Abstract
Rheumatoid arthritis (RA) is an autoimmune disease, in which the abnormal activation and proliferation of effector T cells play a pivotal role in its pathogenesis. Regulatory T cells (Tregs) are a unique subset of immune cells with immunosuppressive functions, which help to inhibit the differentiation and proliferation of effector T cells in RA and maintain immune tolerance. The interaction between gut microbiota and immune cells has long been a research hotspot in autoimmune diseases. Although gut microbiota metabolites are considered to regulate the host’s immune system as a bridge of the gut-joint axis, how gut microbiota acts on immunosuppressive Tregs remains unclear. This review summarizes that how the gut microbiota directly or indirectly (via metabolites) enhances the immunosuppressive capacity of Tregs. This enhancement is primarily achieved through pathways such as promoting the induction of Tregs, upregulating the expression of characteristic transcription factors of Tregs, and facilitating their secretion of anti-inflammatory cytokines, thereby ameliorating the inflammatory microenvironment and subsequently improving autoimmune conditions in RA.
1 Introduction
Rheumatoid arthritis (RA) is a chronic systemic autoimmune disorder characterized by inflammatory arthritis presenting with symmetrical polyarticular pain and swelling (1). RA predominantly affects small joints in the hands and feet, potentially progressing to joint deformity and functional impairment, significantly impairing the patient’s quality of life and imposing a substantial burden on healthcare resources.
A growing body of research has demonstrated the crucial role of the gut microbiota in both the pathogenesis and therapeutic management of RA across clinical and animal models (2–4). Gut microbiota-derived metabolites serve as pivotal mediators of the gut-joint axis and play essential roles in maintaining intestinal barrier integrity, immune homeostasis, and modulating bone destruction in patients with RA (5). A recent Mendelian randomization study revealed that immune cells act as critical mediators of the intricate mechanisms linking gut microbiota to RA pathogenesis (6).
Regulatory T cells (Tregs), a distinct subset of lymphocytes with immunosuppressive properties, have emerged as promising therapeutic targets (7). Therefore, we aimed to review the mechanistic interplay between gut microbiota-derived metabolites and Tregs and systematically elucidate how microbial regulation enhances Treg-mediated immunosuppression to ameliorate RA progression.
2 Tregs
While most immune system cells function to promote inflammation to fight pathogens, Treg is a class of immune cells that can control immunity to maintain homeostasis (8). The currently accepted definition of Treg primarily involves its specific nuclear expression of the transcription factor FOXP3, along with surface-specific expression of CD25 (IL-2 receptor) and cytotoxic T lymphocyte-associated antigen 4 (CTLA-4). The discovery of the transcription factor FOXP3 represents a significant milestone, enabling the identification of Tregs within the CD4+ T cell subset.FOXP3 drives the differentiation of naïve CD4+ T cells into Tregs and serves as a master transcriptional regulator essential for Treg development and functional maintenance (9, 10). The establishment and maintenance of Treg functionality are strictly dependent on the stable, coordinated expression of lineage-specific genes, particularly FOXP3.
2.1 Treg classification
Based on their cellular origin, Tregs can be classified into three subtypes: thymus-derived natural Tregs (nTregs), peripherally induced Tregs (pTregs) originating from lymphoid organs, and in vitro differentiated induced Tregs (iTregs) generated from naïve T cells (11). Compared to other T-cell subsets, Treg cells exhibit an enhanced recognition capacity for self-antigens.
Tregs undergo antigen priming during thymic development (12). In the thymus, thymocytes with intermediate-affinity TCRs undergo differentiation upon receiving agonist signals from TCR/co-stimulatory molecules. Transforming growth factor-β (TGF-β) can induce FOXP3 expression and promote Treg cell development by disrupting weaker agonist signals (13). Upon thymic egress, Tregs express T-cell receptors (TCR) with high affinity for self-antigens (14). Tregs also demonstrate inhibitory functionality at peptide/MHC concentrations 100-fold lower than those required by conventional T-cell subsets (15). pTreg cells contribute to the maintenance of peripheral tolerance at inflammatory sites, particularly on mucosal surfaces such as the gut and lungs. Under inflammatory conditions, exogenous antigens derived from microbes can promote the generation of pTreg cells (16). However, studies have revealed that pTreg exhibits multiple significant characteristics independent of FOXP3 and can suppress the expansion of colonic effector T cells in a FOXP3-independent manner (17). This means FOXP3 is not the only gene required to maintain the development and function of Tregs. For instance, Helios can synergize with FOXP3 to enhance the function of Treg cells, augment the suppressive capacity of induced Treg cells, and upregulate the expression of various Treg cell-associated molecules (18, 19).
Additionally, there are also Treg cells that mediate immunosuppression without expressing FOXP3, such as Type 1 regulatory T cells (Tr1 cells), which are characterized by secreting IL-10 (20). Tr1 cells also possess immunosuppressive functions and can inhibit the expansion of pathogenic collagen-specific T cells in the collagen-induced arthritis (CIA) mouse model (21). Studies suggest that FOXP3+ Treg cells are indispensable during the initial phase of tolerance induction in inflammatory target organs, whereas Tr1 cells contribute to the maintenance of long-term tolerance (22). In addition to CTLA-4, Tregs also express various surface markers such as glucocorticoid-induced TNFR-related protein (GITR), latency-associated peptide (LAP), and/or lymphocyte-activation gene 3 (Lag-3), among others (23). The specific subsets of Tregs are classified based on cell surface or intracellular markers and their secreted cytokines, as shown in Table 1. Different subsets of Treg cells exhibit variations in the expression of chemokine receptors and transcription factors. There is no specific marker that can be used to distinguish all Tregs. However, the fact that some subgroups are similar, overcategorization may hinder the study of Treg. A comprehensive definition of human Tregs requires the integration of both phenotype and suppressive function (33). Although some Treg cell signature genes are indirectly regulated, most genes responsible for Treg cell stability and lineage determination are dependent on FOXP3 (34).
