Narrowband ultraviolet B light treatment changes plasma concentrations of MMP-3, MMP-9 and TIMP-3 in psoriatic patients

Abstract

Background

Matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs) are thought to be associated with the pathogenesis and spread of psoriatic disease. This study was designed to investigate the plasma levels of MMP-3, MMP-9 and TIMP-3 in plaque psoriasis patients prior to and following a course of ultraviolet B narrowband treatment with respect to disease advancement.

Methods

Plasma samples of 49 patients suffering from plaque psoriasis and 40 healthy volunteers were evaluated. Concentrations of MMP-3, MMP-9 and TIMP-3 were determined using enzyme-linked immunosorbent assay, while Psoriasis Area and Severity Index was used to define disease advancement.

Results

Plasma levels of MMP-3, MMP-9 and TIMP-3 were significantly elevated in psoriasis patients compared to healthy individuals. A course of ultraviolet B narrowband treatment resulted in a significant decline in the studied metalloproteinases. Furthermore, the concentration of selected tissue inhibitors was negatively correlated with baseline Psoriasis Area and Severity Index score.

Conclusion

Our research highlights the meaningful role of MMP-3, MMP-9 and TIMP-3 in psoriasis pathogenesis and clearance of disease symptoms. Furthermore, plasma levels of the analyzed metalloproteinases seem to be a valuable psoriasis biomarker.

Keywords:

• gelatinase B
• stromelysin 1

Background

Psoriasis is a chronic, immune-mediated, inflammatory skin disease, affecting ~3% of the world’s population and requiring long-term treatment.¹ The condition occurs with a different frequency according to ethnicity and geographic region. The disease is known to impair the patients’ quality of life by causing considerable physical discomfort and psychological distress.^2–4

The exact etiopathogenesis of psoriasis remains unidentified. It is assumed that the development of psoriatic scales may be triggered by several environmental factors, a genetic predisposition or medication. It may also be associated with other diseases. To date, a number of factors of potential importance in the pathogenesis and spread of the condition have been proposed.⁵ Having analyzed the data presented in the available literature, we hypothesized that matrix metalloproteinases (MMPs) and their tissue inhibitors may be one of these factors.

MMPs are a family of metal-dependent (Zn²⁺, Ca²⁺) enzymes that are classified based on their minor structural differences and substrate specificity into the following subgroups: collagenases, gelatinases, stromelysins, matrilysins, transmembrane MMPs, “other MMPs” and ADAM metalloproteinases.⁶ These proteins are involved in a number of physiologic and pathologic processes, thanks to their remarkable ability to degrade and rebuild proteins forming the extracellular matrix and the basal membrane.⁷ MMPs have been found to be implicated in psoriasis pathogenesis by changing intracellular contacts, extracellular matrix and basal membrane components, cleaving, promoting the formation of new vessels and stimulating immune cells infiltration. Fibroblasts, endothelial cells, keratinocytes, infiltrating immune cells and cancer cells are the main sources of MMPs in the human body.⁸

The adverse effects of MMPs overexpression are suppressed by their tissue inhibitors (TIMPs), a group which comprises four members among mammals.⁹ What is significant, the physiologic MMP:TIMP ratio is strictly defined and any disturbance in this proportion affects tissue homeostasis and the maintenance and function of skin cells in extreme conditions.¹⁰

Since its first application in 1988, narrowband ultraviolet B (NBUVB) therapy has become one of the safest and most commonly utilized methods of psoriasis treatment. The method is also highly effective since a reduction in psoriatic scales with the use of UVB-311 nm light can be achieved after as short a period of time as 5–8 weeks. The treatment is recommended as a second-line psoriasis therapy when the first-line therapy fails or is contraindicated or impractical.¹¹

Considering the fact that psoriatic biomarkers presented in the available literature are not entirely specific or sensitive, researchers are attempting to find parameters implicated in the pathogenesis of psoriasis, whose levels would correlate more closely with disease presence and severity. In this study, we examined the plasma levels of MMP-3 (stromelysin 1), MMP-9 (gelatinase B) and TIMP-3 in psoriatic patients with respect to disease advancement. Moreover, we aimed to reveal the impact of the commonly administered NBUVB treatment on the concentration of selected parameters.

Materials and methods

Table 1 shows the tested groups. This prospective study included 49 plaque psoriasis patients whose condition was diagnosed and treated in the Outpatient Clinic of the Department of Dermatology, University Hospital, Bialystok, Poland, between 2013 and 2015. Participants were assigned to specific groups of disease advancement on the basis of Psoriasis Area and Severity Index (PASI) formulated by Fredriksson and Pettersson.¹² Furthermore, patients with a mild form of the disease were divided into two subgroups – Ia (PASI <5) and Ib (PASI 5–10).

Table 1 Characteristics of psoriatic patients and the control group

Study group	Number of patients
Psoriasis patients
Plaque type	49 (23 females, 26 males)
Median age (range)	39 (18–76)
Severity
Mild	34
PASI <5	15
PASI 5–10	19
Moderate	15
PASI >10–<30	15
Control group
Healthy subjects	40 (19 females, 21 males)
Median age (range)	36 (18–75)

Note: Reproduced from Głażewska EK, Niczyporuk M, Ławicki S, et al. Therapy Of Psoriasis With Narrowband Ultraviolet-B Light Influences Plasma Concentra tion Of MMP-2 And Timp-2 In Patients. Ther Clin Risk Manag. 2016;12:1579–1585.²⁹

Abbreviation: PASI, Psoriasis Area and Severity Index.

All patients underwent a course of NBUVB phototherapy consisting of 20 sessions. Considering the fact that this kind of treatment is suitable for patients with mild and moderate forms of psoriasis, the study included patients with a PASI score between 2 and 30.

The control group consisted of 40 healthy volunteers who had never suffered from any autoimmunologic or chronic dermatologic diseases. The key exclusion criterion in both groups was any additional pharmacotherapy.

All patients gave their informed consent for participation in the study. The study was approved by the Biochemical Committee of the Medical University of Bialystok (No R-I-002/74/2014).

Radiation source

Whole-body irradiation was performed in a Cosmedico GP-36 phototherapy cabinet (Cosmedico Medical System, Stuttgart, Germany), equipped with NBUVB 311 nm TL-01 100W tubes (Heine.Med, Baden-Württemberg, Germany). The energy output was measured with a standard intrinsic UV meter.

Phototherapy protocol

Individual minimum erythema doses of NBUVB were determined prior to the commencement of exposure to prevent burns. The patients underwent two to three treatments weekly (up to a total number of 20), starting with an NBUVB dose of 0.018–0.025 J ⁄cm² and increasing it by ~10%–20% per week, up to a maximum dose of 2.015 J/cm².

Biochemical analyses

Venous blood samples were collected from each patient twice – prior to the commencement and following the last (20th) NBUVB phototherapy treatment – into a heparin sodium tube, centrifuged for 15 min at 1,000× g to obtain plasma samples and stored at −85°C until the assay. The tested parameters were measured with enzyme-linked immunosorbent assay (MMP-3 and MMP-9 with Quantikine Human HGFs Immunoassay, R&D Systems, Inc., Minneapolis, MN, USA; TIMP-3 with Quantikine Human MMP-3 Immunoassay, Wuhan EIAab Science Co., Wuhan, People’s Republic of China), according to the manufacturer’s protocols. Duplicate samples were assessed for each patient.

The intraassay coefficient of variation (CV%) of MMP-3 is reported to be 6.1% at a mean concentration of 3.21 ng/mL, standard deviation (SD) =0.197, for MMP-9 1.9% at a mean concentration of 2.04 ng/mL, SD =0.039 and for TIMP-3 it is 6.1%.

The interassay coefficient of variation (CV%) of MMP-3 is reported to be 7.0% at a mean concentration of 3.08 ng/mL, SD =0.217, for MMP-9 7.8% at a mean concentration of 2.35 ng/mL, SD =0.184 and for TIMP-3 it is 8.4%.

The assay showed no significant cross-reactivity or interference with numerous human cytokines and other growth factors.

