Psoriasis is a common chronic inflammatory skin disease that affects 2% to 3% of the population worldwide. Its etiology is unknown, but it is believed to involve a complex network of cytokines and chemokines produced by various types of immune and tissue cells. Although the pathogenesis of psoriasis is not fully understood, there is growing evidence which indicates that T helper 1 (Th1) and 17 (Th17) cells play a critical role in the development of this disease.
Interleukin (IL)-18, is a potent pro-inflammatory cytokine of the IL-1 family. When synergized with IL-23, IL-18 promotes the development and maintenance of Th17 cells that have been implicated in autoimmune inflammatory diseases.[5,6] IL-18 also plays an important role in activating Th1 cells which can then produce interferon γ (IFNγ) mediated inflammation in psoriatic lesions.
Results from previous studies have indicated that serum or plasma levels of IL-18 correlate well with the Psoriasis Area and Severity Index (PASI).[8,9] The expression of IL-18 was elevated in initially active and progressive plaque-type psoriatic lesions. Moreover, in cooperation with IL-23, IL-18 induced prominent inflammation and enhanced psoriasis-like epidermal hyperplasia. Although it has been clearly demonstrated that IL-18 may aggravate psoriatic inflammation, the specific mechanisms of this process remain unknown. Few studies have been directed toward investigating the means through which IL-18 affects disease severity. In this report, IL-18 knockout (KO) mice were used to investigate the effects of IL-18 within a mouse model of psoriasis-like skin inflammation as induced by imiquimod.
Mice and treatment
C57BL/6 and IL-18 KO (C57BL/6 background) mice were obtained from the Jackson Laboratory (stock No. C57BL/6: 000664-JAX; IL-18 KO: 004130-JAX, Bar Harbor, ME, USA). These mice were bred in house within a pathogen free animal facility and allowed plenty of water and food. Mice were divided into four groups: wild-type (WT) control group (n = 12), IL-18 KO control group (n = 12), WT + imiquimod (IMQ) group (n = 13), and IL-18 KO + IMQ group (n = 11). All mice were shaved on their dorsal surface to expose a 2 cm × 3 cm area. The IMQ-treated mice received a daily application of IMQ using a dose of 62.5 mg IMQ cream (5%, Aldara, 3M, USA). The control mice received an identical volume of vaseline cream. A sample of skin was collected from all mice at 8 days after treatment.
All experimental procedures in this study abided by the Guide for the Care and Use of Laboratory Animals (NIH Publication, 8th Edition, 2011) and were conducted according to the guidelines provided by the Institutional Animal Care and Use Committee at China Medical University (IACUC No. 16008M).
Scoring severity of skin inflammation
To score the severity of IMQ-induced inflammation an objective scoring system was developed based on the clinical PASI. Erythema, scaling and thickening were scored independently from 0 to 4 as follows: 0 = none, 1 = slight, 2 = moderate, 3 = marked and 4 = very marked. The cumulative score (erythema plus scaling plus thickening) served to indicate the severity of inflammation (cumulative scale = 0–12). The scoring process was performed by three investigators.
Real-time polymerase chain reaction
Total RNA was extracted from whole biopsies of the exposed skin from the dorsal area of euthanized mice using a miRNeasy mini kit (Qiagen, Germany). The mRNA was then transcribed to cDNA by the GoScript™ Reverse Transcription System (Promega, USA). The sequences of primers are shown in Table 1. Real-time polymerase chain reaction (PCR) was performed in 384-well plates with use of a 7900HT Fast Real-Time PCR system (Applied Biosystems Industries, Foster city, USA). cDNA (1 μL) was mixed with 5-μL GoTaq®qPCR Master Mix, 0.1-μL CXR Reference Dye, 0.4-μL primer, and 3.5-μL Ruclease-free water to a final volume of 10 μL. The Ct value was calculated using RQ Manager Software (Applied Biosystems Industries, USA). Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) was used as the internal control and expression levels of target genes were calculated by applying 2-ΔΔCT methods. The experiments were repeated three times.
