Journal of Immunology Research
Volume 2021 (2021), Article ID 6683411, 15 pages
https://doi.org/10.1155/2021/6683411

Review Article

Research Progress on the Mechanism of Natural Product Ingredients in the Treatment of Uveitis

Sicong Li,¹ Fang Liu,² Kai Zhang,³ Yujia Tong,⁴ and Xin Liu⁵

¹School of Pharmacy, Peking University Health Science Centre, Beijing, China
²Department of Pharmacy, China-Japan Friendship Hospital, Beijing, China
³Department of Rheumatology and Immunology, Peking University People’s Hospital, Beijing, China
⁴Institute of Medical Information, Chinese Academy of Medical Sciences/Peking Union Medical College, Beijing, China
⁵School of Traditional Chinese Medicine, Beijing University of Traditional Chinese Medicine, Beijing 100029, China

Correspondence should be addressed to Xin Liu; xinliu1011@126.com

Received 31 December 2020; Revised 16 June 2021; Accepted 7 July 2021; Published 16 July 2021

Academic Editor: Chiara Posarelli

Copyright © 2021 Sicong Li et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Background. As the spectrum of ophthalmic diseases keeps changing, uveitis has gradually become one of the major blinding eye diseases in the world. In recent years, it has become a research hotspot to select effective components for uveitis treatment from natural drugs. Methods. We searched PubMed and EMBASE databases for studies written in English as well as Chinese National Knowledge Infrastructure (CNKI), CQVIP, and Wan Fang database for studies written in Chinese (inception through 30 December 2020). Results. Eight kinds of natural product ingredients were included in this article. They were found to not only regulate the expression of cytokines, proliferation, and differentiation of T help cells but also inhibit the damage of cytokines and inflammatory cells to uvea, blood aqueous barrier, and blood retinal barrier. Conclusion. Natural product ingredients have their unique advantages in the treatment of uveitis. They have good anti-inflammatory effects without causing serious adverse reactions, which enables them to be promising choices for preventive and therapeutic strategy of uveitis.

1. Introduction

Uveitis refers to various intraocular inflammatory diseases occurred in uvea (i.e., iris, ciliary body, and choroid) and its adjacent structures (including cornea, vitreous body, retina, and optic nerve) [1]. Without timely diagnosis and treatment on chronic inflammation in the eye, it will lead to cataracts, glaucoma, corneal lesion, macular edema, or even permanent vision loss [2]. Uveitis can be divided into three categories according to its pathogenesis: infectious uveitis caused by pathogens like bacteria, viruses, and fungi and autoimmune-related uveitis as well as camouflage syndrome. Rheumatoid arthritis, Behcet’s disease, and inflammatory bowel disease as well as juvenile idiopathic arthritis are often accompanied by uveitis [3].

The abnormal number and function of cluster of differentiation 4 + (CD4 +) T cells play important roles in the immunopathogenesis of uveitis [4]. As is shown in Figure 1, retinal S antigen, vitamin A binding protein between photoreceptors, and uveal melanin-associated antigen excessively activate dendritic cells that promote the differentiation of CD4 + T cells into different subtypes, such as T helper 1 cells (Th1 cells), T helper 2 cells (Th2 cells), regulatory T cells (Tregs), and T helper 17 cells (Th17 cells) [5].

Figure 1: T lymphocytes and related immune responses in uveitis.

Interferon-γ (IFN-γ), interleukin-12 (IL-12), and interleukin-27 (IL-27) induce differentiation of Th1 cells that secrete cytokines, including interleukin-2 (IL-2), IFN-γ, and tumor necrosis factor (TNF-α) and participate in cellular immunity [6]. The expression levels of TNF-α and IFN-γ are positively correlated with the severity of uveitis [7]. IL-1β, transforming growth factor-β (TGF-β), interleukin-12 (IL-12), interleukin-6 (IL-6), and interleukin-23 (IL-23) induce differentiation of Th17 cells that mediate the immune response. Both Th1 and Th17 cells play important roles in the pathogenesis and recurrence of uveitis [8]. IL-2, IL-4, and IL-13 induce differentiation of Th2 cells that participate in humoral immunity [9]. Functions of Th-2 can be inhibited by IFN-γ that secreted by Th1 cells [10]. TGF-β and IL-10 can induce the differentiation of regulatory T cells (Treg cells) that inhibit the function of Th1 and Th17 cells by secreting TGF-β and IL-10 [11]. Less and impaired functions of Tregs are observed in uveitis patients [12]. It can be concluded that regulating immune function is an effective way in the treatment of uveitis.

Most of the current research on uveitis drugs focuses on biological agents. Infliximab, a tumor necrosis factor antagonist, can effectively treat vitreous opacity, active retinal vasculitis, and macular cystic edema caused by uveitis and scleral inflammation [13, 14], but it can lead to tuberculosis and aggravate demyelination disease. Adalimumab has been proved to be effective and safe for uveitis treatment in many trials [15–18] but has not been approved by the National Medical Products Administration (NMPA) for clinical treatment of uveitis in China. The main drugs currently available in China to treat uveitis include immunosuppressants and glucocorticoids. Immunosuppressants such as cyclophosphamide, cyclosporin, and azathioprine not only inhibit bone marrow function but also have nephrotoxicity or hepatotoxicity [19]. Subconjunctival injection, peribulbar injection, retrobulbar injection, and vitreous cavity injection of glucocorticoid can improve visual impairment, inhibit the formation of adhesion, and relieve eye pain but can lead to adverse reactions including ptosis, cataract, and increased intraocular pressure [20]. Oral administration of corticosteroids can treat uveitis by inhibiting the destruction caused by the inflammatory response. Expansion of capillaries and proliferation of fibroblasts can be inhibited by corticosteroids [21]. On the other hand, corticosteroids can lead to peptic ulcers, hypertension, and hyperlipidemia [22]. In recent years, it has become a hot spot in the research field of uveitis to extract immunomodulators with high efficiency and low toxicity from natural products. In this article, the therapeutic effects of alkaloids, glycosides, polysaccharides, and polyphenols on uveitis and their mechanisms were discussed in detail, to provide a reference for drug development and clinical research.

2. Materials and Methods

2.1. Search Strategy

PubMed and EMBASE databases were searched for studies written in English. Chinese National Knowledge Infrastructure (CNKI), CQVIP, and Wan Fang databases were searched for studies written in Chinese. We searched for articles published before 30 December 2020. Keywords including “Uveitis” or “Panuveitis” plus any of the following: “natural product”, “Matrine”, “Berberine”, “Total glucosides of paeony”, “Tripterygium wilfordii polyglycoside”, “Astragalus polysaccharide”, “Hedysari polysaccharide”, “Rhubarb polysaccharide”, and “Curcumin” were used to search for articles in Chinese database. The search strategy for articles written in English is shown in Tables 1 and 2.

Table 1: Search strategy in PubMed.

Number
Search terms

1
Uveitis (MeSH Terms)

2
Uveitis (ALL field)

3
Panuveitis (MeSH Terms)

4
Panuveitis (ALL field)

5
1 OR 2 OR 3 OR 4

6
natural product [MeSH Terms]

7
natural product [ALL field]

8
Matrine [ALL field]

9
Berberine (MeSH Terms)

10
Total glucosides of paeony [ALL field]

11
Tripterygium wilfordii polyglycoside [ALL field]

12
Astragalus polysaccharide [ALL field]

13
Hedysari polysaccharide [ALL field]

14
Rhubarb polysaccharide [ALL field]

15
Curcumin [ALL field]

16
6 OR 7 OR 8 OR 9 OR 10 OR 11 OR 12 OR 13OR 14 OR 15

17
5 AND 16

Table 2: Search strategy in EMBASE.

Number
Search terms

1
Uveitis (ti,ab,kw)

2
Panuveitis (ti,ab,kw)

3
Uveitis

4
Panuveitis

5
1 OR 2 OR 3 OR 4

6
natural product [ti,ab,kw]

7
natural product

8
Matrine [ti,ab,kw]

9
Berberine [ti,ab,kw]

10
Total glucosides of paeony [ti,ab,kw]

11
Tripterygium wilfordii polyglycoside

12
Astragalus polysaccharide [ti,ab,kw]

13
Hedysari polysaccharide [ti,ab,kw]

14
Rhubarb polysaccharide [ti,ab,kw]

15
Curcumin [ti,ab,kw]

16
6 OR 7 OR 8 OR 9 OR 10 OR 11 OR 12 OR 13OR 14 OR 15

17
5 AND 16

2.2. Study Inclusion and Exclusion Criteria

2.2.1. Inclusion Criteria

The inclusion criteria are the following: (1) articles about studies of natural product ingredients’ therapeutic effect on uveitis, (2) written in Chinese or English, and (3) abstract and full text available.

2.2.2. Exclusion Criteria

The exclusion criteria are the following: (1) study protocols, conference abstracts without data in detail, comments, or letters; (2) no data reported; and (3) therapeutic drug is a decoction of medicinal ingredients. Process of literature screening is revealed in Figure 2.

Figure 2: Flow chart of literature screening.

3. Results and Discussion

3.1. Alkaloids

Alkaloids are nitrogen-containing alkaline compounds widely found in natural products. Among them, matrine and berberine have anti-inflammatory effects.

3.1.1. Matrine

Extracted from the dried root of Sophora flavescens Alt., matrine has antibacterial, anti-inflammatory, antitumor, and antiarrhythmia effects. Matrine has an inhibitory effect on the inflammatory reactions caused by liposaccharides (LPS) [23, 24] LPS, a component of the cell wall of gram-negative bacteria, acts on the Toll-like receptors 4 (TLR4) receptor to induce myeloid differentiation factor88 (MyD88) recruitment, followed by activation of nuclear factor kappa-B (NF-κB) through a series of phosphorylation cascades [25]. After the inflammatory factors destroy the blood-aqueous barrier or blood-retinal barrier, some macromolecular protein substances and cells in the blood infiltrate into the interstitial or intracavity of the eye (anterior chamber or vitreous body), giving rise to different degrees of tissue damage [26]. The breakdown of the blood-aqueous barrier leads to iris neovascularization. The wall of the neovascularization is susceptible to rupture and leads to hyphema [27]. Matrine eye drops (low dosage group (0.50 g/L), middle dosage group (0.75 g/L), high dosage group (1.00 g/L)) decreased the IL-6, IL-1, and TNF-α level in serum and aqueous humor of the uveitis model rabbits induced by LPS; inhibited the expression of the TLR4, MyD88, and NF-κB p65 in retinal tissue; and improved rabbit ciliary hyperemia, retinal edema, and retinal fundus bleeding [28]. Subconjunctival injection of matrine (0.8 mg) inhibited the expression of vascular endothelial growth factor (VEGF) mRNA in the corneal tissue burnt by alkali [29].