Statistical analysis

Statistical analysis was performed using STATISTICA 12.0 PL Program. Preliminary statistical analysis revealed that MMP-3, MMP-9 and TIMP-3 failed to follow a normal distribution. Consequently, the Mann–Whitney U test was used for comparative statistical analysis between psoriatic patients and the control group. Additionally, statistical analysis between the groups with different severity of psoriasis was performed with the use of the Bonferroni correction. Moreover, the Wilcoxon matched pair test was used for statistical analysis of changes in parameters occurring throughout the period of the NBUVB phototherapy treatment. The data were presented as median, mean and range. Spearman rank correlation was used in correlation analysis. Statistically significant differences were defined as comparisons resulting in P<0.05.

Results

Mean PASI value of patients enrolled in the study was 8.53 (range 2.0–25.0). After the completion of the treatment, the mean PASI decreased to 4.74 (range 0–18.2). Mean PASI improvement was 52%.

Plasma levels of MMP-3, MMP-9 and TIMP-3 are summarized as the mean, median value and range in Table 2. Prior to the commencement of NBUVB treatment, the concentrations of all the analyzed parameters were significantly elevated in the total psoriatic patients group when compared to the healthy controls.

Table 2 Plasma levels of tested parameters in psoriatic patients and the control group

Groups tested	MMP-3 (ng/mL)		MMP-9 (ng/mL)		TIMP-3 (ng/mL)
	Before treatment	After treatment	Before treatment	After treatment	Before treatment	After treatment
Psoriatic patients
Total group	a,c		a,c		a	a
Median	14.97	14.70	73.47	57.39	562.0	608.39
Mean	18.80	15.86	112.42	77.72	845.03	821.50
Range	2.96–49.2	1.36–39.57	10.86–569.8	6.41–336.49	246.78–2,340.92	235.50–2,377.03
Mild					a,d	a,d
Median	13.73	13.00	72.82	52.93	1,021.28	763.23
Mean	16.88	14.47	108.87	66.60	1,005.39	946.47
Range	2.96–49.20	1.36–32.46	10.86–569.80	6.40–195.00	246.78–381.67	381.67–2,377.03
Mild – subgroup Ia			a		a,b,e	a,b
Median	12.51	12.19	82.00	57.39	1,286.69	1,154.15
Mean	15.78	13.53	134.76	75.62	1,351.44	11,61.67
Range	4.19–49.20	2.52–26.64	25.87–569.80	37.69–193.29	490.71–2,340.92	447.90–2,323.39
Mild – subgroup Ib						a
Median	14.52	15.82	67.61	49.84	537.5	492.33
Mean	17.75	15.22	88.43	59.46	732.19	776.58
Range	2.96–48.42	1.36–32.46	10.86–306.54	6.41–195.00	246.78–1,725.51	381.67–2,377.03
Moderate	a,c		a
Median	22.04	19.15	91.36	72.23	453.96	491.92
Mean	23.13	19.00	120.48	102.93	481.57	538.23
Range	7.95–46.91	5.60–39.58	21.77–318.012	31.78–336.49	335.42–940.85	235.50–1,137.75
Control group
Healthy subjects
Median	13.04		49.46		411.63
Mean	13.33		65.44		431.63
Range	2.76–32.05		12.84–233.88		287.66–753.27

Notes:

a Statistically significant when psoriatic patients are compared with healthy subjects (P<0.05).

b Statistically significant when subgroup Ia is compared to moderate cases (P<0.05).

c Statistically significant when pretreatment concentration is compared to posttreatment levels (P<0.05).

d Statistically significant when patients with mild scales are compared to subjects with moderate lesions (P<0.05).

e Statistically significant when subgroup Ia is compared to subgroup Ib.

Abbreviations: MMP, matrix metalloproteinase; TIMP, tissue inhibitor of metalloproteinase.

Following the classification of the total group according to disease severity, we found significantly increased levels of MMP-3 and MMP-9 in subjects with moderately severe psoriasis in comparison with the healthy controls. Moreover, significantly higher concentrations of the tested inhibitor were found in the patients with mild scales and in subjects from subgroup Ia, when compared to healthy individuals.

A comparison of the subgroups of untreated psoriatic subjects showed significant differences in TIMP-3 levels between mild and moderate cases, between subgroups Ia and Ib and between patients from subgroup Ia and subjects with moderately severe psoriasis.

Spearman rank correlations were used to explore the associations between selected factors. Pretreatment (R=0.26, P<0.05; Figure 1) as well as posttreatment (R=0.22, P<0.05; Figure 2) plasma levels of TIMP-3 were positively correlated with the analogous concentrations of MMP-9. Also, the levels of the selected factors were negatively correlated with a PASI score (R=−0.54, P<0.05; Figure 3) and positively correlated with the age of the studied individuals (R=0.30, P<0.05), both prior to the commencement and following the completion of NUVB treatment (R=−0.30, P<0.05 and R=0.42, P<0.05, respectively). Furthermore, we noticed a positive correlation between the pretreatment plasma levels of MMP-3 and the cohorts’ sex (R=0.53, P<0.05).

Figure 1 Correlation of baseline plasma MMP-9 with baseline plasma TIMP-3 in patients with psoriasis.

Abbreviations: MMP, matrix metalloproteinase; TIMP, tissue inhibitor of metalloproteinase.

Figure 2 Correlation of posttreatment plasma MMP-9 with posttreatment plasma TIMP-3 in patients with psoriasis.

Abbreviations: MMP, matrix metalloproteinase; TIMP, tissue inhibitor of metalloproteinase.

Figure 3 Correlation of baseline plasma TIMP-3 with baseline PASI in patients with psoriasis.

Abbreviations: PASI, Psoriasis Area And Severity Index; TIMP, tissue inhibitor of metalloproteinase.

A course of 20 NBUVB radiation treatments influenced the concentrations of the tested parameters. Following treatment competition, the plasma levels of MMP-3 and MMP-9 in the total group of psoriatic patients were statistically significantly lower than prior to the commencement of therapy. In contrast, the concentration of TIMP-3 in the total group increased, but this change was not significant.

Interestingly, only TIMP-3 posttreatment values were significantly higher in the total group, subjects with a mild form of the disease and both subgroups, when compared to the controls. Analogous to the pretreatment correlations, we found statistically significant differences of TIMP-3 posttreatment levels between the groups of mild and moderate cases, between the patients from subgroups Ia and Ib and between subgroup Ia individuals and moderately severe cases.

Disscusion

The multifunctionality of MMPs condition their implication in a variety of physiologic processes, which include angiogenesis, embryogenesis and wound healing. On the other hand, significant disturbances in the concentration and activity of the analyzed endopeptidases have been detected among patients suffering from, for example, inflammatory and degenerative conditions, cancer, skin and kidney diseases.¹³

MMP-9, belonging to the gelatinases subfamily, is distinct from the other MMPs, thanks to its ability to digest elatins, collagen types I, IV, V, VII, XI and aggrecans. Moreover, the described factor takes part in interleukin (IL)-1 and plasminogen activation. In contrast, stromelysin 1 does not degrade fibrillar collagen, although it possesses a unique ability to activate MMP-1, -3, -7, -8, -9 and -13 proenzymes.^8,14–16

MMPs are inhibited by TIMPs, one which TIMP-3 efficiently inhibits membrane-type metalloproteinases. Remarkably, this factor is also the most effective inhibitor of MMP-9 among all TIMPs.¹⁷

The clinical manifestations of psoriasis are associated with modifications in the cellular composition of the epidermis by the infiltrating immune cells. Interestingly, the eruption of the disease results in the migration of ~20 million of the total 28–30 million body lymphocytes to the sites of damage. The dermis contains an inflammatory infiltrate composed of lymphocytes, macrophages, mast cells and neutrophils.^18,19 Altered MMP production may occur as a consequence of the disturbed cytokine synthesis (eg, tumor necrosis factor-alpha, IL-1, interferon-γ, IL-6, TGF-α, EGF) by those cells.²⁰

Our research demonstrated that the levels of MMP-9 and MMP-3 were significantly higher in the plasma of psoriatic patients compared to those of healthy individuals, and the value of this concentration increased with disease advancement. Elevated plasma levels of gelatinase B were also detected among an analogous cohort by Altrichter et al²¹ and Sigurdardottir et al.²² Moreover, the overexpression of this factor in psoriatic skin has been repeatedly confirmed by other researchers.^23,24 Furthermore, an increased concentration of MMP-3 has been found in the sera of psoriatic subjects.²⁵

