained the capacity to induce activation of cytotoxic T cells (72). Tao et al. described the use of a blocking antibody against IL-10 to specifically inhibit Bregs and increased the efficiency of CD40-activated B cell transfer, with increased migration of CD8+ T cells into the TME and B cell dependent FasL-mediated tumor cell killing (74). Similarly, in a murine breast tumor model, use of the phytoalexin resveratrol induces a decrease in Bregs and reduction in lung metastases (75). Lastly, Lipoxin A4 (LXA4), a metabolite of the arachidonic acid pathway, has been shown to selectively prevent differentiation of Bregs and also Breg-induced Treg differentiation (76).
B cells can predict response to anti-cancer therapies
Systemic treatment of lung cancer may involve chemotherapy, targeted molecular therapy, or immunotherapy. There have been reports of associations between tumor-infiltrating B cell populations and response to these therapies.
The action of chemotherapies to damage tumor cells may precipitate an immune response that results in therapy resistance. In murine models of squamous cell carcinoma, Affara et al. demonstrated increased infiltration of immunosuppressive CD20+ B cells, which may play a role in resistance to platinum- (cisplatin and carboplatin) and taxol- (paclitaxel) based chemotherapy as their removal using an anti-CD20 antibody improved chemoresponsiveness (77).
Targeted molecular therapies act to modulate specific oncogenic pathways. However, despite good initial response rates, a significant proportion of patients will develop resistance. In a study of melanoma treated with inhibitors to oncogenic BRAF mutation, tumor-associated B cells were observed to mediate drug resistance through secretion of insulin-like growth factor 1 (IGF-1). Furthermore, in therapy-resistant metastatic melanoma patients, depletion of B cells by anti-CD20 antibody may result in tumor control (78).
ICIs have improved cancer treatment by overcoming the inhibition of T cell effector functions. However, a significant proportion of patients do not respond to such therapies, and there is increasing interest in the impact of B cells upon outcome with ICIs. Supporting this, in the blood of non-progressing patients with different forms of metastatic cancers (NSCLC, melanoma, renal cell carcinoma) treated with immune checkpoint blockade immunotherapy (anti-PD-1 or anti-CTLA4), an active humoral response has been detected with somatic hypermutation, IgG class switch and expansion of anti-tumor plasmablasts (79).
Recently, the presence of B cells have been described as a predictive marker for improved response to immune checkpoint blockade. In studies of melanoma and sarcoma, Helmink et al. and Petitprez et al. respectively demonstrated that the presence of B cells in TLS in the tumor before treatment was associated with increased chance of response to immunotherapy (80,81). Furthermore, these findings were more prominent than typical T cell signatures that are currently used to guide immunotherapy outcomes. In lung cancer, similar findings of B cell density as predictive of response to checkpoint blockade are yet to be observed. As discussed above characterization and specific investigation of B cells in other solid tumors has revealed avenues for novel application of therapeutics. These findings cannot be directly translated to lung cancer in the absence of the careful characterization of B cells and subsets proposed in the current review.
Through its activation of the immune system to exert anti-tumor effects, immunotherapy is also associated with multi organ immune-related adverse effects (irAEs) (82). There is early evidence to suggest that B cells may have a potential role as a predictive biomarker for irAEs, where in melanoma patients treated with combination immune checkpoint blockade (with anti-CTLA4 and anti-PD-1 antibodies), patients demonstrating enrichment of specific B cell populations showed an increased risk of developing irAEs (83). Conversely, B cell depletion using Rituximab has been used successfully to treat irAEs in NSCLC (84,85).
In addition to their capacity as a predictive biomarker to lung cancer treatments, tumor-infiltrating B cells and their immunoglobulin repertoires may have a role in prognostication. One significant example is the association of a high ratio of intratumoral IgG1 to IgA with improved survival in KRAS-mutant lung adenocarcinoma (45). Furthermore, abundant IgG4 is associated with a favorable prognosis in lung squamous cell carcinoma (41) and in STK11-mutant and proximal proliferative lung adenocarcinoma (45). Lastly, positive prognosis has been associated with a high ratio of IgH to MS4A1 (which encodes CD20) expression in proximal proliferative lung adenocarcinoma (45).
The phenotypical and functional diversity of B cells make it challenging to clearly define their role in tumor prognosis and response to treatment. Few studies that identify B cells in solid tumors have conducted detailed characterization of B cells by developmental status or functionality, instead relying on detection of pan-B cell markers such as CD19 or CD20, which are not constitutively expressed across all maturation and differentiation stages. Furthermore, B cell subtypes may undergo change with the process of metastasis. Therefore, future studies are needed to perform comprehensive profiling of B cell subpopulations in the specific context of the primary TME as well as sites of metastases to unravel the roles of B cells and subsets in promoting early tumor growth and to harness anti-tumor activity.
The roles of B cells in lung cancer are poorly understood in comparison with T cells. This is largely due to the phenotypical and functional diversity of tumor-infiltrating B cells, with different B cell subsets exerting anti- and pro- tumor effects. Meticulous and systematic characterization of B cell subpopulations and immunoglobulin repertoires in the TME will yield fundamental insights into the influence of different intratumoral contexts which polarize B cells to these opposing functions. This understanding will identify site-specific B cell infiltrates and unravel the specific intrinsic and extrinsic roles of B cells in contributing to disease pathogenesis to redefine B cells as active participants, and not merely bystanders, in the lung cancer microenvironment.
We thank Associate Professor MLAL for critical review of the manuscript. Manuscript figures were created with BioRender.com.
Provenance and Peer Review: This article was commissioned by the Guest Editor (Daniel Steinfort) for the series “Lung cancer and the immune system” published in Translational Lung Cancer Research. The article has undergone external peer review.
Reporting Checklist: The authors have completed the Narrative Review reporting checklist. Available at http://dx.doi.org/10.21037/tlcr-20-788
Peer Review File: Available at http://dx.doi.org/10.21037/tlcr-20-788
Conflicts of Interest: Both authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/tlcr-20-788). The series “Lung cancer and the immune system” was commissioned by the editorial office without any funding or sponsorship. TLL reports grants from David Bickart Clinician Researcher Fellowship, outside the submitted work. VLB reports grants from Sir Clive McPherson Family Fellowship, grants from DW Keir Fellowship, grants from NHMRC Project grant 1127198, grants from Homes Foundation, grants from Rae Foundation, grants from Graty family Foundation, grants from MJ Maughan Foundation, grants from Victorian State Government Operational Infrastructure support, outside the submitted work. The authors have no other conflicts of interest to declare.
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