If inflammatory cells and mucin deposits in aqueous humor block trabecular meshwork and impede the outflow of aqueous humor, it will increase intraocular pressure and give rise to glaucoma in uveitis patients. Trabeculectomy is a commonly used treatment. After trabeculectomy, putting 1.0 g/L matrine cotton tablets under the scleral flap for 28 days reduced the proliferation of fibroblasts and reduce the formation of filter bubble scar [30].

3.1.2. Berberine (BBR)

Extracted from Coptis chinensis Franch., berberine is a kind of isoquinoline alkaloid with anti-inflammatory, antitumor, antibacterial, and antiviral effects. The therapeutic effect of berberine on uveitis has been confirmed in animal and in vitro experiments.

T helper cell 17 (Th17) cells play an important role in the pathogenesis of ocular Behcet’s disease and uveitis [31]. IL-6, IL-21, IL-23,TGF-β, or IL-1β drive the production of IL-17 in Th17 cells by activating signal transducer and activator of transcription-3 (STAT-3) and retinoid-related orphan nuclear receptor γt (RORγt) [32]. In vitro, berberine (5 μM) not only inhibited Th17 and Th1 cell differentiation and secretion of IL-17 and IFN-γ but also regulated the balance of T regulatory cell (Treg)/T helper cell (Th17) in patients with ocular Behcet’s disease [33]. Cytokines such as IL-6, IL-1, and IL-23 secreted by dendritic cells (DC cells) drive the differentiation and production of interleukin-17 by activating STAT-3 [33, 34]. BBR downregulated the expression of costimulatory molecules, including clusters of differentiation 40 (CD40), clusters of differentiation 80 (CD80), and clusters of differentiation 86 (CD86) and inhibited DC cells’ maturation and the secretion of IL-6, IL-1, and IL-23 [35]. Uveitis may be accompanied by retinal pigment epithelium lesions, retinal edema, thinning, and hemorrhage. Berberine dose-dependently inhibited dysfunction of the blood-retina barrier induced by IL-1 and improved retinal edema in rats [36].

In vivo, berberine’s therapeutic effect on uveitis has also been proved. Interleukin-8 and monocyte chemotactic protein-1 (MCP-1) play important roles in LPS-induced uveitis. Cytokine-induced neutrophil chemokine-1 (CINC-1) is a rat analog of IL-8. The role of IL-8 and CINC-1 in endotoxin-induced uveitis has been confirmed by many studies [37, 38]. Orally taking a 0.8 mL berberine solution before injecting LPS in Wistar rats inhibited the expression of MCP-1 mRNA and CINC-1 mRNA of the iris ciliary and the damage of the iris ciliary body caused by inflammatory cells [39]. Li et al. [40] intraperitoneally injected berberine (2 mg/kg) into experimental autoimmune uveitis (EAU) rats for two weeks and found only a slight inflammatory reaction in the eyes, while in the normal saline group, serious vasodilation, iris hemorrhage, and purulent exudation were observed. The therapeutic effect of berberine on experimental autoimmune retinitis is also related to regulating intestinal flora. After 14 days of intragastrically administrating berberine (100 mg/kg), the number of Th1 and Th17 cells in the spleen of mice significantly decreased, while the number of Treg cells increased. Berberine inhibited the breakdown of the blood-retinal barrier, and corneal edema, retinal folding, iris congestion, and iris adhesion were significantly improved, which was related to the significant changes in the composition of the spleen transcriptome and intestinal microorganisms. The dominant microbiome in the experimental autoimmune uveitis (EAU) group was Lactobacillus aceae, while in the BBR group was Muribaculaceae. By means of MetaStat analysis, five genera, including Lactobacillus, was reduced, with thirteen genera, including Akkermansia and Oscillibacter, increased in the BBR group. Compared with the EAU group, 249 differentially expressed genes (DEGs) were downregulated, and 227 DEGs were upregulated. The downregulated biological processes mainly included nucleosome assembly, chromatin assembly, myelin differentiation, and antigen processing and expression. It suggested that berberine led to significant changes in the overall transcription profile of genes [41].

3.2. Glycosides

Glycosides are compounds formed by the attachment of end-group carbon atoms of a sugar or sugar derivative to another type of nonsugar substances (called glycosides, ligands, or glycosides). Most of the glycosides are colorless and soluble in water. With good anti-inflammatory activity, total glucosides of paeony (TGP) and Tripterygium wilfordii polyglycoside (TWP) are widely used in the clinical treatment of rheumatic immune diseases in China.

3.2.1. Total Glucosides of Paeony (TGP)

Extracted from the dried root of Paeonia lactiflora Pall., TGP have anti-inflammatory, analgesic, immunomodulatory, and antitumor effects. TGP capsule has been approved for clinical treatment of rheumatoid arthritis in China since 2005. Moreover, TGP have been reported to be used in the clinical treatment of rheumatoid arthritis [42], idiopathic arthritis [43], systemic lupus erythematosus [44], and Sjogren’s syndrome [45] in China.

The occurrence of uveitis is closely related to the dysfunction of T lymphocytes, especially autoreactive T lymphocytes. Activation-induced cell death pathway (AICD) plays a crucial role in maintaining immune tolerance and clearance of autoreactive T lymphocytes [46, 47]. Fas/FasL can induce faster apoptosis of T lymphocytes. TGP enhanced Bcl-2 expression in the EAU group’s retinal tissues, which was very weak in the normal retinal tissues [48]. In cell experiments, total glucosides of paeony significantly inhibited T lymphocyte proliferation and promoted activation-induced T lymphocyte death by upregulating Fas and downregulating Bcl-2 expression [49].

In animal experiments, total glucosides of paeony (4.8 g/kg, once every 6 h, three times in total) were administered to rats with uveitis before LPS injection, which not only inhibited the invasion of inflammatory cells into the anterior chamber and vitreous body but also inhibited the swelling of iris and ciliary body and thickening of retinal edema, as well as fibrinoid exudation in the anterior chamber. Besides, it significantly alleviated iris bleeding, anterior chamber pus, and pupil narrowing [50]. Total glucosides of paeony (orally taken for 12 days) regulated the expression levels of IL-4 and IFN-γ genes in experimental autoimmune uveitis (EAU) rats and increased the expression levels of natural killer T cells [51].

In clinical trials, Xu et al. [52] treated 38 patients who suffered from systemic lupus erythematosus associated with uveitis, with compound tropicamide eye drops (four times a day) and local administration of tobramycin eye drops (four times a day). In addition to the medicines above, total glucosides of paeony (0.6 g, three times a day) were administered orally to 40 patients in the treatment group. Two months later, the total effective rate of patients in the treatment group was significantly better than that in the control group (95.00% vs. 78.95%, ); the first withdrawal time of glucocorticoids in the treatment group was earlier than that in the control group ( days vs. days, ).

3.2.2. Tripterygium wilfordii Polyglycoside (TWP)

Extracted from the dried roots of Tripterygium wilfordii Hook. F., Tripterygium wilfordii polyglycoside (TWP) has anti-inflammatory, antitumor, and immunomodulatory effects. TWP tablets have been approved in the treatment of nephrotic syndrome, Behcet’s disease, and autoimmune hepatitis in China. Moreover, TWP has been used in the clinical treatment of immune diseases such as rheumatoid arthritis [53], systemic lupus erythematosus [54], and lupus nephritis [55] in China.

TWP can act on the TLR-NF-κB signaling pathway in vitro [56]. TWP (15.27 μmol/L) downregulated the expression of TLR4 and NF-κBp65, inhibited the endotoxin-induced inflammatory response in macrophages, and suppressed the release of TNF-α, IL-1β, IFN-γ, intercellular adhesion molecule 1 (ICAM-1), and monocyte chemotactic protein 1 (MCP-1), with effects superior to those of 0.19 μ mol/L of dexamethasone and 6.62 μmol/L of azathioprine [57]. Matrix metalloproteinase 9 (MMP-9) can regulate the activity of cytokines like IL-8 and promote the release of vascular endothelial growth factors to participate in angiogenesis. Increased expression of MMP-9 is associated with experimental autoimmune uveitis [58] and endotoxin-induced uveitis [59]. Tripterygium wilfordii polyglycosides can dose-dependently inhibit the expression of MMP-9 and proinflammatory cytokine IL-32 [60]. IL-37 significantly inhibits the production of IL-1β, IL-6, IL-10, IL-21, IL-23, TNF-γ, and IFN-γ [61]. Tripterygium wilfordii polyglycosides (15 μg/mL) also upregulated the expression of anti-inflammatory cytokine IL-37 through extracellular regulated protein kinases1/2 (ERK1/2) and p38 mitogen-activated protein kinase (MAPK) signaling pathways [62].

In clinical studies, Huang et al. [63] conducted a randomized controlled trial that proved the efficacy of Tripterygium wilfordii polyglycosides in the treatment of acute uveitis. The basic treatment was 1% atropine eye drops +0.05% dexamethasone eye drops. On this basis, 50 patients in the treatment group orally took Tripterygium wilfordii polyglycoside tablets (TWP) (20 mg, bid, for 4 weeks), while 50 patients in the control group orally took dimorpholine (0.4 g, TID, for 4 weeks). The effective rate of the two groups was 95.7% vs. 95.8%, without statistically significant difference. Ma [64] gave 1% atropine eye drops (three times a day) to 22 patients with recurrent uveitis combined with oral Tripterygium wilfordii polyglycoside tablets (20 mg, three times a day). The clinical effective rate was 95.6% after one week of treatment.

