TYK2 in Immune Responses and Treatment of Psoriasis

Abstract

Tyrosine kinase 2 (TYK2), a key part of the Janus kinase-signal transducer and activator of transcription (JAK-STAT) pathway, plays an integral role in the differentiation and immune responses of intrinsic immune cells and regulates the mediation of cytokines. TYK2 leads to inflammatory cascade responses in the pathogenesis of immune-mediated inflammatory diseases (IMIDs), especially psoriasis. Small-molecule TYK2 inhibitors are considered to be an effective strategy for modulating psoriasis. Here, we attempt to review the pro-inflammatory mechanisms of the JAK-STAT signaling pathway, the regulatory roles of TYK2 in the pathogenesis of psoriasis, and provide updates on ongoing and recently completed trials of TYK2 inhibitors.

Introduction

Psoriasis is a chronic, multifactorial, immune-mediated inflammatory skin disease with a global prevalence of approximately 2%, affecting approximately 125 million people worldwide.^1,2 Psoriasis is characterized by persistent inflammation leading to uncontrolled proliferation and dysfunctional differentiation of keratinocytes.^3,4 The pathogenesis of psoriasis has not been fully elucidated. It is considered that the interaction between innate and adaptive immunity mediated by inflammatory mediators has been the focus of research in recent years. Among them, the Janus kinase-signal transducer and activator of the transcription (JAK-STAT) pathway is involved at multiple levels of the IL-23/Th17 signaling pathway, which is thought to be the core of the pathogenesis.^5–8 A member of the JAK family, Tyrosine kinase 2 (TYK2) transmits a variety of extracellular cytokine signals, which contribute to disorders of immune-mediated inflammatory diseases (IMIDs), leading to inflammatory cascade responses, followed by induction of keratinocyte proliferation and other distinguishing features of psoriasis.^9–11

Current treatments for psoriasis include topical drugs, phototherapy, traditional systemic drugs, biological agents, and novel small-molecule drugs. Biological agents such as TNF-α inhibitors, IL-17 inhibitors, and IL-23 inhibitors have been used for the clinical treatment of psoriasis. However, due to the adverse events (AEs) intolerable in some patients, the decrease in long-term application effect, and the limitations of biological agents in drug administration,¹² people have begun to pay attention to small-molecular drugs that can be administered orally or topically. JAK inhibitors can block the Janus signaling pathway and thus improve the clinical symptoms of psoriasis. This review attempts to provide an overview of the pro-inflammatory mechanisms of the JAK-STAT signaling pathway, the role of the TYK2 signaling pathway in immune responses, and also presents recent advances in the treatment of immune-mediated inflammatory diseases (IMIDs) with JAK inhibitors, focusing on the efficacy and safety of three TYK2 inhibitors (BMS-986165, PF-06700841, PF-06826647) in clinical trials.

JAK-STAT Signaling Pathway

The members of the JAK-STAT family include four JAKs (JAK1, JAK2, JAK3, and TYK2), plus seven STAT proteins (STAT1, STAT2, STAT3, STAT4, STAT5A, STAT5B, and STAT6).^6,13 The JAK-STAT pathway mediates the signal transduction downstream of type I and type II cytokine receptors, including ILs, IFNs, and various growth factors.^13,14 When the intracellular domain of the cytokine receptor binds to JAK, JAK is phosphorylated, which leads to the attachment of signal transmitter and transcription activator STAT protein. Subsequently, STAT becomes phosphorylated and dimerized. The dimerized STAT translocates into the nucleus of the cell to modify and regulate gene transcription and expression.^15–17 Each member of the STAT family can be activated by multiple cytokines and their related JAKs⁸ (Figure 1).

Figure 1.

Janus kinase-signal transducer and activator of transcription pathway. Cytokines bind to receptors on the cell membrane, activating JAKs and phosphorylating them. This subsequently leads to phosphorylation and dimerization of STAT. Activated STAT dimers translocate to the nucleus and regulate gene transcription and expression, ultimately leading to changes in cellular function.

