|
|
ORIGINAL ARTICLE |
|
Year : 2014 | Volume
: 34
| Issue : 1 | Page : 10-14 |
|
The effect of narrow-band ultraviolet-B phototherapy on soluble intercellular adhesion molecule-1 and soluble E-selectin in psoriasis vulgaris patients
Ahmed A Saleha1, Jehan H Sabry2, Neveen E Sorour1
1 Department of Dermatology and Andrology, Benha Faculty of Medicine, Benha, Egypt 2 Department of Clinical Pathology and Chemistry, Benha Faculty of Medicine, Benha, Egypt
Date of Submission | 21-Jan-2014 |
Date of Acceptance | 17-Feb-2014 |
Date of Web Publication | 24-Jul-2014 |
Correspondence Address: Neveen E Sorour MD, Department of Dermatology and Andrology, Benha Faculty of Medicine, Benha Egypt
 Source of Support: None, Conflict of Interest: None  | Check |
DOI: 10.4103/1110-6530.137247
Background Increased levels of soluble E-selectin (sE-selectin) and soluble intercellular cell adhesion molecule-1 (sICAM-1) have been reported in patients with psoriasis vulgaris compared with controls. Objective The aim of this study was to investigate the effects of narrow-band ultraviolet-B (NB-UVB) phototherapy on sE-selectin and sICAM-1 serum levels in patients with psoriasis vulgaris. Patients and methods This case-control study included 30 patients with psoriasis vulgaris and 20 apparently healthy participants as a control group. Both patients and controls were subjected to full history taking, dermatological examination, and measurement of sE-selectin and sICAM-1 using enzyme-linked immunosorbent assay kits. In the patient group, sE-selectin and sICAM-1 were measured after treatment with NB-UVB phototherapy, and the response was assessed by the Psoriasis Area and Severity Index (PASI) score. sE-selectin and sICAM-1 serum levels were compared before and after treatment and correlated with PASI scores. Results In this study, sE-selectin and sICAM-1 serum levels were significantly higher in the patient group than in the control group (P = 0.001 for both). There were statistically significant reductions in sE-selectin and sICAM-1 serum levels after NB-UVB phototherapy (P = 0.001 for both), but still the levels were higher than those of controls. PASI scores significantly decreased after treatment, confirming the efficacy of NB-UVB phototherapy. Both sE-selectin and sICAM-1 serum levels were positively correlated with PASI scores before and after NB-UVB phototherapy (P = 0.001 for both). Conclusion The present study emphasizes the complex nature of the roles played by cell adhesion molecules in the immune-pathogenesis of psoriasis and the effect of NB-UVB phototherapy on their values in relation to the PASI score. Also, results of this study provide a rationale for the possible application of sE-selectin and sICAM-1 measurements as biomarkers of psoriasis activity and predictors of possible exacerbation. Keywords: Narrow-band ultraviolet-B, Psoriasis Area and Severity Index, psoriasis vulgaris, soluble cell adhesion molecule-1, soluble E-selectin
How to cite this article: Saleha AA, Sabry JH, Sorour NE. The effect of narrow-band ultraviolet-B phototherapy on soluble intercellular adhesion molecule-1 and soluble E-selectin in psoriasis vulgaris patients. Egypt J Dermatol Venerol 2014;34:10-4 |
How to cite this URL: Saleha AA, Sabry JH, Sorour NE. The effect of narrow-band ultraviolet-B phototherapy on soluble intercellular adhesion molecule-1 and soluble E-selectin in psoriasis vulgaris patients. Egypt J Dermatol Venerol [serial online] 2014 [cited 2023 Mar 31];34:10-4. Available from: http://www.ejdv.eg.net/text.asp?2014/34/1/10/137247 |
Introduction | |  |
The pathogenesis of psoriasis is multifactorial, with genetic, environmental, and immunological factors contributing to the disease [1]. It includes excessive proliferation and altered differentiation of epidermal keratinocytes, mediated by the immune system and characterized by a dense inflammatory infiltrate composed of clusters of CD4 + Th cells and antigen-presenting dendritic cells in the dermis and CD8 + T cells and neutrophils in the epidermis [2]. Also, there is increased expression of adhesion molecules such as intercellular cell adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1, and E-selectin [3]. ICAM-1 is an immunoglobulin-like adhesion molecule that is expressed on the surface of several cell types, including endothelial cells and cells involved in the immune response [4]. It plays a role in transendothelial migration and adhesion processes involved in the pathogenesis of psoriasis, through interaction with lymphocyte function-associated antigen-1, leading to the entry of T cells into the epidermis [5]. The molecule of E-selectin mediates adhesive contacts between blood cells and vessel walls. These interactions are loose and reversible, operate under conditions of shear flow, and result in leukocyte rolling along the vessel wall [6].