Table 1
| Subgroup name | Markers | Factors | References |
|---|---|---|---|
| FOXP3+Treg | CD25+ FOXP3+,Helios+ CTLA4+,Nrp1+,GITR |
TGF-β,IL-10,IL-35 | (24) |
| Tr1 | FOXP3- CD49b+,LAG3+,CD226+,PD-1+,CTLA-4+ |
IL-10,TGF-β,IFN-r | (20) |
| Th3/Tr2 | CD25+ CD69+,FOXP3- LAP+ |
TGF-β,IL-10 | (25) |
| iTr35 | FOXP3+,p35+ | IL-35 | (26) |
| B cell-derived Treg | CD25+ ,LAG3+,PD1v,ICOS+,CTLA4+,GITR+,CD49b+、FOXP3-、OX40+ |
IL-10,PD-1, CTLA4,LAG3, |
(27) |
| T follicular regulatory (Tfr) cells | FOXP3+,CXCR5+,PD-1+,ICOS+ | IL-10, TGF-b, and granzyme B | (28) |
| ExTreg (cytotoxic Treg) | CD16+,CD56+ CD25+,FOXP3+; |
IL-17,IFN-y | (29) |
| Th1-like Treg | CD25+,FOXP3+,T-bet+,CXCR3+ | IFN-γ | (30) |
| Th2-like Treg | CD25+, FOXP3+, CTLA-4+, GATA3+ CD44+, ICOS+, GITR+, | IL-4, IL-10;IL-5, IL-13 | (31) |
| Th17-like Treg | CD25+,FOXP3+,RORγt+,CCR6+,CCR4,CD103+,ICOS+,Helios+ | IL-10, TGF-β,IL-17A | (32) |
Treg subgroup.
2.2 Epigenetic modification
Epigenetic modifications are critical for Treg functionality, as they regulate the transcriptional control of Treg lineage-specific genes (24). The FOXP3 locus harbors three evolutionarily conserved non-coding sequences (CNS1-CNS3), and subsequent studies have identified an additional regulatory element (CNS0) positioned upstream of the transcriptional start site. These conserved regions contain dense clusters of hypomethylated CpG motifs that epigenetically regulate FOXP3 expression via DNA methylation-sensitive transcriptional modulation. CNS0 is epigenetically activated by the chromatin organizer SATB1 to initiate FOXP3 expression (35); CNS1 serves as a critical enhancer region mediating TGF-β-induced FOXP3 transcriptional activation (36); CNS3 is an indispensable regulatory element involved in FOXP3 induction; and CNS2 plays a non-redundant role in maintaining Treg lineage stability via sustained FOXP3 expression (37). IL-2 signaling induces STAT5 recruitment to the CNS2, driving Treg differentiation through chromatin remodeling (38).
The acetylation of FOXP3 is crucial for its functionality as it promotes the formation of FOXP3 dimers, enhances DNA-binding capacity, increases chromatin accessibility, and facilitates the interaction with transcription factors like FOXP3 (39). These processes regulate the immunosuppressive role of Treg cells. Histone acetyltransferases (HATs) and Histone deacetylase (HDACs) collectively maintain the dynamic equilibrium of acetylation in Treg cells. More than 10 HDAC enzymes are expressed in Treg cells. Histone deacetylase (HDAC) inhibition elevates histone acetylation at both the FOXP3 promoter and its cis-regulatory elements, potentiating Treg suppressive in vitro and in vivo functions (40).
3 Treg-mediated suppression of effector T-cell activation ameliorates RA
3.1 Central role of effector T cells in RA pathogenesis
Synovitis, a hallmark of RA, is histologically characterized by synovial hyperplasia, neovascularization, and heterogeneous inflammatory infiltrates, including lymphoid aggregates and germinal center-like structures (41). Infiltrating cells include T and B cells, macrophages, and dendritic cells. The pathogenesis of RA is not fully understood, but is primarily associated with immune dysregulation. The production of autoantibodies, including anti-citrullinated protein antibodies (ACPAs), and the presence of rheumatoid factor in both blood and synovial structures are considered prominent features of RA (42).
Autoimmune processes related to RA precede the onset of clinical disease by several years (43). Genetics is the most significant risk factor for the development of RA, with the HLA-DR locus facilitating the involvement of citrullinated antigens in CD4+ T-cell antigen presentation through shared epitopes. Binding to citrulline-modified peptides leads to the production of ACPAs, which further induces T-cell activation and cytokine production (34). Additionally, epigenetic factors, such as DNA methylation and histone acetylation, contribute to the pathogenesis of RA (44).
Cellular interactions within the synovium constitute a critical component of RA pathogenesis, with T cells playing a central role in the immune pathogenesis of rheumatoid arthritis (34) (Figure 1). Evaluation of a large array of cell lineages in synovial specimens from patients with RA have identified over 20 transcriptionally defined T-cell subtypes (45). Pathologically expanded peripheral T-helper cell subsets can induce plasma cell differentiation through IL-21 secretion and SLAMF5 interactions (46), subsequently leading to the production of ACPAs and other autoantibodies. These autoantibodies are then presented to T cells by antigen-presenting cells, including dendritic cells and macrophages, which activate and induce T-cell differentiation, along with the production of cytokines (47). In particular, helper T cells (Th cells), such as Th1 cells, promote inflammatory responses by secreting interferon-γ (IFN-γ), while Th17 cells exacerbate inflammation and tissue damage by producing cytokines like IL-17 and IL-22 (48). These cytokines, in turn, activate neighboring cells, including monocytes, macrophages, and synovial fibroblasts, to produce additional pro-inflammatory factors. These cytokines can stimulate the expression of RANKL, and the upregulation of RANKL further activates the NF-κB pathway, leading to the proliferation and activation of inflammatory cells, as well as the activation of osteoclasts. This leads to bone erosion and joint damage (49). In contrast, Tregs inhibit T-cell proliferation, activation, and effector function through multiple pathways.
Figure 1
Pathologically, APCs (DCs and macrophages) present antigens to CD4+ T cells, which abnormally activate their differentiation into Th1 and Th17 subtypes. These two subtypes secrete pro-inflammatory factors such as IFN-γ and IL-17, which in turn lead to the proliferation of fibroblast-like synoviocytes, and ultimately bone destruction. In contrast, Treg cells inhibit abnormal antigen presentation by competitively binding to CD80/CD86 and MHC on the DCs surface; secreting anti-inflammatory factors and inhibiting Th proliferation through the CD39/CD73/A2a adenosine pathway. (DCs, Dendritic Cells;MHC, Major Histocompatibility Complex;TCR, T Cell Receptor; FOXP3, Foxhead Pox protein 3; HDAC, Histone deacetylase; CNS, conserved non-coding sequences; CTLA4, Cytotoxic T-Lymphocyte Associated protein 4;GITR, Glucocorticoid-induced TNFR-related protein; LAP, latency-associated peptide; Lag-3, lymphocyte-activation gene 3; PD-1, programmed cell death protein 1; NRP1, Neuropilin-1;RANK, receptor activator of NF- κB; RANKL, receptor activator of NF- κB ligand).