Hematoxylin and eosin staining
Hematoxylin and eosin (HE) staining was performed using standard procedures. Each section subjected to HE staining was repeatedly microphotographed using light microscopy (original magnification, ×200) to achieve quality control. Three microphotographs (the first, middle, and last fields) were then chosen to assess psoriasis-like skin lesions in each sample using Image-pro Plus software 6.0 (Media Cybernetics, Rockville, USA). The specific items for assessment included: (1) Measurement of acanthosis thickness, (2) measurement area of scales, (3) measurement area of Munro microabscesses, and (4) counting of cells within the dermal layer.
Measurements of microphotographs were then averaged to calculate each sample's mean value for all four items. Some processes of measurements were manually performed (semi-automated). Two independent investigators who were blind as to each other's measurements and treatment groups of the mice performed these analyses.
Immunohistochemistry was performed with use of a BenchMark®GX Automated Slide Stainer (Roche, Switzerland, sequence No. 815700). Tissue sections were incubated with IL-1β polyclonal rabbit antibody (dilution 1:500, cat.no.ab9722, Abcam, UK), mouse CXCL1 rabbit polyclonal antibody (dilution 1:200, cat.no.ab86436, Abcam), mouse Ly6g rat monoclonal antibody (dilution 1:100, cat.no.ab25377, Abcam), and mouse IL-27 rabbit polyclonal antibody (dilution 1:200, cat.no.GTX54307, GenTex, USA). Image Pro-plus 6.0 software (Media Cybernetics, USA) was used to assess immunohistochemical sections by measuring the integrated optical density (IOD).
The tested variables with a normal distribution were presented as mean ± standard deviation (SD), and difference between two groups were compared as using of Student's t test. Otherwise, variables with skewed distributions were expressed as median (Q1, Q3), and differences between the analysis groups were compared using the Kruskal-Wallis test or Mann-Whitney U test. A statistical significance was defined as P < 0.05. All analyses were performed by SPSS software (version 19.0, IBM SPSS, Inc. Chicago, IL, USA).
IL-18 is associated with extent of skin lesions and PASI scores and enhances IMQ-induced inflammation and acanthosis
IMQ-induced skin lesions in WT mice showed evidence of erythema and epidermal thickness with silvery thick scales, whereas no obvious skin lesions were present in IL-18 KO mice [Figure 1A]. As based upon PASI scores, the skin of IMQ-induced WT mice began to display signs of thickness, erythema and scales on day 2. These symptoms continued from days 2 to 4, increased in severity up to day 7, but regressed on the eighth day. However, in IMQ-induced IL-18 KO mice these symptoms continued to increase for 8 days [Figure 1B–D]. Cumulative PASI scores revealed that IL-18 KO mice had significantly lower scores than WT mice on days 3 to 7 in response to IMQ (day 3: 0.00 [0.00, 0.50] vs. 4.00 [3.25, 4.00], Z = −3.248, P = 0.001; day 4: 1.67 ± 0.52 vs. 4.50 ± 1.19, t = −5.410, P < 0.001; day 5: 2.33 ± 1.37 vs. 6.62 ± 1.41, t = −5.714, P < 0.001; day 6: 3.83 ± 1.47 vs. 8.38 ± 1.30, t = −6.113, P < 0.001; day 7: 5.83 ± 1.17 vs. 10.00 ± 1.07, t = −6.939, P < 0.001; Figure 1E). Control mice showed no visible inflammation within the exposed areas of their dorsal surface [Figure 1A].
Histopathological evaluations of skin specimens obtained from mice treated with IMQ showed acanthosis and moderate cellular infiltration in the dermis as reported previously. IMQ-induced IL-18 KO mice showed a milder degree of acanthosis (98.46 ± 14.12 vs. 222.68 ± 71.10 μm, t = −4.500, P = 0.003) and cellular infiltration (572.25 ± 47.45 vs. 762.47 ± 59.59 cells/field, t = −5.182, P = 0.001) as compared with that observed in WT mice [Figure 2]. The epidermis of control mice contained only 1 to 2 layers of cells and there was no infiltration of inflamed cells within the dermal layer of these mice.