Abbreviations: JAK, Janus kinase; STAT, signal transducer and activator of transcription; TYK2, tyrosine kinase 2; IFN, interferon; IL, interleukin; EPO, erythropoietin; GH, growth hormone; TPO, thrombopoietin; GM-CSF, granulocyte macrophage colony-stimulating factor.

The pathological mechanisms of psoriasis include pathogenic T cell drive, the interaction between innate and adaptive immunity, and the “feed-forward” inflammatory loop of adaptive immunity.^1,18 The activation of the Th17 cytokine pathway mediated by IL-23 is the key.^12,19 IL-23 and many pathogenic factors of psoriasis mediate intracellular conduction through the JAK-STAT pathway, resulting in inflammatory cascade reactions, leading to the proliferation of epidermal cells and the recruitment of leukocyte subpopulation, and increased expression of vascular endothelial factors and endothelial adhesion molecules.^5,20 Therefore, the JAK-STAT pathway is involved in many critical targets of regulating the pathogenesis of psoriasis, and the small-molecule JAK inhibitor is considered an effective treatment.

TYK2 Signaling Pathway in Psoriasis

TYK2, a non-receptor tyrosine-protein kinase encoded by the TYK2 gene, induces intracellular signal transduction.²¹ TYK2 plays an integral role in the differentiation and immune responses of innate immunity cells, regulates the mediation of type I IFNs, IL-12, IL-23, IL-10, and IL-6, and participates in the regulation of multiple vital targets in the pathogenesis of psoriasis^22–24 (Figure 2).

Figure 2.

TYK2 mediates IFN-α/β, IL-12, IL-23, IL-10, IL-22, and IL-6 signaling.

Abbreviations: TYK2, tyrosine kinase 2; IFN, interferon; IL, interleukin; JAK, Janus kinase; STAT, signal transducer and activator of transcription; Th, T-helper; R, receptor.

TYK2 and Innate Immunity

In psoriasis, the crosstalk between innate and adaptive immunity leads to the production of inflammatory mediators, causing the induction of inflammation with keratinocyte hyper-proliferation.²⁵ DCs, NK cells, macrophages, and neutrophils produce TNF-α and IFN-γ.²⁶ DC subsets present antigens to T cells and trigger up-regulation of inflammatory cytokines to be increased in psoriatic skin lesions.²⁷

Adoptive transfer experiments showed that the generation of IFN-γ producing specific CD8+ T (Tc1) cells was impaired in the spleen of Tyk2−/− mice infected with Listeria monocytogenes. It was confirmed that Tyk2 signaling was important in inducing restricted CD8+ T (Tc1) cells.²⁸ In DCs pre-infected with Dengue virus (DV), the antiviral response is antagonized by DV due to inhibition of TYK2 phosphorylation.²⁹ It has been reported that in Tyk2−/− DCs, the ability to differentiate Th1 and Th17 cells are diminished, as well as the regulatory mechanisms of multiple cytokines and interferon production are affected.^30,31 Therefore, we have reasons to believe that the immune responses of DCs against pathogens are partly dependent on the presence of TYK2, and TYK2 affects the tandem between DCs and T cells.

Current animal experiments confirmed that IFN-g production by NK cell activity induced by IL-12 and IL-18 were reduced in knockout mice for Tyk2. TYK2 promotes NK cell maturation and anti-cytotoxicity, which is also indispensable for immune defense against Listeria monocytogenes and Lactobacillus monocytogenes.^32,33 Another study showed that NK cell immunity was not particularly affected in patients lacking TYK2. TYK2 deficiency does not affect IL-12-mediated activation of NK cells. This is contrary to the experimental results of animal trials. This may be due to the presence of two different antiviral defense mechanisms in NK cells that attenuate the viral susceptibility. However, the relevant mechanisms are still unclear.³⁴ We still need to continue exploring the significance of TYK2 for NK cells, but at present, it seems that TYK2 may not be necessary for NK cells to perform functions such as immune defense and tumor surveillance in humans.