Approximately 50-87% of patients with Behcet’s disease initially present with uveitis in one eye. Among them, anterior uveitis is the most common type [65]. 30 patients with ocular Behcet’s disease orally took Tripterygium wilfordii polyglycoside tablets (30 mg/d) for 3 months, the serum levels of IL-1β, TNF-α, and IFN-γ significantly decreased, and the clinical effective rate was 86.6% [66]. Yang et al. [67] found that oral administration of Tripterygium wilfordii polyglycoside tablets (20 mg, bid, 2 months) could inhibit the expression of nitric oxide, soluble intercellular adhesion molecule (sICAM-1), and soluble vascular cell adhesion molecule (sVCAM-1) in plasma of 30 patients with ocular Behcet’s disease and improve endothelial dysfunction.

3.3. Polysaccharide

With the characteristics of biodegradability, little toxicity, and side effects, the polysaccharide is a kind of important biological macromolecule composed of a variety of same or different monosaccharides with α- or β-glycosidery bonds [68].

3.3.1. Astragalus Polysaccharide (APS)

Extracted from the root of Astragalus mongolica, Astragalus polysaccharide has pharmacological effects such as immune regulation, anti-inflammatory, antibacterial, antioxidant, improvement of microcirculation, and antitumor effects.

In cell experiments, APS inhibited LPS-induced inflammatory response by inhibiting the TLR4/NF-κB pathway [69]. APS dosage-dependently inhibited the activation of NF-κB and phosphorylation of ERK and c-Jun N-terminal kinase (JNK) to inhibit the production of TNF-α and IL-1β in LPS-stimulated macrophages [70]. APS (1.0 mg/mL) inhibited LPS-induced inflammatory response in mouse retinal ganglion cells by inhibiting tumor necrosis factor-associated receptor factor 6 (TRAF6)/transforming growth factor-β activated kinase 1 (TAK1) pathway [71].

Caspase-3 is a key effector in apoptosis. Caspase-3 also induces apoptosis in the nucleus, resulting in fragmentation of DNA and chromatin consolidation. In vitro experiments, by inhibiting the production of apoptotic factor caspase-3, 250 μg/mL APS inhibited the necrosis of human retinal pigment epithelial cells caused by 100 μmol/L hydrogen peroxide [72, 73]. Uveitis can be complicated by glaucoma. Injecting 1 mL methylcellulose after extracting 0.1 mL aqueous humor could produce acute high intraocular pressure model rats. In this model, APS (500 mg/kg) intragastric administrated for 14 days lowered intraocular pressure and relieved retinal edema. Moreover, APS inhibited retinal caspase-3 expressions to reduce retinal ganglion cell apoptosis. The thickness of the whole retinal layer, optic fiber layer, and the outer granular layer of the Astragalus polysaccharide group was significantly larger than that of the uveitis model group [74].

3.3.2. Hedysari Polysaccharide (HPS)

Extracted from the dry root of Hedysarum polybotrys Hand.-Mazz., Hedysari polysaccharide has antitumor, antioxidation, anti-inflammation, and antivirus effects [75]. Hedysari polysaccharide (400 mg/kg) reduced the clinical severity of endotoxin-induced uveitis in rats and inhibited the fibrin exudation and inflammatory cell infiltration in the eyes.

Toll-like receptor 4 (TLR-4) is the primary signal cell receptor recognized and activated by lipopolysaccharide. TLR-4 plays a key role in the onset of uveitis and eventually leads to the activation of inflammatory cytokines and inflammation pathological reactions [76]. Li et al. [77] found that the TLR4 signaling pathway involved in the pathogenesis of acute anterior uveitis. After bound to LPS, TLR4 produced proinflammatory cytokines that upregulated costimulators and major histocompatibility complex (MHC). After that, dendritic cells got activated, and their antigen presentation capacity got enhanced, followed by the initial T cells activated [78]. Activation of the NF-κB signaling pathway was closely associated with inflammatory factor expression and extracellular matrix metabolic imbalance [79]. The TLR4/NF-κB signaling pathway was an important pathway for regulating TNF-α and IL-1β expression. Activation of the TLR4-MD2-CD14 complex led to phosphorylation of the NF-κB p65 subunit through a cascade of MyD88-dependent pathways [80], which allowed NF-κB to be colonized in the nucleus and activate the expression of a variety of inflammatory mediators, including TNF-α and IL-1β. HPS significantly reduced the mRNA and protein expressions of TLR4, MyD88, tumor necrosis factor receptor-associated factor 6 (TRAF6), and NF-κB65 [75, 81]. The glycogen synthase kinase 3-β (GSK3-β) in the TLR4 signaling pathway plays an important role in maintaining the immune system’s balance. Yang et al. [82] found that intraperitoneally injecting HPS (400 mg/kg) into rats with uveitis induced by endotoxin upregulated the phosphorylation level of GSK3-β protein and inhibited the expression of nuclear factor-κB (NF-κB) P65 mRNA. As a result, the level of the anti-inflammatory factor IL-10 in the anterior chamber water was upregulated, while inflammatory cytokines such as TNF-β, IL-6, and lL-1β were inhibited, thereby inhibiting the damage of the uveium caused by the inflammatory response.

3.3.3. Rhubarb Polysaccharide (RP)

Extracted from the dried roots and rhizomes of Rheum palmatum L., Rheum officinale Baill., and Rheum tanguticum Maxim. ex Balf., Rhubarb polysaccharide has anti-infection, anti-inflammation, immune regulation, hypoglycemia, and antitumor effects. Rhubarb polysaccharides inhibited CD4 T cell proliferation and regulated cytokines produced by Th1 and Th2. Human leukocyte antigen-B27- (HLA-B27-) associated acute preuveitis is a common kind of uveitis, accounting for 18% to 32% of all cases. It is an acute inflammatory exudative disease of the iris ciliary body, with an urgent onset and rapid progression. If not effectively treated in time, patients can develop into severe intraocular complications, such as glaucoma, which eventually leads to blindness. After activated by LPS, TLR4 activated NF-κB through the MyD88-dependent pathway to promote the release of cytokines such as NO and TNF-α, thus initiating the damage of immune cells towards the uveal membrane. In vitro, rhubarb polysaccharide (100 mg/L) had a protective effect on monocytes of rats with HLA-B27-associated acute preuveitis [83]. Rhubarb polysaccharide inhibited the TLR4/NF-κB signaling pathway and inhibited the secretion of TNF-α, IL-10, IL-17, INF-γ, and IL-1β, with no significant difference from the therapeutic effect of monoclonal antibody against TLR4 (5 mg/L) [25].

3.4. Polyphenol

Having phenolic structures with multiple hydroxyls, polyphenols are the secondary metabolites of plants that widely existed in fruits, vegetables, and herbal medicines. Among them, curcumin has an anti-inflammatory effect.

3.4.1. Curcumin

Extracted from the tuberous root of Curcuma Salisb., the rhizome of turmeric (C. aromatica L.), curcumin has antioxidation, anti-inflammation, antivirus, antitumor, and anticoagulation effects. Curcumin’s therapeutic effect on uveitis is related to its antioxidant, anti-inflammatory, and antifibrinolysis properties. Kowluru and Kanwar [84] found that curcumin had antioxidant properties and could downregulate IL-1β and VEGF levels. Curcumin inhibited the release of IL-1, IL-6, IL-8, and tumor cytokine-α (TNF-α) by inhibiting NF-κB expression, thus protecting iris ciliary cells and retinal pigment epithelial cells from inflammatory responses induced by lipopolysaccharide [85]. Curcumin inhibited choroid and retinal neovascularization by inhibiting vascular endothelial growth factor receptor [86]. Zhang et al. found that curcumin eye drops (10 mg/mL) administrated for 2 weeks could inhibit the axis of stromal cell-derived factor-1 (DF-1) and CXC chemokine receptor 4 (CXCR-4), protect retinal ganglion cells, significantly improve vitreous turbation, and inhibit retinal detachment [87]. Also, curcumin not only inhibited the proliferation of retinal pigment epithelial cells and epithelial-mesenchymal transition by inhibiting AKT, MAPK, and TGF-β pathways [88] but also protected retinal pigment epithelial cells from oxidative stress damage by upregulating heme oxygenase-1 (HO-1) and reducing ROS levels [89]. Curcumin’s antioxidation effect is related to regulating Nrf-2/HO-1pathways.

Retinal ischemia-reperfusion injury (RIRI) is common in patients with uveitis and can cause retinal structure and function disorders. By regulating the Bcl-2/Bax/caspase-3 signaling pathway, curcumin could downregulate the expression of Bax and caspase-3 proteins and upregulate the expression of Bcl-2 proteins [90, 91]. Besides, curcumin could downregulate the expression levels of IL-23 and IL-17 in the retina.

In terms of clinical studies, Lal et al. [92] treated 18 patients with chronic anterior uveitis with curcumin (375 mg TID). After 12 weeks of continuous treatment, vision got improved in all patients, and pain, redness of eyes, congestion of the ciliary body, keratinized deposits, aqueous humor, and vitreous opacity disappeared without adverse reactions. Allegri et al. [93] included 106 patients with recurrent uveitis after receiving glucocorticoids, immunosuppressants, antiherpetic drugs, and nonsteroidal anti-inflammatory drugs (NSAIDS) before participated in this study. They had the patients take curcumin phosphatidylcholine complex (Meriva, 1200 mg, bid) orally, in addition to the former medications. After 12 months, only 19 patients relapsed. The study also found that oral administration of curcumin phosphatidylcholine complex significantly improved symptoms such as eye pain, blurred vision, pericorneal congestion.

In recent years, to solve the problem of curcumin’s poor solubility and bioavailability, a variety of different dosage forms were reported besides curcumin phosphatidylcholine compounds, including curcumin/sodium alginate hydrogel nano-emulsion [94], curcumin nano-emulsion [95], new curcumin chitosan nanoparticle capsules [96], curcumin liposomes [97], and curcumin nanoparticles [98]. Dosage forms above were proved to improve the absorption of curcumin.

4. Summary

Natural products play a therapeutic role in uveitis in various ways, including anti-inflammation, antiapoptosis, antioxidation effects, and inhibiting neovascularization. Pharmacological actions on uveitis and related signal pathways of natural products have been summarized in Table 3. Anti-inflammatory effects are the main ways how natural products treat uveitis. Regulating TLR4/NF-κB pathway can protect uvea from the destruction of inflammatory cells and cytokines induced by LPS. Plant polysaccharides, like APS and HPS, have structures similar to lipopolysaccharide. They can inhibit the production of downstream inflammatory factors caused by overexpression of the TLR4/NF-κB signaling pathway in vivo. Besides, curcumin and matrine can also protect uvea from the damage of inflammatory reaction by regulating the TLR4/NF-κB pathway. Th17 cells are the main pathogenic cells that mediate autoimmune diseases, including psoriasis, uveitis, and rheumatoid arthritis. Berberine can improve Behcet’s disease symptoms by regulating the IL-17 signaling pathway. Tumor necrosis factor-related receptor 6 (TRAF6) is a kind of adaptor protein, which can conduct signals mediated by many receptors on the membrane, including the Toll/IL receptor family. LPS stimulation can induce the ubiquitination of TRAF6 and then form a complex with transforming growth factor-beta activated kinase 1 (TAK1), which further activates the IKKS family and promotes the nuclear transfer of NF-κB, leading to the occurrence of inflammatory reactions. APS and HPS can protect retinal ganglion cells from damage of inflammatory response by regulating the TRAF6/TAK1 signaling pathway. IL-37 has a significant positive correlation with disease activity of HLA-B27 associated acute anterior uveitis (AAU). TWP can upregulate anti-inflammatory cytokine IL-37 expression by regulating ERK/MAPK signaling pathway. Moreover, the regulatory effects of natural products on cytokines have been summarized in Table 4.

Table 3: Pharmacological actions on uveitis and related signal pathways of natural products.

Natural products
Pharmacological actions related to uveitis
Signal pathways
Symptoms that can be improved

Matrine
Anti-inflammation, inhibited proliferation of fibroblasts and neovascularization
TLR4-NF-κB signaling pathway
VEGF signaling pathway
Ciliary congestion, retinal edema, fundus hemorrhage, glaucoma, corneal neovascularization

Berberine
Anti-inflammation, regulation of gene expression, regulation of intestinal flora
IL-17 signaling pathway
Retinal edema and hemorrhage, corneal edema, retinal folding, iris congestion, iris adhesions

TGP
Anti-inflammation, antiapoptotic
Fas/FasL signaling pathway
Iris ciliary swelling, retinal edema, iris hemorrhage, hypopyon, miosis

TWP
Anti-inflammation, antiapoptotic
TLR-NF-κB signaling pathway
ERK/MAPK signaling pathway
Keratic precipitate, anterior chamber flare, iris edema, vision loss

APS
Anti-inflammation, antiapoptotic
TLR-NF-κB signaling pathway
TRAF6/TAK1 signaling pathway
Glaucoma

HPS
Anti-inflammation
TLR-NF-κB signaling pathway
TRAF6/TAK1 signaling pathway
Hypopyon, vision loss

RP
Anti-inflammation
TLR-NF-κB signaling pathway
Unknown

Curcumin
Antioxidation, anti-inflammation, antiapoptotic, antifibrinolytic effects
TLR4-MAPK/NF-κB signaling pathway
SDF-1/CXCR-4 signaling pathway
Bcl-2/Bax/caspase-3 signaling pathway
Nrf-2/HO-1 signaling pathway
Keratic precipitate, eye pain, blurred vision, ciliary congestion, aqueous and vitreous opacity

Table 4: Regulatory effect of natural products on cytokines in uveitis.

Cytokines
Major secretory cells
Effect of cytokines in uveitis
Regulatory effect of natural product components

IL-1
Macrophages, epithelial cells
IL-1 can promote the activation of CD4 + T cells and the expression of IL-2 receptor 2 and the antigen presentation ability of APC such as monocyte macrophage [10]. Synergized with IL-2 or interferon, IL-1 can enhance NK cell activity. Moreover, it can recruit neutrophils and promote the release of inflammatory mediators [99]. Intravitreal injection of recombinant IL-1 receptor antagonist anakina (ANA) can inhibit the increase of laser-induced neovascularization choroidal area in a concentration-dependent manner and improve the uveitis symptoms such as iris edema, adhesion, atrophy, and neovascularization [100].
Matrine ↓ Berberine ↓
TWP ↓
APS ↓
HPS ↓
RP ↓
Curcumin ↓

IL-2
T cells
Il-2 can stimulate the proliferation and differentiation of Th17 cells, activate NK cells, and macrophages [101].

IL-4
T cells, mast cells
IL-4 can induce the initial T cells to differentiate into Th2 cells and participate in the humoral immune response. Moreover, it can promote the proliferation and differentiation of activated B cells and induce immunoglobulin E (IgE) antibodies’ production [102, 103].
TGP ↑

IL-6
T cells, macrophages, endothelial cells
IL-6 mediates the differentiation of Th1 to Th17 cells and inhibits physiological intraocular T cell apoptosis [104]. Intravitreal injection of anti-IL-6 (MP5-20F3) twice significantly relieved experimental autoimmune uveitis in mice [105].
Matrine ↓
Berberine ↓
TWP ↓
HPS ↓
Curcumin ↓

IL-8
Monocytes, macrophages, endothelial cells, fibroblasts, T cells
IL-8 takes part in chemotactic signals to recruit leukocytes, leading to directional migration and exocytosis of stored proteins [106, 107]. Intravitreal injection of IL-8 (100 ng) can induce uveitis in the rabbit [108]. Anti-IL-8 antibody treatment partially treated EIU in rabbits [109]. Gene polymorphisms of IL-8 may lead to different susceptibility to ocular Behcet’s disease OBD and increase the risk of developing the disease [110]. IL-8 was found to be the best marker for the diagnosis of children’s idiopathic anterior uveitis [111].
Berberine ↓
Curcumin ↓

IL-10
Monocytes
IL-10 can inhibit the expression of major histocompatibility complex (MHC) and costimulatory molecules in APC and inhibit the production of cytokines by activated Th1 cells [76]. IL-10 polymorphisms +434 T/C, +504G/T, and -2849C/T are predisposing factors for uveitis in children [112].
TWP ↓
HPS ↑
RP ↓

IL-12
Macrophages, dendritic cells
IL-12 can stimulate T cells and NK cells to produce IFN-γ and promote CD4 + helper T cells to differentiate into Th1 cells that produce IFN-γ [113].

IL-17
Th17 cells, NK cells, CD8 T cells, neutrophils
As a proinflammatory cytokine, IL-17 can recruit and activate neutrophils and has synergistic effects with TNF, IL-1β, IFN-γ, granulocyte-macrophage colony stimulating factor (GM-CSF), and IL-22 [114, 115].
Berberine ↓
RP ↓
Curcumin ↓

IL-18
Activated macrophages
Interleukin-12 and interleukin-18 synergically promote the production of interleukin-17A and interleukin-17F, which is independent on IL-23 [116]. IL-18 was found to be a good biomarker for monitoring activity and regression of uveitis [117].

IL-21
Th2 cells
IL-21 promotes the differentiation of Th17 cells that participate in the pathogenesis of autoimmune diseases such as scleritis, uveitis, and Behcet’s disease [118]. Also, it can promote the proliferation and differentiation of B cells, NK cells, and effector CD8 + T cells [119, 120].
Berberine ↓
TWP ↓

IL-23
Macrophages, dendritic cells
IL-23 participates in the occurrence, recurrence, and chronicity of uveitis by promoting the production of IL-17. Moreover, it takes part in the recruitment and differentiation of myeloid cells, which is considered an upstream pathway in intermediate uveitis pathogenesis [121].
Berberine ↓
TWP ↓
Curcumin ↓

IL-27
Macrophages, dendritic cells, monocytes
IL-27 promotes the differentiation of Th1 but inhibits the proliferation of Th2, Th17, and Treg cells [109].

IL-32
NK cells, macrophages, monocytes, and T lymphocytes, epithelial cells, endothelial cells, mesenchymal stromal cells, fibroblasts, and hepatocytes
IL-32 can induce proinflammatory cytokines like TNF-α, IL-8, and IL-1β and induce anti-inflammatory cytokines like IL-10 [122]. Moreover, it can mediate the differentiation of monocytes into dendritic cells [123].

IL-33
Endothelial cells, smooth muscle cells
Both IL-33 and IL-33R were expressed in RPE cells, IL-33 can inhibit the production of IFN-γ, and IL-17 promote Th2 to secrete cytokines and significantly reduce the severity of EAU mice [124, 125].

IL-35
Regulatory T cells
IL-35 can significantly increase the expression of IL-10 and TGF-β and decrease the expression of INF-γ, IL-12, and IL-17 [126]. Moreover, it can promote Treg cells’ proliferation and inhibit the proliferation of Th17 cells [127].

IL-37
Epithelial cells, dendritic cells, monocytes
IL-37 significantly inhibits IL-1β, IL-6, IL-10, IL-21, IL-23, TNF-α, and IFN-γ. IL-37 has a significant positive correlation with disease activity of HLA-B27 associated acute anterior uveitis (AAU) [61] as well as chronic primary angle-closure glaucoma [128].
TWP ↓

TNF-α
Macrophages, T cells, NK cells
TNF-α can directly kill cells infected by virus, activate monocyte macrophages, and enhance their phagocytic and bactericidal ability. Moreover, TNF-α can promote antigen processing and presentation pathways and increase Th1 and Th17 cytokines level [129]. Adalimumab and infliximab have become the most widely used biological agents in the treatment of noninfectious uveitis [130]. TGF-β can induce the differentiation of Th0 towards Treg and inhibit the differentiation of Th17 cells at high concentrations. At low concentrations, with the presence of IL-6, it can induce Th0 to differentiate into Th17 [131]. In patients with uveitis, the expression of TGF-β in aqueous humor decreases, which is considered a potential factor to promote uveitis. Similar changes are observed in the aqueous humor of patients with Vogt Koyanagi Harada during the active phase [132]. Adalimumab and infliximab have become the most widely used biological agents in the treatment of non- infectious uveitis [133].
Matrine ↓
TWP ↓
APS ↓
HPS ↓
RP ↓
Curcumin ↓

TGF-β
Monocytes, T cells, chondrocytes
TGF-β can induce the differentiation of Th0 towards Treg and inhibit the differentiation of Th17 cells at high concentrations. At low concentrations, with the presence of IL-6, it can induce Th0 differentiate into Th17 [131]. In patients with uveitis, the expression of TGF-β in aqueous humor decreases, which is considered a potential factor in promoting the development of uveitis. Similar changes are observed in the aqueous humor of patients with Vogt Koyanagi Harada during the active phase [132].
Berberine ↓

IFN-γ
T cells, NK cells
It can activate macrophages, promote MHC expression and antigen presentation, promote Th1 differentiation, and inhibit Th2 differentiation [133]. IFN-γ can induce VEGF expression in retinal cells through PI-3 K/Akt/mTOR/p70S6 kinase pathway [134]. Deficiency in IFN-gamma can inhibit the development of uveitis induced by muramyl dipeptide [133].
TGP ↓
TWP ↓
RP ↓

VEGF
Tumor cells
VEGF can not only promote the increase of vascular permeability and the degeneration of the extracellular matrix but also promote the neovascularization of choroid, iris, and retina, leading to severe visual loss, even blindness.
Matrine ↓
Curcumin ↓

MCP-1
Immature DC cells, monocytes/macrophages, T cells, NK cells
MCP-1 can recruit immature DC cells, T cells, and monocytes/macrophages to participate in immune response and inflammatory response. Alteration of MCP-1 in aqueous humor was associated with glaucoma secondary to Fuchs uveitis syndrome [8, 135].
Berberine ↓
TWP ↓

MMP-9
Neutrophils, monocytes/macrophages
MMP-9 can remodel the dynamic balance of the extracellular matrix and promote the release of TGF-β1 and VEGF [136]. MMP-9 levels peak at the most severe uveitis stage and then return to baseline as the inflammation subsides [136].
TWP ↓

In terms of antiapoptosis, Fas/FasL expression on T cells’ surface is associated with uveitis. FasL expressed in the corneal epithelium blocks inflammatory cells from the conjunctiva and anterior chamber; FasL expressed in the iris ciliary body blocks inflammatory cells from invading blood vessels; FasL expressed in the retina induces rapid apoptosis of invading inflammatory cells, which is important for the protection of visual function and also has a killing effect on invading lymphocytes. By regulating Fas/FasL signaling pathway, TGP can inhibit the apoptosis of retinal cells. Caspase-3 is one of the important apoptotic executors in the caspase family. It is activated by protein hydrolysis in response to various apoptotic signals and promotes apoptosis in ocular tissue cells. By regulating the Bcl-2/Bax/caspase-3 signaling pathway, curcumin can inhibit the retinal cell apoptosis induced by endoplasmic reticulum stress and inflammatory cell invasion.

Oxidative stress can cause mitochondrial DNA damage, protein nitrification, and membrane lipid oxidation in uveal tissue. Heme oxygenase-1 (HO-1) is a ubiquitous and redox-sensitive induced stress protein that can protect cells from oxidative stress. With strong antioxidant activity similar to vitamins C and E, curcumin can protect RPE cells from oxidative stress by regulating the Nrf-2/HO-1 signaling pathway.

Ocular neovascularization is one of the main causes of severe visual impairment. Regulated by a series of molecular signals, neovascularization is a complex multistep process in which endothelial cells of mature vessels proliferate, migrate, and gradually remodel to form new small vessels. Curcumin and matrine inhibit choroidal, retinal, and iris neovascularization by regulating VEGF signaling pathway. The interaction between SDF-1 secreted by corneal stromal cells, epithelial cells, and inflammatory cells and its receptor CXCR4 are involved in regulating corneal wound repair and inflammatory corneal neovascularization proliferation. Curcumin can protect retinal ganglion cells by inhibiting the SDF-1/CXCR4 signaling pathway.

Although the total glucosides of paeony, TWP, and curcumin have their evidence in clinical trials, the available literature has a high risk of research bias. Natural products like berberine, matrine, and Astragalus polysaccharide are only reported in animal experiments in the field of uveitis. Randomized controlled clinical trials of the natural products above are still lacking. Their efficacy and safety in children and elderly patients remain uncertain.

5. Conclusions

Natural products have been proved effective in the treatment of uveitis in animal experiments. Further efforts are still needed to explore the therapeutic effects of natural products in clinical practice and search for new drugs with anti-inflammatory effects.

Data Availability

The data used to support the findings of this study are included within the article.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Authors’ Contributions

Sicong Li and Fang Liu were responsible for the initial outline, draft writing, and revisions for intellectual content, and final approval. Kai Zhang and Yujia Tong were responsible for data interpretation, presentation, draft writing, and revisions for intellectual content. Xin Liu was the corresponding author and responsible for draft writing and final approval.

Acknowledgments

The authors would like to thank all the scholars who deeply love, popularize the basic knowledge, and expand the influence of natural products.

References

A. Radosavljevic, M. Agarwal, S. P. Chee, and M. Zierhut, “Epidemiology of viral induced anterior uveitis,” Ocular Immunology and Inflammation, vol. 22, pp. 1–13, 2021.

J. T. Rosenbaum, B. Bodaghi, C. Couto et al., “New observations and emerging ideas in diagnosis and management of non- infectious uveitis: a review,” Seminars in Arthritis and Rheumatism, vol. 49, no. 3, pp. 438–445, 2019.

S. Tendolkar, S. I. Murthy, P. Bhatia, and S. Senthil, “Cytomegalovirus endotheliitis with recurrent anterior uveitis and secondary glaucoma misdiagnosed as HLA-B27 uveitis,” BML Case Reports, vol. 14, no. 2, article e240061, 2021.

T. Tsirouki, A. Dastiridou, C. Symeonidis et al., “A focus on the epidemiology of uveitis,” Ocular Immunology and Inflammation, vol. 26, no. 1, pp. 2–16, 2018.

S. J. Bing, I. Shemesh, W. P. Chong et al., “AS101 ameliorates experimental autoimmune uveitis by regulating Th1 and Th17 responses and inducing Treg cells,” Journal of Autoimmunity, vol. 100, pp. 52–61, 2019.

X. Huang, S. Yi, J. Hu et al., “Analysis of the role of palmitoleic acid in acute anterior uveitis,” International Immunopharmacology, vol. 84, article 106552, 2020.

W. Chi, P. Yang, B. Li et al., “IL-23 promotes CD4⁺ T cells to produce IL-17 in Vogt- Koyanagi-Harada disease,” The Journal of Allergy and Clinical Immunology, vol. 119, no. 5, pp. 1218–1224, 2007.

J. Xu, Y. Qin, R. Chang et al., “Aqueous cytokine levels in four common uveitis entities,” International Immunopharmacology, vol. 78, article 106021, 2020.

B. Zhao, W. Chen, R. Jiang et al., “Expression profile of IL-1 family cytokines in aqueous humor and sera of patients with HLA-B27 associated anterior uveitis and idiopathic anterior uveitis,” Experimental Eye Research, vol. 138, pp. 80–86, 2015.

C. Fabiani, J. Sota, G. M. Tosi et al., “The emerging role of interleukin (IL)-1 in the pathogenesis and treatment of inflammatory and degenerative eye diseases,” Clinical Rheumatology, vol. 36, no. 10, pp. 2307–2318, 2017.

M. Q. Zheng, Y. Q. Wang, S. J. Xiang, and Y. Li, “Levels of IL-10, IL-23, TNF-α and INF-γ in patients with HLA-B27-related acute anterior uveitis,” Journal of Medical Research, vol. 40, no. 6, pp. 76–79, 2011.

X. F. Feng, X. J. Chen, J. Gong, and X. Chao, “Expression and significance of Th1/Th2 cells and their cytokines in peripheral blood of patients with uveitis,” Chinese Journal of Health Inspection, vol. 26, 2016.

L. Joshi, L. Talat, S. Yaganti et al., “Outcomes of changing immunosuppressive therapy after treatment failure in patients with noninfectious uveitis,” Ophthalmology, vol. 121, no. 5, pp. 1119–1124, 2014.

R. Lopez-Gonzalez, E. Loza, J. A. Jover et al., “Treatment of refractory posterior uveitis with infliximab: a 7-year follow-up study,” Scandinavian Journal of Rheumatology, vol. 38, no. 1, pp. 58–62, 2009.

N. Ashkenazy, U. S. Saboo, A. Abraham, C. Ronconi, and J. H. Cao, “Successful treatment with infliximab after adalimumab failure in pediatric noninfectious uveitis,” Journal of American Association for Pediatric Ophthalmology and Strabismus, vol. 23, no. 3, pp. 151.e1–151.e5, 2019.

Q. D. Nguyen, P. T. Merrill, G. J. Jaffe et al., “Adalimumab for prevention of uveitic flare in patients with inactive non- infectious uveitis controlled by corticosteroids (VISUAL II): a multicentre, double-masked, randomised, placebo-controlled phase 3 trial,” The Lancet, vol. 388, no. 10050, pp. 1183–1192, 2016.

J. Sheppard, A. Joshi, K. A. Betts et al., “Effect of adalimumab on visual functioning in patients with noninfectious intermediate uveitis, posterior uveitis, and panuveitis in the VISUAL-1 and VISUAL-2 trials,” JAMA Ophthalmology, vol. 135, no. 6, pp. 511–518, 2017.

E. B. Suhler, A. Adán, A. P. Brézin et al., “Safety and efficacy of adalimumab in patients with noninfectious uveitis in an ongoing open-label study: VISUAL III,” Ophthalmology, vol. 125, no. 7, pp. 1075–1087, 2018.

J. R. Smith, J. M. Matthews, D. Conrad et al., “Recommendations for the management of childhood juvenile idiopathic arthritis-type chronic anterior uveitis,” Clinical & Experimental Ophthalmology, vol. 49, no. 1, pp. 38–45, 2021.

U. Pleyer, P. Neri, and C. Deuter, “New pharmacotherapy options for noninfectious posterior uveitis,” International Ophthalmology, vol. 41, no. 6, pp. 2265–2281, 2021.

B. M. Burkholder and D. A. Jabs, “Uveitis for the non-ophthalmologist,” BMJ, vol. 372, article m4979, 2021.

G. J. Jaffe, A. D. Dick, A. P. Brézin et al., “Adalimumab in patients with active noninfectious uveitis,” The New England Journal of Medicine, vol. 375, no. 10, pp. 932–943, 2016.

Y. Z. Li, X. Peng, Y. H. Ma, F. J. Li, and Y. H. Liao, “Matrine suppresses lipopolysaccharide-induced fibrosis in human peritoneal mesothelial cells by inhibiting the epithelial-mesenchymal transition,” Chinese Medical Journal, vol. 132, no. 6, pp. 664–670, 2019.