IL-18 is associated with Munro microabscesses and scale formation in IMQ-induced skin inflammation
Munro microabscesses, as a characteristic hallmark of psoriasis pathology, are reported to be located in the epidermis and contain substantial numbers of neutrophils. Here, we found that Munro microabscesses (11,467.83 ± 5112.09 vs. 4093.19 ± 2591.88 μm2, t = 3.309, P = 0.008) and scales (100,935.24 ± 41,167.77 vs. 41,604.41 ± 14,184.10 μm2, t = 3.586, P = 0.005) were present in a significantly greater amount of area in IL-18 KO vs. WT mice in response to IMQ [Figure 3].
IL-18 upregulates mRNA levels of pro-inflammatory cytokines but downregulates protective cytokines and IL-1β
To determine some of the potential mechanisms underlying the milder psoriasis-like skin inflammation of IL-18 KO mice, we analyzed the profiles of cytokines that have been reported to be involved in the pathogenesis of psoriasis. RT-PCR analysis showed that expressions of IL-1β (343.04 [220.69, 459.12] vs. 54.99 [13.87, 179.90], Z = −2.021, P = 0.043), IL-27 (1360.68 [985.52, 2549.14] vs. 373.15 [47.85, 1011.42], Z = −2.415, P = 0.016) and IL-4 (6276.45 [3811.54, 7510.34] vs. 1312.03 [207.67, 3524.04], Z = −2.882, P = 0.004) were all significantly increased in IMQ-induced IL-18 KO as compared to WT mice [Figure 4A]. IL-17 was decreased in IL-18 KO vs. WT mice (89.29 ± 30.06 vs. 188.34 ± 62.64, t = −2.851, P = 0.029, Figure 4A). The mRNA levels of IFNγ, TNFα, IL-23, IL-12, IL-15, and IL-18R were not significantly different between IMQ-induced IL-18 KO and WT mice. Immunohistochemical assays were then performed to clarify protein expression levels of IL-1β and IL-27. The results of these assays showed that in response to IMQ treatment, significantly increased expressions of IL-1β (0.61 [0.53, 0.64] vs. 0.02 [0.01, 0.26], Z = −2.661, P = 0.009) and IL-27 (0.59 ± 0.18 vs. 0.08 ± 0.10, t = 5.082, P = 0.002) were obtained in IL-18 KO compared to WT mice [Figure 5]. Accordingly, these results were consistent with those of the mRNA analysis.
IL-18 promotes production of CXCL1 and inflammatory forms of neutrophils
As an obvious cellular infiltration was found within the dermis, immunohistochemistry was used to measure expression of the chemokine, CXCL1. Compared with IMQ-treated WT mice, significantly lower expression levels of CXCL1 were present in IL-18 KO mice (0.19 ± 0.01 vs. 0.75 ± 0.14, t = −6.943, P = 0.019, Figure 5). Based upon these findings we presumed that neutrophil infiltration may be decreased in IL-18 KO mice. As Ly6g is a surface protein that is expressed predominantly on neutrophils, it is considered to serve as a marker for neutrophils in mice. We found that IMQ-induced IL-18 KO mice had significantly increased expressions of Ly6g within the epidermis as compared with that of WT mice (0.23 [0.13, 0.62] vs. 0.01 [0.00, 0.03], Z = −2.739, P = 0.006, Figure 5).
The results of our study indicate that IL-18 may aggravate psoriatic inflammation and the immunological effects of IL-18 upon IMQ-induced psoriasis-like skin inflammation. Using an IL-18 gene deficiency to establish a psoriatic mouse model, we found that IMQ-induced IL-18 KO mouse showed milder psoriasis-like skin lesions, acanthosis and cellular infiltration compared with WT mice. IL-18 might affect pathological features of psoriasis-like skin inflammation. In addition, IL-18 promoted IL-17 mRNA expression, while exerting negative effects on mRNA of IL-1β, IL- 4, and IL-27. IL-18 might be involved in the formation of Munro microabscesses and scales, the specific mechanisms remain unknown.
This study represents to employ an IL-18 deficient mouse model as an approach to examine the effects of IL-18 in psoriasis. IL-18, as a member of the IL-1 family of cytokines, plays a strong proinflammatory role in chronic inflammatory diseases. IL-18 receptor (IL-18R) is a heterodimer, composed of α and β chains, and active IL-18 can bind to either IL-18Rα or IL-18Rβ. After forming the heterodimer, the intracellular Toll-IL-1 receptor (TIR) domain binds to myeloid differentiation factor 88 (MYD88) and IL-1 receptor-associated kinase (IRAK). Finally, the inflammatory pathway, nuclear factor-kappa B (NF-κB), would be activated by triggering a cascade of reaction.[6,16]
IMQ, a Toll-like-receptor (TLR), 7/8 ligand and potent immune activator used for the treatment of actinic keratosis and superficial basal cell carcinomas. In 2009, van der Fits et al reported that application of imiquimod cream to the back skin of mice caused phenotypes with remarkable resemblance to human psoriasis pathology including the presence of Munro microabscesses. It was further established that the disease in mice was dependent upon the IL-23/IL-17 axis. IL-18 is considered as having a major role in the Th1 response, which induces Th1 cells to produce large amounts of IFNγ. Importantly, IL-18, also stimulates γδT and Th17 cells, which then secretes IL-17.[3,16,18] Under Th1 conditions, IL-18 can recruit dendritic cells expressing IL-18R and IL-23 to areas of inflammation.
We presumed that IL-18 might upregulate pro-inflammatory cytokine expression. As a result, IFNγ, IL-23, and IL-17 mRNA would all be decreased within the skin lesions of IL-18 KO mice. However, our results revealed that IFNγ and IL-23 were not significantly downregulated within the skin lesions of these IL-18 KO mice [Figure 4B]. Although IL-18 can stimulate Th1 cells to produce large amounts of IFNγ (results not shown), which appears to be important in early stage of psoriasis, its expression was inhibited by Treg cells in plaque stage of psoriasis.[3,4] In this study, IFNγ mRNA was tested at the eighth day after IMQ application, which showed no significant difference between IL-18 KO mice and WT mice, possibly due to the tolerance of IMQ stimuli in such time. IL-23 is a key molecule that promotes the development and maintenance of Th17 cells that have been implicated in autoimmune inflammatory diseases, especially psoriasis. Under inflammatory conditions, myeloid dendritic cells producing IL-23 are regulated by several pro-inflammatory cytokines including IL-18, IL-1β, and IFNγ. It seems possible that IL-18 is just one of the factors that contribute to the production of IL-23 within dendritic cells.
IL-1β, a pro-inflammatory cytokine of the IL-1 family, possesses a sequence that highly resembles of IL-18 and signaling pathway as that of IL-18. As a result, IL-18 appears to be related to IL-1β in several processes. IL-1β induces CD4+ and CD8+T cell activation and stimulates γδT cell transformation into Th17 cells. Except driving the Th17 response, IL-1β promotes keratinocyte proliferation and production of chemokines involved with recruiting neutrophils. Here, we show that IL-1β mRNA and IL-1β protein were significantly increased in IMQ-induced IL-18 KO compared to WT mice [Figures 4A and 5]. In IL-18 deficient mice, skin lesion cells could enhance the production of IL-1β to compensate for immunological dysfunctions due to its extreme similarity in structure and function to IL-18. The high levels of IL-1β expression in IL-18 KO mice might partly result from IMQ stimulating keratinocytes to produce IL-1β.
The results of our current study also demonstrate that the protective cytokines, IL-4 and IL-27, were increased in IMQ-induced IL-18 KO mice. Serum IL-4 levels in active psoriatic patients are significantly lower than that of patients in stable stage. IL-4 has anti-inflammatory properties, which can then downregulate IL-1β, TNFα, IL-18, IL-23, and IL-17 production within many different cell types such as keratinocytes, monocytes, DC, and macrophages.[24–26] Inflammatory cytokines can, in turn, inhibit IL-4 gene expression. The results of our study indicate that IL-18 might decrease the production of IL-4, which may then inhibit the Th2 response. IL-27 reduces the production of IL-18 by robustly enhancing IL-18 binding protein (IL-18BP), which then inhibits the expression and activation of IL-18. It should be noted that there exist conflicting results regarding IL-27's role in the pathogenesis of psoriasis. IL-27 exerts anti-inflammatory effects by inhibiting Th17 cell differentiation, but also stimulates Th1 cell activation. It appears that IL-18 might reduce the expression of IL-27, however, the major role of IL-27 in psoriasis-like skin inflammation clearly requires further investigation.