In macrophages, TYK2 mainly affects IFN signaling. TYK2-deficient macrophages exhibited loss of IFN-α, IFN-β or IFN-γ mediated responses and reduced gene expression. Furthermore, TYK2 is necessary for the activation of STAT1 and STAT2.^35,36

TYK2 Mediates IFN-α/β Receptors

Different types of type I IFNs show different tissue expression and binding affinities for the heterodimeric receptor complex (IFNAR1/2) so that the different isoforms produce various outcomes in terms of antiviral, antiproliferative, and immunomodulatory activities.³⁷ In psoriasis, type I IFNs promote significant inflammatory effects, including DCs maturation and activation, Th1 and Th17 polarization, reduced regulatory T cells (Treg) function, B cell activation, and subsequent increased antibody production.³⁸

Different types of IFNs signals are emitted through different receptor complexes on the cell surface. IFN-α/β binds to receptor IFNAR1/2 complex and activates JAK1 and TYK2 to phosphorylate them, which in turn allowing reposition and phosphorylate STAT1, STAT2, and STAT3 proteins through Src homology 2 (SH2) domain interactions, and interacting with IFNs regulatory factor (IRF) to translocate to the nucleus.³⁷ STAT1 homodimers bind to gamma-activated sequences (GASs) to induce pro-inflammatory genes. STAT3 homodimers indirectly inhibit the expression of pro-inflammatory genes, possibly by inducing unknown transcription repressors.³⁹

TYK2 Mediates IL-12/IL-23 Receptors

IL-12 binds to IL-12Rb1 and IL-12Rb2 receptors to induce TYK2 and JAK2, resulting in the activation of STAT4.⁴⁰ Then they bind to the STAT binding site in the IFN-g promoter to induce the transcription of the IFN-g gene. IL-12 promotes the differentiation of CD4+ T cells into Th1 cells, which produce IFN-g.⁴¹ The receptors of IL-23 consist of IL-12Rb1 and IL-23R, with STAT3 as their main STAT. IL-23 also activates STAT4, but to a lesser extent than IL-12.^10,42 IL-23 is central to the value-added of innate immune Th17 cells, resulting in the secretion of IL-17, IL-22, and TNF-α by Th17 cells.^40,41

Recent studies have demonstrated that TYK2 deficiency leads to specific impairment of immune responses pathways in mice. Reduced ability of IFN-α to induce gene expression, antiviral and immune responses, an inability of IL-12 to promote Th1 cell differentiation and IFN-g gene transcription, and an inability of IL-23 to stimulate the secretion of other inflammatory factors by Th17 cells, which subsequently leads to the absence of adaptive immune responses.⁴³ The experiment also showed that the IL-6 and IL-10 responses of Tyk2−/− mice were not affected.⁴³ The studies of TYK2 in human cytokine responses are still insufficient. A patient with TYK2 protein deficiency due to mutation of the TYK2 is related to the defects of IFN-α, IL-23, IL-12, IL-6, and IL-10 pathways.^44,45 It is now considered that TYK2 protein plays a broader role in human cytokine pathways compared to mice. In another study, by establishing a mouse model of psoriasis-like skin inflammation induced by imiquimod (IMQ) and IL-23, the results showed that Tyk2−/− mice could eliminate the thickening of the ear margins due to epidermal hyperplasia caused by IMQ-induced inflammatory cell infiltration. Also, in the IL-23-induced mouse model, ear margin swelling was significantly reduced in Tyk2−/− mice compared to Tyk2+/+ mice. The absence of TYK2 could reduce the production of psoriasis-related cytokines and antibacterial peptides. IL-23 and IL-22 synergistically induce psoriasis skin inflammation through the TYK2 signaling pathway, leading to epidermal hyperplasia, infiltration of large numbers of leukocytes, and production of inflammatory factors.⁴⁶