G. Wu, W. Zhou, J. Zhao et al., “Matrine alleviates lipopolysaccharide-induced intestinal inflammation and oxidative stress via CCR7 signal,” Oncotarget, vol. 8, no. 7, pp. 11621–11628, 2017.

X. Zhang, J. Wang, Z. Xu, Z. Li, S. Feng, and H. Lu, “The impact of rhubarb polysaccharides on Toll-like receptor 4-mediated activation of macrophages,” International Immunopharmacology, vol. 17, no. 4, pp. 1116–1119, 2013.

N. X. Nguyen, M. Küchle, and G. O. Naumann, “Quantification of blood-aqueous barrier breakdown after phacoemulsification in Fuchs’ heterochromic uveitis,” Ophthalmologica, vol. 219, no. 1, pp. 21–25, 2005.

I. C. Kuo and E. T. Cunningham Jr., “Ocular neovascularization in patients with uveitis,” International Ophthalmology Clinics, vol. 40, no. 2, pp. 111–126, 2000.

Z. Deng, Y. F. Wu, L. Jiang et al., “Matrine eye fluid regulates TLR4/NF- B pathway and affects the expression of cytokines associated with experimental uveitis in rabbits,” Chinese Journal of General Practice, vol. 18, no. 4, pp. 568–572, 2020.

J. Yu and M. C. Chang, “Inhibitory effect of matrine on corneal neovascularization in rats,” New Advances in Ophthalmology, vol. 32, no. 6, pp. 532–535, 2012.

T. Rao and Y. L. Zhang, “Effect of matrine on the scar of filtration vesicle after trabeculectomy in rabbits,” New Progress in Ophthalmology, vol. 37, no. 5, pp. 428–430, 2017.

A. J. St Leger, A. M. Hansen, H. Karauzum et al., “STAT-3-independent production of IL-17 by mouse innate-like αβ T cells controls ocular infection,” The Journal of Experimental Medicine, vol. 215, no. 4, pp. 1079–1090, 2018.

K. Ghoreschi, A. Laurence, X. P. Yang et al., “Generation of pathogenic TH17 cells in the absence of TGF-β signalling,” Nature, vol. 467, no. 7318, pp. 967–971, 2010.

Y. Yang, Q. Wang, M. Xie et al., “Berberine exerts an anti-inflammatory role in ocular Behcet’s disease,” Molecular Medicine Reports, vol. 15, no. 1, pp. 97–102, 2017.

J. S. Cho, E. M. Pietras, N. C. Garcia et al., “IL-17 is essential for host defense against cutaneous Staphylococcus aureus infection in mice,” The Journal of Clinical Investigation, vol. 120, no. 5, pp. 1762–1773, 2010.

Y. Yang, J. Qi, Q. Wang et al., “Berberine suppresses Th17 and dendritic cell responses,” Investigative Ophthalmology & Visual Science, vol. 54, no. 4, pp. 2516–2522, 2013.

P. Tian, H. Ge, H. Liu et al., “Leukocytes from diabetic patients kill retinal endothelial cells: effects of berberine,” Molecular Vision, vol. 19, pp. 2092–2105, 2013.

Y. Guex-Crosier, A. J. Wittwer, and F. G. Roberge, “Intraocular production of a cytokine (CINC) responsible for neutrophil infiltration in endotoxin induced uveitis,” The British Journal of Ophthalmology, vol. 80, no. 7, pp. 649–653, 1996.

M. D. Becker, L. M. O'Rourke, W. Blackman, S. R. Planck, and J. T. Rosenbaum, “Reduced leukocyte migration, but normal rolling and arrest, in interleukin-8 receptor homologue knockout mice,” Investigative Ophthalmology & Visual Science, vol. 41, no. 7, pp. 1812–1817, 2000.

H. S. Cui, S. Hayasaka, L. S. Zheng, Y. Hayasaka, X. Y. Zhang, and Z. L. Chi, “Effect of berberine on monocyte chemotactic protein-1 and cytokine-induced neutrophil chemoattractant-1 expression in rat lipopolysaccharide-induced uveitis,” Ophthalmic Research, vol. 39, no. 1, pp. 32–39, 2007.

M. Li, X. Chen, J. Liu et al., “Treatment of experimental autoimmune uveoretinitis with different natural compounds,” Molecular Medicine Reports, vol. 13, no. 6, pp. 4654–4658, 2016.

Z. du, Q. Wang, X. Huang et al., “Effect of berberine on spleen transcriptome and gut microbiota composition in experimental autoimmune uveitis,” International Immunopharmacology, vol. 81, article 106270, 2020.

J. Luo, D. E. Jin, G. Y. Yang et al., “Total glucosides of paeony for rheumatoid arthritis: a systematic review of randomized controlled trials,” Complementary Therapies in Medicine, vol. 34, pp. 46–56, 2017.

P. Liu, L. Wei, M. Tian, S. F. Zhang, and G. H. Cao, “Effect of total glucosides of paeony on the expression of IL6, interleukin-1 and tumor necrosis factor-α in children with juvenile idiopathic arthritis,” Rheumatism and Arthritis, vol. 9, no. 1, pp. 10–13, 2020.

Y. Zhang, “Efficacy of total glucosides of paeony capsule combined with tacrolimus in the treatment of systemic lupus erythematosus,” Journal of Contemporary Medicine, vol. 18, no. 6, pp. 146-147, 2020.

L. Jin, C. Li, Y. Li, and B. Wu, “Clinical efficacy and safety of total glucosides of paeony for primary Sjögren’s syndrome: a systematic review,” Evidence-based Complementary and Alternative Medicine, vol. 2017, 9 pages, 2017.

U. Khan and H. Ghazanfar, “T lymphocytes and autoimmunity,” International Review of Cell and Molecular Biology, vol. 341, pp. 125–168, 2018.

R. Arakaki, A. Yamada, Y. Kudo, Y. Hayashi, and N. Ishimaru, “Mechanism of activation-induced cell death of T cells and regulation of FasL expression,” Critical Reviews in Immunology, vol. 34, no. 4, pp. 301–314, 2014.

G. S. Zhou, H. Ren, G. J. Wei et al., “Expression of Bcl-2 and FasL in autoimmune uveoretinopathy,” Harbin Medical University, vol. 42, pp. 31–33, 2008.

C. F. Xiong, J. Y. Qi, R. Deng, L. F. Xie, C. Z. Li, and X. L. Nie, “Total glucosides of paeony inhibits T cell proliferation in vitro and promotes activation-induced cell death in mice lymphocyte,” Journal of Southern Medical University, vol. 40, no. 1, pp. 118–124, 2020.

W. Wu, M. F. He, Z. L. Guo, X. K. Huang, and J. W. Zhong, “Protective effect of total glucosides of paeony on uveitis model rats,” Chinese Pharmacy, vol. 25, no. 11, pp. 994–996, 2014.

C. Y. Jing, J. K. Song, B. B. Wang, Q. M. Tian, and X. F. Xie, “Effect of total glucosides of paeony on expression of natural killer T cells in liver of experimental autoimmune uveitis rats,” Chinese Journal of optometry and Visual Science, vol. 20, no. 11, pp. 669–676, 2018.

Q. B. Xu, L. Y. Zhong, L. W. Zhu, and Y. Zhang, “Adjuvant treatment of systemic lupus erythematosus with uveitis by total glucosides of paeony,” Modern Applied Pharmacy in China, vol. 32, no. 2, pp. 202–205, 2015.

J. Long, T. Wang, C. Qu, and C. Liang, “Effect of Tripterygium glycosides combined with methotrexate on rheumatoid arthritis,” China Medical News, vol. 16, no. 7, pp. 71–75, 2019.

G. K. Li, J. Li, Y. Yuan, Y. W. Zhao, and G. Wang, “Effect of Tripterygium wilfordii polyglycoside combined with prednisone on CD 4 ~ + CD 25 ~ +T cells in SLE patients and its therapeutic effect,” Laboratory Medicine and Clinical Medicine, vol. 15, no. 6, pp. 798–801, 2018.

Y. D. Ding, J. J. Zhu, and L. D. Zhang, “Clinical study of Tripterygium glycosides combined with leflunomide in treatment of lupus nephritis,” Chinese Medicine and Clinical Practice, vol. 19, no. 3, pp. 85–87, 2019.

M. Zhang, S. A. Wang, and L. X. Liu, “Tripterygium glycosides interfere with TLR-NF-κB pathway to exert immunosuppressive effect,” Chinese Herbal Medicine, vol. 45, no. 9, pp. 1288–1292, 2014.

D.-P. Qin, Y. J. Zhou, S. Z. Zhang, J. M. Cao, and L. Y. Xu, “Anti-inflammatory effects of Tripterygium wilfordii polyglycosides on macrophages and regulation of TLR4/NF-κB,” Chinese Journal of Traditional Chinese Medicine, vol. 40, no. 16, pp. 3256–3261, 2015.

S. M. Zhou, F. Q. Kong, and S. Chen, “Preliminary study of matrix metalloprotein-9 inhibitor blocking CD73 shedding on retinal pigment epithelium cells to prevent experimental autoimmune uveitis,” Chinese Journal of Fundus Diseases, vol. 20, no. 4, 2020.

Y. Q. Wang, W. K. Hu, X. N. Zhang, and Y. L. Wang, “No content and expression of matrix metalloproteinase-9, tissue type protease inhibitor-1 and inducible NO synthase in lipopolysaccharide-induced uveitis eyes,” Chinese Journal of Ocular Fundus Diseases, vol. 6, pp. 29–32, 2005.

A. Cai, S. Qi, Z. Su, H. Shen, W. Ma, and Y. Dai, “Tripterygium glycosides inhibit inflammatory mediators in the rat synovial RSC-364 cell line stimulated with interleukin-1β,” Biomedical Reports, vol. 3, no. 6, pp. 763–766, 2015.

B. Zhao, S. Zhang, W. Chen et al., “Elevated interleukin 37 expression associated with disease activity in HLA-B27 associated anterior uveitis and idiopathic anterior uveitis,” Current Molecular Medicine, vol. 17, no. 7, pp. 460–467, 2018.