3.2 Immunosuppressive mechanisms of Tregs in RA pathogenesis
Treg-mediated immunosuppression is primarily executed through three mechanistically distinct pathways: (1) regulatory cytokine secretion, (2) direct cell–cell contact-dependent suppression, and (3) metabolic modulation of target cells (50) (Figure 1). Treg cells elaborate upon an array of immunomodulatory cytokines critical for their suppressive functions, including interleukin-10 (IL-10), transforming growth factor-beta (TGF-β), and IL-35. IL-10 downregulates MHC-II and CD86 surface expression on dendritic cells and macrophages, impairing their antigen-presenting capacity to CD4+ T cells, thereby attenuating inflammatory responses in RA (51). TGF-β can inhibit T-cell proliferation, activation, and effector functions through dual mechanisms: downregulating dendritic cell function, interfering with antigen presentation, and concurrently inhibiting IL-2 production (52). IL-35 can inhibit Th17 differentiation and reduce the production of pro-inflammatory factors, thereby improving the inflammatory response in RA (53).
Cell–cell contact mediates immunosuppression. Dendritic cells (DCs) are the most effective antigen-presenting cells (APCs) in the immune system and possess bidirectional immune functions. While mature DCs activate effector T cells to drive inflammation, tolerogenic DCs upregulate anti-inflammatory cytokines (IL-10/TGF-β) with reduced co-stimulatory molecule expression, thereby promoting Treg differentiation and immunosuppression (54, 55). Treg surface-expressed CTLA-4 competitively antagonizes CD28 costimulation by binding to CD80/CD86 on DCs and transmitting inhibitory signals that suppress effector T-cell activation and clonal expansion (56). The transmembrane protein lymphocyte activation gene-3 (LAG-3) binds to MHC-II on APCs and inhibits DC activation through an ITAM-mediated inhibitory signaling pathway (57) and is currently emerging as an immunomodulatory target for various therapeutic approaches in RA (58). Furthermore, programmed cell death protein 1 (PD-1), a member of the CD28 superfamily, binds to its ligands, thereby inhibiting T-cell proliferation and IFN-γ production. PD-1 also plays a role in the regulation of osteoclast development in RA (59, 60).
Another mechanism of Treg cell-mediated suppression is disruption of target cell metabolism. CD39 and CD73 on the surface of Tregs act synergistically to produce adenosine, which binds to the adenosine receptor A2A on activated T cells, driving the inhibition of T-cell proliferation (61, 62). Studies have demonstrated the anti-inflammatory effects of adenosine on synovial cells in RA (63). Furthermore, the high expression levels of the IL-2 receptor (CD25) on the surface of Treg cells can bind to IL-2, reducing the activation and proliferation of effector T cells (64).
In RA pathogenesis, impairment of Treg migration and homeostasis may inhibit anti-inflammatory effects. IL-6-induced vasodilator-stimulated phosphoprotein phosphorylation inhibits Treg migration to inflammatory sites, thereby limiting their immunosuppressive functions (65). G protein signaling modulator 2 (GPSM2) is almost completely absent in RA, leading to abnormal G protein-coupled receptor signaling, which further weakens Treg migration (56). Additionally, abnormal expression of chemokines and adhesion molecules, such as CCR4, CCR6, and LFA-1 also affects the homing of Tregs to synovial tissue. A review summarized the existing research and concluded that strategies aimed at increasing the number of Tregs or enhancing their suppressive functions are effective in treating RA (7). Glucocorticoid drugs can upregulate FOXP3 expression to promote Treg expansion and enhance Treg function by modulating the TCR signaling pathway and cytokine milieu (66). Traditional antirheumatic drugs such as methotrexate (MTX) and cyclophosphamide (CTX) in combination therapy can enhance the suppressive function of Tregs (67). In addition to conventional drug therapies, low-dose IL-2 therapy has been demonstrated to alleviate symptoms by restoring Treg levels in RA patients (68). The underlying mechanism may involve selective expansion of Tregs through activation of the STAT5 signaling pathway (69).
4 The gut microbiota and RA
Abnormal immune responses at mucosal sites in vivo may be associated with the onset and progression of RA. The intestinal mucosa accounts for a significant portion of the mucosal content of the body, and microbial dysbiosis may interact with immune dysregulation, leading to more severe systemic immune disorders. The intestine is the largest immune organ in the human body and plays a crucial role in autoimmune diseases (70). The gut microbiota is a complex microbial ecosystem vital for maintaining host health and forming a mutually beneficial relationship. In the human body, the host provides a living environment for microorganisms that can supply nutrients and, more importantly, mount immune responses against pathogens to protect the body (71).
Researchers believe that the microbiota is crucial for various aspects of host immunity, including immune maturation, prevention of pathogen overgrowth, host cell proliferation and angiogenesis, regulation of intestinal physiological functions, and energy synthesis (72). Healthy gut microbiota is primarily characterized by diverse colonization, high microbial gene abundance, and stable core functions (73). Although its specific composition varies among individuals owing to factors such as genetics, age, diet, and environment, the functions of the adult gut microbiota remain relatively consistent in healthy individuals (74). In the gut, bacterial populations are predominantly anaerobic and include phyla such as Firmicutes and Bacteroidetes.
A dysbiotic gut microbiota is pathologically characterized by reduced microbial diversity, overrepresentation of specific taxa, compromised intestinal barrier integrity, and concomitant metabolic dysregulation (75). In clinical studies, significant changes in the gut microbiota composition have been observed in patients with RA. Xing et al. (76) found that both the Shannon diversity and Simpson index of gut bacteria were significantly lower in patients with RA than in healthy controls, indicating a reduction in prokaryotic diversity within samples under disease conditions and the presence of pronounced gut bacterial dysbiosis. At the phylum level, patients with RA exhibit a higher abundance of Actinobacteria and lower levels of Bacteroidetes and Proteobacteria. At the genus level, Ruminococcus, Collinsella, Gemmiger, and Dorea are significantly enriched, whereas Bacteroides, Prevotella, Roseburia, Clostridium, Lactobacillus, Parabacteroides, and Megamonas are markedly reduced. Similar alterations in the gut microbiota have been observed in animal studies. Compared to normal mice, a model group showed an increased relative abundance of Lactobacillus, Candidatus_Arthromitus, UCG-005, and Anaerofustis, whereas the relative abundance of Bacteroides, Alistipes, Mucispirillum, unclassified_o_Bacteroidales, and norank_f:norank_o:Rhodospirillales decreased (77). Due to the variety and large number of intestinal flora, and significant individual differences, coupled with the limitations of existing experimental methods, the results obtained from various experiments on flora changes are not completely consistent. More advanced technical means may need to be introduced to clarify the changes of flora. A Mendelian randomization study demonstrated that eight bacterial taxa were positively correlated with the risk of developing RA, whereas six taxa were negatively correlated with RA risk (78). Alterations in gut microbiota are highly evident in the pathogenesis of RA.