A study conducted by Altrichter et al suggested that the general inflammatory status, that is, a combination of cell destruction, inflammatory cells migration and tissue remodeling, occurring in the course of psoriasis resulted in an increase in MMP-9 plasma levels.²¹ Reiss et al were the first to report that the overexpression of MMP-9 was strongly correlated with skin damage and its expression declined rapidly in response to the healing of lesions in a mouse model. Furthermore, they proved that a chronically elevated gelatinase B level delayed wound healing.²⁶ Interestingly, a different research group has advocated that the upregulation of MMP-3 suppresses dermis contraction and prolongs the wound healing process.²⁷ The data obtained in our study appear significant since we demonstrated that the concentrations of gelatinase B and stromelysin 1 stimulate the growth and spread of psoriatic scales.

Additionally, in this study, we observed a significantly elevated level of TIMP-3 in the analyzed group compared to the controls. These findings are in accordance with data from other available studies. As previously stated, TIMP-3 is the most effective suppressor of MMP-9. Moreover, our findings releaved a strong positive correlation between these factors. Interestingly, we also found a negative correlation between TIMP-3 levels and disease advancement. These findings prove the hypothesis that elevated MMP-9 levels, increasing with the advancement of psoriasis without a relevant increase in its tissue inhibitor levels, contribute to the development of the condition.

Studies concerning other metalloproteinases and tissue inhibitors have also been conducted in the plasma of psoriasis patients. In our previous research, we detected elevated levels of MMP-2 with no significant changes in TIMP-2 concentration, and decreased levels of MMP-12, while Flisiak et al pointed to a significantly elevated concentration of MMP-1 and TIMP-1 in psoriatic patients when compared to healthy subjects.^28–30 These findings indicate a strong relationship between the analyzed condition and changes in the concentrations of MMPs and TIMPs.

The efficacy of UVB narrowband phototherapy in the treatment of psoriasis and a number of other skin disorders is determined by a multisite action of this type of treatment, which includes alteration of the cytokine profile, induction of apoptosis and promotion of immunosuppression.^11,31 Furthermore, the clinical improvement of psoriasis achieved by NBUVB is associated with the downregulation of the IL-17 pathway and also, type I and type II interferon signaling pathways, which is crucial to the pathogenesis of the condition. Additionally, a clinically effective NBUVB therapy involves the suppression of numerous significant molecular pathways in psoriatic skin.^32,33

In this study, we found that a successful NBUVB course resulted in a significant decline in MMP-3 and MMP-9 concentrations. Simultaneously, the phototherapy treatment caused an increase in TIMP-3 levels, although this change was not statistically significant. Our results are in line with those obtained by other authors who analyzed the influence of different kinds of psoriasis treatment on these parameters.^8,34 In contrast, a study by Sigurdardottir et al did not find significant changes in MMP-9 concentration after NBUVB treatment.²² Moreover, other studies have demonstrated that NBUVB causes a decrease in plasma MMP-2 levels as well as a reduction in psoriatic scales.^29,35

As it was previously highlighted, the available literature demonstrates that the wound healing process is strongly connected with the levels of selected endopeptidases. Our study is the first one to show that the plasma concentrations of MMP-3 and MMP-9 increase together during disease eruption and decline significantly after successful treatment, which constitutes convincing proof of a connection between the analyzed factors and the healing process of psoriatic lesions.

Conclusion

In summary, elevated levels of MMP-3, MMP-9 and TIMP-3 occurring during psoriasis eruption and significant decline of mentioned metalloproteinases following successful NBUVB treatment resulting in the clearance of the disease symptoms indicate that these proteins are implicated in the etiopathogenesis and spread of the condition. Therefore, plasma concentrations of gelatinase B and stromelysin 1, and TIMP-3 appear to be a valuable candidate as the biomarkers of psoriasis.

Acknowledgments

This work was supported by grants from the Medical University of Białystok (143–30737F and N/ST/MN/16/001/2230).

Disclosure

The authors report no conflicts of interest in this work.