Qifeng Ou1
Matthew D. Griffin- 1Regenerative Medicine Institute (REMEDI) at CÚRAM SFI Research Centre for Medical Devices, School of Medicine, College of Medicine, Nursing and Health Sciences, University of Galway, Galway, Ireland
- 2Nephrology Department, Galway University Hospitals, Saolta University Healthcare Group, Galway, Ireland
Regulatory T cells (Treg) are known to be critical for the maintenance of immune homeostasis by suppressing the activation of auto- or allo-reactive effector T cells through a diverse repertoire of molecular mechanisms. Accordingly, therapeutic strategies aimed at enhancing Treg numbers or potency in the setting of autoimmunity and allogeneic transplants have been energetically pursued and are beginning to yield some encouraging outcomes in early phase clinical trials. Less well recognized from a translational perspective, however, has been the mounting body of evidence that Treg directly modulate most aspects of innate immune response under a range of different acute and chronic disease conditions. Recognizing this aspect of Treg immune modulatory function provides a bridge for the application of Treg-based therapies to common medical conditions in which organ and tissue damage is mediated primarily by inflammation involving myeloid cells (mononuclear phagocytes, granulocytes) and innate lymphocytes (NK cells, NKT cells, γδ T cells and ILCs). In this review, we comprehensively summarize pre-clinical and human research that has revealed diverse modulatory effects of Treg and specific Treg subpopulations on the range of innate immune cell types. In each case, we emphasize the key mechanistic insights and the evidence that Treg interactions with innate immune effectors can have significant impacts on disease severity or treatment. Finally, we discuss the opportunities and challenges that exist for the application of Treg-based therapeutic interventions to three globally impactful, inflammatory conditions: type 2 diabetes and its end-organ complications, ischemia reperfusion injury and atherosclerosis.
Introduction
Regulatory T cells (Treg), classically identified in humans and other species as CD4+/Foxp3+ lymphocytes, comprise only 5-10% of total CD4+ T cells, but are essential for balancing immune system activity throughout life. The immunosuppressive and immune modulatory functions of Treg have been unequivocally established in the context of adaptive immunity and have become fundamental to our understanding of autoimmunity, transplant rejection, tumor antigen-specific immune responses and the distinction between harmful and commensal microorganisms (1). Less well appreciated has been the accumulating research evidence that Treg directly modulate activity of the innate immune system through cross-talk with mononuclear phagocytes (monocytes/macrophages), granulocytes (neutrophils), dendritic cells (DC) and innate lymphocytes (NK cells, NKT cells, γδ T cells and other innate lymphocytic cells (ILC)) (2). The impacts of innate immune cell interactions with Treg may include modifications to cell survival, proliferation, cytokine production, phagocytosis, cytotoxicity and other effector functions. Although Treg-mediated suppressive effects on innate immune cells can be implicated in their regulation of antigen-specific T- and B-cell responses, they may also be more broadly relevant to immune-mediated inflammatory diseases (IMID) and disorders of tissue homeostasis, such as diabetes, atherosclerosis, Parkinson’s disease, wound healing and aging (3). This suggests that a deeper understanding of the Treg phenotypic and functional properties that underlie their modulation of innate immune responses could open new translational pathways for the burgeoning field of regulatory immune cell therapies (4).
In this review, we aim to summarize current knowledge of the direct modulatory effects of Treg on diverse innate immune cells types with an emphasis on mechanisms and clinically-meaningful contexts in humans as well as experimental animals. We also discuss the relevance of these insights to common human diseases and health challenges for which non-autoimmune inflammation is a key component and reflect on the prospects for Treg-based therapies to be applied to their treatment.
Although the majority of the studies described here focus on the canonical CD4+CD25+CD127- Foxp3+ Treg phenotype, it is important to acknowledge that there is considerable heterogeneity in regard to Treg subtypes and functionality. Most clearly, CD4+ Treg may be divided into “natural” or thymic-derived (tTreg), peripherally-derived (pTreg) and in-vitro induced Treg (iTreg). In addition, however, sub-populations defined on the basis of specific surface markers, transcription factors, functional properties or disease associations have been described, including type 1 regulatory T cells (Tr1), Th3 cells, FoxA1+ Treg (5), CD39+ Treg, CD8+ Treg, Treg-of-B and others (6, 7). Where relevant, therefore, we highlight Treg subpopulations that have been described to regulate specific aspects of innate immune response.
Regulatory T cell interactions with mononuclear phagocytes and granulocytes
Mononuclear phagocytes
Accumulating evidence supports the existence of a biologically significant role for Treg in regulating monocyte- and macrophage-mediated inflammation in diverse contexts. For example, the co-occurrence of decreased Treg proportions and increased monocyte inflammatory mRNA expression was identified in the blood of adults with major depressive disorders (8). In contrast, in patients with acute HIV-1 infection, increased proportions of Foxp3+Helios+CD45RA+ Treg were reported along with decreased frequencies of CD14++CD16+ (intermediate) monocytes and increased proportions of PD-1+ cells among both CD14++CD16+ and CD14+CD16++ (non-classical) monocytes (9). In scurfy mice, an animal model in which Foxp3 mutation results in profound Treg deficiency, increased myelopoiesis and monocyte homing receptor expression, phagocytic activity and cytokine production occurs (10). Recently, Hand et al. reported that diurnal variations of Treg numbers occur within joints of mice and that depletion of Treg resulted in increased joint inflammation at night in association with enhanced production of IL-1β by Ly6Chi monocytes (11). These observations of inverse relationships between Treg and monocyte activities indicate a potential role of Treg in directly regulating the inflammatory profile of mononuclear phagocytes. In both ex vivo human cell experiments and in vivo animal models, Treg have been demonstrated to promote monocyte differentiation toward alternatively activated/anti-inflammatory (M2) macrophage phenotypes characterized by high phagocytic activity and expression of related marker proteins (CD206, CD163, and heme oxygenase-1); low antigen-presentation capacity (CD40, CD80/86, and class II MHC); increased secretion of anti-inflammatory cytokines (IL-10) and decreased production of pro-inflammatory molecules (TNF, IL-6, nitric oxide (NO) and reactive oxidative species (ROS)). Such influences of Treg on mononuclear phagocyte differentiation have been reported to be both cell contact- (12, 13) and cytokine-dependent. In the case of soluble mediators, Treg IL-10 (14), IL-13 (15), TGF-β, IL-4 (16), arginase (17), and soluble fibrinogen-like protein 2 (18) have all been shown to play a role in various experimental settings. The transcription factor Krüppel-like factor 10 (KLF10) (19) and the signaling pathway mediated by mammalian target of rapamycin complex 1 (mTORC1) have also been reported to be necessary for Treg suppression of macrophage-mediated inflammation (20). Recently, exosome-based cross-talk between Treg and macrophages has also been documented. In a mouse model of acute myocardial infarction, Hu et al. reported that infusion of Treg-derived exosomes reduced infarct size and improved cardiac function by promoting macrophage polarized towards M2 phenotypes in myocardial tissue (21). In a reverse interaction, Zhou et al. demonstrated that macrophage-derived exosomes transferred miR-29a-3p and miR-21-5p into CD4+ T cells to promote their differentiation into Treg, in a mouse tumor microenvironment (22). Furthermore, Treg-supported M2 macrophages can induce CD4+CD25- T cell to acquire a suppressive phenotype, forming a positive feedback loop in immune regulation (23). Mechanistically, macrophage promotion of Treg induction, proliferation and migration has been linked to an IL-10 and TGF-β-secreting (M2c) phenotype, to the secretion of resistin-like molecule (Relm)-α and to the induction of CD62L on Treg (24–26). Figure 1 illustrates a range of reported interactions between Treg and mononuclear phagocytes along with their key mediators and outcomes.
