Rheumatoid arthritis (RA) is a chronic inflammatory disease characterized by inflammation of the synovial membrane. The release of pro-inflammatory cytokines as well as other pro-inflammatory molecules results in joint destruction and disability [1, 2]. To date, the exact cause of RA has not been identified but several studies pointed out that pro-inflammatory cytokines, including tumor necrosis factor (TNF)-α, interleukin (IL)-1, IL-6, IL-17 and the mediators produced through downstream pathways in the arthritic joints, constitute the milieu driving cartilage and bone destruction [3]. On this basis, therapeutic possibilities for RA patients include monoclonal antibodies, fusion proteins or antagonists against these molecules. However, partial and non-responses to these compounds, together with the increasing clinical drive to remission induction, requires that further therapeutic targets are identified [4]. In recent years, a growing number of new cytokines as well as their function in health and disease have been identified [5]. Cytokines serve as the mediators of cellular differentiation, inflammation, immune pathology, and regulation of the immune response. In particular, novel inflammatory mediators with their associated cell signaling events have now been proven to have a role in experimental arthritis and in RA, including members of the IL-1 (IL-33, IL-36, IL-37, IL-38) and IL-12 (IL-27, IL-35) superfamilies, and other cytokines such as IL-32, IL-34. The aim of this review article is to provide an overview on these recently identified cytokines, emphasizing their pathogenic role and therapeutic potential in RA. Table 1 summarizes all the available data in animal models and RA patients for each cytokine.

Table 1 Data on different cytokines in experimental arthritis and patients with rheumatoid arthritis

New members of IL-1 family


IL-1 cytokine includes 11 pro-inflammatory and anti-inflammatory members, chronologically named according to their discovery, IL-1 family member 1 (IL-1F1) to IL-1F11. More commonly, they are also known as IL-1α, IL-1β, IL-1 receptor antagonist (IL-1Ra), IL-18, IL-33, IL-36α, IL-36β, IL-36γ, IL-36Ra, IL-37, and IL-38 [6]. All IL-1 cytokines bind to similar receptors consisting of extracellular immunoglobulin domains and intracellular Toll/IL-1 (TIR) domains. The signal is transduced via cytoplasmic myeloid differentiation primary response protein 88 (MyD88) and IL-1R associated kinase 4 (IRAK4), ending up in the activation of transcriptions factors like NF-kB or MAPK [7]. IL-33 (IL-1F11) was identified in high endothelium venules in 2003 [8]. Subsequent studies revealed that IL-33 acts as alarmin, being modulated by inflammatory stimuli. Indeed, IL-33 is up-regulated during the inflammatory response and can be released by necrotic cells. On the other hand, IL-33 is inactivated by caspase-1 during apoptosis [9]. IL-33R ST2 belongs to the family of IL-1R and, upon binding to the ligand, triggers the transduction signal via the NF-kB or MAPK pathways [10]. ST2 is expressed by several immune cells including basophils, mast cells, eosinophils, DCs and NK cells. However, the most important target of IL-33 is represented by Th2 cells. Besides its trans-membrane form, ST2 can be released in a soluble form (sST2) by different immune and non-immune cell types thereby blocking IL-33 effects [11]. Being involved in Th2 immune response, IL-33 has been extensively investigated in the field of allergic diseases [12]. Circulating and tissue levels of IL-33 are increased in experimental models of asthma [13, 14] and blockade of this pathway is able to ameliorate airway inflammation [13, 15,16,17], thereby confirming an in vivo inhibition of IL-33-mediated effects. With regard to experimental arthritis, the development and severity of CIA in IL-33 KO mice is comparable to that of WT mice [18]. However, mice lacking ST2 develop attenuated CIA and AIA and treatment of WT mice with recombinant (r) IL-33 significantly exacerbated both [19, 20]. Therefore, data from animal models do not provide univocal evidence. In RA patients, IL-33 serum levels are increased compared to normal and disease controls (OA and psoriatic arthritis (PsA)) [21,22,23,24]. Evidence from RA SF is conflicting as IL-33 was found to be either increased [25] or comparable [23] to OA SF. Conflicting results were also obtained with regard to the correlation of serum and SF IL-33 in RA paired samples. In fact, both an inverse [21] and a direct association have been reported [25]. Of interest, RA patients with higher active disease display higher levels of this cytokine in serum [21] and SF [26] and higher IL-33 serum levels were also associated to bone erosions and RA-ILD [22]. In this regard, and also in general when measuring cytokines in the serum of RA patients, it should be taken in mind that discrepancies could be due to false measurements caused by heterophilic antibodies [27] or differences in patient population. Serum sST2 levels were found to be increased in RA compared to OA [23]. IL-33, IL-33R ST2 and sST2 expression has been claimed as possible markers of response to treatment in RA. First, RA patients achieving a good response with an anti-TNF-α treatment display lower levels of IL-33 in serum and SF and IL-33R on immune cells compared to patients treated with methotrexate or non-responders to TNF-α inhibitors [28, 29]. This is further supported by the evidence that neutrophils of anti-TNF-α responder patients respond to a lesser extent to IL-33 in vitro compared to methotrexate-treated patients. Secondly, RA patients with lower sST2 levels at baseline are those who more likely achieved remission following 12 months of treatment with disease modifying anti-rheumatic drugs (DMARDs) and anti-TNF-α agents [30]. Finally, baseline detectable serum IL-33 levels have been associate to a good clinical response to rituximab [31]. Interestingly, baseline IL-33 and sST2 levels have been also associated to cardiovascular risk factors. Cardiovascular risk is a severe comorbidity in RA patients being the first cause of death in these patients and persistent inflammation is one of the main determinants. In this regard, baseline level of serum IL-33 is also a predictor for atherosclerotic plaque progression in patients with early RA, independently of other traditional risk factors and other inflammatory biomarkers [30]. Currently available data regarding IL-33 axis in RA do not allow to draw definitive conclusion about its actual role in RA pathogenesis and consequently about its possible therapeutic targeting in this disease.

IL-36 and IL-38

The new IL-1 family members IL-36α, IL-36β, IL-36γ, IL-36Ra (IL-1F5) and the antagonist IL-38, bind to the IL-36R consisting of the IL-1 receptor-related protein 2 (IL-1RrP2) and its accessory protein IL-1RAcP. IL-36R is expressed by DCs, CD4+ T-cells and macrophages. Binding of the agonists to the membrane bound IL-1RrP2 leads to the recruitment of the co-receptor IL-1RAcP. This triggers an intracellular signaling cascade via JNK, ERK1/2, and NF-kB which results in the production of pro-inflammatory mediators. On the contrary, the binding of the natural inhibitors IL-36Ra and IL-38 prevents the signaling [32, 33]. During the last few years, IL-36 cytokines as well as IL-37 and IL-38 raised growing interest, as they have been involved in various diseases, including RA [34]. IL-37 and IL-38 have been shown to play an anti-inflammatory role in several diseases, whereas IL-36 exerts pro-inflammatory effects. All the three IL-36 agonists induce pro-inflammatory mediators such as cytokines, chemokines and co-stimulatory molecules thereby promoting Th1 and Th17 cell commitment, neutrophil influx and DC activation [35]. In particular, IL-36 and its receptor can stimulate DC and can promote their maturation; DC precursors exposed to IL-36 release IL-12 and contribute to differentiation of T cells to Th1 cells. In vivo, IL-36β can act as an adjuvant to promote Th1 response [36]. In humans, the three IL-36 isoforms and their receptor are over-expressed in psoriasis; moreover, IL-36 can induce the release of pro-inflammatory cytokines, such as IL-6 or IL-8 as well as IL-17, IL-22, and. These cytokines can induce IL-36 release, creating a feedback loop [33, 37]. In mouse models of RA, such as CIA, collagen antibody-induced arthritis (CAIA), and AIA, all of the IL-36 family members are upregulated during acute inflammation. However, treatment with an IL-36R-blocking antibody of TNF-transgenic mice, another experimental model of RA, resulted in no changes in symptoms or clinical onset, suggesting that the severity of experimental arthritis is independent of IL-36R signaling [38, 39]. This evidence can be attributable to the redundancy of IL-1 family member downstream signaling, mainly those of IL-1, which is a major player in experimental arthritis. It is unclear whether this redundancy is similar in human arthritis. Of note, the magnitude of stimulatory effect of IL-36 in synovial fibroblasts and articular chondrocytes was markedly lower than those of IL-1 [40], suggesting that IL-36 is probably not a key player in human arthritis. IL-36β is constitutively expressed in human articular chondrocytes, and stimulation of both synovial fibroblasts and articular chondrocytes by recombinant IL-36β induces proinflammatory cytokine responses [40]. In mice with CIA and in the synovium of patients with RA, IL-36α, IL-36β, IL-36γ, IL-36Ra and IL-38 were all elevated and correlated with IL-1β, CCL3, CCL4 and macrophage (M)-CSF, but not with Th17 cytokines [41]. Expression of IL-36R and its ligands IL-36α and IL-36Ra has been detected in the synovial lining layer and cellular infiltrates of patients with inflammatory arthritis [42]. IL-36α was upregulated in the synovium of patients with PsA and RA, compared to patients with OA. Conversely, IL-36R and its natural antagonist IL-36Ra were expressed at similar levels in the synovial tissue in all three diseases. In the same study, synovial CD138+ plasma cells seem to be the main source of IL-36α, and IL-36α is able to induce IL-6 and IL-8 production in synovial fibroblasts [42]. IL-38 (IL-1F10) is released as a 152-amino acid precursor having a molecular weight of 16 kDa. IL-38 shares 41% homology with IL1-Ra and 43% with IL-36Ra [43, 44]. IL-38 binds to IL-36 receptor, as does IL-36Ra, and has similar biological effects on immune cells. Thus, in vitro, IL-38 inhibits the production of Th1 cytokines, IL-17, and IL-22. IL-38, similarly to IL-36Ra, has an anti-inflammatory effect on PBMCs, contrasting with a clearly pro-inflammatory effect on DC with increased IL-6 production [45]. IL-38 is selectively secreted by human apoptotic cells to counteract inflammation. The depletion of IL-38 in apoptotic cells leads to an increase of pro-inflammatory cytokine release by macrophages and to the subsequent expansion of Th17-cell at expense of IL-10-producing T cells [46]. Interestingly, in this study, full length recombinant IL-38 induced IL-6 production by macrophages, whereas truncated IL-38 decreased IL-6 expression after X-linked interleukin-1 receptor accessory protein-like 1 (IL-1RAPL1) binding. However, it is still unclear whether IL-38 is an inflammatory or an anti-inflammatory cytokine. IL-38 seems to have either pro- or anti-inflammatory effects depending on the dose. Whereas IL-38 gene deficiency enhanced arthritis, systemic administration of recombinant IL-38 protein did not inhibit arthritis development. Therefore, it is possible that IL-38 may have dose-dependent effects in inflammatory vs. anti-inflammatory responses. Further analysis is required to test this hypothesis. Takenaka et al. investigated AIA in IL-38 KO and observed greater disease severity, accompanied by higher IL-1β and IL-6 gene expression in the joints compared to control mice [47]. Recently, Boutet et al. demonstrated that adeno-associated virus-mediated IL-38 overexpression exerted moderate but significant anti-inflammatory effects in CIA and K/BxN serum transfer-induced arthritis (STIA) [48]. In addition to the reduced macrophage number, a significant decrease in the expression of Th17 cytokines (IL-17, IL-22), IL-6, TNF-α and CXCL1 was observed in this study, without any modification in IL-1β expression. Of note, IL-38 overexpression did not induce the production of other anti-inflammatory cytokines, but reduced significantly IL-10 expression. IL-38 levels are increased in the synovial membrane and sera from patients with RA compared with healthy controls [47, 49] IL-38 is expressed by keratinocytes, synovial fibroblast from patients with RA, as well as by human monocytes and type I macrophages polarized in vitro [41].

Taken together, data about IL-36 in RA seem to support the pursuit of its blockade for therapeutic purposes in this disease, Conversely, whether the anti-inflammatory cytokine IL-38 should be considered a new therapeutic option in arthritis or other inflammatory diseases deserves further experiments.


IL-37, previously known as IL-1 family member 7 (IL-1F7), is a member of the IL-1 family initially identified in early 2000s [49]. IL-37b is the largest of the 5 different splice variants (from a to e) and its precursor is cleaved by caspase-1 into mature IL-37b. IL-37 is expressed in several tissues, is associated with plasma cells and it is constitutively expressed in the cytoplasm of monocytes and PBMCs [50]. TLR agonists and pro-inflammatory cytokines, including IL-1β, TNF-α and IFN-γ can upregulate IL-37 in PBMCs [51]. Upon binding to its receptor shared with IL-18, IL-18R, IL-37 is able to inhibit the transcription of several pro-inflammatory cytokines, including IL-17, via the suppression of the MAPK pathway [52, 53]. Recent data demonstrated that IL-37 also needs IL-1R8, a member of the IL-1R family, to exert such anti-inflammatory activity. In fact, transgenic mice overexpressing IL-37 are protected from lipopolysaccharide (LPS)-induced shock [53], but only if the IL-1R receptor is correctly expressed in order to form the tripartite IL-37–IL-1R8–IL-18Rα complex on the surface of PBMCs upon stimulation with LPS [54]. Similarly, the administration of recombinant IL-37 consistently reduced LPS-induced inflammation [54]. In addition, IL-37 transgenic mice develop less severe colitis and psoriasis [55, 56]. Based on the anti-inflammatory activity of IL-37, several studies have been performed to investigate whether the administration of IL-37 may ameliorate chronic inflammation [57]. Studies performed in patients reported an overall increase of circulating as well as tissue IL-37 in inflammatory bowel disease [58], systemic lupus erythematosus [59], Graves’ disease [60] and AS [61]. With regard to experimental arthritis, systemic and intra-articular administration of recombinant IL-37 was able to inhibit the development of synovitis by reducing pro-inflammatory cytokines and modulating Th17 cells [62, 63]. In striking contrast with experimental RA, but in line with the results obtained in patients with other autoimmune disease, studies performed in RA patients revealed higher serum and plasma levels of IL-37 compared to normal and OA controls [63,64,65,66]. Such increase is particularly evident in patients with active disease, compared to patients in remission [65], and in patients with positive RF and anti-CCP [66]. Furthermore, IL-37 levels have been correlated to pro- and anti-inflammatory cytokines (IL-4, IL-7, IL-10, IL-12, IL-13, IL-17A, TNF-α) as well as to disease activity and bone erosions. Moreover, they are reduced by DMARD and anti-TNF-α treatment in patients with a good clinical response [64,65,66]. The only available study assessing IL-37 levels in RA SF reported increased levels of this cytokine compared to paired serum samples [66]. IL-37 is also consistently expressed in the synovial tissue of RA patients with active disease [63]. These findings may be explained, at least in part, by the evidence that IL-37 plasma concentration in RA is directly correlated with pro-inflammatory cytokines, including IL-17 and TNF, as well as with disease activity and radiographic bone erosion score and bone loss [64, 67]. It is therefore reasonable to speculate that such increase of IL-37 may be a compensatory mechanism to counteract the effector immune response, likely occurring also in other autoimmune diseases. This mechanism is not effective of course either because IL-37 levels are insufficient or because the cytokine is neutralized by factors that need to be elucidated.

Based on this, the potentiation of IL-37 as well the identification of its agonists may represent an intriguing approach for therapeutic purposes in RA.

New members of IL-12 family


IL-27 is a newly identified heterodimeric cytokine belonging to the IL-12 family, which includes IL-12, IL-23, IL-27, and IL-35 [68]. The IL-12 cytokine family is part of the IL-6 superfamily of type I cytokines. However, while IL-6 family members are secreted as single-subunit monomers, those of the the IL-12 family are heterodimeric. The four members of the IL-12 cytokine family are consisted of an α chain (p19, p28, or p35) and a β chain (p40 or Epstein-Barr virus induced gene 3 (EBI3)) [69]. In detail, p35 and p40 subunits constitute IL-12, p19 and p40 subunits constitute IL-23 and p28 combines with EBI3 forming IL-27. The latest recognized member, IL-35, consists of p35 and EBI3. For the sake of completeness, it should be mentioned that very recently another family member, IL-39, has been described. IL-39 is composed of IL-23p19 and EBI3 heterodimer, is secreted by activated B lymphocytes and seems to play a pathogenic role in mouse models of systemic lupus erythematosus [70, 71], but no data on RA or other diseases are available so far. These cytokines transduce the signal through unique pairings of 5 receptor chains: IL-12Rβ1, IL-12Rβ2, IL-23R, IL-27Rα (or WSX-1) and gp130. IL-12 signals through IL-12Rβ1 and IL-12Rβ2, IL-23 signals through IL-23R and IL-12Rβ1, and IL-27 signals through gp130 and IL-27Rα [72]. In T cells, IL-35 signals through IL-12Rβ2 and gp130, although it can also signal through IL-12Rβ2/IL-12Rβ2 and gp130/gp130 homodimers [73]. Signal transduction through these receptor chains is mediated by the Janus kinase (JAK)-signal transducer and activator of transcription (STAT) pathway. Despite similarities in the structural cytokine subunits, receptor components, and downstream signaling, IL-12 family members display diverse but balanced functions. IL-12 and IL-23 represent the strictly pro-inflammatory members with key roles in T helper (h) 1 and Th17 development [26, 74], while IL-27 carries out its role in inflammation supporting Th1 development and interferon (IFN)-γ production and inhibiting Th2 and Th17 differentiation programs [75, 76]. IL-27 is mainly produced by antigen presenting cells (APCs), including dendritic cells (DCs) and macrophages, as well as by endothelial cells. Besides the JAK/STAT pathway, IL-27 can also activate other pathways including p38- mitogen-activated protein kinase (MAPK) and AKT in specific cell types, such as liver and intestinal epithelial cells [77]. gp130 is ubiquitously express in a wide range of cell types including mast cells and natural killer (NK) cells while WSX-1 is consistently expressed by naïve T cells and to a greater extent by activated and memory cells, the latter being therefore highly susceptible to the effects of this cytokine [78]. Indeed, IL-27 is a pivotal cytokine in the commitment of naïve T cells. It was first described as a Th1-polarizing cytokine being able to induce expression of T-bet and suppression of GATA-3 [77]. However, the evidence that IL-27R knockout (KO) mice develop a hyper-inflammatory phenotype, prompted to explore possible effects of this cytokine on other T-cell subsets. The subsequent demonstration that IL-27 can both increase the secretion of IL-10 by naïve T cells, thereby inducing regulatory T (Treg) cells, and directly antagonize the development of pro-inflammatory Th17-cell responses, allowed to speculate that IL-27 may have a protective role in chronic immune mediated inflammatory diseases [79]. Interestingly, studies evaluating the contribution of each receptor subunit function revealed that the lack of WSX alone does not affect the anti-inflammatory properties of IL-27 [80, 81]. With regard to RA animal models, collagen induced arthritis (CIA) in IL-27Rα KO mice is characterized by a more severe clinical picture with synovial germinal center -like structures, increased leukocyte infiltration, synovial hypertrophy, and cartilage/bone erosion compared to wild type (WT) mice [82]. Conversely, in proteoglycan-induced arthritis (PGIA), IL-27 seems to be crucial to trigger the inflammatory response [83]. Therefore, although the majority of studies agree that both systemic and local administration of IL-27 ameliorates CIA and adjuvant induced arthritis (AIA) [84,85,86,87], still the negative effect observed in PGIA requires additional evaluation. With regard to the human counterpart, serum IL-27 levels are increased in RA and seem to be directly correlated with disease activity and RA-associated interstitial lung disease (ILD) [88]. Wong et al. reported that IL-27 is higher in RA plasma compared to normal subjects [89], while Tanida et al. failed to observe any difference between RA, osteoarthritis (OA) and healthy controls [90]. Of interest, however, the latter study revealed that IL-27 is highly expressed in RA synovial fluid (SF) and synovial tissue. Synovial IL-27 mainly derives from CD14+ mononuclear cells (MNC) rather than from fibroblast-like synoviocytes (FLS). These IL-27 producing CD14+ MNCs are virtually absent in OA synovium where IL-27 is barely detectable. The production of pro-inflammatory cytokines and chemokines including IL-6 by RA-FLS in vitro is inhibited by IL-27. Therefore, it may be hypothesized that IL-27 exerts, or at least attempts to, an anti-inflammatory effect in RA synovial environment via the inhibition of Th17-cell commitment. In light of the well-established role of Th17 cells in RA pathogenesis, and in particular in the development of synovial germinal center-like structures, Jones et al. demonstrated that synovial IL-27 expression is more pronounced in germinal center-negative RA synovium compared to germinal center-positive RA synovium and OA synovium, and that it is inversely correlated to the expression of molecules involved in ectopic lymphoid neogenesis. These findings, are in line with those obtained in experimental RA and allow to speculate that IL-27 may have a protective role in this disease [82].

Currently available data about IL-27 highlight that this is another cytokine owing an anti-inflammatory activity and therefore the identification of molecules acting as IL-27 agonists may represent an intriguing option to be explored in RA.


IL-35 is a heterodimeric cytokine belonging to the IL-12 family together with IL-12, IL-23, IL-27 and IL-35 [91]. In T cells, IL-35 signals through IL-12Rβ2 and gp130, although it can also signal through IL-12Rβ2/IL-12Rβ2 and gp130/gp130 homodimers [92]. Interestingly, although all the receptors for IL-35 induce suppression of T-cell proliferation, the homodimeric receptors are unable to mediate the generation of IL-35 induced regulatory T cells (iTr35) [92]. IL-35 signals both through gp130 and IL-12Rb2 homodimers and through an IL-12Rb2:gp130 heterodimeric receptor but only the latter can mediate T-cell suppression and iTr35 induction through the formation of pSTAT1:pSTAT4 heterodimers [92]. Furthermore, IL-35 signaling through an IL-12Rβ2:WSX-1 heterodimer and the induction of pSTAT1 and pSTAT3 is peculiar of B cells [93]. IL-35 is mainly released by Treg cells, is required to potentiate the suppressive activity of murine and human Treg cells and therefore inhibits T-cell proliferation in vitro and in vivo disease models [94]. Recently, it has been reported that also regulatory B (Breg) cells can produce IL-35 [93, 95]. Finally, as shown for IL-10 and transforming growth factor (TGF)-β, IL-35 can also induce the conversion of naïve T cells into iTr35 cells [96]. The CIA mouse model shares many similarities with human RA as synovial cells proliferate in a tumor-like manner and cause synovitis. Angiogenesis is a shared pathogenic process, hence vascular endothelial growth factor (VEGF) is a crucial player in tissue injury/repair, inflammation and eventually in RA development [97]. IL-35 plays an anti-inflammatory role by inducing Treg-cells and inhibiting Th17 cell commitment in several experimental models of inflammatory diseases including CIA [98]. Moreover, IL-35 treatment inhibited proliferation and promoted apoptosis in cultured FLS from CIA mice in a dose-dependent manner [99]. Finally, IL-35 seems to inhibit angiogenesis of CIA mice as well as downregulate the expression of VEGF and its receptors, ameliorating the severity of synovitis [100]. Unfortunately, data on IL-35 in patients affected by RA remain controversial. In particular, while some Authors support anti-inflammatory activities of IL-35, others suggest its pro-inflammatory properties. IL-35 was found to be higher in patients with treatment naïve early RA compared to those with established disease and to be reduced after 3 months treatment with glucocorticoids and conventional synthetic (cs) DMARDs [101]. IL-35 was found to be also higher in SF RA compared to PsA and control OA patients and correlated with higher disease activity, supporting a potential role of IL-35 in the pathogenesis of RA [101, 102]. Moreover, TNF-α can induce the expression of both p35 and EBI3 subunits in FLS and MCs, and since the latter express both subunits of IL-35 receptor can secrete several pro-inflammatory molecules (IL-1β, IL-6 and MCP-1) upon IL-35 stimulation [102]. Nakano et al. reported that serum levels of IL-35 are decreased in RA patients, when compared with normal controls, mainly in patients with active disease, with an inverse correlation between serum IL-35 levels and the 28-joint disease activity score (DAS) based on CRP [103]. The function of IL-35 was also evaluated in a suppression assay using T cells isolated from human RA patients; recombinant IL-35 facilitated the function of natural Treg cells in vitro and restrained pro-inflammatory cytokines such as IL-17 and IFN-γ [103]. These conflicting results may be explained at least in part by the heterogeneity of patient cohorts, also from a genetic point of view, and different disease activity scoring systems. Further studies, especially in larger cohorts of patients are required to clearly explore the immunosuppressive role and potential therapeutic benefits of targeting IL-35 in RA.


IL-32 is a cytokine produced by immune and non-immune cells, and has recently gained popularity because of its important biological functions [104]. IL-32 gene was found to be located on human chromosome 16p13.3 and was reported to exist in nine different isoforms by mRNA alternative splicing including IL-32훼, IL-32훽, IL-32훾, IL-32훿, IL-32휀, IL-32휁, IL-32휂, IL-32휃, and IL-32 s (small), with specific activities and properties. Moreover, these isoforms can interact with each other intracellularly to control their respective activities and IL-32훾 is the most active isoform [105,106,107]. IL-32 is not assigned to any of the cytokine families, due to the lack of homology with other well-known cytokines. IL-32 was originally described as an mRNA called NK cell transcript 4 (NK4), which encoded a protein with many characteristics of a cytokine, derived from IL-2 activated natural killer cells [108]. NK cells, monocytes/macrophages, T lymphocytes, as well as epithelial cells, endothelial cells, fibroblasts, and hepatocytes, express IL-32 [109], mainly intracellularly, although some reports suggest that the IL-32γ isoform, could be secreted in limited amounts [110]. However, depending on the cell type and stimulus, IL-32 may be released after necrotic cell death or in vesicles such as exosomes [111, 112]. One problem that remains associated with IL-32 is the identification of cell surface receptor of IL-32. IL-32 is a pleiotropic cytokine and an important player in innate and adaptive immune responses, involved in a number of biological functions, including cell differentiation, stimulation of pro- or anti-inflammatory cytokines and cell death, especially apoptosis [113]. In detail, this cytokine induces other pro-inflammatory cytokines and chemokines such as TNF-α, IL-1β, IL-6, and IL-8 by means of the activation of NF-kB and p38-MAPK. IL-32, via caspase-3 activity, induces differentiation of monocytes into macrophage-like cells with characteristics of generating pro-inflammatory cytokines such as IL-6, TNFα and chemokines [114]. IL-32γ, via a phospholipase C (PLC)/ c-Jun N-terminal kinases (JNK)/NF-kB-dependent pathway, induces maturation and activation of DCs, leading to increased production of IL-12 and IL-6, Th1- and Th17-polarizing cytokines [115]. Moreover, IL-32 synergizes with nucleotide oligomerization domain (NOD) 1 and NOD2 ligands for IL-1β and IL-6 production, through a caspase 1-dependent mechanism [116]. Finally, IL-32β, increasing adhesion of inflammatory cells to activated endothelial cells with consequent induction of pro-inflammatory cytokines, is involved in the propagation of vascular inflammation [117]. Its production is predominantly induced by IL-1β, TNF-α, IL-2 or IFN-γ in blood monocytes and epithelial cells [39]. In addition to cytokines, microbial products, including viruses, have emerged as potent inducers of IL-32 in human monocytes, macrophages, and monocyte-derived DCs [109]. All the above mentioned data clearly point out that IL-32 and TNF-α are strongly linked to each other and being TNF-α a key cytokine in RA pathogenesis, IL-32 may play profound effects in this process [118]. Studies from animal models demonstrated that human IL-32, when injected in joints of naïve mice, leads to increased expression of inflammatory molecules (IL-1β, TNF-α, IL-18, IFN-γ, IL-17, IL-21 and IL-23), recruitment of inflammatory cells, cartilage derangements and joint swelling [119]. Conversely, joint swelling and presence of inflammatory cells drastically decreased in a TNF-α deficient mouse model [120]. This observation further supports the key interplay between TNF-α and IL-32 in RA pathogenesis. Furthermore, the unmasking of the molecular mechanism of the IL-32/ TNF-α in RA open new avenues for their potential therapeutic targeting. Several studies confirmed an overexpression of IL-32 and IL32γ in RA patients, when compared to osteoarthritis or healthy volunteers [121, 122]. In particular, the IL-32γ level was found significantly upregulated in CD14+ monocytes and synovial membrane of RA patients [123, 124]. High levels of IL-32 in synovial biopsies of RA, as compared to its absence in OA patients, suggested that IL-32 is potent mediator of active osteoclastogenic activity. In particular, the synergism between IL-32 and soluble receptor activator of nuclear factor κ-B ligand (sRANK-L) enhances the activity of osteoclasts and consequently tissue resorption [124]. Both IL-32 and IL-17 can reciprocally influence each other’s production and amplify the function of osteoclastogenesis in RA synovium [124]. RA FLS seem to have a key role in osteoclastic activity, as well as in pannus formation in the joint [125]. IL-32β, δ, and γ mRNA overexpression in RA FLS is primarily induced by TNF-α, IFN-γ and toll-like receptor (TLR)-2, −3, and −4 ligands, and the overexpression of IL-32 seems to stabilize the mRNA transcripts of other cytokines, in particular TNF-α, IL-1β and IL-8 [110, 126]. In FLS, TNF-α-activates Syk/PKC-d/JNK/c-Jun pathway to induce IL-32 (isoforms α, β, δ, and γ) [127], suggesting a splicing of IL-32γ into IL-32β [110]; interestingly, IL-32β is associated with lower inflammation and less severity of RA when compared with IL-32γ. IL-32 stimulates the synthesis of prostaglandin E2, an important mediator of cartilage and bone destruction in RA [128]. Very few clinical data regarding IL-32 response in patients treated with anti-TNF-α therapy are available; in particular, synovial knee biopsies showed a significant decrease in IL-32 expression in RA patients treated with a TNF-α blocker [129]. This observation fits with the evidence of a direct correlation between IL-32, TNF-α and disease activity in RA [130]. Additional studies, especially in human systems, are necessary to resolve the inconsistency of IL-32 in RA as well as to explore the therapeutic potential of this cytokine in RA.


IL-34 has been discovered in 2008 [131] and the receptor to which IL-34 binds with the highest affinity, colony stimulating factor (CSF)-1R, is shared with CSF-1. However, IL-34 and CSF-1 do not share sequence homology and have different expression patterns being IL-34 restricted to few tissues (brain, epidermis, spleen, bone marrow, lymph nodes) and CSF-1 widespread [132]. Upon binding to CSF-1R, IL-34 stimulates monocytes and macrophages through extracellular signal-regulated kinase (ERK) 1/2 or AKT phosphorylation. Recent data, however, demonstrated that IL-34 could also bind chondroitin sulphate chains, such as PTP-ζ and syndecan-1, but with lower affinity [133, 134]. This is of particular importance in tumor biology as these receptors are up-regulated in several cancer types. IL-34 can be induced by a variety of pro-inflammatory cytokines, including IL-1β and TNF-α, and its main function of that to promote monocyte survival, proliferation and differentiation to macrophages. Recent studies revealed that IL-34 drives the differentiation of monocytes into immunosuppressive M2 and that human macrophages cultured in the presence of IL-34 are able to expand Treg cells. Interestingly, IL-34-expanded Treg cells display a stronger suppressive activity compared to non–IL-34–expanded Treg cells [135, 136]. This widens the spectrum of action of IL-34 towards immune tolerance. Moreover, IL-34 is involved in RANK-L mediated osteoclastogenesis by inducing the proliferation and adhesion of osteoclast progenitors in vitro and by inducing the formation of osteoclasts from murine splenocytes in vivo, thereby reducing trabecular bone mass [137,138,139]. IL-34 deficient mice selectively lack Langerhans cells and microglia and display weak immune responses to skin antigens and central nervous system-selective viruses, but they display neither osteopetrosis nor any autoimmune manifestation [140, 141]. Mice lacking CSF-1R receptor are toothless and severely osteopetrotic and display circulating monocyte depletion, total depletion of microglia, significant impairment of olfactory function, defects in reproductive function and reduced bone marrow hematopoietic progenitor cells [142,143,144]. Conversely, the neutralization of CSF-1R in adult mice leads to a reduction of mature monocytes in blood and bone marrow, without affecting precursors [145]. With regard to experimental arthritis, it is interesting to note that the lack/blockade of CSF-1 as well as the blockade of CSF-1R is associated with less severe methylated bovine serum albumin (mBSA)-induced arthritis and CIA [146,147,148]. In RA patients, all available studies pointed to increased serum and SF levels of IL-34 with respect to normal and disease controls (OA, PsA, ankylosing spondylitis (AS)) [149,150,151,152,153]. Of interest, ser0075m IL-34 levels correlated with immunological markers of more severe disease including rheumatoid factor (RF), anticyclic citrullinated peptide antibody (anti-CCP) titers, erythrocyte sedimentation rate (ESR), C-reactive protein (CRP), and with disease activity and smoking [149,150,151,152]. In this regard, serum IL-34 levels have been also associated with radiographic progression and appear to be good predictors of radiographic damage in RA patients [150, 152]. Interestingly, treatment with DMARDs or TNF-α inhibitors is able to reduce serum IL-34 levels [151, 154]. IL-34 levels are also higher in RA SF compared to OA SF and increased in RA patients with higher disease activity [149, 153]. Of interest, SF IL-34 levels are directly correlated with those of SF RANK-L, further supporting the link between IL-34 and RANK-L mediated osteoclastogenesis [149]. Finally, IL-34 is also consistently expressed in RA ST, mainly in the sublining and the intimal lining layer, with its expression being associated to synovitis severity [148, 154, 155]. All these observations about IL-34 raise the question whether the blockade of its pro-inflammatory and bone remodeling effects are worth the loss also of the strongly suppressive IL-34 driven Treg cells. Therefore additional data are needed to clarify its therapeutic potential in RA.


The progression and severity of inflammation in RA is associated with a consistent production of pro-inflammatory cytokines and a deregulation of anti-inflammatory cytokines. Although several biologic agents with different mechanisms of action are available for the treatment of RA, even now a consistent number of patients either do not respond or respond only partially to these compounds. Therefore, the advance of our understanding of mediators involved in the pathogenesis of RA and in consequence, the development of novel targeted therapies, are compelling. Forty years after the discovery of IL-1, the never-ending quest to identify ‘the’ culprit of RA development is still a fascinating field under intense investigation. In recent years, the landscape of pro- and anti-inflammatory cytokines has rapidly expanded with the identification of new members proven to be involved at different extent in the pathogenesis of RA. In some cases, evidence from animal models and RA patients is already consistent to move forward into drug development. In others, conflicting observation and the paucity of data require further investigations.