CXCL1, an important neutrophil recruiting chemokine, was significantly decreased in IL-18 KO compared to WT mice. A study involving oral keratinocytes showed that IL-1 network upregulates CXCL1. Our results indicate that IL-18 may promotes epidermal cells to secrete CXCL1.
The IMQ-induced IL-18 KO mice showed a milder degree of skin lesions and dermal cell infiltration compared with that observed in WT mice. The leukocyte infiltrate in psoriasis consists predominantly of T cells, and their infiltration precedes epidermal hyperplasia.[30,31] As T cells are associated with the formation of psoriatic lesions, the milder phenotype observed in IL-18 KO mice may be related to lower levels of T cell infiltration rather than that attributable to neutrophils. Larger areas in Munro microabscesses were obtained in IL-18 KO vs. WT mice. In addition, Ly6g, a surface protein of neutrophils, showed higher expression levels in IL-18 KO mice. These results indicate that neutrophils may be increased in IL-18 KO mice. The role of neutrophils in psoriasis is not entirely understood. Although they appear to recruit T lymphocytes, they may not be directly related to severity of skin lesions. The mechanisms responsible for the lack of a significant phenotype effect and increased area of Munro microabscesses will require further investigation.
Results of our HE staining revealed that IL-18 KO mice showed increased areas of scale formation as compared with WT mice. However, such differences were not apparent when gross observations were performed in these mice. It indicated that IL-18 might affect the adhesiveness of keratin, but there are few reports on IL-18 and scales in IMQ-induced psoriasis-like skin inflammation. The mechanisms involved in this process are unclear.
Our study represents an initial attempt at examining the functions of IL-18 protein in psoriasis. With the use of a conventional IL-18 KO mouse, the IL-18 gene will be knocked out in all cells. Such a condition would affect all immune-associated cells and organ functions related to IL-18, which may then result in a dysfunction of the IMQ-induced skin inflammation response. Therefore, a specific conditional gene knock-out mouse model might provide a more accurate model in which to assess the role of IL-18 in the development of psoriasis. While the analyses of sections resulting from HE staining and immunohistochemistry provide important information, their semi-quantitative parameters lack the rigor of methods that can provide more robust quantitative measures. Nevertheless, we believe the data presented in this initial report on IL-18 and psoriasis provide a strong foundation for future work on the specific mechanisms of IL-18 in human psoriasis and for the development of new therapeutic approaches in the treatment of this condition. For future research, we will further explore the specific mechanism that IL-18 affect formation of scales and Munro microabscesses in IMQ-induced mouse model of psoriasis.
This work was supported by National Natural Science Foundation of China (Nos. 81673070, 81872538).
Conflicts of interest
1. Zhou F, Cao H, Zuo X, Zhang T, Zhang X, Liu X, et al. Deep sequencing of the MHC region in the Chinese population contributes to studies of complex disease. Nat Genet
2016; 48:740–746. doi: 10.1038/ng.3576.
2. Grozdev I, Korman N, Tsankov N. Psoriasis
as a systemic disease. Clin Dermatol
2014; 32:343–350. doi: 10.1016/j.clindermatol.2013.11.001.
3. Elloso MM, Gomez-Angelats M, Fourie AM. Targeting the Th17 pathway in psoriasis
. J Leukoc Biol
2012; 92:1187–1197. doi: 10.1189/jlb.0212101.
4. Dinarello CA, Novick D, Kim S, Kaplanski G. Interleukin-18
and IL-18 binding protein. Front Immunol
2013; 4:289doi: 10.3389/fimmu.2013.00289.
5. Lowes MA, Russell CB, Martin DA, Towne JE, Krueger JG. The IL-23/T17 pathogenic axis in psoriasis
is amplified by keratinocyte responses. Trends Immunol
2013; 34:174–181. doi: 10.1016/j.it.2012.11.005.