Figure 1 Regulatory T cell interactions with mononuclear phagocytes. Regulatory T cells (Treg) interact with mononuclear phagocytes including monocytes and macrophages, through a range of mechanisms leading to a diverse array of consequences. As shown in the upper part of the figure, Treg modulate several aspects of monocyte behavior, including their survival (through death receptor and cytolytic pathways), migration/infiltration (through inhibition of MCP-1) and differentiation into M2-type macrophages. Such functions may be dependent on specific Treg transcriptional (KLF-10) and signaling (mTORC1) programs. As depicted in the lower part of the figure, Treg and macrophages may engage in complex cross-talk including release/expression of signature modulatory cytokines (IL-10, IL-13, IL-4 and TFG-β), arginase, RELMα and sFGL2; and exchange of extracellular vesicles (EVs). Outcomes of this cross-talk may include enhanced macrophage phagocytosis, release of pro-inflammatory mediators (TNF, IL-1β and nitric oxide) and modulation of the communication between macrophages and fibroblasts, as well as increased Treg proliferation and expression of CD62L. EVs, extracellular vesicles; RELMa, resistin-like molecule α; MCP-1, monocyte chemoattractant protein-1; KLF-10, Krüppel-like factor 10; mTORC1, mechanistic target of rapamycin complex 1; sFGL2, soluble fibrinogen-like protein 2; HO-1, haemoxygenase 1.
From a therapeutic perspective, Romano et al. have reported that ex vivo expanded human Treg may be more potent in suppressing monocyte activation than freshly-isolated Treg. In this study, the effects of ex vivo expanded Treg on activated human monocytes were manifested as reduction of NF-κB signaling, a higher proportion of CD14+CD206+CD163+CD86− (M2-like) cells and compromised potency to induce Th17 cell responses (27). Using a CD28 super-antagonist, Cai et al. recently showed that in vivo-expanded endogenous mouse Treg adoptively transferred to diabetic animals undergoing ischemic stroke induced an increase in CD206+ M2 microglia/macrophages in ischemia tissue detected by real-time visualization using an optical imaging probe (28).
In addition to the initiation and resolution of inflammation, monocytes and tissue macrophages also play an important role in the development of post-inflammatory fibrosis through direct effects or via interactions with fibroblasts. In the short-term, the pro-fibrotic effects of alternatively-activated macrophages are beneficial to wound healing and tissue repair, whereas their prolonged pro-fibrotic activity contributes to the pathogenesis of a range of disease processes (29). For example, fibrosis of lung (30) and liver (31) as well as chronic kidney disease (32) and systemic sclerosis (33), have all been reported to be linked with macrophage-induced fibrosis. Currently, the potential influence of Treg interactions with mononuclear phagocytes on physiological and pathological tissue fibrosis is not well understood. Of interest, Song et al. recently reported that adoptively transferred Treg accelerated tissue repair and kidney function recovery in mice following reversal of unilateral ureteral obstruction in association with higher intra-renal proportions of M2 macrophages (34). Nonetheless, the concept of Treg ameliorating fibrosis through M2-like polarization of macrophages is not entirely in accordance with current understanding of M1/M2 balance in disease-associated fibrosis. For example, in animal models of diabetic kidney disease, pharmacological interventions which alleviated renal fibrosis and preserved kidney function have variously been reported to promote M1 (35) or M2 (36) macrophage phenotypes. Furthermore, Kim et al. demonstrated that M2c macrophages, induced with IL-10 and TGF-β from mouse bone marrow-derived macrophages, exacerbated renal fibrosis following acute kidney injury (32). Bhandari et al. also reported that a subset of human macrophages capable of activating fibroblasts and promoting fibrosis exhibited both M1- and M2-associated surface marker expression and cytokine production in the setting of systemic sclerosis (33), while Tan-Garcia et al. observed enrichment of TNF-secreting, CD206+ macrophages in fibrotic liver of hepatocellular carcinoma (31). Such results indicate that the classical dichotomy of macrophage M1/M2 polarization frequently fails to explain the various roles of macrophages in fibro-inflammatory disease and, by extrapolation, raise the possibility that Treg modulation of mononuclear phagocyte activation and differentiation could also exacerbate disease in some settings (37). In keeping with this, pro-fibrotic Treg subtypes have been identified as participating in ventricular remodeling after heart failure (38) and in lymphatic tissue fibrosis after HIV infection (39). In addition, adoptively transferred Treg have been reported to worsen the pro-fibrotic environment in bleomycin-induced lung injury models (40). In non-fibrotic diseases also, the effects of Treg on macrophage phenotype may be more ambiguous than simply modulating from M1 to M2. For example, Treg have been shown to decrease macrophage infiltration in lesional skin, resulting in reduced disease progression in a model of psoriasis (41). However, the macrophage phenotypes that predominate in psoriasis progression may include CD68+iNOS+ (M1), CD206+ (M2), or phenotypes distinct from M1/M2 (42). These studies highlight the complexity of predicting the outcome of Treg/mononuclear phagocyte cross-talk in different contexts as well as the need for carefully designed pre-clinical studies to guide the development of Treg-based therapies for non-autoimmune acute and chronic inflammatory diseases. Further investigation of the phenotypes, origin, migration and pro/anti-inflammatory function of monocytes and macrophages will help to develop a deeper understanding of how Treg modulate their activity in specific disease settings.
Regulatory T cells also express multiple mediators of programmed cell death and may suppress inflammation through induction of apoptosis in mononuclear phagocytes (Figure 1). While the killing of CD4+ T cells by Treg is thought to be based on TRAIL/TRAILR and galectin pathways (43), the mechanisms underlying monocyte killing by Treg is controversial. Venet et al. reported that human Treg induced CD14 down-regulation – a marker of apoptosis - in LPS-activated monocytes through a FasL/Fas interaction (44). In contrast, however, Jagger et al. concluded from co-culture experiments that FasL/Fas-mediated killing of activated human monocytes is mediated by effector T cells (Teff) rather than Treg, and that the effects of Treg were predominantly suppressive rather than pro-apoptotic (45). Nevertheless, Grossman et al. have also reported Treg to be capable of inducing apoptosis via perforin in multiple cell types, including CD14+ monocytes (46). Thus, the significance of Treg-mediated killing in modulating mononuclear phagocyte-associated inflammation requires further investigations.
Effects of Treg on phagocytosis in the context of inflammatory disease have also been reported (Figure 1). In atherosclerosis, for instance, phagocytosis by macrophages contributes to the resolution of arterial wall plaques and, in this context, Sharma et al. have recently demonstrated, in mice, that Treg prime resident macrophages to be phagocytic and pro-resolving. Mechanistically, this effect was mediated by Treg-secreted IL-10 and macrophage-derived IL-13 (47). Finally, there is evidence that resident Treg have specialized functions for local regulation of mononuclear phagocyte activity in inflammation-sensitive tissues. For example, Xie et al., reported that cerebral, but not splenic, Treg modulated the phenotype (upregulated CD163, downregulated RTIB) and cytokine production (downregulated TNF, IL-1β, and IL-6) of resident macrophages (microglial cells) in an IL-10-dependent manner, to maintain immune homeostasis in the central neuron system (14).
Granulocytes
In comparison to mononuclear phagocytes, there has been relatively limited investigation of Treg interactions with granulocytes. Nonetheless, it has been proposed that Treg can mediate anti-inflammatory and pro-tolerogenic effects through their influences on neutrophils. As described by Lewkowicz et al., Treg activated by LPS or CD3/CD28 ligation induced expression of a range immune suppressive pathways in neutrophils through different mediators in addition to promoting their apoptosis (48). In a subsequent study, these authors showed that human neutrophils co-cultured with activated Treg, had increased expression of anti-inflammatory molecules (IL-10, TGF-β1, IDO and HO-1). Upregulation of IDO was dependent on Treg expression of CTLA-4, although the corresponding target on neutrophils was not clear (49). In a mouse model of sepsis complemented by human co-culture experiments, Okeke et al., demonstrated that a PI3Kσ-dependent Treg function limited severe inflammation by promoting neutrophil apoptosis (50). Adoptively transferred Treg have also been shown to improve intestinal barrier function in association with decreased frequency of neutrophils in the intestinal tissue in the setting of heatstroke (51). In a meticulous study of mouse autoimmune hepatitis, Umeshappa et al. observed that autoantigen-specific Tr1 cells together with B regulatory cells (Breg), orchestrated neutrophil recruitment to the liver and reprogrammed them to myeloid-derived suppressor cell (MDSC) subtypes via GM-CSF, IL-10, and TGF-β. These regulatory neutrophils subsequently protected liver tissue from autoimmune injury via cathelin-related anti-microbial peptide (CRAMP) (52). Of interest, human Treg have been shown to recruit neutrophils in vitro by secretion of CXCL8 (53). Furthermore, neutrophils have been found to be spatially distributed closer to Foxp3+ Treg and to potentially modulate CD4+ T cell differentiation via PD-L1/PD-1 interactions (54). Less well understood, however, is the relationship of Treg with NETosis, a process by which neutrophil extracellular traps (NETs) are extruded by neutrophils prior to cell death. A positive correlation between Treg with high-risk NETosis score was identified in ANCA glomerulonephritis (55). However, it has also been reported that Treg tend to have no impact on NETosis of polymorphonuclear neutrophils stimulated by either immune complex or PMA (56). Inversely, in diverse animal model settings, NETs have been shown to promote Treg differentiation from naive CD4+ T cells and to be supportive of Treg suppression potency (57). Nonetheless, NETs have also been reported to promote differentiation of naïve CD4+ T cells towards Th17-like phenotype either in vitro or in vivo (58).
As is clear from these studies, different Treg subtypes are capable of complex cross-talk with neutrophils during acute and chronic immune/inflammatory responses. How such interactions influence disease outcomes or could be exploited in therapeutic contexts remains unclear and it should be acknowledged that some of the published work in this area indicates a potential for detrimental effects. For example, Treg in skin expressing the integrin αVβ8 use latent-activated TGF-β in a cell contact-dependent manner to induce CXCL5 expression by keratinocytes, recruiting neutrophils and, as a result, contributing to a delayed epithelial regeneration (59). Figure 2 summarizes reported Treg granulocyte interactions along with their key mediators and functional outcomes.
Figure 2 Interactions of various regulatory T cell subtypes with granulocytes. TGF-β1, transforming growth factor beta 1; IDO, indoleamine-2,3-dioxygenase; HO-1, hemoxygenase 1; ICAM-1, intercellular adhesion molecule 1; LPS, lipopolysaccharide; GM-CSF, granulocyte macrophage colony stimulating factor; αVβ8, integrin alphaVbeta8.
Mast cells (MC), as a type of tissue-resident granulocytes, play a pro-inflammatory role in parasite infection and anaphylaxis in addition to mediating regulatory effects on innate and adaptive immune responses under other conditions. In the past two decades, it has become increasingly clear that Treg modulate MC activation and migration in different clinical settings and by numerous mechanisms. A prototypical mechanism is cell-cell contact based on OX40 (on MC) and OX40L (on Treg) resulting in downregulation of the Fyn/Gab2/PI3K pathway and suppressed degranulation of MC, halting allergic inflammation (60). Treg-derived TGF-β has been reported to prime MC IL-6 production, which facilitates clearance of neutrophils in innate lung inflammatory (61) – an effect that is dependent on membrane-bond rather than soluble TGF-β (62). Treg-derived TGF-β is also reported to function in counterpart with IL-4 to modulate MC activation by reciprocal downregulation of their receptors (63). Unlike TGF-β, Treg-secreted IL-9, in a soluble form, promotes MC migration to skin allografts to promote immune tolerance (64), or to draining lymph node to promote renal protection in the nephrotoxic serum nephritis model (65). However, one study has reported that Treg suppressed rather than enhanced IL-9 production, resulting in abrogation of IL-9-dependent MC degranulation and aggravation of intestinal nematode burden in S. ratti infected mice (66).
Mast cells, in turn, influence Treg phenotype and function in similar fashion to Treg cross talk with monocytes and neutrophils. For example, MC-derived IL-2 is indispensable for maintaining resident Treg/Teff ratio for skin homeostasis in chronic allergic dermatitis (67). Similar effects on Treg were also observed for MC-secreted TGF-β (68). In contrast, MC-derived histamine muted Treg suppressive potency on effector T cells by signaling through the H1 receptor in vitro (69). Mast cells, in particular stimulated by IL-33 (70), may also drive Treg into Th17-like phenotypes via OX40/OX40L-mediated cell contact in presence of MC-derived IL-6 (71). Overall, therefore, the interplay between Treg and MC is clearly complex with diverse potential outcomes, necessitating further, context-dependent research before it can be directly exploited for therapeutic purposes. A recent comprehensive review focused on therapeutic opportunities for cholangiopathies provides a more detailed delineation of Treg/MC cross talk (72).
Regulatory T cell interactions with dendritic cells
Dendritic cells represent a key interface between innate and adaptive immunity, sensing microbial and other threats in tissues through pattern recognition and responding by producing soluble mediators of inflammation as well as by migrating to secondary lymphoid organs while processing and presenting foreign peptides to activate naïve antigen-specific CD4+ and CD8+ T cells (73). The interplay between DC and Treg has been extensively studied and Treg/DC cross-talk has been established to be an important pathway by which Treg support immune tolerance to self- and non-threatening foreign antigens (74). Although the focus of this review is on Treg effects on innate immunity, the complex mechanisms underlying Treg interactions with DC and their downstream influences on both innate and adaptive aspects of DC functions merit some description as they provide important insights into the potential for Treg-based therapies to be applied to a range IMID.
In this regard, both surface interactions and exchange of soluble mediators between Treg and DC are of significant interest. As potent antigen-presenting cells, activated DC abundantly express the B7 family surface proteins CD80 and CD86 which mediate co-stimulation for initialization of Teff activation by binding to the CD28 receptor (75). In contrast, Treg inherently express higher levels of CTLA-4 (CD152) which competes with CD28 for binding to CD80/CD86 and, thereby, limits DC-stimulated Teff responses. In addition to competing with CD28, however, Treg are also known to directly downregulate DC expression of CD80/CD86 through CTLA-4 (76). Of interest, one mechanism for this downregulation has been directly visualized as a physical process by which CD80/CD86 molecules are removed from the DC surface by Treg and internalized (trans-endocytosis) (77) or incorporated into the Treg surface membrane (trogocytosis) (78). Depletion of CD80 from the DC surface may lead to an increase of free PD-L1 surface expression, favoring co-inhibition of Teff activation (79). Thymic-derived Treg have also been shown to induce endocytosis of CD70 from the surface of DC, thereby inhibiting the CD70/CD27 pathway which is required for DC-primed Th1 responses (80). It is also noteworthy that the mechanisms and outcomes of these interactions could vary between secondary lymphoid tissues and inflamed organs such as autoimmune target organs or transplants. For example, Dai et al. recently reported in an allogeneic islet transplant model that, while Treg contacts with DCs and suppression of DCs/T effector interactions within the inflamed allograft were dependent on adenosine generated by the ecto-nucleotidase CD73, contacts between Treg and DCs within the spleen were independent of CD73 (81).
Soluble factors secreted by Treg, in particular IL-10 and TGF-β, also suppress DC surface expression of key proteins including HLA-DR, CD80/CD86 and CD40 as well as their production of pro-inflammatory cytokines such as TNF and IL-12 (82, 83). Another cytokine, IL-35, produced predominantly by thymic Treg, has been reported, in mice, to induce tolerogenic DC characterized by increased expression of CD11b and IL-10 and decreased MHC-II (84). Zhang et al., have demonstrated the combined roles of human Treg cell surface proteins (CTLA-4) and soluble factors (IL-10 and TGF-β) in inducing a type of tolerogenic DC from primary monocytes in the presence of T helper cells (85). Another mechanism for non-contact-dependent modulation of DC by Treg occurs through release and uptake of extracellular vesicles (EVs). For example, Tung et al. reported that murine CD4+Foxp3+Treg-derived EVs induced increased IL-10 and decreased IL-6 production in LPS-activated DCs, and this modulated cytokine production is in association with evidence of EV-mediated trafficking of miR-150-5p and miR-142-3p (86).
The question of whether Treg modulation of DC functions is dependent on recognition of DC-presented MHC II/peptide complexes by the Treg remains under investigation and is of particular importance to the clinical translation of Treg therapies for immune-mediated diseases without a well characterized auto- or allo-immune basis. In this regard, it is reasonable to hypothesize that antigen-specific Treg mediate more potent modulation of inflammatory processes than polyclonal Treg if DCs presenting their cognate antigens are present. Indeed, in the setting of experimental autoimmune (type 1) diabetes, antigen-specific Treg, based on a unique TCR repertoire capable of recognizing specific class II MHC-presented peptide antigens, have been clearly shown to prevent disease more potently than polyclonal Treg (87, 88). Furthermore, adoptively transferred or in vivo-induced antigen-specific Treg are considered to have enhanced potency to contribute to disease-specific immune regulation, consequently necessitating a lower dose of infused Treg and reducing the potential for systemic immunosuppression (89). In keeping with this, Akkaya et al. observed, in co-cultures, that mouse antigen-specific iTreg formed stable compact clusters around cognate antigen-pulsed DCs and stripped off MHC-II peptide complexes from the DC surface to compromise DC-induced activation of naïve antigen-specific Teff. This interaction was not present in co-cultures of polyclonal Treg with DC. The findings were replicated in in vivo experiments, further supporting the conclusion that Treg capture of MHC/peptide complexes from DC was antigen-specific (90). In a study by Liang et al., Treg expanded by culture with antigenic peptide-bearing DCs, subsequently suppressed DC maturation through Lag-3:MHC-II-based cell contact only in the presence of peptide (91). Of note, however, polyclonally expanded Treg were not used as controls in these studies. Furthermore, others, have provided evidence that Treg suppress DC antigen presenting potency in an MHC-independent manner. For example, Chen et al. and Yan et al, reported that polyclonal Treg suppress DC interaction with conventional T cells, by inducing changes in cytoskeletal polarization through stable integrin-mediated contact independent of antigen and MHC-II (92, 93). In the study of Yan et al., IL-2 conditional polyclonal Treg were shown to build stable connections with MHC-II-deficient DCs and such conditioned DCs were incapable of activating CD8+ T cells (93). Specific molecular interactions reported to be involved in the strong adhesion between Treg and DC include LFA-1/ICAM-1 (92, 94); integrin α4β1 (95) and Nrp1 (96), regardless of MHC restriction. Overall, more investigation is needed to characterize and validate the mechanisms underlying Treg/DC physical interactions and to exploit non-antigen-specific Treg modulation of DC in inflammatory diseases that lack an auto- or allo-immune component. More broadly, whether TCR/MHC peptide engagement is necessary for or enhances Treg suppression of the pro-inflammatory functions of other MHC II-expressing innate immune effectors such as monocytes/macrophages and granulocytes merits additional study.
Besides canonical CD4+Foxp3+ Treg, regulation of DC by other types of Treg has also been documented. In a study involving mouse and human experiments, Liu et al. reported that FoxA1+ Treg with a deficiency in Foxp3 expression yet a higher expression of PD-L1, reduce IL-12 and IL-17 production by LPS-activated HLA-DR+ antigen presenting cells (APC) (5). Other studies have investigated the cross-talk between IL-10-secreting DC (DC-10) and Tr1 cells (97), demonstrating that co-culture of human DC-10 with CD4+ T cells results in the induction of antigen-specific Tr1 in the setting of autoimmune disease (98) and organ transplantation (99). Initially identified and purified as CD14+CD11c+CD83+ cells (100), DC-10 could also be generated from bead-selected CD14+ monocytes by culture in presence of GM-CSF and IL-4 (99). Recently, a better-defined DC-10 population (CD14+CD16+CD141+CD163+) has been purified from blood and shown to exhibit similar IL-10 production and Tr1 induction potency (101). Importantly, ex vivo generated Tr1 have been recognized as a promising anti-inflammatory cell therapy and may modulate DC to more tolerogenic phenotypes characterized by higher expression of ILT-3, ILT-4 and HLA-G. Induced Tr1 can also release granzyme B and perforin through CD2/CD58- and CD226/CD155-based cell contact, to induce cell death in myeloid cell-derived APC. Despite lack of Foxp3 expression, Tr1 express key Treg-associated receptors (e.g. CTLA-4, PD-1 and ICOS) and are capable of similar suppressive regulation of DC through cell-cell contact (102). A range of the reported mechanisms of Treg modulation of DC phenotype and function are summarized in Figure 3.
Figure 3 Regulatory T cell interactions with dendritic cells. EVs, extracellular vesicles; CTLA-4, cytotoxic T lymphocyte antigen 4; TCR, T cell receptor; MHC II, major histocompatibility complex II; ICAM-1, intercellular adhesion molecule 1; LFA-1, lymphocyte function-associated antigen 1; DC, dendritic cells; TGF-β1, transforming growth factor beta 1; TNF, tumor necrosis factor.
Regulatory T cell interactions with innate or innate-like lymphocytes
Natural killer cells
Natural killer cells, a subset of innate immune cells derived from lymphoid progenitors, play important roles in the control of viral infection and tumorigenesis in an MHC-independent manner. The effector functions of NK cells include cytolysis and induction of programmed cell death in target cells as well as production of pro-inflammatory cytokines. Numerous studies have provided evidence that Treg counteract NK cell effector functions by decreasing cytolytic activity and proliferation, downregulating activation receptors (NKG2D and NKp44), upregulating inhibitory receptors (CD158a, CD158b, and NKG2A) (103), and suppressing production of IL-12 and IFN-γ (104). Mechanistically, membrane-bound TGF-β on Treg has been shown to be an important mediator of Treg suppression of NK cells response in the setting of cancer (104). In a mouse model of hepatitis B, Treg-mediated inhibition of NK cell cytotoxicity was attenuated by blockade of OX-40L, identifying a role for the OX-40/OX-40L pathway in protecting against NK cell-mediated chronic liver injury in this infection (105). Intrahepatic Treg also suppressed NK cell degranulation and NKG2D expression in a CTLA-dependent manner, contributing to decreased liver fibrosis by regulating NK cell interactions with hepatic stellate cells (106). Secretion of IL-37 by Treg is reported to suppress NK cell proliferation, cytotoxicity and IFN-γ production through its receptor IL-1R8 in association with NK cell downregulation of TIM-3 and upregulation of PD-1 (107). In a mouse model of autoimmune diabetes, an indirect mechanism of suppression of NK cells by Treg has been described by which Treg consumed IL-2 produced by islet-infiltrating CD4+ cells, thereby curbing the localized expansion of NK cells (108). A recent study also suggested that IL-10+ Treg suppress cytolytic activity of NK cells in acute retroviral infection. In this study, Littwitz-Salomon et al. showed that Treg were activated with increased expression of ICOS, IL-10 and TGF-β during the early, acute phase of Friend Retrovirus (FV) infection in mice. Depletion of Treg or neutralization of IL-10 (but not TGF-β) resulted in increased NK cell anti-viral activity (109). Figure 4A illustrates various reported mechanisms of Treg modulation of NK cell cytolytic and pro-inflammatory functions.
Figure 4 Regulatory T cell interactions with four main types of innate or innate-like lymphocytes: (A) Natural Killer (NK) cells, (B) Natural Killer T (NKT) cells, (C) Gamma delta (γδ) T cells (D) type 2 innate lymphoid cells (ILC-2). TGF-b – transforming growth factor beta 1; NKG2A, natural killer group 2A; PD-1, programmed cell death 1; NKG2D, natural killer group 2D; TIM3, T cell immunoglobulin and mucin domain-containing protein 3; NKp44, natural killer p44; IFNγ, interferon gamma; ICAM – intercellular adhesion molecule; TCR, T cell receptor; TNF, tumor necrosis factor; ST-2, suppression of tumorigenicity 2; IL-10R, interleukin 10 receptor; Ebi3, Epstein Barr virus-induced; ICOS, inducible T cell costimulatory; ICOSL, inducible T cell costimulatory ligand; IL-4Rα, interleukin 4 receptor alpha.
Modulation of NK cells by Treg has also been reported to contribute to the maintenance of immune tolerance in models of allo-transplantation and autoimmune disease. For example, in mouse cardiac allografts, depletion of Treg resulted in increased graft infiltration by both NK cells and CD4+ T cells in association with more severe transplant vasculopathy. Of interest, the exacerbation of vasculopathy following Treg depletion was ameliorated by depletion of NK cells, implying an important role for Treg suppression on NK cells in allograft survival (110). A similar protective role for Treg-mediated NK cells suppression has been reported in bone marrow transplantation (111) and autoimmune hepatitis (112).