Ecological disturbances in the gut and autoimmune mechanisms may be involved in the development of RA (79). The interactions between mucosal sites and probiotic bacteria may play a role in the pathogenesis of RA (80). For instance, in the intestines of patients with RA, there is a reduction in certain beneficial bacteria, such as those from the Bacteroidetes phylum, and an increase in potentially pathogenic bacteria, such as Prevotella spp.; this imbalance in the microbiota may promote the development of RA by activating immune cells, fostering inflammatory responses, and affecting gut barrier function. An increase in Lactobacillus may drive joint inflammation by activating Th17 cells to secrete IL-17 (67), whereas a decrease in Bacteroides and Alistipes leads to insufficient differentiation of CD4+ T cells into Tregs (81). In addition, gut microbial dysbiosis can stimulate autoreactive cells to relocate to the joints, leading to inflammation (82).
Therefore, restoration of dysbiosis can alleviate inflammation levels. Bacteria in the gut can traverse the mucus layer and stimulate epithelial cells, thereby modulating immune function and enhancing the gut barrier (83). Zhao et al. found that Escherichia coli and Streptococcus bovis significantly influence levels of TNF-α and IL-6, with increased abundance of these bacteria enhancing ascorbic acid degradation, thereby mitigating the progression of RA (84). Gut microbiota can also interact directly with the host through microbial metabolites such as short-chain fatty acids (SCFAs) to regulate the immune system (85, 86). Through polysaccharide therapy, the gut microbiota breaks down polysaccharides into SCFAs (such as butyrate), which, by activating G-protein-coupled receptors (like GPR43), inhibit the NF-κB pathway and reduce the release of pro-inflammatory cytokines, thereby alleviating arthritis (77).
5 Gut microbiota and regulatory T cells
The intestine harbors a vast array of immune cells, including Tregs, which are abundant in the large intestine and are primarily represented as FOXP3+ Tregs (87). In the small intestine Tr1 cells are in relative abundance (88). Tregs are typically thought to be primed in the mesenteric lymph nodes before migrating to the gut. Additionally, FOXP3+ Tregs acquire secondary activation signals and expand in the small intestine to produce IL-10 (89). Intestinal epithelial cells are in close contact with immune cell populations, and secrete high levels of cytokines. For instance, IL-33 promotes the stability and function of Tregs (90) and modulates IL-18 secretion to help regulate CD4+ T cells in the colon, limiting their differentiation into Th17 cells, and enhancing the role of FOXP3+ Tregs in inflammation (91). The mucus layer above the intestinal epithelium is rich in large molecules called mucins. Upon inflammation, this layer can promote the production of IL-10 and TGF-β while reducing the production of pro-inflammatory cytokines, thereby facilitating Treg development (92). Intestinal mucosal dendritic cells can synergistically induce FOXP3+ Treg cells through the production of TGF-β and retinoic acid (93). Mice with specific knockout of TGF-β receptors exhibit reduced generation of FOXP3+ Tregs (94). Furthermore, microbial metabolites such as SCFAs can promote the development of peripheral Tregs (95). Intestinal microbiota can directly influence immune cells, and their metabolites affect immune cells. This complex interplay underscores the significance of the gut microbiota in shaping immune responses and maintaining immune homeostasis.
5.1 Bifidobacterium
Bifidobacterium is one of the most predominant physiological bacteria in the gastrointestinal tract of humans and animals and exerts its effects by reducing intestinal pH, inhibiting the growth of pathogens, maintaining the balance of intestinal flora, and preserving the integrity of the intestinal barrier (96). Bifidobacteria can alleviate RA by suppressing the production of IL-17 and other pro-inflammatory mediators (97). Furthermore, early administration of bifidobacteria can restore the healthy state of the intestinal flora in RA rat through histidine metabolism, thereby delaying the onset and progression of RA (98).
Treg cells serve as crucial mediators through which Bifidobacterium regulates the structure of intestinal flora. Bifidobacterium breve increases the expression of interleukin-10 receptor alpha (IL-10Rα) and the secretion of IL-10 in mouse Treg cells, forming an IL-10/IL-10Rα auto-stimulatory loop, thereby enhancing their immunosuppressive function (99). This process is associated with the enhanced mitochondrial activity of Tregs. Ravi Verma et al. (100) proposed that Bifidobacterium >bifidum is an effective inducer of FOXP3+ Tregs, with its cell surface glucan/galactan (CSGG) polysaccharide as a key component for Treg induction. CSGG activates intestinal dendritic cells (particularly CD103+CD11b+ DCs) through the TLR2 receptor, inducing their phenotypic transformation into regulatory dendritic cells (rDCs), which secrete IL-10 and TGF-β1, promoting the differentiation of naïve CD4+ T cells into Treg cells. This process is likely dependent on the MyD88 signaling pathway, a joint adapter protein within dendritic cells. A team from Jiangnan University discovered that B. breve CCFM1078 could alleviate joint inflammation in rat by modulating the intestinal flora and strengthening the intestinal barrier (101). Experimental results demonstrated that CCFM1078 increased the abundance of beneficial bacteria (such as Bifidobacterium spp. and Faecalibaculum), promoted the production of SCFAs, and enhanced the expression of FOXP3. Additionally, the genomic DNA of B. longum subsp. infantis significantly induces Tregs through unique methylated CpG motifs oligodeoxynucleotide (ODN) (102). CpG methylation is a crucial epigenetic mechanism that regulates Treg stability and function, promotes FOXP3 expression, enhances Treg differentiation, and bolsters their immunosuppressive capabilities. However, the latest research results show that ODN induces Treg most obviously at a certain dose, and excessive ODN will reduce the induction of Treg (103). It is therefore hypothesized that the effect of different levels of flora on Treg may also be different, which requires more research to verify.
Bifidobacterium can produce a variety of metabolites that are beneficial to the host, including vitamins, polyphenols, conjugated linoleic acids, and SCFAs. These metabolites, such as organic acids, bacteriocins, and biosurfactants, also exert detrimental effects on pathogenic microorganisms, thereby hindering the proliferation of harmful microbes (104). Yang et al. confirmed that Bifidobacterium can mitigate RA by suppressing inflammatory responses in CIA rat, regulating intestinal barrier function, and downregulating specific metabolites via the histidine metabolism pathway (98). Zhao et al. discovered that Bifidobacterium can mediate bile acid metabolism, wherein unconjugated bile acids can activate the TGR-5 receptor(, triggering the cAMP-PKA signaling pathway, which subsequently induces CREB to secrete IL-10 and promotes the Treg cell population in mouse (105).