S. Wang, R. Li, S. He et al., “Tripterygium wilfordii glycosides upregulate the new anti-inflammatory cytokine IL-37 through ERK1/2 and p38 MAPK signal pathways,” Evidence-based Complementary and Alternative Medicine, vol. 2017, Article ID 9148523, 6 pages, 2017.

Q. S. Huang, Z. L. Zhang, and Y. M. Liu, “Effect of Tripterygium wilfordii polyglycoside on serum IL-2 and TNF-alpha in patients with acute anterior U-veitis,” Zhongguo Zhong Xi Yi Jie He Za Zhi, vol. 22, no. 6, pp. 432–434, 2002.

G. Ma, “Effect of Tripterygium wilfordii on recurrent uveitis,” Journal of Integrative Ophthalmology, vol. 2, pp. 86-87, 1996.

J. Gueudry and M. Muraine, “Anterior uveitis,” Journal Français d'Ophtalmologie, vol. 41, no. 1, pp. e11–e21, 2018.

Q. Song, J. Z. Lu, and J. Li, “Effect of Tripterygium glycosides on serum interleukin-1beta, interleukin-2, tumor necrosis factor alpha, and interferon-gamma levels in patients with Behcet’s disease,” Zhongguo Zhong Xi Yi Jie He Za Zhi, vol. 30, no. 6, pp. 598–600, 2010.

H. Z. Yang, N. Liu, and C. Dai, “Detection of endothelium function in patients with Behcet’disease and effect of Tripterygium glycosides,” Chinese Journal of Integrative Dermatology and Venereology, vol. 15, no. 2, pp. 94–96, 2016.

J. Song, M. Chen, Z. Li et al., “Astragalus polysaccharide extends lifespan via mitigating endoplasmic reticulum stress in the silkworm, Bombyx mori,” Aging and Disease, vol. 10, no. 6, pp. 1187–1198, 2019.

J. Wu and X. Z. Yao, “Anti-inflammatory effect of Astragalus polysaccharide and its mechanism of inhibiting TLR4/NF-κB pathway in COPD,” Journal of Xi’an Jiaotong University, vol. 39, no. 5, pp. 760–764, 2018.

X. He, J. Shu, L. Xu, C. Lu, and A. Lu, “Inhibitory effect of Astragalus polysaccharides on lipopolysaccharide-induced TNF-a and IL-1β production in THP-1 cells,” Molecules, vol. 17, no. 3, pp. 3155–3164, 2012.

L. Lai and H. Qin, “Astragalus polysaccharides modulate the inflammatory response of retinal ganglion cell via Traf6 TAK1 signaling pathway,” Chinese Journal of Ophthalmology of Traditional Chinese medicine, vol. 29, no. 6, pp. 434–437, 2019.

T. Napso and F. Fares, “Zebularine induces prolonged apoptosis effects via the caspase-3/PARP pathway in head and neck cancer cells,” International Journal of Oncology, vol. 44, no. 6, pp. 1971–1979, 2014.

J. K. Si, J. G. Guo, D. D. Guo, K. Tang, Y. X. Du, and X. R. Wang, “Protective effects of Astragalus polysaccharides on hydrogen peroxide-induced oxidative damage in human retinal pigment epithelium cells,” New Advances in ophthalmology, vol. 35, no. 1, pp. 18–21, 2015.

A. Q. Wang and Y. He, “Effects of Astragalus polysaccharides on intraocular pressure, retina, inner and outer granular layer, optic nerve fiber, caspase-3 and retinal ganglion cell apoptosis in acute ocular hypertension rats,” Journal of Practical Chinese Medicine, vol. 32, no. 1, pp. 61–64, 2018.

S. Yu, W. Zhang, J. Yu, S. Feng, T. Guo, and H. Lu, “Inhibiting effect of Radix Hedysari polysaccharide (HPS) on endotoxin-induced uveitis in rats,” International Immunopharmacology, vol. 21, no. 2, pp. 361–368, 2014.

Y. Sun, D. Guo, B. Liu et al., “Regulatory role of rno-miR-30b-5p in IL-10 and Toll-like receptor 4 expressions of T lymphocytes in experimental autoimmune uveitis in vitro,” Mediators of Inflammation, vol. 2018, Article ID 2574067, 11 pages, 2018.

S. Li, H. Lu, X. Hu, W. Chen, Y. Xu, and J. Wang, “Expression of TLR4-MyD88 and NF- B in the iris during endotoxin-induced uveitis,” Mediators of Inflammation, vol. 2010, Article ID 748218, 7 pages, 2010.

C. Tong, Z. Cui, X. Sun et al., “Mannan derivatives instruct dendritic cells to induce Th1/Th2 cells polarization via differential mitogen-activated protein kinase activation,” Scandinavian Journal of Immunology, vol. 83, no. 1, pp. 10–17, 2016.

J. Xie, B. Li, P. Zhang, L. Wang, H. Lu, and X. Song, “Osteogenic protein-1 attenuates the inflammatory cytokine-induced NP cell senescence through regulating the ROS/NF-κB pathway,” Biomedicine & Pharmacotherapy, vol. 99, pp. 431–437, 2018.

M. E. Spehlmann and L. Eckmann, “Nuclear factor-kappa B in intestinal protection and destruction,” Current Opinion in Gastroenterology, vol. 25, no. 2, pp. 92–99, 2009.

J. Wang, X. L. Liu, H. R. Wu, H. Y. Jia, and H. Lu, “Mechanism of Radix Hedysari polysaccharide on endotoxin-induced uveitis in rats,” New Advances in Ophthalmology, vol. 39, no. 7, pp. 606–610, 2019.

S. Yang, S. Yu, X. L. Liu, W. L. Zhang, and J. R. Guo, “Effects of Astragalus polysaccharide on expression of glycogen synthase 3-in lipopolysaccharide-induced uveitis model and its mechanism,” New Advances in Ophthalmology, vol. 39, no. 2, pp. 123–128, 2019.

F. Juan, L. Yan, S. Yang, S. Xiaopeng, and W. Aidong, “Rhubarb polysaccharide inhibits the activation of TLR-4/NF-κB pathway induced by lipopolysaccharide,” Advances in modern Biomedicine, vol. 14, no. 31, pp. 6035–6038, 2014.

R. A. Kowluru and M. Kanwar, “Effects of curcumin on retinal oxidative stress and inflammation in diabetes,” Nutrition and Metabolism, vol. 4, no. 1, p. 8, 2007.

Y. Li, H. Li, and S. B. Zhou, “Curcumin inhibits lipopolysaccharide-induced inflammatory response of retinal pigment epithelium cells,” Journal of Chongqing Medical University, vol. 43, no. 7, pp. 994–998, 2018.

X. J. Lin, P. Xie, D. Q. Yuan, and Q. H. Liu, “Curcumin inhibits choroidal neovascularization in mice,” Advances in Modern Biomedicine, vol. 14, no. 1, pp. 52–56, 2014.

C. Zhang, H. Z. Yu, D. J. Yang, and H. Q. Jia, “Effect of curcumin on SDF-1 / CXCR4 axis in rats with proliferative vitreoretinopathy,” Sichuan Traditional Chinese Medicine, vol. 38, no. 3, pp. 80–84, 2020.

X. Zhou, X. Kuang, C. Long et al., “Curcumin inhibits proliferation and epithelial-mesenchymal transition of retinal pigment epithelial cells via multiple pathways,” Current Molecular Medicine, vol. 17, no. 4, pp. 312–319, 2017.

J. M. Woo, D. Y. Shin, S. J. Lee et al., “Curcumin protects retinal pigment epithelial cells against oxidative stress via induction of heme oxygenase-1 expression and reduction of reactive oxygen,” Molecular Vision, vol. 18, pp. 901–908, 2012.

D. L. Peng, X. N. Wang, and J. Yang, “Effects of curcumin on endoplasmic reticulum stress in rats with retinal ischemia/reperfusion injury,” World Traditional Chinese Medicine, vol. 13, no. 4, pp. 929–935, 2018.

H. J. Zhang, Y. Q. Xing, W. Jin, D. Li, K. Wu, and Y. Lu, “Effects of curcumin on interleukin-23 and interleukin-17 expression in rat retina after retinal ischemia-reperfusion injury,” International Journal of Clinical and Experimental Pathology, vol. 8, no. 8, pp. 9223–9231, 2015.

B. Lal, A. K. Kapoor, O. P. Asthana et al., “Efficacy of curcumin in the management of chronic anterior uveitis,” Phytotherapy Research, vol. 13, no. 4, pp. 318–322, 1999.

P. Allegri, A. Mastromarino, and P. Neri, “Management of chronic anterior uveitis relapses: efficacy of oral phospholipidic curcumin treatment. Long-term follow-up,” Clinical Ophthalmology, vol. 4, pp. 1201–1206, 2010.

J. H. Park, E. Y. Shin, M. E. Shin et al., “Enhanced retinal pigment epithelium (RPE) regeneration using curcumin/alginate hydrogels: In vitro evaluation,” International Journal of Biological Macromolecules, vol. 117, pp. 546–552, 2018.

B. Zheng, S. Peng, X. Zhang, and D. J. McClements, “Impact of delivery system type on curcumin bioaccessibility: comparison of curcumin-loaded nanoemulsions with commercial curcumin supplements,” Journal of Agricultural and Food Chemistry, vol. 66, no. 41, pp. 10816–10826, 2018.

E. Marin, M. I. Briceño, A. Torres, and C. Caballero-George, “New curcumin-loaded chitosan nanocapsules: in vivo evaluation,” Planta Medica, vol. 83, no. 10, pp. 877–883, 2017.

Z. Y. Ng, J. Y. Wong, J. Panneerselvam et al., “Assessing the potential of liposomes loaded with curcumin as a therapeutic intervention in asthma,” Colloids and Surfaces B, Biointerfaces, vol. 172, pp. 51–59, 2018.

A. Ubeyitogullari and O. N. Ciftci, “A novel and green nanoparticle formation approach to forming low-crystallinity curcumin nanoparticles to improve curcumin's bioaccessibility,” Scientific Reports, vol. 9, no. 1, article 19112, 2019.

J. L. Olson, R. J. Courtney, B. Rouhani, N. Mandava, and C. A. Dinarello, “Intravitreal anakinra inhibits choroidal neovascular membrane growth in a rat model,” Ocular Immunology and Inflammation, vol. 17, no. 3, pp. 195–200, 2009.