6. Lee JH, Cho DH, Park HJ. IL-18 and cutaneous inflammatory diseases. Int J Mol Sci
2015; 16:29357–29369. doi: 10.3390/ijms161226172.
7. Sedimbi SK, Hagglof T, Karlsson MC. IL-18 in inflammatory and autoimmune disease. Cell Mol Life Sci
2013; 70:4795–4808. doi: 10.1007/s00018-013-1425-y.
8. Pietrzak A, Lecewicz-Torun B, Chodorowska G, Rolinski J. Interleukin-18
levels in the plasma of psoriatic patients correlate with the extent of skin lesions and the PASI score. Acta Derm Venereol
2003; 83:262–265. doi: 10.1080/00015550310016508.
9. Takahashi H, Tsuji H, Hashimoto Y, Ishida-Yamamoto A, Iizuka H. Serum cytokines
and growth factor levels in Japanese patients with psoriasis
. Clin Exp Dermatol
2010; 35:645–649. doi: 10.1111/j.1365-2230.2009.03704.x.
10. Companjen A, Van Der Wel L, Van Der Fits L, Laman J, Prens E. Elevated interleukin-18
protein expression in early active and progressive plaque-type psoriatic lesions. Eur Cytokine Netw
11. Shimoura N, Nagai H, Fujiwara S, Jimbo H, Yoshimoto T, Nishigori C. Interleukin (IL)-18, cooperatively with IL-23, induces prominent inflammation and enhances psoriasis
-like epidermal hyperplasia. Arch Dermatol Res
2017; 309:315–321. doi: 10.1007/s00403-017-1735-2.
12. Van Der Fits L, Mourits S, Voerman JS, Kant M, Boon L, Laman JD, et al. Imiquimod-induced psoriasis
-like skin inflammation in mice is mediated via the IL-23/IL-17 axis. J Immunol
2009; 182:5836–5845. doi: 10.4049/jimmunol.0802999.
13. Prasad K, Prabhu GK. Image analysis tools for evaluation of microscopic views of immunohistochemically stained specimen in medical research-a review. J Med Syst
2012; 36:2621–2631. doi: 10.1007/s10916-011-9737-7.
14. Uribe-Herranz M, Lian LH, Hooper KM, Milora KA, Jensen LE. IL-1R1 signaling facilitates Munro's microabscess formation in psoriasiform imiquimod-induced skin inflammation. J Invest Dermatol
2013; 133:1541–1549. doi: 10.1038/jid.2012.512.
15. Bucher K, Schmitt F, Autenrieth SE, Dillmann I, Nurnberg B, Schenke-Layland K, et al. Fluorescent Ly6G antibodies determine macrophage phagocytosis of neutrophils and alter the retrieval of neutrophils in mice. J Leukoc Biol
2015; 98:365–372. doi: 10.1189/jlb.1AB1014-488RR.
16. Novick D, Kim S, Kaplanski G, Dinarello CA. Interleukin-18
, more than a Th1 cytokine. Semin Immunol
2013; 25:439–448. doi: 10.1016/j.smim.2013.10.014.
17. Rabeony H, Pohin M, Vasseur P, Petit-Paris I, Jegou JF, Favot L, et al. IMQ-induced skin inflammation in mice is dependent on IL-1R1 and MyD88 signaling but independent of the NLRP3 inflammasome. Eur J Immunol
2015; 45:2847–2857. doi: 10.1002/eji.201445215.
18. Cai Y, Shen X, Ding C, Qi C, Li K, Li X, et al. Pivotal role of dermal IL-17-producing gammadelta T cells in skin inflammation. Immunity
2011; 35:596–610. doi: 10.1016/j.immuni.2011.08.001.
19. Boehncke WH, Schon MP. Psoriasis
2015; 386:983–994. doi: 10.1016/S0140-6736(14)61909-7.
20. Zaba LC, Fuentes-Duculan J, Eungdamrong NJ, Johnson-Huang LM, Nograles KE, White TR, et al. Identification of TNF-related apoptosis-inducing ligand and other molecules that distinguish inflammatory from resident dendritic cells in patients with psoriasis
. J Allergy Clin Immunol
2010; 125:1261–1268. e1269. doi: 10.1016/j.jaci.2010.03.018.
