Qi Jiang
Guocan Yang
Fan Xiao
Jue Xie
Shengjun Wang
Liwei Lu
Dawei Cui- 1Department of Blood Transfusion, Shaoxing People’s Hospital (Shaoxing Hospital, Zhejiang University School of Medicine), Shaoxing, China
- 2Department of Pathology and Shenzhen Institute of Research and Innovation, The University of Hong Kong; Chongqing International Institute for Immunology, Chongqing, China
- 3Department of Blood Transfusion, The First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China
- 4Department of Laboratory Medicine, The Affiliated People’s Hospital, Jiangsu University, Zhenjiang, China
- 5Department of Immunology, Jiangsu Key Laboratory of Laboratory Medicine, School of Medicine, Jiangsu University, Zhenjiang, China
Upon antigenic stimulation, naïve CD4+T cells differentiate into different subsets and secrete various cytokines to exert biological effects. Th22 cells, a newly identified CD4+T cell subset,are distinct from the Th1, Th2 and Th17 subsets. Th22 cells secrete certain cytokines such as IL-22, IL-13 and TNF-α, but not others, such as IL-17, IL-4, or interferon-γ (IFN-γ), and they express chemokine receptors CCR4, CCR6 and CCR10. Th22 cells were initially found to play a role in skin inflammatory diseases, but recent studies have demonstrated their involvement in the development of various autoimmune diseases. Here, we review research advances in the origin, characteristics and effector mechanisms of Th22 cells, with an emphasis on the role of Th22 cells and their main effector cytokine IL-22 in the pathogenesis of autoimmune diseases. The findings presented here may facilitate the development of new therapeutic strategies for targeting these diseases.
Introduction
CD4+ T cells mainly include Th1, Th2, Th17, Th9, Th22, follicular helper T (Tfh) cells and regulatory T (Treg) cells (1–4), and they were initially divided into two categories: Th1 and Th2 cells (5). This classification does not explain the pathogenesis of certain diseases; for example,neutralizing or eliminating IL-12 or Th1 cells and the cytokine IFN-γ could not prevent or alleviate experimental autoimmune encephalomyelitis (EAE) and collagen-induced arthritis (CIA); however, the discovery of Th17 cells explains this paradox. Th17 cells do not express IL-4 or IFN-γ but secrete IL-17 at a high level (6, 7). Previous studies have shown that both Th17 and Th1 cells secrete IL-22 (8, 9). A recent report identified that a group of special T cell subsets that could secrete IL-22 and IL-13 but not IL-17 and IFN-γ (10). Mouse T lymphoma cells stimulated with IL-9 expressed a cytokine very similar to the secondary structure of IL-10, and it is named interleukin-10-related T cell-derived inducible factor (IL-TIF) (11). Further studies identified a new sequence from human T cells that encodes 23% amino acids homologous to IL-10 and is 87% similar to IL-TIF, and it is named IL-22 (12). The expression of IL-22 has been suggested to be associated with Th1 (8, 13) and Th17 cells (9, 14). However, Th22 cell clones in the induced environment of Th1, Th2, Th17 and Treg cells do not secrete their characteristic cytokines but can secrete IL-22, which demonstrates that Th22 cells represent an independent T cell subset. It is named Th22 because of its high level of IL-22 secretion (15). Plank et al. performed a whole gene chip analysis and found differences between Th22 and Th17 cells, and they determined that Th22 cells were an independent cell lineage (16).
Th22 cells can differentiate into Th1 or Th2 cells under appropriate conditions. In an in vivo IFN-γ-rich inflammatory microenvironment or in vitro Th1-promoting conditions, Th22 cells have obvious plasticity. In an in vitro Th2 culture environment, Th22 cells showed increased secretion of IL-13 (16). The conditions for the transformation between Th22 and Th17 cells have not been clarified (17). Since other cells, such as Th17 cells, also secrete IL-22, the identification of Th22 cells is particularly important. Mousset et al. suggested that when using flow cytometry to identify Th22 cells, Th22 cells can be identified by integrating cell surface markers (CCR4+, CCR6+ and CCR10+), combining cell transcription factors (AhR+ and/or STAT3+) and/or cytokine staining (IL-22+), and requiring IFNγ-, IL- 4-, IL-9-, IL-10- and IL-17- (18). Here, we review the characteristics and effector mechanisms of Th22 cells, with an emphasis on the role of Th22 cells and their main effector cytokine IL-22 in the pathogenesis of autoimmune diseases, including rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), psoriasis,multiple sclerosis (MS), immune thrombocytopenia (ITP), immunoglobulin A nephropathy (IgAN), autoimmune hepatitis (AIH), autoimmune thyroid diseases (AITD), myasthenia gravis (MG), and systemic sclerosis (SSc).
Characteristics of Th22 Cells
Th22 cells secrete IL-22, IL-13, IL-26, TNF-α and granzyme B but not IL-17, IFN-γ or IL-4 (16). Activation of the transcription factor aryl hydrocarbon receptor (AhR) significantly promotes the differentiation of naïve CD4+T cells into Th22 cells (19). The expression of the signature cytokines and transcription factors of Th1, Th2 and Th17 cells was absent in Th22 cells (10, 15, 19). Th22 cells are abundant in human skin and play important roles in epidermal wound healing (15). These cells are tissue homing CD4+T cells and exhibit anti-inflammatory, antibacterial and antiviral activities. Emerging evidence has shown the critical roles of Th22 cells in allergies, autoimmune diseases, intestinal diseases and tumors (20–22).
IL-22 is the main effector molecule of Th22 cells and belongs to the IL-10 family, and it acts by binding to IL-22 receptors which are composed of IL-22R1 (main high affinity chain) and IL-10R2 (helper receptor chain) subunits (23). IL-22R1 is mainly expressed in nonhematopoietic organs, such as the skin, lung,intestine and pancreas, but not in lymphoid organs including thymus, bone marrow and spleen (24). IL-22 has little effects on immune cells, and mainly acts on mucosal barriers of skin,respiratory system and digestive system. IL-22 binding protein (IL-22BP) or IL-22RA2, the soluble receptor of IL-22, is expressed in various tissues around the lung, colon and breast. IL-22BP blocks the binding of IL-22 to IL-22R and is the receptor antagonist of IL-22 (25). IL-22 can also be produced by lymphoid cells, including Th17 cells, innate lymphocytes (ILCs), dermis γδ T cells, Tc17 cells, nonlymphatic macrophages (26), neutrophils (27–29) and even fibroblasts of RA patients (28, 30–33). IL-22 in the intestine is mainly produced by ILCs. ILCs migrate from mucosal associated lymphoid tissue to the lamina propria after stimulation (12). γδT cells are the primary source of IL-22 in the skin, intestinal tract, lung, reproductive tract and other epithelial tissues, where they respond quickly to exotic pathogens at an early stage (34, 35). Moreover, IL-22 can induce the production of different antimicrobial proteins by keratinocytes, intestinal epithelial cells,bronchial epithelial cells and other different parts of the human body (36). In addition, IL-22 can directly act on endothelial cells through the activation of STAT3 and ERK pathways,stimulate endothelial cell proliferation and migration,and stimulate angiogenesis (37). IL-22 can also act on colonic subepithelial myofibroblasts (SEMFs) to produce inflammatory mediators such as chemokines, inflammatory cytokines and matrix metalloproteinases (MMPs) (38).
The binding of IL-22 to IL-22R activates downstream signal transduction (Figure 1) (39). IL-22 transmits phosphorylation signals downstream through Janus kinase (JAK) 1 and tyrosine kinase (TYK) 2, including the mitogen-activated protein kinase (MAPK) pathway (p38 kinase, ERK1/2, MEK1/2 and JNK),STAT3, STAT1 and STAT5 (39–41). Similar to other members of the IL-10 family, IL-22 phosphorylates STAT3 mainly at Ser727 and Tyr705 (23, 42, 43). IL-22 is also unique in that it induces the phosphorylation of serine residues in addition to tyrosine residues, and activates the ERK1/2 pathway (40), whereas IL-10 induces the phosphorylation of tyrosine residues on STAT3. This difference may be caused by the difference inreceptor R1. The binding of SRC homologous phosphatase 2 (Shp2) to Tyr-251 phosphorylation residues and the activation of IL-22R1 on Tyr-301 are necessary for the activation of STAT3 (39, 44). Moreover, the phosphorylation of STAT3 is essential for IL-22 to exert its effects on epithelial cells (45). IL-22 also induces the expression of suppressor cytokine signaling1 and 3 (SOCS1/3), which in turn inhibits the activity of STAT3 (39). Activation of STAT1 and/or STAT5 can be observed in tumors (46–48). IL-22 can also activate the PI3K-Akt-mTOR pathway, which is essential for the migration of hepatocytes and colonic epithelial cells (39, 49). The activation of Akt is important for the proliferation of human fibroblast-like synoviocytes and epidermal keratinocytes (50). IL-22 induces osteoclast formation in RA by p38MAPK/NF-κB and JAK2/STAT3 signaling (51).
Figure 1 Signaling pathways mediated by IL-22. The IL-22 receptor complex consists of IL-22R1 and IL-10R2. By binding to its receptor, IL-22 activates TYK2 and JAK1and triggers multiple intracellular pathways, including p38MAPK, MEK1/2, ERK1/2 and AKT, by phosphorylating serine and tyrosine in STAT3, STAT1 and STAT5, which can ultimately lead to immune homeostasis. IL-22BP is a soluble receptor antagonist that specifically neutralizes the activity of IL-22. AhR, aryl hydrocarbon receptor; APCs, antigen-presenting cells; JAK1, Jenus kinase 1; TYK2, tyrosine kinase 2; MAPK, mitogen-activated protein kinase; IL-22BP, IL-22 binding protein.
Differentiation of Th22 Cells
The differentiation of Th22 cells is regulated by many factors,which are different from other CD4+T cell subsets including Th1, Th17 and Tfh cells (Figures 2A, B). Both IL-6 and TNF-α can induce the differentiation of Th22 cells, IL-6 alone drives the differentiation of naïve CD4+T cells into Th22 cells. TNF-α further promotes the differentiation of Th22 cells induced by IL-6, while a high dose of TGF-β inhibits the differentiation of Th22 cells (10). In the presence of anti-IL-4/IFN-γ, IL-17A secretion still occurs when combined with IL-6,IL-23, IL-1β and 6-formylindolo (3, 2-b) carbazole (FICZ). The TGF-βR inhibitor (galunisertib) effectively inhibits the production of IL-17Abutdoes not affect the secretion of IL-22. Under this culture condition, the levels of IL-13 and granzyme B also increase significantly. Under this culture condition,the levels of granzyme B and IL-13 also increased significantly (16). IL-21 alone or in combination with IL-1β or IL-23 can induce Th22 cell differentiation and IL-22 expression (52). Many reports show that differentiated Th22 cells can be identified by integrating cell surface markers (CCR4+, CCR6+ and CCR10+) or its correlated intracellular cytokines including IL-22+, IL-17- and IFN-γ- (Figure 3) (15–19).
Figure 2 Regulation of Th22 cells differentiation. (A) The diagram illustrates the differentiation of Th cell subsets from naïve CD4+ T cells. (B) IL-21, IL-21 combined with IL-23 or IL-1β can induce the differentiation and IL-22 expression of Th22 cells; IL-6 and TNF-α secreted by DCs or external IL-6 or IL-6 and TNF- α can promote the differentiation of naïve CD4+T cells into Th22 cells, and IL-1β promotes the differentiation; IL-6, IL-23, IL-1β, FICZ and TGF-βR inhibitor can promote the differentiation of naïve CD4+T cells into Th22 cells. Both TGF-β and T-bet inhibit the expression of IL-22 in Th22 cells.
Figure 3 Schematic diagram illustrates the flow cytometric analysis of Th22 cells. Th22 cells are identified as CD3+CD4+IL-17-IFN-γ-IL-22+, as well as high expressions of CCR4,CCR6 and CCR10.
In addition,plasmacytoid-like dendritic cells (pDCs) could induce Th22 cells more strongly than conventional dendritic cells (cDCs), and both of them release high concentrations of TNF-α and IL-6 after activation. Blocking TNF-α and IL-6 inhibited 70% of Th22 cells in culture, which indicates that DCs may promote Th22 differentiation in both direct and indirect ways (10). Foreign antigens, such as microorganisms,can also activate DCs. After stimulation by the serotypes of A. actinomycetemcomitans, the levels of AhR and IL-22 in T lymphocytes were increased,and the levels of TNF-α and IL-6 in DCs were significantly increased. This type of actinomycete can trigger the polarization of Th22 cells, which may be an important part of the subgingival biofilm (53). Langerhans cells (LCs) from the human epidermis and dermis can also induce naïve CD4+T cells and peripheral blood T cells to differentiate into Th22 cells,and the effect of LCs on the epidermis is stronger than that of dermal DCs (54). Endogenous TLR4 ligands stimulate keratinocytes to secrete IL-23 which activates DCs and induces the differentiation of Th22 cells and IL-22 production (55). Activated B cells and initial T cells significantly inhibit the expression of RORγt and the production of IL-17, but significantly increase the differentiation of Th22 cells and the production of IL-22 by cultured Th17 cells in vitro. Further in vivo experiments showed that MRL/lpr lupus mice treated with activated B cells exhibited reduced levels of anti-dsDNA antibody and urinary protein. Meanwhile, Th17 cell differentiation was inhibited and Th22 cell differentiation was enhanced in these mice (56).
AhR is an important transcription factor in the differentiation of Th22 cells. However, the expression of IL-22 in naïve CD4+T cells was reduced in the absence of RORc (γt) but increased in Tbx21-deficient cells. Therefore, RORγt is considered a positive regulator of Th22, while T-bet is considered a negative regulator (16). Runt-related transcription factor 3 (RUNX3) is a runt-domain family transcription factor. The number of Th22 cells decreased significantly with the inhibition of RUNX3 (57). Recent studies have shown that miR-31 mimic transfection can increase the levels of AhR and IL-22 and promote the differentiation of Th22 cells in coronary heart disease. Overexpression of miR-31 promotes the differentiation of Th22 cells by inhibiting the BTB domain and CNC homolog-2 (Bach2) pathway (58). Medroxyprogesterone acetate (MPA) can also enhance the Th22 cell response and decrease the expression of Th1 and Th17 cell signature genes by activating AhR signaling, thus affecting susceptibility to inflammatory diseases and infectious diseases (59).
Th22 Cells in Autoimmune Diseases
Recent studies have shown that Th22 cells play a regulatory role in the initiation and development of many diseases, such as kidney disease (60), cardiovascular disease (61), tumors (62) and infectious diseases (63). IL-22, the main effector of Th22 cells,also exerts different functions in different autoimmune diseases. Cytokines of the IL-10 family mainly act on interstitial cells and tissue epithelial cells, which can promote the proliferation and repair of tissues and organs, protect the integrity of the barrier, and play a patrolling role (23). These cytokines have both proinflammatory and anti-inflammatory functions. Here, the roles of Th22/IL-22 in the pathogenesis of autoimmune diseases are reviewed (Table 1).
Table 1 Dual role of Th22/IL-22 in autoimmune diseases.
RA
RA is a common autoimmune disease that is characterized by uncontrolled joint inflammation, bone erosion and cartilage damage. The levels of Th22 cells, Th17 cells and IL-22 in patients with RA were significantly higher than those in healthy controls. The numbers of Th22 cells were positively correlated with the IL-22 levels. Moreover, the percentages of Th22 cells and Th17 cells were positively correlated with the disease activity score in 28 joints (DAS28) scores and C-reactive protein (CRP) levels in RA patients (20, 64, 65). Not only did the levels of IL-17 and IL-22 in plasma increase, but the levels of IL-17 and IL-22 in the subchondral bone marrow of patients with RA were also significantly higher than those in plasma. The percentage of Th1,Th17 and Th22 cells and the levels of IL-17 and IL-22 in bone marrow were also positively correlated with DAS28 (95). The frequency of Th22 and Th17 cells in peripheral blood and the levels of IL-22, IL-17 and IFN- γ in plasma were decreased in RA patients who received effective treatment with methotrexate and leflunomide, although significant changes were not observed in patients with nonresponsive RA (96).
However,there are different views on whether Th22/IL-22 is involved in T cell-mediated synovitis. Researchers have found that the disease severities of wild-type mice and IL-22-deficient mice are comparable to those of T cell-mediated arthritis,Th17 cells have a strong effect on synovial fibroblasts while targeting Th17 cells and IL-17A but not Th22/IL-22 has been suggested as a focus treatment for T cell-mediated synovial inflammation (97). Recently, IL-22 neutralization was shown to inhibit osteoclast formation. Th22 cells promote osteoclast differentiation by producing IL-22 and play an important role in bone destruction in patients with RA (98). High levels of IL-22 in synovial tissue induce the proliferation of synovial fibroblasts and produce chemokines to enhance the inflammatory response of synovial tissue (29). IL-22 also induces osteoclast formation by inducing the p38MAPK/NF-κB and JAK2/STAT3 signaling pathways in synovial fibroblasts. Moreover, Th22 cells migrate to synovial tissues, which might be associated with the high expression of C-C chemokine ligand 28 (CCL28) in RA patients (98). IL-22 induces osteoclast formation by p38MAPK/NF-κB and JAK2/STAT3 signaling in RA development (51). In an animal model of CIA, blocking chemokine receptors was able to effectively inhibit the progression of RA. After treatment with the selective CXCR3 antagonist AMG487, the percentage of Treg cells in CIA mice was increased while the percentages of Th1, Th17 and Th22 cells were decreased. The expression of T-bet, IL-17A, IL-22 and RORγt was down-regulated, and the expression of Foxp3 was up-regulated. Chemokine receptor antagonists have been suggested as an effective strategy for the treatment of RA (99). Current studies support the hypothesis that Th22/IL-22 plays a pathogenic role in RA pathogenesis, although this mechanism requires further study. Blocking IL-22 may serve as a novel effective therapeutic method for the treatment of the disease.
SLE
SLE is another common autoimmune disease that is characterized by increased autoantibodies and immune disorders leading to tissue and organ damage. The role of Th22 cells in SLE is still controversial. Zhao et al. found that the plasma levels of IL-17A and IL-22 in patients with SLE were higher than those in healthy controls, and they showed that Th17 and IL-22 levels were positively correlated with the SLE disease activity index (SLEDAI), indicating that IL-22 and IL-22+CD4+ T cells play an important role in the pathogenesis of SLE (66). In 2014, the team further found that the levels of IL-22 and IL-22+CD4+ T cell before and after immunosuppressant and glucocorticoid (GC) treatment did not differ compared with the healthy controls (100). In 2017, this group also found that the levels of CCR6+ T cells, CCR6+Th22 cells and plasma IL-22 increased in SLE patients. The percentage of Th22 cells was positively correlated with the area of lupus erythematosus and the severity index (RCLASI) of the skin. The percentage of Th22 cells in SLE patients with renal damage was positively correlated with ESR, suggesting that CCR6+ Th22 cells may be a therapeutic target for SLE treatment (67). Defects in TGF-β1 signaling in patients with active SLE are also associated with the over-production of IL-22 (101). Yang et al. found that the IL-22 levels increased in MRL/LPR mice while treatment with anti-IL-22 monoclonal antibody significantly decreased the urinary protein, urea nitrogen and serum creatinine in these mice (68). Moreover, Th22 cells might be a better predictor of SLE tissue involvement than Th17 cells (102). Other studies have shown that the level of IL-22 is decreased in patients with SLE (69–71) and significantly lower in patients with primary SLE (70). Urinary IL-22 mRNA levels are decreased in SLE patients with proliferative glomerulonephritis. IL-22 mRNA can also be used to evaluate the activity of lupus nephritis (71). In Chinese SLE patients, IL-22 gene polymorphisms may increase susceptibility to SLE by reducing the expression of IL-22 (103). In addition, recent studies have shown that activated B cells suppress the development of lupus by promoting Th22 cell differentiation and inhibiting Th17 (56). These results show that both Th22 cells and IL-22 levels are related to SLE; however, the exact mechanism is still unclear. Moreover,these studies show that IL-22 levels differ at different stages of SLE (70) and indicate its involvement in tissue inflammation and damage to different organs (102). The currently available results suggest the complexity of IL-22 and the heterogeneity of SLE, which needs to be further explored.
PSORIASIS
Psoriasis is a chronic inflammatory autoimmune disease mediated by T cells, and it is characterized by the abnormal proliferation of keratinocytes. IL-22 is considered an activator of keratinocyte over-proliferation (104, 105). The levels of Th22 cells and plasma IL-22 in patients with psoriasis are increased and positively correlated with the severity of the disease (72–74). High levels of IL-22 can induce the expression of antimicrobial proteins (AMPs), antimicrobial peptides such as S100A7,S100A8, S100A9 and β-defensin, and neutrophil chemoattractants CXCL8, CXCL5 and CXCL1 in the epidermis (106, 107). It can also inhibit keratinocyte differentiation, interfere with the normal skin healing process, and induce the production of MMPs, which is conducive to extracellular tissue degradation (108, 109). IL-22 also induces dermatitis and acanthosis by activating the STAT3-mediated IL-23 pathway (9, 110). In addition, IL-22 neutralizing antibody treatment decreased antimicrobial peptide levels and inhibited disease development in a psoriasis mice model, suggesting the therapeutic potential of IL-22 inhibitors in psoriasis (111).
Psoriasis is characterized by recurrent lesions in the same anatomic area. New lesions appear in areas that have healed after successful treatment because even if the psoriatic plaque disappears, tissue resident memory cells (TRMs) are still present in the skin (105, 112). In the active stage of psoriasis,the expression of IFN-γ, IL-17A and IL-22 in CD4+ and CD8+ T cells in the epidermis is increased. IL-22 is mainly produced by CD4+ epidermal T cells, where it activates keratinocytes and leads to acanthosis. IL-17A is mainly produced by epidermal CD8+ T cells, and it drives keratinocytes to participate in the recruitment of neutrophils and produces chemokines and proinflammatory cytokines (113). TNF-α promotes the differentiation of Th22 cells, while TNF-α blockade has achieved satisfactory results in the treatment of psoriasis patients. However, Th22 cells in the healed skin epidermis still produce IL-22 after 6 years of remission. Therefore, Th22 cells play an important role in the memory of psoriatic relapse (113). Previous findings suggest that IL-22 in the psoriatic epidermis is produced by IL22+IL-17+ Th17 cells. Recent studies show that there is no significant correlation between the expression of IL-17A and IL-22 in psoriasis, which does not support the existence of double-secreted IL-17A/IL-22 Th17 cells (114).
MS
MS is an autoimmune disease of the central nervous system (CNS), and it is characterized by the loss of the axonal myelin sheath and inflammation of the CNS, showing clinical symptoms such as muscle spasm and paralysis. Proinflammatory cytokines such as IL-22, IL-17, TNF-α and IFN-γ are involved in MS pathogenesis through multiple signaling pathways. The proportion of Th22 cells (75, 76) and the level of IL-22 in the serum of patients with MS increased (75, 76, 115–121), and the level of IL-22 in recurrent stage was significantly higher than that in progressive stage and remission stage (115, 116, 119, 122). The level of IL-22 in cerebrospinal fluid is also increased, and IL-22 increases the survival rate of brain astrocytes. The IL-22 receptor subunit IL-22R is mainly expressed on astrocytes (119), suggesting that astrocytes may play an important role in IL-22-mediated pathological changes in MS. IL-22 also inhibits the expression of Foxp3 by activating the NF-κB pathway and promotes the expression of Fas in oligodendrocytes, which leads to apoptosis of oligodendrocytes (123). Large-scale studies of 5019 MS patients in Norway and Sweden by Beyenet et al. identified IL-22RA2 as a risk gene for MS (124). The high expression of T-bet and CCR6 in Th22 cells of MS patients suggests that Th22 cells may migrate to the central nervous system. The infiltration of Th22 cells leads to an increase in T cell infiltration and contributes to the destruction of the blood-brain barrier (76, 125). In addition, the resistance to IFN-β therapy in MS patients may be related to the low expression of IFN receptor 1 on the surface of Th22 cells, and similar findings have been observed in the MS animal model of EAE (115).
A study in 2014 suggested that IL-22 played a protective role in CNS inflammation (126). The severity of inflammation was positively correlated with the level of IL-22BP in the cerebrospinal fluid of patients with MS. IL-22BP has a pathogenic effect on EAE in both mice and rats, and IL-22BP is theoretically an antagonist of IL-22. IL-22BP has been proposed to reduce IFN-γ produced by brain-derived T cells in lymph nodes (92). Previous studies showed that the histopathological features of EAE in IL-22-deficient mice were comparable to those in wild-type mice (14). Hannes et al. conducted EAE experiments on wild-type mice, IL-22 deficient mice, IL-22BP deficient mice, and IL-22 and IL-22BP double deficient mice and concluded that the loss of control of IL-22 signal in IL-22BP deficient mice reduced the severity of EAE,which supported the protective effect of IL-22 in MS; thus, they suggested that IL-22BP could be used as a new target for MS (92).
ITP
ITP is an autoimmune disease that is characterized by increased destruction and decreased production of platelets (127). The frequency of Th22 cells and the level of plasma IL-22 in patients with ITP were significantly higher than those in the control group (77, 78, 128). The increase in plasma IL-22 levels in ITP patients was reported to be associated with the dysregulation of Th1 and Th22 cells (128). Furthermore, Th22 cells in ITP patients were positively correlated with Th1 and Th17 cells (77, 79), and patients treated with high-dose dexamethasone (HD-DXM) exhibited significantly decreased frequencies of Th1 and Th22 cells and plasma concentrations of IL-22 (78). The level of IL-22 was also increased in pediatric ITP patients compared with healthy populations (129). A recent study showed that the frequencies of Th22, Th17, Tfh and Th1 cells in the bone marrow of ITP patients were significantly higher than those in the control group; moreover, the frequency of Th22 cells in bone marrow was significantly higher than that in peripheral blood (130). Notably, ITP patients with negative autoantibodies showed a higher percentage of Th22 cells than patients with positive detection of autoantibodies (77). In summary, Th22 plays a proinflammatory effect in ITP and acts synergistically with Th1/Th17 and Tfh cells. Th22 cells play an important role in the pathophysiological process of ITP patients. Therefore, blocking IL-22 may serve as a potential therapeutic target for treating ITP patients.
IGAN
IgAN is the most common primary glomerular disease characterized by inflammatory cell infiltration and IgA deposition in the mesangial area of the glomerulus, which is an important cause of renal failure (131). Although the exact pathogenesis is still unclear, the involvement of T cells has been confirmed. IgAN has a higher proportion of circulating Th2, Th17, Th22, Tfh and γδ T cells, but a lower proportion of Treg and Th1 cells (80). Peng et al. also showed that Th17 and Th22 cell frequencies in peripheral blood and plasma IL-22 levels were significantly increased in patients with IgAN, and Th22 cells were positively correlated with Th17 cells and plasma IL-22 levels. In addition, compared with IgAN patients without proteinuria, IgAN patients with proteinuria showed a higher percentage of Th22 cells (81). Th22 cells in patients with IgAN are higher than those in healthy controls, and the percentage of increase is positively correlated with the degree of kidney disease in patients with IgAN. Moreover,tonsillitis aggravates the over-expression of Th22 cells and the chemokines CCL20, CCL22 and CCL27 and aggravates kidney damage in IgAN (132). Xiao et al. confirmed that streptococcal infection can increase the chemotaxis of Th22 cells and aggravate kidney inflammation (133). Chronic inflammation is a common sign of chronic fibrosis,and fibrosis is one of the common pathological changes of IgAN. IL-22 binds to kidney IL-22R1 to activate STAT3, JAK and other signaling pathways, and regulate renal fibrosis through the ERK, Akt, and p38MAPK signaling pathways. Therefore,Th22 cells promote renal fibrosis in IgAN (134, 135). Treatment is mainly reflected in the reduced chemotaxis of Th22 cells. After treatment with cordyceps (CS), dexamethasone and losartan, the frequency of Th22 cells in the IgAN mouse model decreased and the expression of CCR10, CCL27 and IL-22 was also significantly reduced (60, 136). The above treatments all regulate the chemotaxis of Th22 cells to inhibit inflammation and improve renal function in patients. Acteoside (the main component of Rehmannia glutinosa) can also inhibit Th22 cell proliferation and inhibit Th22 cell chemotactic factors to regulate Th22 cell chemotaxis (137). In addition, the IL-22R1 gene polymorphism is genetically associated with the development of childhood IgA nephropathy (138).
AIH
AIH is a chronic autoimmune inflammatory liver disease that is characterized by high autoantibodies, high liver enzyme levels,and liver damage (139). Hepatocytes are one of the target cells of IL-22. IL-22 has dual effects on hepatocytes: protecting hepatocytes and inducing acute phase proteins. IL-22 acts on liver progenitor cells (LPCs), which is beneficial for liver reconstruction after injury. In human and mouse chronic HBV-infected livers, IL-22 promotes hepatocyte proliferation through the STAT3 pathway (140, 141). Patients with drug-induced liver injury (DILI) have increased intrahepatic and peripheral Th22 cells and IL-22 levels, and the liver IL-22 level is positively correlated with regeneration. Th22/IL-22 has a hepatoprotective effect in DILI (142). Studies have indicated that the increase in Th22/IL-22 is related to the severity of hepatitis B virus-related chronic liver failure (HBV-ACLF) and suggested that Th22/IL-22 can be used as a biomarker for the prognosis of HBV-ACLF (143). Few studies have focused on the pathogenesis of Th22/IL-22 in AIH. Studies have shown that compared with healthy controls, the serum levels of IL-6,IL-10,IL-17F, IL-21, IL-23 and TNF-α in AIH are significantly increased while those of IL-22 and IL-17A are not. According to the grouping of immunoserological markers, the cytokines of type 2 AIH patients are characterized by elevated levels of IL-21 and IL-22 (144). The mouse experimental autoimmune hepatitis (EAH) model and AIH patients present reduced serum IL-10 and Treg levels. The number of Th22, Th17 and Th1 cells and the number of corresponding cytokines IL-22, IL-17A and IFN-γ were all reduced. Moreover, the number of Tregs was negatively correlated with the number of Th22, Th17 and Th1 cells and cytokine levels. More interestingly, the serum IL-22 and IL-17A levels were positively correlated with liver injury in patients with AIH, suggesting that the imbalance between Th1/Th17/Th22 and Treg cells may be involved in the process of AIH (82).
AITD
AITD mainly includes Graves’ disease (GD) and Hashimoto’s thyroiditis (HT). GD manifests as hyperthyroidism caused by the overproduction of thyroid hormone, while HT manifests as hypothyroidism (145). T cell dysfunction and/or corresponding cytokine abnormalities cause the destruction of immune tolerance, which leads to abnormal immune responses in AITD. Research on Th22/IL-22 in AITD is also limited. The study by Peng et al. showed that the percentage of Th17 and Th22 cells and plasma IL-17 and IL-22 in GD patients were increased and positively correlated with serum TSAb levels (83, 84). GD patients not only have higher Th22 cell frequencies and serum IL-22 levels than healthy people but also have higher IL-22 mRNA and AhR expression, whereas HT patients do not show an increase in Th22/IL-22 (146). However, different results have also been presented. Bai et al. found that the circulating Th22 cell level of HT patients was significantly higher than that of the healthy control group and the GD patient group, and was positively correlated with the serum IL-22 level and thyroid peroxidase antibody (TPOAb) titer. Under TNF-α and IL-6 stimulation,the T lymphocytes of HT patients showed an enhanced ability to differentiate into Th22 cells in vitro (85). Ruggeri et al. also believed that serum IL-22 levels in untreated,newly diagnosed HT patients were higher than those in healthy controls (86). The level of Th22/IL-22 in AITD patients is elevated,and Th22 cells may participate in the pathogenesis of AITD by secreting IL-22, IL-6 and other proinflammatory cytokines; however, the exact mechanism remains to be further confirmed.
MG
MG is an autoimmune disease that produces anti-acetylcholine receptor (ACHR) autoantibodies and neuromuscular transmission disorders and manifests as skeletal muscle fatigue and weakness (147). Thymectomy (TE) represents one of the treatment methods. The frequency of Th22 cells in patients treated with TE was not significantly different from that of the healthy controls. After TE surgery, the frequency of Th22 cells was significantly reduced (93). Studies have also shown that the levels of IL-17 mRNA in PBMC and IL-17 concentrations in serum increase while levels of IL-22 mRNA and serum IL-22 decrease in MG patients. In addition, the level of serum IL-22 is negatively correlated with the level of serum anti-ACHR antibody, suggesting that IL-22 plays a protective role in MG (94). A recent study showed that the levels of IL-22 in the PBMCs of MG patients did not differ from those in the control group (148). Thus, further research is required to clarify the specific role of Th22/IL-22 in MG.
Other Autoimmune Diseases
SSc is an autoimmune connective tissue disease with skin and visceral organ fibrosis due to excessive deposition of extracellular matrix and vascular lesions (149). The increased frequency of circulating Th22 cells is positively associated with pulmonary interstitial disease in SSc patients (87). Moreover, the excessive production of IL-22 in injured skin was independent of IL-17 (88). Other studies have shown that IL-22 can enhance the response of fibroblasts to TNF-α, promote the inflammatory phenotype of fibroblasts, and enhance the ability of TNF-activated keratinocytes to stimulate fibroblasts (89). Th22 cells express massive amounts of fibroblast growth factor, suggesting that targeting the IL-22 signaling pathway may be effective for preventing fibrogenesis (150). Th22/IL-22 may be related to skin and visceral fibrosis in patients with SSc. Primary Sjogren’s syndrome (pSS) is a chronic autoimmune disease that is characterized by lymphocyte infiltration in lacrimal and salivary glands, and it also presents elevated IL-22 levels (43, 151, 152). IL-22 plays a proinflammatory role in pSS pathogenesis and promotes salivary gland inflammation at an early stage (152, 153). IL-22 is predominantly secreted by Th17 and NKp44+ NK cells in pSS patients (152). Studies have shown that the frequency of Th22 cells in the peripheral blood of ankylosing spondylitis (AS) patients is increased (20, 154), while other studies have shown that there is no difference in IL-22+CD4+ and IL-22+CD8+ T cells between AS patients and healthy controls; however, the secretion of IL-22 by circulating mucosal-associated invariant T (MAIT) cells is increased in AS patients (90). A number of types of vasculitis have been identified, and several studies have focused on Th22/IL-22 in vasculitis. A study by Zerbini et al. showed that the levels of IL-22 and IL-22R1 were higher in giant cell arteritis (GCA) patients who were confirmed to be positive for temporal artery biopsy (TAB) than in TAB-negative patients and normal controls. IL-22 is expressed in spindle cells and infiltrating immune cells, while IL-22R1 is expressed in endothelial cells; moreover, IL-22 is involved in B cell proliferation, differentiation and arterial remodeling of GCA (91).