S. C. Teoh, S. Sharma, A. Hogan, R. Lee, A. V. Ramanan, and A. D. Dick, “Tailoring biological treatment: anakinra treatment of posterior uveitis associated with the CINCA syndrome,” The British Journal of Ophthalmology, vol. 91, no. 2, pp. 263-264, 2007.

A. Amadi-Obi, C. R. Yu, X. Liu et al., “TH17 cells contribute to uveitis and scleritis and are expanded by IL-2 and inhibited by IL-27/STAT1,” Nature Medicine, vol. 13, no. 6, pp. 711–718, 2007.

L. Tian, B. Lei, J. Shao, L. Wei, A. Kijlstra, and P. Yang, “AAV2-mediated combined subretinal delivery of IFN-α and IL-4 reduces the severity of experimental autoimmune uveoretinitis,” PLoS One, vol. 7, no. 6, article e37995, 2012.

L. V. Rizzo, R. A. Morawetz, N. E. Miller-Rivero et al., “IL-4 and IL-10 are both required for the induction of oral tolerance,” Journal of Immunology, vol. 162, no. 5, pp. 2613–2622, 1999.

J. Tode, E. Richert, S. Koinzer et al., “Intravitreal injection of anti-interleukin (IL)-6 antibody attenuates experimental autoimmune uveitis in mice,” Cytokine, vol. 96, pp. 8–15, 2017.

S. J. Curnow, D. Scheel-Toellner, W. Jenkinson et al., “Inhibition of T cell apoptosis in the aqueous humor of patients with uveitis by IL-6/soluble IL-6 receptor trans-signaling,” Journal of Immunology, vol. 173, no. 8, pp. 5290–5297, 2004.

J. S. Mo, A. Matsukawa, S. Ohkawara, and M. Yoshinaga, “Role and regulation of IL-8 and MCP-1 in LPS-induced uveitis in rabbits,” Experimental Eye Research, vol. 68, no. 3, pp. 333–340, 1999.

I. Goczalik, E. Ulbricht, M. Hollborn et al., “Expression of CXCL8, CXCR1, and CXCR2 in neurons and glial cells of the human and rabbit retina,” Investigative Ophthalmology & Visual Science, vol. 49, no. 10, pp. 4578–4589, 2008.

L. Akduman, H. J. Kaplan, O. Ataoglu, M. Or, A. Bilgihan, and B. Hasanreisoglu, “Comparison of uveitis induced by interleukin-8 (IL-8) and endotoxin in rabbits,” Ocular Immunology and Inflammation, vol. 2, no. 4, pp. 223–229, 1994.

M. J. Verma, N. Mukaida, U. Vollmer-Conna, K. Matsushima, A. Lloyd, and D. Wakefield, “Endotoxin-induced uveitis is partially inhibited by anti-IL-8 antibody treatment,” Investigative Ophthalmology & Visual Science, vol. 40, no. 11, pp. 2465–2470, 1999.

A. Atalay, S. Arıkan, O. Ozturk et al., “The IL-8 gene polymorphisms in Behçet’s disease observed in Denizli Province of Turkey,” Immunological Investigations, vol. 45, no. 4, pp. 298–311, 2016.

B. Zelazowska-Rutkowska, M. Mrugacz, and B. Cylwik, “Comparison of the diagnostic power of serum IL-6, IL-8 and TNF-α for the idiopathic anterior uveitis in children,” Clinical Laboratory, vol. 63, no. 11, pp. 1889–1895, 2017.

S. Rytkönen, J. Ritari, J. Peräsaari, V. Saarela, M. Nuutinen, and T. Jahnukainen, “IL-10 polymorphisms +434T/C, +504G/T, and -2849C/T may predispose to tubulointersititial nephritis and uveitis in pediatric population,” PLoS One, vol. 14, no. 2, article e0211915, 2019.

H. Keino, T. Watanabe, Y. Sato, M. Niikura, Y. Wada, and A. A. Okada, “Therapeutic effect of the potent IL-12/IL-23 inhibitor STA-5326 on experimental autoimmune uveoretinitis,” Arthritis Research & Therapy, vol. 10, no. 5, p. R122, 2008.

R. Chang, S. Yi, X. Tan et al., “MicroRNA-20a-5p suppresses IL-17 production by targeting OSM and CCL1 in patients with Vogt-Koyanagi-Harada disease,” The British Journal of Ophthalmology, vol. 102, no. 2, pp. 282–290, 2018.

J. M. G. Ruiz de Morales, L. Puig, E. Daudén et al., “Critical role of interleukin (IL)-17 in inflammatory and immune disorders: an updated review of the evidence focusing in controversies,” Autoimmunity Reviews, vol. 19, no. 1, article 102429, 2020.

S. Cole, J. Murray, C. Simpson et al., “Interleukin (IL)-12 and IL-18 synergize to promote MAIT cell IL-17A and IL-17F production independently of IL-23 signaling,” Frontiers in Immunology, vol. 11, article 585134, 2020.

H. Belguendouz, D. Messaoudene, K. Lahmar-Belguendouz et al., “Production de l’IL-18 in vivo et ex vivo pendant l’uveite associee a la maladie de Behçet: effet de la corticotherapie,” Journal Français d'Ophtalmologie, vol. 38, no. 3, pp. 206–212, 2015.

L. Wang, C. R. Yu, H. P. Kim et al., “Key role for IL-21 in experimental autoimmune uveitis,” Proceedings of the National Academy of Sciences of the United States of America, vol. 108, no. 23, pp. 9542–9547, 2011.

R. Zeng, R. Spolski, S. E. Finkelstein et al., “Synergy of IL-21 and IL-15 in regulating CD8+ T cell expansion and function,” The Journal of Experimental Medicine, vol. 201, no. 1, pp. 139–148, 2005.

M. T. Kasaian, M. J. Whitters, L. L. Carter et al., “IL-21 limits NK cell responses and promotes antigen-specific T cell activation: a mediator of the transition from innate to adaptive immunity,” Immunity, vol. 16, no. 4, pp. 559–569, 2002.

Y. J. Sepah, G. Velez, P. H. Tang et al., “Proteomic analysis of intermediate uveitis suggests myeloid cell recruitment and implicates IL-23 as a therapeutic target,” American Journal of Ophthalmology Case Reports, vol. 18, article 100646, 2020.

J. W. Kang, S. C. Choi, M. C. Cho et al., “A proinflammatory cytokine interleukin-32β promotes the production of an anti-inflammatory cytokine interleukin-10,” Immunology, vol. 128, 1, Part 2, pp. e532–e540, 2009.

M. Schenk, S. R. Krutzik, P. A. Sieling et al., “NOD2 triggers an interleukin-32-dependent human dendritic cell program in leprosy,” Nature Medicine, vol. 18, no. 4, pp. 555–563, 2012.

M. Barbour, D. Allan, H. Xu et al., “IL-33 attenuates the development of experimental autoimmune uveitis,” European Journal of Immunology, vol. 44, no. 11, pp. 3320–3329, 2014.

S. Ali, A. Mohs, M. Thomas et al., “The dual function cytokine IL-33 interacts with the transcription factor NF-κB to dampen NF-κB-stimulated gene transcription,” Journal of Immunology, vol. 187, no. 4, pp. 1609–1616, 2011.

C. Hou, Q. Wu, C. Ouyang, and T. Huang, “Effects of an intravitreal injection of interleukin-35-expressing plasmid on pro-inflammatory and anti-inflammatory cytokines,” International Journal of Molecular Medicine, vol. 38, no. 3, pp. 713–720, 2016.

Y. Zongyi, Z. Funian, L. Hao et al., “Interleukin-35 mitigates the function of murine transplanted islet cells via regulation of Treg/Th17 ratio,” PLoS One, vol. 12, no. 12, article e0189617, 2017.

J. L. Zhang, X. Y. Song, Y. Y. Chen et al., “Novel inflammatory cytokines (IL-36, 37, 38) in the aqueous humor from patients with chronic primary angle closure glaucoma,” International Immunopharmacology, vol. 71, pp. 164–168, 2019.

A. Psarras, A. Antanaviciute, A. Alase et al., “TNF-α regulates human plasmacytoid dendritic cells by suppressing IFN-α production and enhancing T cell activation,” Journal of Immunology, vol. 206, no. 4, pp. 785–796, 2021.

M. Leclercq, A. C. Desbois, F. Domont et al., “Biotherapies in uveitis,” Journal of Clinical Medicine, vol. 9, no. 11, p. 3599, 2020.

Y. Zhu, H. Yu, Y. Qiu et al., “Promoter hypermethylation of GATA3, IL-4, and TGF-β confers susceptibility to Vogt-Koyanagi-Harada disease in Han Chinese,” Investigative Ophthalmology & Visual Science, vol. 58, no. 3, pp. 1529–1536, 2017.

Y. Ke, G. Jiang, D. Sun, H. J. Kaplan, and H. Shao, “Anti-CD3 antibody ameliorates experimental autoimmune uveitis by inducing both IL-10 and TGF-β dependent regulatory T cells,” Clinical Immunology, vol. 138, no. 3, pp. 311–320, 2011.

H. L. Rosenzweig, T. Kawaguchi, T. M. Martin, S. R. Planck, M. P. Davey, and J. T. Rosenbaum, “Nucleotide oligomerization domain-2 (NOD2)-induced uveitis: dependence on IFN-γ,” Investigative Ophthalmology & Visual Science, vol. 50, no. 4, pp. 1739–1745, 2009.

B. Liu, L. Faia, M. Hu, and R. B. Nussenblatt, “Pro-angiogenic effect of IFNγ is dependent on the PI3K/mTOR/translational pathway in human retinal pigmented epithelial cells,” Molecular Vision, vol. 16, pp. 184–193, 2010.

D. Bauer, M. Kasper, K. Walscheid et al., “Alteration of MCP-1 and MMP-9 in aqueous humor is associated with secondary glaucoma in Fuchs uveitis syndrome,” Ocular Immunology and Inflammation, vol. 28, no. 4, pp. 688–698, 2020.

C. Cuello, D. Wakefield, and N. Di Girolamo, “Neutrophil accumulation correlates with type IV collagenase/gelatinase activity in endotoxin induced uveitis,” The British Journal of Ophthalmology, vol. 86, no. 3, pp. 290–295, 2002.