In contrast to the settings described above, the crosstalk between Treg and NK cells within the uterus during pregnancy appears to form a positive feedback loop in which depletion or dysfunction of either cell type can result in miscarriage (113). The canonical pro-inflammatory role of NK cells has also been challenged in autoimmune disease. While NK cells can be characterized as pathogenic through direct cytotoxicity and production of inflammatory cytokines, they may regulate adverse immune response by eliminating autoreactive immune cells and by serving as a source of anti-inflammatory mediators such as IL-10, TGF-β, and IL-4 (114). Thus, the combined immunological roles of NK cells and Treg are likely to be complex and highly contextual, necessitating more disease-specific research in human subjects to better understand the likely effects of Treg-based therapies on NK cell-mediated innate immune responses. This may be of particular interest in auto-inflammatory diseases in which sterile inflammation and dysfunctional innate immunity occur in the absence of autoantibodies and autoreactive T cells (115, 116).
Natural killer T cells
Natural killer T (NKT) cells are a specialized type of innate-like lymphocytes, yet have the property of both NK cells and T cells by recognizing glycolipid ligands bound to the MHC class I-like protein CD1d via a restricted T cell receptor (TCR) repertoire and by widely participating in immune responses to infection, cancer, transplantation and fetal-maternal immunity (117). It was shown 20 years ago that human CD4+CD25+ Treg suppressed Vα24+NKT cell proliferation, cytotoxicity to tumor cells lines and cytokine production (IFN-γ, IL-4, IL-10, and IL-13) upon stimulation by α-galactosylceramide (αGalCer)-pulsed Mo-DCs. This suppression was dependent on direct contact between Treg and NKT cells and could be neutralized by antibody against ICAM but not IL-10 or TGF-β (118). Subsequently, Venken et al. reported that Treg suppressed proliferation and modulated cytokine production of human invariant (i)NKT cells in response to glycolipid or to innate stimuli. Conversely, Treg were induced to produce high amounts of IL-10 following contact with stimulated iNKT cells, indicating cross-talk between the two cell types (119). Evidence for direct Treg/NKT cell cross-talk in vivo has been reported by Hua et al., who demonstrated that CD1d deficient mice had reduced Treg number and function in the liver and that adoptively transferred Treg ameliorated NKT cell-mediated liver injury in a CD1d-dependent manner (120). In co-cultures of blood-derived human cells, induced Treg were shown to increase the proportion of CD4+ NKT cells with lower cytotoxicity and pro-inflammatory cytokine production than their CD4- counterparts. Of interest, αGalCer-stimulated PBMC cultures from cancer patients contained higher proportions of both CD4+ NKT cells and effector Treg than those of patients with benign tumors (121).
In addition to the findings from studies such as these that Treg suppress NKT cell activation and function, predominantly through contact-dependent interactions, there is also experimental evidence that activated NKT cells delete or suppress the counter-regulatory functions of Treg in settings such as allergic asthma and pregnancy loss (122, 123). Of interest, NKT cells were also reported to promote Treg expression of negative costimulatory receptors PD-1 and IL-10 production through secreting IL-4 (124), and NKT cell-secreted IL-2 helped sustain Treg survival (125). Type 2 NKT cells, a subset with a more diverse TCR repertoire, have been documented to have immunomodulatory potential and to protect from autoimmune disease (126). Figure 4B summarizes aspects of Treg/NKT cell cross-talk described above. Overall, there is compelling evidence for direct, clinically-relevant interactions between Treg and NKT cells that merit further investigation – particularly in relation to diseases and treatment strategies in which NKT cells participate in dictating the nature of tissue inflammation.
Gamma Delta T cells
γδ T cells represent a T cell subset which express TCRs consisting of γ and δ chains rather than the canonical TCR composed of α and β chains. They are typically categorized as innate immune cells because their activation via the TCR is MHC-independent and because they also express a range of surface NK receptors which modulate their responses to stress-associated antigens (127). The effector functions of γδ T cells include target cell cytolysis and production of inflammatory cytokines including IFNγ, TNF, IL-17A and IL-6. Accumulating evidence indicates that Treg exert regulatory effects on γδ T cells. For example, in a mouse model of ischemic stroke, the beneficial effect of intracerebral administration of IL-10 was shown, in part, to be mediated by induction of FoxP3+ Treg to suppress IL-17A production by γδ T cells (128). Similarly, IL-10-dependent Treg effects have been shown to reduce γδ T cell proliferation in a model of spontaneous colitis (129), and to inhibit human γδ T cell IFNγ secretion in response to the Mycobacterium tuberculosis antigen ESAT-6 (130). Direct Treg suppression of proliferation and production of IL-17A and IFNγ by γδ T cells was also observed in a mouse model of mucosal inflammation, although the mechanism was not elucidated (131). Along with IL-10, TGF-β has also been reported to participate in Treg suppression γδ T cell responses. In patients with hepatocellular carcinoma (HCC), compromised anti-tumor potency of γδ T cells was observed and Treg isolated from HCC tissue were suppressive of IFNγ production and tumor cell cytotoxicity by γδ T cells. Importantly, these effects were abrogated by anti-IL-10 or anti-TGF-β1 antibodies (132).
The role of specific Treg subpopulations in suppressing γδ T cells has been investigated in some disease settings. In a mouse model of myocardial infarction (MI), Blanco-Domínguez et al. used depletion and adoptive transfer of Treg to demonstrate that CD69+ Treg, through CD39 ectonucleotidase activity, protected against myocardial inflammation by suppressive effects on γδ T cells including induction of apoptosis, inhibition of IL-17A production and reduced migration to infarcted myocardium. In human subjects, higher proportions of circulating CD69+ Treg were shown to be associated with reduced risk of re-hospitalization for heart failure following acute MI (133). In a model of respiratory mucosal injury, Faustino et al. observed that depletion of GATA3+ Treg expressing the IL-33 receptor, ST2, resulted in increased IL-17-secreting γδ T cells and exacerbation of allergic lung inflammation. Mechanistically, the suppressive effect of ST2-expressing Treg on pulmonary γδ T cells was dependent on Treg exposure to allergen peptide and IL-33 resulting in Treg-secretion of Ebi3 (a component of IL-35). The inhibition of γδ T cells was associated with decreased eosinophil recruitment to the lungs (134). Figure 4C provides a summary of Treg markers, pathways and mediators shown to be relevant their modulatory interactions with γδ T cells.