21. Fuentes-Duculan J, Suarez-Farinas M, Zaba LC, Nograles KE, Pierson KC, Mitsui H, et al. A subpopulation of CD163-positive macrophages is classically activated in psoriasis
. J Invest Dermatol
2010; 130:2412–2422. doi: 10.1038/jid.2010.165.
22. Lalor SJ, Dungan LS, Sutton CE, Basdeo SA, Fletcher JM, Mills KH. Caspase-1-processed cytokines
IL-1beta and IL-18 promote IL-17 production by gammadelta and CD4 T cells that mediate autoimmunity. J Immunol
2011; 186:5738–5748. doi: 10.4049/jimmunol.1003597.
23. Khandpur S, Gupta V, Das D, Sharma A. Is there a correlation of serum and tissue T helper-1 and -2 cytokine profiles with psoriasis
activity and severity? A cross-sectional study. Indian J Dermatol Venereol Leprol
2018; 84:414–418. doi: 10.4103/ijdvl.IJDVL_471_17.
24. Wong HL, Costa GL, Lotze MT, Wahl SM. Interleukin (IL) 4 differentially regulates monocyte IL-1 family gene expression and synthesis in vitro and in vivo. J Exp Med
1993; 177:775–781. doi: 10.1084/jem.177.3.775.
25. Racz E, Kurek D, Kant M, Baerveldt EM, Florencia E, Mourits S, et al. GATA3 expression is decreased in psoriasis
and during epidermal regeneration; induction by narrow-band UVB and IL-4. PLoS One
2011; 6:e19806doi: 10.1371/journal.pone.0019806.
26. Onderdijk AJ, Baerveldt EM, Kurek D, Kant M, Florencia EF, Debets R, et al. IL-4 Downregulates IL-1beta and IL-6 and Induces GATA3 in psoriatic epidermal cells: route of action of a Th2 cytokine. J Immunol
2015; 195:1744–1752. doi: 10.4049/jimmunol.1401740.
27. Wittmann M, Doble R, Bachmann M, Pfeilschifter J, Werfel T, Muhl H. IL-27 Regulates IL-18 binding protein in skin resident cells. PLoS One
2012; 7:e38751doi: 10.1371/journal.pone.0038751.
28. Shibata S, Tada Y, Asano Y, Yanaba K, Sugaya M, Kadono T, et al. IL-27 activates Th1-mediated responses in imiquimod-induced psoriasis
-like skin lesions. J Invest Dermatol
2013; 133:479–488. doi: 10.1038/jid.2012.313.
29. Wu T, Du R, Hong Y, Jia L, Zeng Q, Cheng B. IL-1 alpha regulates CXCL1, CXCL10 and ICAM1 in network form in oral keratinocytes. Clin Lab
2013; 59:1105–1111. doi: 10.7754/Clin.Lab.2012.121029.
30. Coimbra S, Figueiredo A, Castro E, Rocha-Pereira P, Santos-Silva A. The roles of cells and cytokines
in the pathogenesis of psoriasis
. Int J Dermatol
2012; 51:389–395. quiz 395–388. doi: 10.1111/j.1365-4632.2011.05154.x.
31. Gottlieb SL, Gilleaudeau P, Johnson R, Estes L, Woodworth TG, Gottlieb AB, et al. Response of psoriasis
to a lymphocyte-selective toxin (DAB389IL-2) suggests a primary immune, but not keratinocyte, pathogenic basis. Nat Med
1995; 1:442–447. doi: 10.1038/nm0595-442.
32. Terui T, Ozawa M, Tagami H. Role of neutrophils in induction of acute inflammation in T-cell-mediated immune dermatosis, psoriasis
: a neutrophil-associated inflammation-boosting loop. Exp Dermatol
2000; 9:1–10. doi: 10.1034/j.1600-0625.2000.009001001.x.
Keywords:© 2019 Chinese Medical Association
Interleukin-18; Psoriasis; Cytokines; Scales