TYK2 Mediates Other Cytokines Receptors

IL-10 binds to IL-10R2 and IL-20R2 receptors to induce JAK1, JAK2, and TYK2, resulting in the activation of STAT1, STAT3, and also in STAT5.⁴⁷ IL-22 belongs to the IL-10 cytokine family and mediates its action through a heterodimeric transmembrane receptor complex composed of IL-22R1 and IL-10R2, activating JAK1 and JAK2, and TYK2.⁴⁸ Like other members of the IL-10 cytokine family, it mediates a common pathway of signaling through STAT3.⁴⁷ In the mouse model of psoriasis-like disease, IL-22 deficient mice significantly reduced squamous skin injury, inflammatory cell infiltration, and the expression of chemokines.^49–51

In addition, TYK2 is an important signaling sensor for IL-6.²⁴ IL-6 binds to the receptor IL-6R on the cell surface to form a complex. Then the complex binds to the receptor subunit homodimer gp130 of IL-6, resulting in selective activation of JAK1, JAK2, and TYK2, which in turn promotes the recruitment and phosphorylation of STAT1, STAT3, and to a lesser extent STAT5.^52–54 Ishizaki et al found various inflammatory cytokines, such as IL-6, IL-1b, and matrix metalloproteinases (MMPs), such as MMP3 and MMP9, were significantly reduced in Tyk2−/− mice.⁵⁵

JAK Inhibitors Progress

In recent years, clinical trials of several oral JAK inhibitors for the treatment of psoriasis have been underway. First-generation JAK inhibitors, non-selective JAK inhibitors, include Tofacitinib, Baricitinib, and Ruxolitinib. Tofacitinib is a JAK1/3 inhibitor, which has been approved by the United States Food and Drug Administration (FDA) for ulcerative colitis, psoriatic arthritis, and rheumatoid arthritis.^{24,56,57,83,84} Baricitinib and Ruxolitinib are JAK1/2 inhibitors. A Phase 2 clinical trial of Baricitinib in patients with psoriasis is underway.⁵⁸ Ruxolitinib has been approved by the FDA and the European Medicines Agency (EMA) to treat myelodysplasia. In psoriasis, its use has only been tested in topical cream, and clinical trials of related oral drugs are still in progress.⁵⁹ Among the first-generation JAK inhibitors, although their efficacy has been confirmed to some extent, the safety problems related to AEs still exist. For example, changes in laboratory parameters including neutrophils, platelets, and creatinine, increased probability of herpes zoster, and gastric perforation.^58,60–64 The mechanisms of many AEs are still unclear, but some of them are due to the inhibition of related cytokine transduction pathways by non-selective JAK inhibitors. Hyperlipidemia, neutropenia, and elevated liver enzymes are thought to be due to the inhibition of IL-6 signaling by JAK1/2 inhibitors. The reduction in platelet, hemoglobin, and reticulocyte counts is due to the inhibition of the EPO-JAK2 pathway by JAK2 inhibitors.^15,65

The second-generation JAK inhibitors are highly selective for related JAKs. Theoretically, different cytokine receptor signal through different JAKs. Selective blockade of one JAK with a JAK inhibitor thus inhibits the function transduced by specific cytokines while allowing other irrelevant cytokines to continue to signal normally. Among them, TYK2 selective inhibitors have attracted much attention in recent years.

TYK2 Inhibitors Progress

A genome-wide association study (GWAS) in 2016 demonstrated that TYK2 transduced signals downstream of type I IFNs, gp130, IL-10R2, IL-13Ra, and IL-12Rb1 cytokine receptors, thus TYK2 gene is associated with several autoimmune diseases. As the pathogenesis of psoriasis is related to the cytokine signal transduction pathway, the deletion of the TYK2 gene locus is related to the susceptibility of psoriasis.⁶⁶ Although IL-17 does not activate the JAK-STAT pathway, TYK2 inhibitors can indirectly suppress IL-23/IL-17 signaling by inhibiting other STAT-dependent cytokines, namely IL-23.⁶⁷ Meanwhile, TYK2 inhibitors lead to decreased IL-12 and type I IFNs signaling, improving inflammatory cell infiltration, epidermal proliferation, and thus psoriasis symptoms.⁶⁸ The latest clinical trial progress of TYK2 inhibitors will be described below (Table 1).