5.2 Lactobacillus
Lactobacillus and other genera are widely used as probiotics, with intestinal glucose aiding their survival in acidic gastrointestinal environments (106). These probiotics alleviate RA through mechanisms such as immunomodulation, metabolite production, and improvement of intestinal barrier function (107, 108). Lactobacillus treatment can prevent the onset of arthritis in preclinical models, reduce arthritis scores in CIA rat and pro-inflammatory cytokines (such as IL-17, IL-1β, IL-6, and TNF-α), and increase the release of anti-inflammatory cytokines like IL-4 and IL-10 in bodily fluids (109). Fan et al. (110) clarified that Lactobacillus casei (particularly CCFM 1074) can alleviate symptoms in arthritic mice by modulating the Th17/Treg balance and enhancing the proportion of Treg cells in mesenteric lymph nodes. The process is primarily through local and systemic immune responses triggered by the production of SCFAs, which can induce the differentiation and proliferation of Treg cells. In rats with RA, following Lactobacillus casei intervention, symptoms were significantly alleviated, with restoration of intestinal flora homeostasis and regulation of oxidative stress balance. Further research revealed that Lactobacillus casei promotes the differentiation of CD4+ T cells into Treg cells by metabolizing tryptophan to produce indole derivatives that activate the aryl hydrocarbon receptor (AHR) on CD4+ T cells. Lactobacillus also maintains Tregs homeostasis through metabolites such as SCFAs (111).
Lactobacillus rhamnosus (LPR), another strain of Lactobacillus, promotes Treg differentiation of Tregs by forming a complex with secretory immunoglobulin A (SIgA) (112). This complex is taken up by DCs in Peyer’s patches (PPs), upregulating negative regulatory proteins of the Toll-like receptor (TLR) pathway (such as SIGIRR, Tollip, and SOCS1), thereby inhibiting the TLR signaling pathway and reducing inflammatory responses (113). Concurrently, the expression of retinaldehyde dehydrogenase 2 (RALDH2) is significantly enhanced, promoting the production of retinoic acid. Conversely, DCs in PP and mesenteric lymph nodes (MLN) secrete substantial amounts of IL-10 and TGF-β upon interaction with the LPR-SIgA complex. These DCs present antigens to naïve CD4+ T cells, and under the combined effects of IL-10, TGF-β, and retinoic acid, promote the differentiation of T cells into FOXP3+ Tregs (114). This entire process occurs within the PPs and MLN.
Lactobacillus salivarius is classified as a member of the genus Ligilactobacillus and is particularly notable for its immunomodulatory functions. L. salivarius has been isolated from patients with RA and has been found to elevate serum levels of IL-10 in arthritic mice, thereby increasing the proportion of Tregs (115). Additionally, Lactobacillus salivarius (especially strain FXJCJ7-2) can increase the proportion of FOXP3+ Tregs in the spleen, and its specific genes (such as LS_0679 and LS_0681) can boost the production of SCFAs (116). SCFAs (such as acetate and butyrate) directly promote Treg differentiation and mitigate inflammation by inhibiting the NF-κB pathway.
5.3 Bacteroides fragilis
Bacteroides fragilis can improve the symptoms of RA and enhance the efficacy of methotrexate (MTX) against arthritis in CIA rats by regulating butyrate metabolism (117). Moreover, Bacteroides fragilis produces a symbiotic factor known as polysaccharide A (PSA), which promotes mammalian immune system development. PSA facilitates the conversion of CD4+ T cells to FOXP3+ Tregs in germ-free mice, induces the expression of anti-inflammatory cytokines (such as IL-10 and TGF-β2), and enhances the suppressive function of Treg cells by directly activating the TLR2 signaling pathway on Treg cells (118). Subsequently, Telesford et al. demonstrated that PSA, mediated by DCs, induces the differentiation of naïve human CD4+ T cells into FOXP3+ Treg cells and significantly enhances the expression of CD39 on Treg cell surfaces (119). Upon activation by PSA, DCs upregulate molecules such as HLA-DR, CD86, CD40, and PD-L1, which promote the expression of FOXP3 and CD39 through direct contact with T cells.
5.4 Faecalibacterium prausnitzii
The abundance of Faecalibacterium prausnitzii is lower in patients with RA (120), whereas in healthy adults, F. prausnitzii constitutes 5–15% of intestinal bacteria (121). In a mouse model of RA, F. prausnitzii intervention reduced the levels of the pro-inflammatory cytokine IL-17, generated the metabolite butyrate, and improved the composition of the gut microbiota (122). Researchers identified a FOXP3-expressing, IL-10-secreting Treg subset in human colonic mucosa and blood, designated as DP8α based on its co-expression of CD4 and CD8α (123). This subset shares similarities with RORγt+ Treg, exhibiting a distinct hybrid profile of Tr1-like/cytotoxic CD4+ T cells. Besides demonstrating robust cytotoxicity, chemotaxis, and IgA-promoting capacity, the subset inhibits effector T-cell proliferation through CD39- and CD73-mediated purinergic metabolic pathways, thereby suppressing effector T-cell activity (124). The TCR on the surface of Tregs is more readily induced by Faecalibacterium prausnitzii within Clostridium cluster IV to trigger immunoregulatory responses (125). Additionally, this bacterium can induce dendritic cells to secrete anti-inflammatory cytokines IL-10 and IL-27 via the TLR2/TLR6 signaling pathway, differentiating into a “tolerogenic” phenotype that drives Tr1 cells differentiation and exerts immunosuppressive effects (126).
5.5 Prevotella
RA is associated with a relative expansion of the Prevotellaceae family in feces. Prior to the onset of RA, Prevotella species increased in individuals during the preclinical phase of RA (127). Colonization with P. copri exacerbates arthritis in a CIA model (128). However, unlike P. copri, P. histicola exhibits immunomodulatory properties and suppresses the production of inflammatory cytokines. Treatment with P. histicola significantly increased the number of CD103+ DCs in the intestinal lamina propria and spleen (129). These DCs possess immunomodulatory characteristics and can induce the differentiation of naïve CD4+ T cells into FOXP3+ regulatory T cells (Tregs) by secreting anti-inflammatory factors (such as IL-10) and expressing co-stimulatory molecules (such as CD80/86). Additionally, glucocorticoid-induced TNF receptor-related protein, which is highly expressed on the surface of Tregs, may maintain immune tolerance by inhibiting the mTOR pathway or promoting IL-10 secretion (130). A recent study found that P. histicola has a unique genetic sequence, and its unique outer membrane protein BtuB sequence may be the key to distinguishing it from pathogenic strains (131). The outer membrane protein is crucial in the interaction between bacteria and immune cells. The dual role of this flora reflects the complexity of intestinal microbial action. Due to the limitation of experimental level, it is not possible to identify and classify all strains, so more research is needed to clarify the classification of flora and its mechanism of action.
6 Gut microbial metabolites and Treg regulation
Intestinal microbes generate various metabolites through complex metabolic interactions that significantly affect various physiological processes within the host (132). In RA, gut microbiota metabolites can mediate communication between the commensal microbiota and the immune system, influencing the balance between anti-inflammatory Tregs and pro-inflammatory Th17 cell differentiation (133, 134).
6.1 Butyrate
SCFAs are primarily produced by specific subgroups of anaerobic bacteria, notably the members of the genera Clostridium, Eubacterium, and Butyrivibrio. Among these, Clostridium clusters IV and XIVa are efficient butyrate producers, with the dominant species Faecalibacterium prausnitzii and Roseburia spp., along with Anaerostipes and Eubacterium species, which play key roles (135). Additionally, dietary fiber serves as an appropriate substrate for the bacterial production of SCFAs (136).
Butyrate, a SCFA with anti-inflammatory and gut-barrier-regulating properties, serves as the primary energy source for colonocytes and plays a crucial role in the maintenance of intestinal homeostasis (137). The immunomodulatory effects on immune cells have attracted considerable attention. Butyrate can modulate T-cell differentiation and function while inhibiting the activation of myeloid cells such as dendritic cells, macrophages, and mast cells (138). As a canonical histone deacetylase (HDAC) inhibitor, butyrate enters cells either via passive diffusion or transmembrane proteins, directly binding to intracellular HDACs to inhibit their activity, or, at lower concentrations, is metabolized into acetyl-CoA to enhance histone acetylation (139). Specifically, butyrate upregulates FOXP3 expression by promoting histone H3 acetylation at the FOXP3 promoter and other conserved non-coding sequence regions within the FOXP3 locus, thereby inducing the differentiation of intestinal Tregs (140). Studies have suggested that butyrate-mediated Treg differentiation is dependent on the FOXP3 CNS1 enhancer (141). Da Som Kim et al. found that butyrate induces Treg expansion and production of the key anti-inflammatory factor IL-10 by inhibiting HDAC8 in T cells (142). Butyrate also induces differentiation of functional follicular regulatory T cells (TFR) directly in vitro, and also promotes histone hyperacetylation in the promoter region by inhibiting HDAC (143). On the other hand, butyrate enhances the differentiation and suppressive functions of FOXP3+ Tregs by activating GPR43 on Treg cells (144). Furthermore, butyrate, through a G protein-coupled receptor 43 (GPR43)-dependent mechanism, activates anti-inflammatory Treg cell responses in the colonic lamina propria. When the GPR43 gene was knocked out, the alleviation of inflammation diminished (145).
In addition to directly modulating Treg cell differentiation, butyrate also exhibits the capacity to regulate the expression of Treg cell-inducing molecules in epithelial cells or dendritic cells (DCs). For instance, it can stimulate epithelial cells to produce retinoic acid, a metabolite of dietary vitamin A, which serves as an essential cofactor for the generation of gut-specific Tregs by intestinal DCs (146, 147). Retinoic acid can induce the generation of antigen-specific Tr1 cells to prevent the occurrence and development of autoimmune diseases, and when combined with IL-2 it can enhance the induction (148). Furthermore, butyrate acts on DCs in the gut through its receptors, such as GPR109A and the butyrate transporter SLC5A8, to support DC-induced Treg cell differentiation (149).
Propionate and acetate are also natural HDAC inhibitors that can enhance lymphocyte activity and promote IL-10 production (150). However, their roles in RA remain poorly investigated. Studies have demonstrated that propionate alleviates disease symptoms in CIA mice, and in vitro experiments indicate that propionate upregulates FOXP3 gene expression and IL-10 production in T cells (151). Acetate has been found to facilitate the development and maturation of Treg cells in fetal mice (152), but its function in RA remains unexplored.
6.2 Bile acids
BA metabolism is mediated by bacteria with bile salt hydrolase activity, primarily Lactobacillus, Bifidobacterium, Clostridium, and Bacteroides (153, 154). These secondary bile acids (SBAs), generated through gut microbial metabolism, are involved in intestinal inflammatory responses (155). Numerous studies have elucidated the immunomodulatory properties of BAs within the gut (156–158). In RA models, BAs inhibit NLRP3 inflammasome activation and reduce the release of pro-inflammatory cytokines (such as IL-1β and IL-6) by binding to and activating the TGR5 receptor, thereby triggering the downstream cAMP-PKA signaling pathway (159).
BAs are signaling molecules that modulate immune homeostasis and exert control over host immune responses through a mechanism involving direct regulation of the balance between Th17 and Treg cells by BA metabolites. Primary BAs such as cholic acid and chenodeoxycholic acid (CDCA), are directly synthesized in the liver, whereas SBAs such as deoxycholic acid (DCA) and lithocholic acid (LCA), are generated via metabolic transformation by the gut microbiota. The positional arrangement of hydroxyl groups (α or β configuration) and the stereochemistry of the rings create structural variations in BAs, leading to the formation of diverse derivatives (160). Hang et al. screened over 30 BA metabolites and identified an LCA derivative, isoallolca, which enhanced Treg cell differentiation (161). Their findings revealed that isoallocalcin promotes Treg differentiation by augmenting mitochondrial reactive oxygen species (mitoROS) production, thereby increasing H3K27 acetylation in the FOXP3 promoter region. This process is regulated by the conserved non-coding enhancer CNS3 and requires TGF-β-induced signaling. Li et al. (156) further discovered that isoalloLCA increases the binding of the nuclear receptor NR4A1 to the FOXP3 locus, leading to enhanced FOXP3 gene transcription and subsequent Treg cell differentiation. Another DCA derivative, isoDCA, inhibits the immunostimulatory properties of dendritic cells (DCs) by antagonizing the activity of the farnesoid X receptor, shifting the balance toward immune tolerance and promoting the expansion of peripheral RORγt+ Treg cells in the colon. This process is dependent on CNS1 rather than on CNS3 (158).
6.3 Tryptophan
Tryptophan can be metabolized through two major pathways: kynurenine (Kyn) and indole. An imbalance in the kynurenine pathway, characterized by an increase in pro-inflammatory metabolites (such as QUIN) and a decrease in anti-inflammatory metabolites (such as KYNA and XANA), promotes synovial inflammation, cell proliferation, and joint destruction (162). Kynurenine is recognized as an endogenous ligand of the AhR and can activate AhR (163). Upon activation, AhR can facilitate the induction and differentiation of peripheral Tregs through the modulation of TGF-β and IL-2 signaling pathways (164). Tryptophan deficiency (such as excessive tryptophan consumption by IDO1/TDO enzymes in the tumor microenvironment) can directly trigger an increase in the transcription and protein expression of the AhR (165). Simultaneously, tryptophan depletion activates GCN2 kinase, which triggers the downstream transcription factor ATF4, subsequently upregulating amino acid transporter LAT1 (SLC7A5). This leads to a significant increase in kynurenine uptake, which further activates the AHR pathway. This dual sensitization enhances the induction of Tregs.