As for other innate immune effectors, γδ T cells may also compete with and inhibit Treg functions. For example, IL-23 secretion by γδ T cells was shown to reduce Treg numbers and suppression of CD4+ αβT cells during mouse autoimmune encephalomyelitis (135). Similarly, secretion of IFNγ by γδ T cells may suppress the induction of Treg differentiation from CD4+ T cells as well as Treg expansion and suppression of effector T cells in vitro and in vivo (136–138). Importantly, in some settings, γδ T cells may also mediate regulatory effects on immune responses (139). Nonetheless, the weight of experimental evidence to date indicates that Treg can serve an important role in regulating the potent pro-inflammatory effects of γδ T cells in a range of diseases and that development of Treg-based therapies that replicate this function may be a promising translational goal.
Innate lymphoid cells
Although NK cells have been characterized as innate lymphoid cells for several decades, additional subtypes of bone marrow-derived cell types with lymphoid morphology and non-antigen specific immunological functions have been described more recently and termed ILC1, 2 and 3. These cells are present in lymphoid organs and blood but occur at higher concentrations at epithelial barriers and other tissue sites and play important roles in regulating the responses to infection or injury and in maintaining tissue homeostasis. They serve as a potent source of cytokines and can be viewed as serving as “helper cells” during evolving immune/inflammatory responses. The analogy to helper cells is strengthened by the associations of ILC1, 2 and 3 with production of signature cytokines that match those of CD4+ Th1, Th2 and Th17 cells respectively (140, 141).
Investigation of the interactions between Treg and ILC is in its infancy and we focus here on recent studies related to ILC2 which represent the most numerous ILC and serve to control extracellular parasitic infection and widely participate in mucosal immunity, by secreting type 2 cytokines including IL-4, IL-5, IL-9, IL-13. Rigas et al. have shown that human TGF-β-induced Treg suppressed IL-5 and IL-13 secretion by ILC2 through contact-dependent (ICOS/ICOS-L) and soluble (TGF-β and IL-10) mediators to control airway inflammation in a humanized model of ILC-2-dependent asthma. Interestingly, this effect was absent in naïve Treg (142). Similarly, in a mouse model of allergic asthma, Khumalo et al. demonstrated that Treg expression of the IL-4 receptor alpha was necessary for Treg-mediated suppression of ILC2 proliferation and secretion of IL-5 and IL-13 (143). In co-culture experiments informed by a mouse model of asthma, Krishnamoorthy et al. observed dose-dependent Treg suppression of IL-13 secretion by ILC-2, which was enhanced by Treg priming with the fatty acid derivative maresin 1 (144). Lui et al. observed increased proportions of ILC2 and related type 2 cytokines in PBMC from patients with allergic rhinitis which was accompanied by reductions in IL-35-producing Treg. Subsequently, IL-35 and induced IL-35-producing Treg were shown to suppress ILC2 in activation cultures. A role for ICOS/ICOSL in Treg suppression of ILC2 was also shown in this study (145). In another recent study of PBMC from allergic rhinitis patients, Treg-secreted IL-10, induced by co-culture with induced pluripotent stem cell-derived mesenchymal stem cells (iPSC-MSC), was shown to suppress ILC-2-secretion of IL-13, IL-9, and IL-5 in an ICOS/ICOSL-dependent manner (146). The key mediators of Treg/ILC2 interactions that have been described to date are summarized in Figure 4D.
The impact of Treg on ILC2 has been investigated in non-allergic pathological contexts as well. For example, in a mouse model of chronic pancreatitis, Treg depletion resulted in increased proportion of ILC2 cells, but not ILC1, in spleen and pancreatic tissue and concomitantly aggravated pancreatic fibrosis (147). Finally, in contrast to other studies described here, Treg and ILC2 were shown by Gao et al. to play complementary roles in reducing the severity of atherosclerosis in a mouse model. In this study, Treg tended to promote rather than suppress ILC2 and ILC2-derived IL-13 in a cell-contact and cytokine-based (IL-10 and TGF-β) manner (148). Notably, ILC2, much like Treg cells, express CD25 and are consumers of IL-2. A consequence of this is that ILC2 may be inadvertently expanded by administration of low-dose IL-2 intended to enhance Treg numbers in vivo (149). Whether there is natural antagonism between Treg and ILC2 during immune responses through competition for IL-2 remains to be directly investigated. Interestingly, it has been reported that IL-2 produced by ILC3 aids in supporting regulatory functions of Treg cells to maintain gut tissue homeostasis (150), while also serving as a cofactor to ILC2 survival/proliferation in lung inflammation (151). Thus, in common with other innate immune cell types reviewed here, the interactions described to date between ILC and Treg reflect a range of mechanisms and outcomes. Nonetheless, consistent striking observations of direct Treg-mediated suppression of maladaptive ILC2 activity in asthma and allergy speak to a distinct area of clinical potential.
Relevance to human diseases and translational opportunities
In contrast to the growing number of clinical trials of Treg-based therapies in patients with autoimmune diseases and organ transplants, little clinical translation has occurred to date of the capacity of Treg to modulate innate immune responses. Nonetheless, as we have reviewed in the preceding sections, there is a wealth of basic and pre-clinical evidence that specific Treg functional characteristics could be exploited as novel treatment strategy for innate immune-mediated inflammatory diseases (152). We conclude this review with short appraisals of evidence in favor of the development of Treg-based therapies for three common inflammatory conditions in which innate immune responses play a key role: type 2 diabetics (T2DM), ischemia reperfusion injury (IRI) and atherosclerosis.
Firstly, in the case of T2DM and its major complications, some human studies have observed numerical defects in circulating Treg in association with the presence or progression of diabetic nephropathy, retinopathy (153) and diabetic foot ulcer (154). In addition, animal studies have demonstrated that adoptive transfer or in vivo expansion of Treg ameliorate the severity of T2DM and its macro- and micro-vascular complications. For example, in diabetic pigs, intravenously injected Treg were shown by Guo et al. to protect tissue-engineered blood vessels from intimal hyperplasia by inhibiting inflammation and cell apoptosis and promoting endothelial progenitor cell mobilization (155). Other studies in rodent models of diabetes have demonstrated that adoptively transferred Treg migrate to retina and reduce neovascular retinopathy (156) or suppress obesity-linked insulin resistance and preserve kidney function (157). In a model of stroke in T2DM, endogenous expansion of Treg by a CD28 superagonist was found to increase M2-type macrophages and to alleviate ischemic brain injury (28). Similarly, in vivo expansion of Treg in mice with T2DM by injection of a novel hybrid cytokine bearing IL-2 and IL-33 activities, reduced diabetic kidney damage (158). Importantly, functional as well as numerical Treg deficits may also occur in T2DM. For example, Zhu et al. observed increased proportions of IL-17-producing Foxp3+Treg in T2DM patients compared to healthy patients which associated with higher body mass index (BMI) and the HbA1c levels (159). Similarly, Sheikh et al. reported that CD4+CD25+CD45RA+ Treg have comparable frequency but reduced suppressive potency in T2DM compared to non-diabetic controls (160). Overall, these and other studies provide evidence that augmentation of the autologous Treg repertoire in T2DM, either through ex vivo or endogenous expansion, has potential to prevent or reverse multiple severe diabetic complications.