Table 1.

Clinical Trials of TYK2 Inhibitors

Drug	Target	Clinical Trial	Research Phase	Description	Primary Endpoint	Key Results
PF-06700841	JAK1/TYK2	NCT02310750	1	30 patients with psoriasis received PF-06700841 30 or 100 mg or placebo QD for 28 days.	__	Change from baseline in PASI for 30 mg and 100 mg QD were −67.92% and −96.31%, respectively in week 4.
		NCT02969018	2a	212 Patients were randomized to PF-06700841 30 mg QD, 60 mg QD, or placebo (4-week induction), then 10 mg QD, 30 mg QD, 100 mg QW, or placebo (8-week maintenance).	PASI score at week 12	Achieving PASI 75 and PASI 90 was the highest in the 30-mg QD(86.2% and 51.7%) for 12 week.
		NCT03850483 (topical)	2b	240 patients received PF-06700841 cream 0.1% QD,0.3% QD,1% QD,3% QD,0.3% BID,1% BID,3% BID or placebo.	PASI score at week 12	__
		NCT03963401	2b	219 patients with active PsA received PF-06700841 30mg QD, 60mg QD for 52 weeks or 10 mg QD for 16 weeks, followed by 30mg,60mg QD until 52 weeks or placebo.	ACR20 response at week 16	__
PF-06826647	TYK2	NCT03895372	2	178 patients with moderate-to-severe psoriasis received PF-06826647 50mg QD, 100mg QD, 200mg QD,400mg QD or placebo for 16 weeks.	PASI 90 at week 16	A greater proportion of patients achieved PASI90 in the 200mg and 400mg groups(33.0% and 46.5%, respectively) versus placebo at week 16._
BMS-986165	TYK2	NCT02931838	2	267 patients with psoriasis received BMS-986165 3mg every other day, 3mg QD,3mg BID,6mg BID,12mg QD or placebo for 12 weeks.	PASI 75 at week 12	BMS-986165 at doses of 3 mg daily and higher resulted in greater PASI75 than placebo for 12 weeks. PASI score was 9% (3mg every other day),39%(3mg QD), 9% (3mg BID),67%(6mg BID),75%(12mg QD),7%(placebo).
		NCT03881059	2	203 patients with PSA received BMS-986165 6mg QD,12mg QD, or placebo for 16 weeks.	ACR20 response at week 16	BMS-986165 at doses of 6 mg and 12mg QD were more likely to achieve ACR20 response at week 16 compared with placebo. ACR20 response was 52.9%(6 mg QD) and 62.7%(12 mg QD).
		NCT03624127	3	666 patients with psoriasis received BMS-986165 6mgQD or Apremilast 30mg BID or placebo for 52 weeks.	sPGA 0/1 at week 16 PASI75 at week 16	BMS-986165 groups resulted in higher response rates versus Apremilast or placebo for PASI75 (58.4% vs 35.1% vs 12.7%); and sPGA 0/1 (53.6% vs 32.1% vs 7.2%).
		NCT03611751	3	1020 patients with psoriasis received BMS-986165 6mgQD or Apremilast 30mg BID or placebo for 16 weeks.	sPGA 0/1 at week 16 PASI75 at week 16	__
		NCT04167462	3	220 patients with psoriasis received BMS-986165.	sPGA 0/1 at week 16 PASI75 at week 16	__
		NCT03924427	3	74 patients with psoriasis received BMS-986165 for 16 weeks.	sPGA 0/1 at week 16 PASI75 at week 16	__
		NCT04036435	3	1470 patients with psoriasis received BMS-986165.	Incidence of AEs up to 244 weeks.	__

Abbreviations: PASI, Psoriasis Area and Severity Index; PASI75, 75% improvement from baseline PASI; ACR, American College of Rheumatology score; sPGA, static Physician’s Global Assessment; AEs, Adverse events; PsA, psoriatic arthritis.