Soluble cell adhesion molecules (sCAMs), including soluble intercellular cell adhesion molecule-1 (sICAM-1) and soluble E-selectin (sE-selectin), among others, may serve as markers for CAMs and represent important biomarkers for inflammatory processes involving activation of or damage to cells such as platelets and the endothelium [7].
sICAM-1 promotes angiogenesis and serves as an indicator of vascular endothelial cell activation or damage [8],[9]; it also functions as an inhibitor of transmembrane ICAM-1-mediated activities, such as monocyte adhesion to activated endothelial cells [10]. sE-selectin is regarded as an adequate marker of endothelial activation [7] and suppresses leukocyte migration by competing with surface-associated E-selectin, and can activate neutrophils and act as a proinflammatory agent [11]. Narrow-band ultraviolet-B (NV-UVB) phototherapy is of proven efficacy in the short-term treatment of moderate and extensive plaque psoriasis [12]. Despite its widespread use, there is little published literature on its impact on sCAMs.
The aim of this study was to investigate the effects of NB-UVB phototherapy on sE-selectin and sICAM-1 serum levels in patients with psoriasis vulgaris.
Patients and methods | |  |
Thirty patients with psoriasis vulgaris were recruited from the Outpatient Clinic of Benha University Hospital and 20 healthy participants served as controls during the period from September 2011 to August 2012. Written informed consent was obtained from all patients and controls before the study. The study was approved by the Research Ethics Committee of the Faculty of Medicine in Benha University. Inclusion criteria were patients with psoriasis vulgaris with at least 20% of their total body surface area involvement and Fitzpatrick skin types III and IV. Their age ranged between 15 and 60 years. Exclusion criteria included patients who had been treated with oral steroids, oral retinoids, and immunosuppressants during the previous 3 months and topical steroids during the previous 4 weeks. Patients with a history of previous failure or intolerance to phototherapy and pregnant and lactating women were excluded.
All patients were subjected to the following: history taking including personal history, present history with special emphasis on the onset, the course, and the duration of psoriasis, and history of previous or current treatment for psoriasis and date of stopping the drug. History of other systemic or skin diseases was also taken into account.
Narrow-band ultraviolet-B phototherapy protocol
All patients were irradiated with Waldmann UV 7001 K light stand (Medizinische Technik, Villingen-Schwenningen, Germany) with Philips TL-01 lamps (312 nm; Philips, Eindhoven, the Netherlands) after determining the 24-h minimal erythema dose. They were treated three times a week with a starting dose according to the skin photo type: skin type III was started with an initial UVB dose of 260 mJ/cm 2 , and then increased by 40 mJ/cm 2 after each treatment. Skin type IV was started with an initial UVB dose of 330 mJ/cm 2 , and then increased by 45 mJ/cm 2 after each treatment. In both skin types, the maximum UVB dose should not exceed 3000 mJ/cm 2 [13]. The treatment continued until clearance of all exposed psoriatic lesions or five consecutive sessions resulted in no further improvement and the patient had at least 16 exposures. The efficacy of treatment was assessed by means of the Psoriasis Area and Severity Index (PASI) score before and after NB-UVB [14]. A score of 4 or less was defined as clear or almost clear [15].
Laboratory investigations
Sample collection
0A 5 ml sample of untreated peripheral blood was obtained by cubital vein puncture from each patient before and after NB-UVB treatment, and from each control subject for comparison. Samples were incubated at room temperature for 30-45 min to coagulate. Samples were centrifuged for about 10-15 min at 3000 rpm. Serum was divided into two Eppendorfs and stored in small tubes at −20°C until analysis.
Determination of serum level
Serum levels of sICAM-1 and sE-selectin were evaluated using a commercial enzyme-linked immunosorbent assay kit. It is a quantitative measurement supplied by IDELISA sE-selectin and sICAM-1 ELISA kit (ID Labs Inc., London, