Neutrophil Function in an Inflammatory Milieu of Rheumatoid Arthritis.
Rheumatoid arthritis (RA) is an autoimmune disease characterized by the presence of autoantibodies against citrullinated protein antigens (ACPAs) and proinflammatory cytokines which cause chronic synovitis, bone erosion, and eventual deformity. In the early stage of RA, there is a large infiltrate of neutrophils to the articular cavity, accumulating in both synovial tissue and fluid . The presence of neutrophils in the synovial area correlates with the early clinical manifestations of joint inflammation, suggesting that neutrophils play a significant role in the initiation of RA . Neutrophils are the first cells attracted by chemotactic cytokines and thus are quickly recruited into sites of infection or inflammation. As a member of the phagocytic innate immune system, neutrophils play an indispensable role during infection, injury, autoimmunity, and chronic disease. Neutrophils within circulating blood are captured by adhesion molecules on the endothelial surface of blood vessels and migrate from the bloodstream into pathological sites where invading pathogens are recognized by the host . Neutrophils fulfill their protective functions through phagocytosis and release of granular enzymes and reactive oxygen species (ROS) as well as producing web-like structures called neutrophil extracellular traps (NETs) . The release of granular enzymes and ROS into the extracellular space can cause damage to host tissues during inflammation . Effective constitutive apoptosis of these cells is required for the resolution of inflammation. NETosis is a special type of neutrophil death which can produce NETs composed of a network of extracellular DNA fibers, histone proteins, elastase, and myeloperoxidase. NETs help neutrophils to immobilize and ensnare bacteria, fungi, or viruses, which results in a more effective elimination of these pathogens. It is reported that RA synovial fluid neutrophils show increased NETosis. Neutrophils from patients with RA are preactivated by immune complexes such as rheumatoid factor (RF), resulting in excessive ROS release, degranulation, and NETosis ex vivo . Thus, the activation of neutrophils is associated with the initial inflammation in RA.
In addition, NETs can serve as a potential major source of citrullinated autoantigens which can trigger the development of autoimmune disease such as RA . In recent years, studies have found that the formation of NETs is associated with autoantigens being detected in patients with RA. NET formation may drive ACPA production in the lung and promote the development of the early stage of RA . Furthermore, it is reported that increased sputum NET levels are related to several citrullinated antibody reactivities in patients with RA . Citrullinated autoantigens contained in NETs can be taken up by fibroblast-like synoviocytes (FLS) and presented to T cells in a major histocompatibility complex (MHC) II-dependent manner, leading to amplified antigenspecific T and B cell responses in RA . Therefore, neutrophils may act as a bridge connecting FLS to T cell-mediated responses. In RA, the hallmark profile is the markedly increased proinflammatory cytokines which may regulate the neutrophil functions such as migration, apoptosis, and the formation of NETs [11-13]. In addition, activated neutrophils in the inflamed tissue can express a wide variety of proinflammatory cytokines and chemokines, which are also important to RA pathogenesis and neutrophils themselves . For example, neutrophil-derived production of IL-8 (also known as CXCL8) leads to further rounds of neutrophil migration from the circulation, which enhances the inflammatory process . In this review, we summarize the advances made in improving our understanding of neutrophil migration, apoptosis, and NET formation in the presence of an RA inflammatory milieu. We will also discuss the most recent strategies in targeting cytokines to modulate the function of neutrophils which may provide alternative novel therapies for RA.
2. Neutrophil Migration in RA
Neutrophils are major components in the synovial fluid of RA patients making up to 90% of cells. These cells are also abundant at the junction of the pannus and cartilage, where invasion occurs . During the past decades, it has been reported that neutrophil depletion can greatly inhibit the development of arthritis in two different murine models, collagen antibody-induced arthritis (AIA) and the K/BxN models [2, 17]. Therefore, it is suggested that neutrophils play a crucial role in initiating the inflammatory response and the progression of arthritis in RA. It is important to know which cytokines can affect the neutrophil migration. By blocking or weakening the migration of neutrophil into the inflamed tissue, one would predict that this would lead to a decrease in disease activity of RA, thereby developing a new strategy for the treatment of RA.
It is well accepted that factors including cytokines, chemokines, and immune complexes (RF and ACPA) can contribute to the process of neutrophil migration. In this review, we focus on the cytokines that can orchestrate neutrophil migration in human RA and animal arthritis models. In RA, cytokines such as tumor necrosis factor alpha (TNF-[alpha]), interleukin-6 (IL-6), IL-17a, IL-22, IL-23, IL-1[beta], IL-8, interferon-y (IFN-[gamma]), granulocyte/macrophage colony-stimulating factor (GM-CSF), granulocyte colony stimulating factor (G-CSF), IL-15, IL-18, IL-33, and IL-37 [11, 13, 18-36] are all detected either in the serum or in the synovial fluids of these patients. Thus, we discuss the impact of these cytokines on neutrophil migration in RA separately (Table 1).
2.1. TNF-[alpha] Enhances the Neutrophil Migration in RA. It is well known that TNF-[alpha] and IL-6 are two of the most predominant proinflammatory cytokines involved in the pathogenesis of RA. Anti-TNF-[alpha] and anti-IL-6R agents have been proven to be clinically useful in the disease control of RA. It is reported that TNF-[alpha] and IL-6 can both enhance the RA neutrophil migration in vitro [11, 21]. An additional study also finds that treatment with an anti-TNF-[alpha] agent can decrease the migratory capacity of neutrophils in patients with RA . However, anti-IL-6R agents do not appear to affect neutrophil migration in vitro . It indicates that TNF-[alpha] is a strong cytokine which can enhance RA neutrophil migration.
2.2. Th17-Related Cytokines Increase Neutrophil Migration in RA. Th17 cells (IL-17 and IL-22) and neutrophils are frequently observed in the synovial fluid of RA patients. A crosstalk exists between Th17 cells and neutrophils. Activated Th17 cells can directly attract neutrophils via the release of IL-8 . Moreover, IL-17 and IL-23 can both induce neutrophil migration after intra-articular injection in a dose-dependent manner. In antigen-induced arthritis, early release of IL-23 can stimulate IL-17 production, in turn, causing a release of TNF-[alpha], a variety of chemokines, and leukotriene B4 (LTB4), which together contribute to neutrophil recruitment. Therefore, IL-23/IL-17-induced neutrophil migration plays an important role in the pathogenesis of a murine model of RA . Furthermore, injection of adenoviral vectors with IL-17 (AdIL-17) into the knee joints before induction of immune complex- (IC-) mediated arthritis has been shown to induce greater neutrophils migrating to the cartilage surface, exacerbating inflammation and cartilage destruction . Interestingly, another Th17-related cytokine IL-22 is highly expressed in the synovial tissue of an antigen-induced arthritis mouse and human RA . Furthermore, IL-22 inhibition and IL-22 genetic deficiency can reduce neutrophil migration in arthritic mice and improve articular pain . Therefore, IL-17 and IL-22 both can promote the neutrophil migrating to the cartilage surface, exacerbating joint inflammation of RA.
2.3. IL-8 Promotes the Neutrophil Migration in RA. IL-8, a potent chemoattractant for neutrophils, plays a vital role in the recruitment and activation of neutrophils. IL-8 is considered to be one of the most crucial inflammatory chemokines involved in the development of arthritis . Injection of lipopolysaccharide (LPS) or IL-1[alpha] into joints of rabbits induces arthritis accompanied by upregulation of IL-8. Blockade of IL-8 by neutralizing antibody can ameliorate arthritis and reduce the infiltration of neutrophils into the joints in the early phase of inflammation . In RA patients, IL-8 is significantly elevated in the [ACPA.sup.high] synovial fluid. The elevated level of IL-8 is associated with worse clinical manifestations of the disease. There is a positive correlation between IL-8 and the number of neutrophils in synovial fluid . So IL-8 enhances the neutrophil migration and promotes the inflammatory response in RA.
2.4. IFN-[gamma] Biphasically Affects Neutrophil Migration, While IL-15 Enhances the Neutrophil Migration in RA. IFN-[gamma] has a dual function in the regulation of neutrophil migration. Firstly, IFN-[gamma] is generally considered to be a proinflammatory factor produced by Th1 cells and natural killer cells. IFN-[gamma] modulates neutrophil migration, as shown by a decrease of neutrophil recruitment in IFN-[gamma]-deficient mice and recovery after reconstitution of the IFN-[gamma] signaling pathway . IFN-[gamma]-induced neutrophil migration in vivo may be mediated by the release of the neutrophil chemotactic factor from resident macrophages . In contrast, IFN-[gamma] can also exert an anti-inflammatory effect in an RA animal model . In the murine AIA model, the arthritis symptoms are exacerbated by the absence of IFN-[gamma]. Furthermore, CXC chemokine receptor 2 [(CXCR2).sup.+] neutrophil recruitment is significantly higher in the joints of IFN-[gamma]-deficient mice. IFN-[gamma] receptor knockout (IFN-[gamma]R KO) mice develop collagen-induced arthritis (CIA) more severely with an increased neutrophil influx, while anti-IL-17 antibody administration can ameliorate arthritis partly by reducing the neutrophil infiltration . Based on these findings, it appears that there is a crosstalk between IFN-[gamma] and IL-17 in inflammation. Meanwhile, IFN-[gamma] modulates TNF-[alpha]-driven chemokine syntheses in RAFLS, resulting in a downregulation of IL-8 production . IL-15 is a proinflammatory cytokine that has a wide variety of functions in autoimmune diseases. IL-15 has been found to be highly expressed in the synovial fluid of RA patients . IL-15 can mediate blood and synovial neutrophil migration by triggering LTB4 production in antigen-induced arthritis models . Furthermore, IL-15 can also induce NF-[kappa]B activation and IL-8 production directly in human neutrophils, thereby activating these cells . In a summary, IFN-[gamma] bilaterally affects neutrophil migration, while IL-15 enhances the migration of neutrophil into joint.
2.5. GM-CSF and G-CSF Both Enhance the Neutrophil Migration in RA. GM-CSF and G-CSF are two hematopoietic growth factors involved in the regulation of hematopoiesis, used to treat neutropenia and to elicit the release of the hematopoietic stem cells from the bone marrow for transplantation . They are both found in human RA serum and synovial fluid [29-31]. GM-CSF can activate and sustain the viability of neutrophils. [GM-CSF.sup.-/-] mice are resistant to K/BxN serum transfer arthritis, whereas blockade of GMCSF can ameliorate the severity of arthritis in the CIA mouse model with a simultaneous reduction in synovial neutrophils . Recently, two clinical studies demonstrate that a monoclonal antibody targeting the GM-CSF receptor a called mavrilimumab is effective in the treatment of RA [49, 50]. However, the effect of this novel agent on neutrophil function has not yet been reported. Interestingly, G-CSF and G-CSF receptor-deficient mice are significantly protected in RA animal models partly due to a reduction in the number of neutrophils [47, 51]. A neutralizing antibody to the G-CSF receptor also prevents the progression of the disease by reducing neutrophil accumulation in the joints and inhibiting STAT3 phosphorylation in collagen Ab-induced arthritis . Furthermore, the production of proinflammatory cytokines and chemokines is decreased in anti-G-CSF receptor-treated mice . As such, targeting either GMCSF or G-CSF may be a promising novel approach to treat RA via the downregulation of neutrophil migration.
2.6. IL-1 Family Cytokines Affect Neutrophil Migration in RA. IL-1 family is a group of 11 cytokines that play a central role in the regulation of immune responses. IL-1[beta] is the most studied member because it is discovered first and it has a strongly proinflammatory effect. Importantly, IL-1[beta] can promote neutrophil migration . This is likely to contribute to RA disease progression since the level of IL-1[beta] in the joint increases with the onset of arthritis and correlates highly with arthritis scores. Moreover, recombinant IL-1[beta] (rIL-1[beta]) administration into mice can induce arthritis, whereas arthritis development is arrested in [IL-1R.sup.-/-] mice . IL-18, another member of the IL-1 family, functions by binding to its receptor to induce IFN-[gamma] production by T cells which can cause a rapid activation of the monocytes and macrophages. Recently, IL-18 is thought to be a potent mediator of inflammation in RA. It has been reported that IL-18 is significantly elevated in sera, synovial tissues, and synovial fluid of RA patients. IL-18 contributes to the inflammatory process by recruiting monocytes, lymphocytes, and neutrophils to the inflamed joints of RA . In the CIA model, IL-18 activates neutrophils through a synthesis of LTB4 in response to TNF-[alpha], which in turn enhances neutrophil recruitment . IL-33 and IL-37 are both new members of the IL-1 family of cytokines. In methylated bovine serum albumin(mBSA-) immunized mice, enhanced local neutrophil infiltration is associated with an increase in IL-33 mRNA expression. When recombinant IL-33 is injected into the joints of mice, it induces local neutrophil infiltration which subsequently resulted in joint damage. Moreover, neutrophil migration is inhibited by systemic and local administration of soluble IL-33R . IL-33-induced neutrophil migration is dependent on increased levels of CXCL1, CCL3, TNF-[alpha], and IL-1[beta] concentrations in the joint . Unlike other cytokines, IL-37 is an anti-inflammatory cytokine which suppresses joint and systemic inflammation . IL-37 has a protective effect in an arthritis mouse model by reducing cell influx and inhibiting joint inflammation . In a short conclusion, IL-1 family members, IL-1[beta], IL-18, and IL-33, all can induce local neutrophil migration, but IL-37 has an opposite effect.
3. Neutrophil Survival in RA
As we know, neutrophils usually have a limited lifespan in the circulation and rapidly undergo constitutive apoptosis when exposed to a stimulator such as TNF-[alpha] or Fas . Once recruited into sites of the inflammation, the activated neutrophils can encounter with a variety of proinflammatory cytokines in the microenvironment that may affect their function and longevity . Many cytokines are generated during inflammation, and these can induce a similar "primed" phenotype in neutrophils affecting their ability to undergo apoptosis. While proinflammatory factors such as GM-CSF, IFN-[gamma], IL-9, and IL-15 can reduce the induction of apoptosis and extend the lifespan of the neutrophils from RA patients in vitro, both IL-8 and IL-18 show no effect on this phenotype [27, 28, 32, 57-59]. In contrast, TNF-[alpha] and IL-6 exert a biphasic effect on neutrophil apoptosis [21, 27, 60-63].
3.1. GM-CSF, IFN-[gamma], IL-9, and IL-15 Delay Apoptosis of RA Neutrophils, but IL-8 and IL-18 Have No Effect. There is strong evidence that supports the role of GM-CSF in prolonging the neutrophil survival and activity in RA in vitro [27, 28, 57]. Both GM-CSF and IL-15 inhibit spontaneous apoptosis by downregulating proapoptotic proteins Bax and caspase-3, but only GM-CSF can abolish immune complex-induced apoptosis . Importantly, IL-15 and IFN-[gamma] can delay the apoptosis of RA neutrophils in vitro [27, 58]. Recently, Th9 cell frequency has been shown to be higher in synovial fluid of RA patients. Synovial IL-9 can decrease the apoptosis by inducing the expression of the antiapoptotic protein, Mcl-1, and prolonging the survival of the neutrophils . IL-1[beta] can reduce the spontaneous apoptosis of neutrophils from healthy controls in vitro, but not RA neutrophils [62, 65]. IL-8 and IL-18 do not affect the apoptosis of RA neutrophils in vitro [27, 59]. In summary, GM-CSF, IFN-[gamma], IL-9, and IL-15 can delay the apoptosis of neutrophils and extend their lifespan which may be harmful to inflammation resolution in RA .
3.2. TNF-[alpha] and IL-6 Exert a Biphasic Effect on Neutrophil Apoptosis. TNF-[alpha] shows an opposing effect where it enhances the rate of apoptosis in human neutrophils during the first 6 hours of exposure, followed by delayed apoptosis after 20 hours in culture [60,61]. Furthermore, the regulation of TNF-[alpha] on human neutrophil apoptosis is dependent on the concentrations of TNF-[alpha] in vitro. Higher concentrations of TNF-[alpha] ([greater than or equal to] 10ng/mL) increase the rate of caspase-dependent turnover of the antiapoptotic protein Mcl-1, which controls neutrophil survival, thereby accelerating neutrophil apoptosis, whereas lower concentrations of TNF-[alpha] ([less than or equal to] 1 ng/mL) can stimulate the expression of the antiapoptotic protein Bfl-1 leading to enhanced neutrophil survival . In contrast, other studies show that TNF-[alpha] can reduce the spontaneous apoptosis in neutrophils from healthy individuals (at [less than or equal to] 1 ng/mL) and RA patients (at 10 ng/mL) in vitro [27,62]. Actually, the concentrations of TNF-[alpha] in RA plasma (<100pg/mL) are far below those required to increase neutrophil apoptosis . Meanwhile, IL-6 can inhibit apoptosis of neutrophils from a healthy donor [62, 64, 66] and RA patients in vitro . However, others find that IL-6 enhances apoptosis in human neutrophils in vitro . Recent evidence reveals that IL-6 indeed does not affect the rate of neutrophil apoptosis in patients with RA . It has been reported that RA patients receiving the anti-IL-6 receptor agent tocilizumab (TCZ) may have decreased neutrophil counts . However, TCZ in vitro does not induce apoptosis or phagocytosis of neutrophils. Also, TCZ does not affect neutrophil functions in RA patients receiving TCZ treatment ex vivo .
The mechanisms underlying the effects of priming cytokines on neutrophil apoptosis have been partially elucidated. GM-CSF reduces the rate of neutrophil apoptosis through activation of ERK1/2 or PI-3K/Akt pathways [68, 69]. GM-CSF has also been shown to decrease mRNA levels of the proapoptotic protein Bad while increasing its phosphorylation . An RNAseq analysis of human neutrophils primed by proinflammatory cytokines (GM-CSF and TNF-[alpha]) in vitro revealed altered levels of 58 transcripts implicated in the control of apoptosis . Synovial fluid of patients with RA contains a variety of antiapoptotic and proapoptotic cytokines. The hypoxic environment within these joints can have beneficial effects on neutrophil survival. Compared to arterial blood, inflamed tissues are usually more hypoxic and acidic. Hypoxia causes delayed apoptosis of neutrophils in humans and mice. Additional studies have found that hypoxia-induced neutrophil survival is mediated by HIF-1[alpha]-dependent NF-[kappa]B activity . Other studies demonstrate neutrophils isolated from RA synovial fluid and blood undergo delayed apoptosis as shown by increased expression of neutrophil survival protein Mcl-1 and decreased levels of activated caspase-9 [56, 57, 72]. The delay of neutrophil apoptosis is restored to control levels after treatment with methotrexate . Interestingly, Janus kinase inhibitor (JAKi) prevents GM-CSF- and IFN-[gamma]-induced apoptosis delay in RA and healthy control neutrophils in a dose-dependent manner. Incubation with JAKi prevents chemotaxis of RA neutrophils towards IL-8 but does not increase the level of apoptosis in vitro . Therefore, the RA neutrophils in synovial fluid and blood undergo delayed apoptosis due to the proinflammatory and hypoxic microenvironment. GM-CSF, IFN-[gamma], IL-9, and IL-15 delay apoptosis of RA neutrophils, but others have no effect or a biphasic effect on neutrophil apoptosis.
4. The Role of NETs in the Pathogenesis of RA
Solid evidence exists that supports the important role of NETs in the pathogenesis of RA [8, 9, 13, 20, 73]. NET formation has been identified as a link between the innate and adaptive immune responses in autoimmunity. NETs provide the immune system with access to enriched sources of citrullinated proteins and thereby representing an early event preceding epitope spreading. Enhanced NETs are observed in both the bloodstream and synovial fluid of RA patients compared to healthy controls and patients with osteoarthritis [13, 73]. However, not all NETs shape the immune response toward disease-specific autoantibodies. One hypothesis speculates that NETs triggered by smoking can be an initiating factor in the pathogenesis of RA . These NETs may drive anti-ACPA production in the lung which can play an important role in the early stage of RA development . Increasing NET levels in the sputum are found to be significantly correlated with several citrullinated and noncitrullinated antibody reactivities in patients with RA . Sera and immunoglobulin fractions from RA patients with high levels of ACPA or RF significantly enhanced NETosis. In vitro incubation of neutrophils with [ACPA.sup.high] synovial fluid results in increased ROS production and extracellular DNA release compared to neutrophils incubated with ACPA-negative synovial fluid .
The inflammatory cytokines such as TNF-[alpha], IL-17a, IL-6, and IL-8 can induce NETs in RA neutrophils. Subsequently, NETs promote more cytokine production and persistent inflammation via activating FLS or macrophages [13, 73, 75-78]. The neutralizing antibodies to TNF-[alpha] or IL-17R can reduce RA serum-induced-NETs . NETs are strong activators of inflammatory responses in RA synovial fibroblasts since they can significantly augment the inflammatory reactions of RA synovial fibroblasts by inducing the production of IL-6, IL-8, chemokines, and adhesion molecules . IL-6 can induce NET formation in neutrophils isolated from healthy individuals . In RA, IL-6 may induce B cell maturation into plasma cells that can produce ACPA, thereby indirectly promoting NET formation . Furthermore, anti-TNF-[alpha] (Infliximab) and anti-IL6R drugs (TCZ) can reduce the production of NETs [73, 76]. Interestingly, IL-8 can affect neutrophils through two different mechanisms of actions in RA. IL-8 recruits neutrophils to the inflammatory site through chemotactic effects while simultaneously triggering NET formation [13, 77].
IFN-[gamma] and complement-5a (C5a) stimulation results in the formation of NETs in mature but not in immature human neutrophil populations . Additional cytokines such as IL-1[beta] and IL-18 are both able to stimulate NETs in human neutrophils [80-83]. CD177 is exclusively expressed in neutrophils and can be upregulated during inflammation. [CD177.sup.+] neutrophils produce NETs through IL-22 signaling . IL-9 and IL-33 are involved in the pathogenesis of several autoimmune diseases, such as RA [11, 32, 33]. Recently, neutrophils isolated from patients with systemic sclerosis (SSc) express IL-9R and exposure of these neutrophils to rIL-9 can significantly induce NET formation . IL-33 enhances noninfectious inflammation in the liver by amplifying NET formation . However, the role of IFN-[gamma], IL-9, IL-1[beta], IL-18, IL-22, and IL-33 in the formation of NETs in RA remains to be studied.
5. Parodontitis, NETs, and Anticitrulline Response in RA
Citrullines are produced not only in the lung but also in the oral cavity. Periodontitis, an oral bacterial infection, is very common in RA . Patients with periodontitis appear to have increased the risk for RA and patients with RA have increased the risk for periodontitis . It has been reported that periodontitis is associated with anti-CCP antibody and RA disease activity . Most importantly, citrullinated proteins can be detected in the periodontium in RA patients with periodontitis . As we know, the formation of citrullinated proteins is catalyzed by peptidylarginine deiminase (PAD) enzymes. Porphyromonas gingivalis (P. gingivalis), an oral bacteria that is a crucial factor for periodontitis and express PAD and citrullinated enolase, can mediate citrullination of bacterial and host protein . It has been shown that deletion of the bacterial PAD gene results in complete abrogation of protein citrullination . Moreover, antibody titers to P. gingivalis are correlated with ACPA titres of RA patients . Therefore, PAD from P. gingivalis may cause citrullinated protein formation, which may elicit an antibody response to these proteins potentially leading to ACPA formation. Although P. gingivalis does not seem to directly regulate NET generation in RA , it has been shown that P. gingivalis could induce human neutrophils to generate NETs in vitro . Interestingly, a pilot case-control study has found that periodontal treatment markedly reduced the serum levels of NETs in patients with RA and periodontitis . Furthermore, Konig et al. find another periodontal germ called Aggregatibacter actinomycetemcomitans (Aa) can induce hypercitrullination in host neutrophils through its leukotoxin A (LtxA). Moreover, LtxA induces neutrophil lysis and the extracellular release of hypercitrullinated proteins mimicking extracellular trap formation. It has been confirmed in patients with RA that serum anti-LtxA antibodies are associated with both anticitrullinated protein antibodies and rheumatoid factor .
6. Neutrophils and Their Anti-inflammatory Effects
NETs have not only proinflammatory effects, but also contribute to the resolution of inflammation. Neutrophils can resolve inflammatory processes via the annexin A1(AnxA1-) mediated pathway . Microvesicles (MVs), those extracellular particles within a size range between 50 nm and 1000 nm, can mediate cell to cell communication by transferring proteins and lipids to target cells. MVs also have a role in antigen presentation and activation of endosomal receptors such as Toll-like receptors. Recently, MVs have been considered a functional molecule with their potential for the treatment of autoimmune disease. Neutrophilderived MVs are present at higher levels in synovial fluids of RA . Neutrophil-derived MVs can protect cartilage degradation through the reduction of interleukin-8 and prostaglandin E2. In addition, it has been demonstrated that synovial MVs overexpress the anti-inflammatory protein annexin A1 (AnxA1). Furthermore, neutrophil-derived MV-associated AnxA1 interacts with its receptor, increasing transforming growth factor-[beta] production by chondrocytes ultimately leading to cartilage protection .
7. Conclusion and Perspectives
Neutrophils play a crucial role in initiating inflammatory response and progression of arthritis in RA (Figure 1). Cytokines which can regulate migration and activation of neutrophils are highly expressed in the inflamed joint tissues of RA patients. Proinflammatory factors such as GMCSF, IFN-[gamma], IL-9, and IL-15 can reduce neutrophil apoptosis and extend their neutrophil lifespan in RA, whereas TNF-[alpha] and IL-6 display a biphasic effect on the apoptosis of neutrophils. NETs can be a source of released self-antigens found in RA. Formation of NETs is closely related to an autoantigen-triggered immune response in patients with RA. Furthermore, the inflammatory cytokines such as TNF-[alpha], IL-6, IL-8, and IL-17a can induce NETs in RA neutrophils. Subsequently, NETs can promote an increase in cytokine production and enable the persistence of inflammation via the licensing of FLS and/or macrophages. Importantly, the anti-TNF-[alpha] and anti-IL-6R have been successful in treating RA by partially acting on neutrophils. Additional cytokines, for example, IL-22, IL-23, IL-18, GCSF, IL-33, and IL-37, may also play an important role in the regulation of neutrophil functions. In addition, neutrophils may also play a role in the resolution of inflammation in RA. In the future, further studies are needed to understand how neutrophils act in an inflammatory milieu in patients with RA and animal models which may be critical for the development of novel treatment strategies.
Conflicts of Interest
The authors declare that they have no conflicts of interest.
Weiqian Chen and Qin Wang equally contributed to this manuscript.
This work was supported by the National Natural Science Foundation of China (81701600), the Natural Science Foundation of Zhejiang Province (LQ17H100001 and LGF18H100001), and the Research Medical and Health Program of Zhejiang Province (2019RC032). The authors would like to thank Dr. Bohdan P. Harvey for his critical review of their manuscript.
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Weiqian Chen, Qin Wang, Yini Ke, and Jin Lin (ID)
Division of Rheumatology, First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, Zhejiang, China
Correspondence should be addressed to Jin Lin; firstname.lastname@example.org
Received 28 June 2018; Revised 31 October 2018; Accepted 15 November 2018; Published 3 December 2018
Guest Editor: Yi Zhao
Caption: Figure 1: Role of neutrophil in the pathogenesis of RA. Proinflammatory cytokines in the joint can influence the migration of neutrophils. Neutrophils are activated by immune complexes and inflammatory cytokines (TNF- [alpha], IL-6, IL-8, and IL-17a) within the synovial fluid, frequently causing enhanced NET formation in RA. In turn, NETs are served as a source of citrullinated autoantigens, further triggering the production of ACPA. Meanwhile, neutrophils undergo delayed apoptosis in an inflammatory milieu (GM-CSF, IL-9, IL- 15, IFN-[gamma], and TNF-[alpha]) leading to persistent inflammation and joint damage in RA. * Controversial.
Table 1: Known cytokines' capacity to induce biological changes in neutrophils in RA. Cytokines/blockade Human RA or mouse Expression model TNF-[alpha] Human RA [up arrow] in serum and synovial fluid [13, 18, 19] Blockade of TNF- Human RA Collagen Ab -- [alpha] and [TNFR.sup.-/-] LPS-induced -- arthritis model IL-6 Human RA [up arrow] in serum and synovial fluid [19-21] Blockade of IL-6 Human RA -- IL-17a AIA mouse model and [up arrow] in the human RA joint [22, 23] Adenoviral vectors IC-mediated -- with IL-17 arthritis mouse model Anti-IL-17 antibody CIA model -- administration IL-23 AIA mouse model and [up arrow] in joint human RA [22, 24] IL-22 AIA mouse model and [up arrow] in human RA synovial tissue [25, 26] Block IL/22 or AIA mouse model -- [IL-22.sup.-/-] rmIL-22 Normal mice -- administration IL-1/3 Human RA and AIA [up arrow] in mouse model synovial fluid  [IL-1R.sup.---] or Collagen Ab and LPS- -- IL-1R antagonist induced arthritis model IL-8 Arthritis rabbit [up arrow] in model and human RA synovial fluid [19, 27] Blockade of IL-8 Arthritis rabbit -- model IL-10 Human RA [up arrow] in synovial fluid  IFN-[gamma] Human RA [up arrow] in synovial fluid  [IFN-[gamma].sup.- AIA, CIA model [up arrow] released 7-] by RAFLS GM-CSF Human RA in vitro , [up arrow] in serum and synovial fluid [18, 29, 30] Blockade of GM-CSF CIA -- [GM-CSF.sup.-/-] K/BxN serum transfer -- arthritis G-CSF Human RA [up arrow] in serum and synovial fluid [30, 31] rhG-CSF CIA [up arrow] serum G- CSF  [G-CSF.sup.-/-] CIA -- mAb to G-CSF Collagen Ab-induced -- receptor arthritis model IL-9 Human RA [up arrow] in serum and synovial fluid [32, 33] IL-15 Human RA [up arrow] in synovial fluid  IL-18 Human RA [up arrow] in serum, synovial tissue and fluid  IL-33 mBSA-immunized mouse [up arrow] mRNA model expression  rmIL-33 rmIL-33 local -- injection Blockade of IL-33 mBSA-immunized mouse -- model IL-37 Human RA [up arrow] in serum and synovial fluid  IL-37 administration CIA and -- streptococcal cell wall fragments induced arthritis Cytokines/blockade Migration or Apoptosis or recruitment survival TNF-[alpha] [up arrow] in vitro Promote or delayed  apoptosis In vitro  Antiapoptotic Mcl-1 Blockade of TNF- [down arrow] in vivo [up arrow] and [alpha]  proapoptotic caspase-9 [down arrow],  [TNFR.sup.-/-] [down arrow], in vivo  IL-6 No effect in vitro No effect in vitro  , delayed apoptosis in vitro  Blockade of IL-6 -- No effect in vivo and ex vivo  IL-17a [up arrow] in vivo --  Adenoviral vectors [up arrow] in vivo -- with IL-17  Anti-IL-17 antibody [down arrow], in -- administration vivo  IL-23 [up arrow] in vivo --  IL-22 [up arrow] in vivo --  Block IL/22 or [down arrow], in -- [IL-22.sup.-/-] vivo  rmIL-22 [up arrow] in vivo -- administration  IL-1/3 [up arrow] in vitro Delayed apoptosis in  vitro*  [IL-1R.sup.---] or [down arrow], in -- IL-1R antagonist vivo  IL-8 [up arrow] in vivo No effect in vitro , [up arrow] in  vitro  Blockade of IL-8 [down arrow], in -- vivo  IL-10 -- -- IFN-[gamma] -- Delayed apoptosis in vitro  [IFN-[gamma].sup.- [up arrow] in vivo Survival [up arrow] 7-] [43, 44] , GM-CSF -- delayed apoptosis in vitro [27, 57, 58] Blockade of GM-CSF [down arrow], -- neutrophils in the joint  [GM-CSF.sup.-/-] [down arrow], -- neutrophils in the joint  G-CSF -- -- rhG-CSF [up arrow] in vivo --  [G-CSF.sup.-/-] [down arrow], in -- vivo  mAb to G-CSF [down arrow], in -- receptor vivo  IL-9 -- Delayed apoptosis  IL-15 [up arrow] in vivo Delayed apoptosis in  vitro  IL-18 [up arrow] in vivo No effect in vitro   IL-33 [up arrow] in vivo --  rmIL-33 [up arrow] in vivo --  Blockade of IL-33 [down arrow], in -- vivo  IL-37 -- -- IL-37 administration [down arrow], in -- vivo  Cytokines/blockade NET formation Outcome TNF-[alpha] [up arrow] in vitro  Blockade of TNF- [down arrow], in Improved [73, 98] [alpha] vitro [13, 73] [TNFR.sup.-/-] Improved  IL-6 [up arrow] in vitro --  [up arrow] in vitro*  Blockade of IL-6 [down arrow], in Improved  vivo and in vitro [73, 76] IL-17a [up arrow] in vitro  Adenoviral vectors -- Deteriorated  with IL-17 Anti-IL-17 antibody [down arrow], in Improved  administration vitro  IL-23 -- -- IL-22 -- -- Block IL/22 or -- Improved  [IL-22.sup.-/-] rmIL-22 -- Deteriorated  administration IL-1/3 [up arrow] in vitro * -- [81-83] [IL-1R.sup.---] or [down arrow], in Improved  IL-1R antagonist vitro * [82, 83] IL-8 [up arrow] in vitro --  Blockade of IL-8 -- Improved  IL-10 [up arrow] in vitro * --  IFN-[gamma] [up arrow] in vitro * --  [IFN-[gamma].sup.- -- Deteriorated 7-] [43, 44] GM-CSF No effect in vitro --  Blockade of GM-CSF -- Improved  [GM-CSF.sup.-/-] -- Improved  G-CSF [up arrow] in vitro * --  rhG-CSF -- Deteriorated  [G-CSF.sup.-/-] -- Improved  mAb to G-CSF -- Improved  receptor IL-9 [up arrow] in vitro * --  IL-15 [up arrow] in vitro *  IL-18 [up arrow] in vitro *  IL-33 [up arrow] in vitro *  rmIL-33 -- Deteriorated  Blockade of IL-33 -- Improved  IL-37 -- IL-37 administration -- Improved [54, 102] RA: rheumatoid arthritis, NETs: neutrophil extracellular traps, TNF-[alpha]: tumor necrosis factor-alpha, Mcl-1: myeloid cell leukemia-1, TNFR: tumor necrosis factor receptor, Ab: antibody, LPS: lipopolysaccharide, IL: interleukin, AIA: antigen-induced arthritis, IC: immune complex, rmIL-22: recombinant murine interleukin 22, IL-1R: interleukin 1 receptor, IFN-[gamma]: interferon gamma, CIA: collagen-induced arthritis, GM-CSF: granulocyte/macrophage colony-stimulating factor, RAFLS: rheumatoid arthritis synovial fibroblasts, G-CSF: granulocyte colony-stimulating factor, mAb: monoclonal antibody, mBSA: methylated bovine serum albumin, rmIL-33: recombinant murine interleukin 33, rhIL-37: recombinant human interleukin 37. * is found in other inflammatory diseases or healthy individuals, but not RA