Bms-986165

BMS-986165 is an emerging, highly selective, and potent oral TYK2 inhibitor that binds to the residual ATP-binding site of the TYK2 pseudokinase domain, also known as the JH2 domain, via an allosteric mechanism rather than to the highly conserved ATP-binding sites in the catalytic domain. This mode of binding, which differs from that of JAK1/2/3 inhibitors, is associated with the high selectivity of BMS-986165.^9,69

In a phase 2 clinical trial, adults with moderate to severe plaque psoriasis were randomized into six groups. Patients received oral medication at 3 mg every other day, 3 mg once daily (QD), 3 mg twice daily (BID), 6 mg BID, 12 mg QD, or placebo. The results showed that, in the 12th week, the proportion of patients who reached the 75% improvement from baseline Psoriasis Area and Severity Index (PASI75) in the above treatment groups were: 9%, 39%, 69%, 67%, 75%, and 7%. AEs occurred in 55–80% of patients in the active drug groups, with the highest incidence in the 6 mg BID group, where nasopharyngitis, headache, nausea, diarrhoea, and upper respiratory tract infections were more common.⁷⁰ Meanwhile, the clinical efficacy of BMS-986165 is associated with a decrease in IL-23/Th17 and IFNs pathway markers.⁷¹ In addition, in the phase 2 clinical trial for patients with psoriatic arthritis, patients were randomly divided into 3 groups to receive oral drugs. The results showed that patients treated with BMS-986165 were more likely to achieve ≥20% improvement in the American College of Rheumatology score (ACR20) than those treated with placebo at week 16.⁸⁵

A large Phase 3 trial demonstrated that a significantly higher proportion with moderate-to-severe psoriasis achieved PASI75 and SPGA 0/1 at week 16 in the BMS-986165 6 mg QD (58.4% and 53.6%) dosage groups compared with Apremilast 30 mg QD (35.1% and 32.1%) or placebo (12.7% and 7.2%). In addition to the primary endpoint, BMS-986165 groups also showed greater improvements compared to Apremilast and placebo, including PASI90, quality of life, psoriasis symptoms, and improvements in scalp psoriasis. The incidence of AE was not significantly different among all 3 treatment groups, and the most common AEs in BMS-986165 groups were nasopharyngitis and upper respiratory tract infection. This experiment further confirmed that no meaningful changes in laboratory parameters associated with JAK1/2/3 inhibitors were detected during treatment with BMS-986165.⁷²

The clinical trial data further confirmed the efficacy, safety and durability of BMS-986165 oral administration compared to placebo and Apremilast, which provides sufficient evidence for its use in the treatment of psoriasis. Three phases 3 trials for plaque psoriasis are still currently underway (NCT03611751, NCT04036435, and NCT03924427).²⁴

Pf-06700841

PF-06700841 is a dual inhibitor of TYK2 and JAK1, inhibiting cytokines mediated through TYK2 and JAK1 signaling pathways.⁷³

In a Phase 1 clinical trial, patients with moderate to severe psoriasis were randomized to 30 mg QD, 100 mg QD, and placebo.⁷⁴ By comparing the changes of gene expression in lesional skin at weeks 2 and 4 with placebo, the changes were significant dose-dependent from baseline in both the 30 mg and 100 mg groups. By week 4, the overall improvement of the IL-17 gene in the 100 mg group reached 124%, while the reduction in IL-17 gene expression was strongly correlated with PASI and Body Surface Area (BSA). No serious AEs occurred in this study, with decreases in reticulocyte, platelet, and neutrophil counts, increases in lymphocyte counts, and increases in serum creatinine observed in healthy subjects and patients with psoriasis.⁷³ In a phase 2a trial, patients with moderate-to-severe plaque psoriasis treated with the oral PF-06700841 were divided into seven treatment groups. Among the seven treatment groups, a higher percentage of patients achieved PASI 75 and PASI90 than in the placebo group, and at week 12, the proportion of patients achieving PASI75 and PASI90 were the highest in the 30 mg QD treatment group, respectively, 86.2% and 51.7%.⁷⁵

A phase 2b clinical trial is currently underway in patients with psoriatic arthritis. Topical application of PF-06700841 cream is also being conducted in patients with mild-to-moderate psoriasis to evaluate its safety and efficacy.