Furthermore, the indole pathway is highly dependent on the gut microbiota (166). Jiang et al. found that sinomenine treatment can elevate the levels of metabolites such as indole-3-acrylic acid (IA), indole-3-propionic acid (IPA), and indole-3-acetic acid (IAA) through the gut microbiota, thereby modulating tryptophan metabolism and activating AhR to regulate the Treg/Th17 balance, improving RA (167). In vitro experiments have also demonstrated that IAA can reduce the ubiquitination of FOXP3 through the AhR-TAZ-Tip60 pathway, promote the differentiation of Treg cells (168).
6.4 Other metabolites
Polyamine metabolites are abundant in the gut and can contribute to gut immunity (169). Spermidine, an antioxidant, can protect chondrocytes from IL-1β-mediated ferroptosis in rheumatoid arthritis (170). An in vitro experiment showed that spermidine can promote the differentiation of naive T cells into Tregs and upregulate the expression of FOXP3 (171). Furthermore, the gut microbiota produces hydrogen sulfide, a gaseous metabolite that enhances the expression of Tet1 and Tet2. This process catalyzes the conversion of 5-methylcytosine (5mC) to 5-hydroxymethylcytosine (5hmC) in FOXP3, establishing a Treg cell-specific hypomethylation pattern and stabilizing FOXP3 expression (172). However, the impact of these metabolites on Tregs has not been confirmed in RA animal models or clinical studies. These metabolites could potentially offer a promising avenue for future RA treatment.
7 Interactions among gut microbiota
There are interactions among microorganisms in the gut, which are dynamic and environment-dependent. These interactions encompass multiple aspects, including positive effects, such as cooperation, commensalism, and cross-feeding; and negative effects, like interference competition (173). Multiple clinical studies have found that probiotic supplements containing a mixture of various strains have improved the clinical symptoms of RA patients (174–176). These mixed strains are mainly Lactobacillus species. Further research found that the mixed strains of Lactobacillus acidophilus could restore the abundances of Lactobacillus and Clostridium in CIA rats and increase the content of the metabolite butyric acid (177). Moreover, the mixed strains were more effective than single strains. Ho - Keun Kwon et al. used a probiotic mixture of five strains, including Lactobacillus acidophilus, Lactobacillus casei, Lactobacillus reuteri, Bifidobacterium bifidum, and Streptococcus thermophilus, to intervene in RA mice. This intervention increased the level of FOXP3 in T cells, thereby increasing the number of CD4+FOXP3+ Tregs and inducing the regulatory dendritic cells (rDCs) to express high levels of IL - 10 and TGF - β, thus promoting the differentiation of FOXP3+Tregs (178). Such probiotics are the main sources of short-chain fatty acids and bile acids. The intervention of multiple strains may enhance the promotion of Tregs to improve RA. Therefore, determining the types and dosages of strains for combined use that can have a better effect on Treg cells and thus improve the therapeutic efficacy may be a direction for further research in the future.
Microbial metabolites also interact with each other in the gut. For example, bile acids and SCFAs may jointly participate in the regulation of cell proliferation through interrelated signaling pathways. They may have different effects at different concentrations. At high concentrations, SCFAs have anti - inflammatory effects, while secondary bile acids have pro - inflammatory effects (179). However, the interaction mechanism of multiple metabolites in the RA model has not been explored. More research designs are needed to investigate the network effects of co-existing metabolites.
8 Factors influencing the interaction between the gut microbiota and Tregs
8.1 Diet
Diet is considered the primary environmental factor influencing the gut microbiota. Therefore, diet-induced alterations in the microbiota can induce changes in host physiology (180). Fopei Ma et al. found that diet affects the inflammation of rheumatoid arthritis (RA) in mice through the circadian fluctuations of gut microbiota, and altering the diet timing reduces the anti - inflammatory effect (181). Teresina Laragione et al. found that a high-magnesium diet increased the number of Treg cells and alleviated the severity of arthritis in mice through an IL - 10-dependent manner mediated by gut microbiota (182). Among them, the level of Prevotella decreased, while the levels of bacteria such as Bacteroides increased.
In addition, a high-fiber diet rich in resistant starch (RS) increases the abundance of Bacteroides and circulating propionate, thereby promoting the increase of Treg cells and the production of IL-10 and improving arthritis in CIA mice (151). Ddietary fiber can also induce the biosynthesis of bile acids (183). The study summarizes that the Mediterranean diet rich in n-3 PUFAs, polyphenols, dietary fiber, and probiotics can regulate the gut microbiota. In particular, it can increase the content of short-chain fatty acids, reduce systemic inflammation, and improve the intestinal barrier function, thereby improving the prognosis of RA (184, 185).
Diet may promote the differentiation and function of Treg by enhancing the healthy metabolism of gut microbiota. Therefore, regular and healthy diet can restore the disrupted gut microbiota, regulate metabolism, and further promote the immunosuppressive function of Treg. However, another study found that the combination of a high-fiber diet and Prevotella could exacerbate the arthritis symptoms in RA mice, possibly because Prevotella leads to the overproduction of pro-inflammatory metabolites such as succinate (128). It is necessary to further determine that different doses and individual differences may yield different outcomes for the disease.
8.2 Other lifestyle
Exercise is considered to improve gut microbial health, and moderate aerobic exercise can increase the abundance of beneficial bacteria such as Bifidobacterium (186). Maintaining regular schedules and increasing sleep time may contribute to the stability of gut microbiota and gut health (187). Psychological stress can alter the composition of gut microbiota, reducing the abundance of some beneficial bacteria like Lactobacillus (188). Tobacco reduces the diversity of gut microbiota. Studies have shown that nicotine leads to an increase in Proteobacteria and Bacteroidetes and a decrease in Actinobacteria and Firmicutes in the mouse gut (189). Alcohol is also an important factor damaging the gut microbial environment. Research indicates that alcohol causes excessive growth of gut bacteria in mice, especially Enterobacteriaceae, thereby triggering gut inflammation (190). Therefore, a healthy lifestyle can enhance the abundance of beneficial bacteria, which are believed to promote the differentiation and function of Treg cells. However, further experimental studies are needed to clarify their correlation.
8.3 Drugs
Traditional anti - rheumatic drugs can regulate the gut microbiota to exert their effects (191). However, studies have found that most traditional anti - rheumatic drugs fail to increase the abundance of relevant flora and metabolites. After MTX intervention, the abundance of Bacteroides fragilis in mice decreased (192). Nevertheless, the absence of Bacteroides fragilis can make MTX treatment ineffective in CIA mice (117). This may be due to beneficial bacteria metabolizing to help drugs work.