Therapeutic Targeting of IL-22
Previous investigations have shown a critical role of IL-22 during the pathogenesis of autoimmune diseases. Preclinical studies indicate that IL-22 may serve as a promising therapeutic target for treating autoimmune diseases. Th22 cells promote osteoclast differentiation while neutralization of IL-22 inhibits osteoclast formation, suggesting that blocking IL-22 could be effective in suppressing bone destruction in RA patients (98). Inhibition of IL-22 by neutralization antibodies has been shown to reduce the expression of chemotactic factors, decrease antimicrobial and hyperproliferative responses of keratinocytes, and prevent the development of imiquimod-induced psoriasis from skin inflammation (111). It has been reported that treatment with cordyceps sinensis, dexamethasone and losartan improves kidney functions associated with a reduction of Th22 cells in mice with IgA nephropathy, suggesting that these drugs may exert their protective effects through modulating Th22 cells (60, 136).
Currently,the safety, tolerability and therapeutic effects of Fezakinumab (ILV-094), a human monoclonal antibody that directly binds to IL-22, have been examined in atopic dermatitis patients in severalclinical studies (155). A small scale randomized,double-blind, phase 2a clinical trial involving 60 patients with moderate-to-severe atopic dermatitis has shown that Fezakinumab is well-tolerated with sustained clinical improvements after last drug dosing. Fezakinumab treatment has shown significant clinical improvements versus placebo in patients with severe disease as reflected by significant reductions of SCORing of Atopic Dermatitis (SCORAD) scores and Investigator Global Assessment (156). Furthermore, transcriptomic and immunohistochemistry analyses reveal that Fezakinumab has profound effects on multiple inflammatory pathways in these patients (157). Fezakinumab broadly decreases immune activation in skin tissues and reduces overall inflammatory burden and epidermal pathologic characteristics. The treatment effects of Fezakinumab are particularly evident in patients with high IL-22 baseline expression, suggesting that a precision medicine-based approach might be needed for improving therapeutic outcomes in patients with atopic dermatitis.
It has been revealed that IL-22 exerts protective roles in certain diseases. A phase II study (NCT02406651) is undergoing to investigate the therapeutic effects of recombinant IL-22 for GVHD after bone marrow transplantation (158). Other potential strategies including the modulation of chemotaxis of Th22 cells,administration of AhR agonists to enhance IL-22 expression,and application of IL-22BP are under investigation. Available results suggest that Th22 cells are involved in autoimmune pathogenesis through multiple effector functions, including the production of various cytokines, such as IL-22, IL-13 and IL-26. Moreover, Th22 cells may have close interactions with Th1, Th2 and Th17 cells during disease progression. Further investigations on the safety,tolerability and therapeutic effects of agents targeting Th22/IL22 pathway are needed for the effective treatment of autoimmune diseases.
Conclusion
Th22 cells and IL-22play diverse roles in the development of autoimmune diseases and have both proinflammatory and anti-inflammatory functions. Th22/IL-22 plays a pathogenic role in most autoimmune diseases, while IL-22 has been shown to have a protective effect in many other diseases involving skin and mucosal barrier. Thus, the function of IL-22 varies depending on the cellular source, types of inflammatory response, the affected tissue (mucosa or solid organ), and the concentration and duration of IL-22 itself in local environment. Emerging evidence supports the notion that Th22 cells may serve as therapeutic targets for autoimmune diseases. However, further studies are needed to elucidate the mechanisms of Th22 cells in disease pathogenesis and validate the therapeutic potential of targeting Th22 cells for the treatment of autoimmune diseases.
Author Contributions
QJ and DC drafted the manuscript and designed the figures. GY and FX reviewed the manuscript structure and ideas. DC, JX, SW, and LL conceived the topic and revised the manuscript. All authors contributed to the article and approved the submitted version.
Funding
This work was supported by the National Natural Science Foundation of China (Grant Nos. 81871709, 81971994, 82071817, 91846103, 31711530025 and 81771759), Funding for Chongqing International Institute for Immunology (2020YJC10), Hong Kong Research Grants Council General Research Fund (17103821, 17113319) and Theme-Based Research Scheme (T12-703/19R), Zhejiang Provincial Key Research and Development Program (Grant No. 2020C03032).
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.
Acknowledgments
We gratefully acknowledge the highly qualified native English speaking editors at American Journal Experts (AJE) for providing reputable English language editing service (Verification code:4EEC-BB22-0394-0139-C5A7) for our manuscript.
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Keywords: Th22 cells, IL-22, rheumatoid arthritis, systemic lupus erythematosus, psoriasis, immune thrombocytopenia, autoimmune diseases, autoimmune hepatitis
Citation: Jiang Q, Yang G, Xiao F, Xie J, Wang S, Lu L and Cui D (2021) Role of Th22 Cells in the Pathogenesis of Autoimmune Diseases. Front. Immunol. 12:688066. doi: 10.3389/fimmu.2021.688066
Received: 30 March 2021; Accepted: 22 June 2021;
Published: 06 July 2021.
Edited by:
Carlo Perricone, Sapienza University of Rome, ItalyReviewed by:
Philippe GUILPAIN, Université de Montpellier, FranceStefania Croci, Local Health Authority of Reggio Emilia, Italy
Copyright © 2021 Jiang, Yang, Xiao, Xie, Wang, Lu and Cui. 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: Dawei Cui, daweicui@zju.edu.cn; Liwei Lu, liweilu@hku.hk; Jue Xie, zyyyxj2011@zju.edu.cn