Pf-06826647

PF-06826647 is a selective oral TYK2 inhibitor.⁷⁶ Several phases 1 studies have been conducted to evaluate its safety and pharmacokinetics in healthy participants and patients with plaque psoriasis.^77,86 The severity of AEs in the current study is mild, but the safety still needs to be further determined.⁷⁷ In a phase 2 clinical trial, patients with moderate to severe plague psoriasis were randomized to 50 mg, 100 mg, 200 mg, 400 mg QD or placebo for 16 weeks. The trial demonstrated that a greater proportion of patients achieving PASI90 in the 200 mg (33.0%) and 400 mg (46.5%) groups versus placebo. Significant increases in secondary endpoints (PASI75, PASI50/100 and PGA responses) compared to placebo could be observed in all treatment groups. The most common AEs were upper respiratory tract infection, nasopharyngitis, and increased blood pressure. There are no serious AEs occurred in this trial.⁷⁸

Discussion

Systemic treatment options for moderate to severe psoriasis include traditional oral immunosuppressive drugs, biologics, and oral small molecule drugs. The efficacy of traditional oral drugs is generally lower than that of biologics, but they are still widely used due to their low price.⁷⁹ Among biologic agents, TNF antagonists, IL-17 inhibitors, and IL-23 are the predominant drug classes currently available for the treatment of moderate-to-severe psoriasis. Though biologics are currently among the most effective options for the treatment of psoriasis, they still have many limitations. A subset of patients with malignancies and chronic infections have restricted access, while others fade of efficacy over time. Additional limitations of biologics include intravenous or subcutaneous administration and expensive expenses, which have kept biologics from being preferred by some patients.^80,81 Oral administration of small molecules, which can partially and reversibly inhibit multiple cytokine pathways with a single small molecule compared to inhibiting a single cytokine pathway with a biologic agent, could provide new treatment ideas for psoriasis. Apremilast, a phosphodiesterase inhibitor, may not be as effective as some biologics, but its lower cost of treatment and fewer AEs have kept its use in a stable range.⁸² JAK inhibitors offer the benefits of Apremilast while providing better efficacy than Apremilast. TYK2 inhibitors bind allosterically to the residual ATP-binding site of the JH2 domain, reducing the AEs such as hematological toxicity caused by the inhibition of the JAK1/2/3 signaling pathway compared with other pan-JAK inhibitors.⁸⁷ Among these, TYK2 inhibitors are considered potential drugs for the treatment of psoriasis. In Table 2, we compare the efficacy, dosage and limitations of several representative systemic treatments.

Table 2.