Although antibiotics have been proven to reduce the abundance of RA-related pathogens (such as Prevotella copri) and short-term treatment can help alleviate inflammation (193), they may cause a decrease in gut microbiota diversity, changes in metabolic activities, and antibiotic resistance (194). Moreover, supplementing probiotics during antibiotic treatment cannot change the diversity index of the gut microbiome (195).
8.4 Chinese medicine
Traditional Chinese medicine can also regulate the immune system through the action of intestinal microorganisms to prevent RA (196). The herbal extract madecassoside promotes differentiation of Treg cells and expression of FOXP3 and IL-10 in mice by regulating intestinal flora and increasing butyric acid levels (197). Total Glucosides of Paeony up-regulated beneficial bacteria abundance and treg cell levels in CIA mice (198) [xx3]. Treatment with Fuzi increased bile acid content in CIA mice (199). In addition, the relative abundance of actinomycetes and lactobacillus in RA mice was significantly increased after acupuncture treatment, and such flora could increase the level of Treg cells (200).
9 Prospects for microbial therapy in RA
In the clinical treatment of RA, therapies targeting gut microbiota can help improve clinical symptoms in RA patients, including probiotic supplementation, prebiotics and fecal bacteria transplantation (134). But there are still a lot of challenges (1). Due to factors such as age, lifestyle, and eating habits, the intestinal flora changes dynamically and has significant individual differences (201), and the uncertainty about the differences between strains and doses makes it difficult to formulate standard personalized treatment plans (2). Probiotics are highly susceptible to environmental influences, and their stability in production, storage and transportation needs to be improved. However, the pharmaceutical development of butyrate faces challenges owing to its pungent odor, limited intestinal absorption, and rapid metabolic clearance as an energy substrate (202). To circumvent these limitations, serine-conjugated butyrate prodrugs have been developed via esterification. Experimental evidence demonstrated that this prodrug formulation enhances bioavailability while effectively modulating key immune cell populations in rat by reducing Th17 cell prevalence and promoting Treg differentiation (203) (3). The first-pass effect of liver and intestinal barrier limit the absorption and entry of metabolites into systemic circulation, and the chemical stability, hydrophilicity and lipophilicity of metabolites also affect systemic delivery efficiency. How to improve their bioavailability is the key issue to improve probiotic therapy (4). Due to the above reasons, the current clinical studies on intestinal microbial RA are of low quality. Most of them only observe their simple efficacy, which makes it difficult to deeply explore the true effect of intestinal microorganisms on Treg in human body. Therefore, there is insufficient evidence to prove its effectiveness and mechanism of action.
10 Conclusions and perspectives
Immunological imbalance is a critical mechanism underlying the pathogenesis of RA. Enhancing the induction of Tregs and maintaining their cellular function and homeostasis can ameliorate the immune imbalance in RA. The gut microbiota can enhance Treg induction and promote immunosuppressive functions. This process primarily occurs by promoting the differentiation of dendritic cells into tolerogenic DCs and inducing the differentiation of CD4+ T cells into Tregs. Increased secretion of anti-inflammatory factors during this process, especially IL-10, allows these beneficial bacteria to provide an anti-inflammatory environment for Treg differentiation and maturation. Additionally, the gut microbiota can directly or indirectly influence Treg surface proteins and intracellular transcription factors through metabolites, thereby strengthening the immunosuppressive pathways (Figure 2). In summary, modulation of the gut microbiota can regulate the overall immune environment, increase the secretion of anti-inflammatory factors, and help mitigate the overall inflammatory milieu. Multiple pathways further enhance the anti-inflammatory effects of Tregs, thereby improving the immune imbalance in RA. A healthy diet and lifestyle can improve symptoms by promoting the action of beneficial bacteria on Treg (Figure 3).
Figure 2
The intestinal microbiota and their metabolites can enhance the homeostasis and functionality of Tregs through direct cellular contact-mediated mechanisms. Concurrently, they promote the differentiation of regulatory DCs, which subsequently stimulate CD4+ T cells to preferentially differentiate into Tregs. Distinct arrow colors are utilized to delineate the differential regulatory pathways mediated by specific microbial taxa or metabolites. (TLR, Toll-like receptor; CSGG, cell surface glucan/galactan; PSA, polysaccharide A; PD-1, programmed cell death protein 1; GPR, G-protein-coupled receptors; TGR-5, Takeda G protein-coupled receptor 5; FXR, Farnesoid X Receptor).
Figure 3
Factors influencing the interaction between the gut microbiota and Tregs.
However, the gut microbiota comprises a wide variety of strains, and the microbiota composition varies significantly among individuals and exhibits dynamic changes. These factors limit in - depth exploration of the direct mechanism by which the microbiota acts on Treg. In the future, more in - vivo and in - vitro experiments are needed to explore more specific mechanisms of Treg, and these mechanisms should be verified in clinical research for translation into clinical practice.
Statements
Author contributions
XX: Writing – review & editing, Writing – original draft. JZ: Writing – review & editing, Writing – original draft. HX: Writing – original draft. RZ: Writing – original draft. BG: Writing – original draft. LL: Writing – review & editing, Funding acquisition. ML: Funding acquisition, Writing – review & editing. XC: Writing – review & editing, Resources.
Funding
The author(s) declare that financial support was received for the research and/or publication of this article. This work was supported by National Natural Science Foundation of China (82274627), the science and technology innovation Program of Hunan Province (No. 2024JK2132, 2024RC1061), the National Administration of Traditional Chinese Medicine 2022 Young Qihang Scholar Training Project (State Administration of Traditional Chinese Medicine Letter (2022) No. 256). Hunan Provincial Natural Science Foundation General Project (2025JJ50569).
Acknowledgments
The authors thank the editor and the reviewers for the insightful suggestions and comments. And give heartfelt thanks to all the people who have ever helped with this paper.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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Summary
Keywords
gut microbiota, metabolites, rheumatoid arthritis, regulatory T cells, autoimmune
Citation
Xu X, Zhou J, Xie H, Zhang R, Gu B, Liu L, Liu M and Chang X (2025) Immunomodulatory mechanisms of the gut microbiota and metabolites on regulatory T cells in rheumatoid arthritis. Front. Immunol. 16:1610254. doi: 10.3389/fimmu.2025.1610254
Received
11 April 2025
Accepted
23 June 2025
Published
07 July 2025
Volume
16 - 2025
Edited by
Fabrizio Bruschi, University of Pisa, Italy
Reviewed by
Yunliang Yao, Huzhou University, China
Tara Fiyouzi, Complutense University of Madrid, Spain
Updates
Copyright
© 2025 Xu, Zhou, Xie, Zhang, Gu, Liu, Liu and Chang.
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: Li Liu, 26134591@qq.com; Mi Liu, newmean@hnucm.edu.cn; Xiaorong Chang, xrchang1956@163.com
Disclaimer
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