Ischemia reperfusion injury refers to an acute compromise to the blood supply of an organ or tissue resulting in cellular damage or necrosis followed by a restoration of blood flow which further aggravates tissue injury by activating inflammatory processes. A significant role for Treg in alleviating inflammation has been demonstrated through Treg depletion and adoptive transfer in animal models of intestinal and renal IRI and of ischemic stroke (161, 162). In keeping with modulatory effects on mononuclear phagocytes summarized in an earlier section, ex vivo expanded Treg have also been shown to modulate the production of TNF and IL-1β by Kuffer cells and, thereby, protect against acute liver injury due to IRI (163). More widely studied has been the impact of Treg on myocardial IRI. A recent detailed review of this topic highlights that Treg, migrating to myocardial tissue after infarction through CCR5, the CXCR4-CXCL12 axis, and the Hippo pathway, may promote myocardial tissue repair through multiple mechanisms including modulation of macrophage phenotypes, direct interactions with cardiomyocytes and increasing collagen content and maturation in the infarct zone (164). A distinct heart-resident HelioshighNrp-1high Treg population, which expresses Sparc and is sustained and expanded by IL-33/ST-2 interaction was also identified and proved to be the primary mediator of Treg-mediated repair following myocardial infarction (165). In acute kidney injury, a CXCR3+ Treg subpopulation was found to be recruited to kidney tissue following reperfusion and to correlate with lower renal tissue injury and better kidney function (166). As evidenced by this predominantly pre-clinical literature, therapeutic strategies aimed at expanding or delivering pro-repair Treg to the site of IRI-related tissue injury have promise for limiting the consequences to brain (162), heart, kidney, liver, intestine and other organs in clinical settings. However, successful translational strategies in this area will likely require highly stable Treg-based therapies with distinct migratory and effector functions.
Atherosclerosis refers to the formation of cholesterol-containing plaques in arterial blood vessels, which may result in severe acute or chronic cardiovascular conditions due to reduced blood flow to tissue or rupture leading to thrombosis. Following initial changes to endothelial cells, increasing evidence indicates that progression of atherosclerotic plaques is driven by inflammatory responses. Indeed, three recent clinical trials of anti-inflammatory agents have proven beneficial effects in patients with atherosclerosis, including reductions in cardiovascular events and mortality (167–169). A number of studies have provided evidence for anti-inflammatory and athero-protective roles for Treg in atherosclerosis, including correlations between disease progression and defects of Treg numbers (170) or function (171). In animal models, Sharma et al, provided more direct evidence that Treg protect from rupture and promote regression of atherosclerotic plaques through modulatory effects on macrophages (47). Adoptively transferred Treg have also been found to contribute to reduced size and contraction of atherosclerotic plaques in hypercholesterolemic mice (172, 173). Studies such as these provide convincing evidence that Treg-enhancing approaches could be of value as a therapeutic strategy for reversing atherosclerosis. It is worth noting, however, that challenges will arise in maintaining the stability and adaptability of Treg in the pro-inflammatory setting of atherosclerosis (174, 175). In this regard, Treg within atherosclerotic aortas have been reported to have a high expression of Foxp3 but also low CD25 levels, expression of Th1-associated factors IFN-γ and T-bet and compromised suppressive potency (176). Understanding Treg metabolism under hypoxic conditions may help to address this issue.
Conclusion
As we have described here, the capacity for Treg to suppress innate immune responses and to ameliorate acute and chronic diseases involving non antigen-specific inflammation is well established. Furthermore, many mechanistic details of the specific modulatory effects of Treg and Treg subpopulations on individual innate immune effectors have been identified in experimental animals as well as human cells. That this body of knowledge could be exploited to develop Treg-enhancing strategies for a much broader range of conditions than that which they have, to date, been applied seems self-evident. Importantly, Treg cell therapies have proven to be safe in early phase clinical trials and are now in the process of overcoming several important obstacles to their more effective use in autoimmune diseases and organ transplants. While this progress should provide a valuable platform for extending Treg therapies to diseases driven primarily by innate immune responses, additional challenges related to tissue targeting, in vivo stability and selection for the required effector mechanisms will almost certainly require an extensive amount of focused research and innovation. Nonetheless, we propose that the existing evidence is sufficient to support a greater investment of time and resources in the development of interventions to augment Treg modulation of innate immunity.
Author contributions
QO: Conceptualization, Funding acquisition, Writing – original draft, Writing – review and editing. RP: Funding acquisition, Writing – original draft. MG: Conceptualization, Funding acquisition, Supervision, Writing – review and editing.
Funding
The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by a China Scholarship Council PhD fellowship to QO (Grant number 202106370032) and by an Academic Internship from the Health Service Executive of Ireland to RP. MG is supported by a Science Foundation Ireland Research Centres grant (CÚRAM, grant number 13/RC/2073_P2) and by the European Regional Development Fund.
Conflict of interest
MG reports honoraria from the American Society of Nephrology; Hebei Medical University, China; Théa Pharma Ltd., Ireland; and Novo Nordisk as well as advisory roles as an Editorial Board member for the journal Transplantation and an Associate Editor for Mayo Clinic Proceedings.
The remaining 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.
The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.
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Keywords: regulatory T cells (Treg), innate immune response, macrophages, dendritic cells, immune regulation, neutrophils, inflammatory diseases, cell therapies
Citation: Ou Q, Power R and Griffin MD (2023) Revisiting regulatory T cells as modulators of innate immune response and inflammatory diseases. Front. Immunol. 14:1287465. doi: 10.3389/fimmu.2023.1287465
Received: 04 September 2023; Accepted: 05 October 2023;
Published: 20 October 2023.
Edited by:
Qizhi Tang, University of California, San Francisco, United StatesReviewed by:
Xuyu Zhou, Chinese Academy of Sciences (CAS), ChinaMaria-Luisa Alegre, The University of Chicago, United States
Copyright © 2023 Ou, Power and Griffin. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Matthew D. Griffin, bWF0dGhldy5ncmlmZmluQHVuaXZlcnNpdHlvZmdhbHdheS5pZQ==