Biologic and Oral Systemic Treatments for Psoriasis

Systemic Treatments	Mechanism of Action	Dosage	PASI75	Safety Considerations
Biologics
Adalimumab	anti-TNF- antibody	80 mg SQ first week, 40 mg SQthe second week, then 40 mg SQevery two weeks	71% at week 16	Serious infection, cancer, induction of autoimmunity,new onset demyelinating disorders;Contraindications: demyelinatingdiseases hepatitis B
Secukinumab	IL-17 monoclonal antibody	300 mg SQ at weeks 0–4; then 300mg every 4 weeks	82% at week 12	Monilial infections;Contraindications: IBD
Ustekinumab	IL-12/23 monoclonal antibody	<100 kg: 45 mg SQ at weeks 0 and4, then every 12 weeks; >100kg: 90mg SQ at the same intervals	67% and 76% at week 12, patients weighing <100kg and ≥100kg, respectively	Cancer, induction of autoimmunity,Candida infections, cardiovascular events;Contraindications: serious infection
Guselkumab	IL-23 monoclonal antibody	100 mg SQ at weeks 0–4; then 100mg every 8 weeks	73% achieve PASI 90 at week 16	Monilial infections;Contraindications: serious infection
Oral systemic
Methotrexate	Dihydrofolate reductase inhibitor	15–20 mg once weekly with folic acid supplementation	36% at week 16	Bone marrow toxicity, hepatotoxic,lymphoma, drug-drug interactions;Contraindications: Pregnancy/nursing, alcoholism
Cyclosporine	Calcineurin inhibitor	5mg/kg as a twice-daily divided dose	65% achieve IGA 0/1 at week 8	Nephrotoxicity, gastrointestinal disturbances,headache, myalgia, cancer, lethargy
Apremilast	Phosphodiesterase-4 inhibitor	Gradual increasing doseto 30 mg PO twice daily	33% at week 16	Gastrointestinal disturbances and weight loss
Tofacitinib	JAK1 and JAK3inhibitor	5 or 10 mg, twice daily	39.9–59.6% at week 12	Increase in LDL, HDL, and Cr, sporadic neutropenia, anemia, possibly increase therisk for infections with varicella zostervirus and malignancies.
BMS-986165	TYK2 inhibitor	6 mg once daily	58.4% at week 16	Nasopharyngitis and upper respiratory tract infection

Abbreviations: TNF, tumor necrosis factor; JAK, Janus kinase; TYK2, tyrosine kinase 2; SQ, subcutaneous; IBD, inflammatory bowel disease; PASI, Psoriasis Area and Severity Index; PASI75, 75% improvement from baseline PASI; IGA, Investigator’s Global Assessment scale.

Conclusion

TYK2, the key part of the JAK-STAT pathway, regulates the mediation of cytokines such as type I IFNs, IL-12, IL-23, IL-10, and IL-6 and plays an indispensable role in the maturation, differentiation, and immune responses of innate immune cells. There are few studies on the concrete functionary mechanisms related to the association of TYK2 and immune immunity, and the physiological significance of TYK2 expression in DCs, NK cells, and macrophages should be explored in depth, then search for new therapeutic targets related to TYK2 and innate immune cells. Small-molecule drugs that selectively inhibit TYK2 may become a new strategy for the long-term treatment of moderate-to-severe psoriasis in the future. We expect the performance of TYK2 inhibitors in clinical trials, and to obtain outstanding results in the future treatment of psoriasis and psoriatic arthritis.

Abbreviations

TYK2, Tyrosine kinase 2; JAK-STAT, Janus kinase-signal transducer and activator of transcription; IFNs, interferons; ILs, interleukins; DCs, Dendritic cells; NK cells, Natural killer cells; IMIDs, immune-mediated inflammatory diseases; TNF-α, tumor necrosis factor-α; AEs, adverse events; DV, Dengue virus; Treg, regulatory T cells; IMQ, imiquimod; MMPs, matrix metalloproteinases; FDA, Food and Drug Administration; EMA, European Medicines Agency; GWAS, genome-wide association study; QD, once daily; BID, twice daily; QW, once weekly; SQ, subcutaneous; PASI, Psoriasis Area and Severity Index; PASI75, 75% improvement from baseline PASI; PASI90, 90% improvement from baseline PASI; ACR, American College of Rheumatology score; ACR20, achieve ≥20% improvement in the ACR; BSA, Body Surface Area; sPGA, static Physician’s Global Assessment; PsA, psoriatic arthritis; IGA, Investigator’s Global Assessment scale; IBD, inflammatory bowel disease.

Ethical Approval

Submitted paper is a mini-review of relevant literature. This article does not contain any studies with human participants or animals performed by any of the authors.

Author Contributions

All authors contributed to conception, data analysis, drafting or revising the article, have agreed on the journal to which the article will be submitted, gave final approval of the version for publication, and agree to be accountable for the contents of the article.

Disclosure

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.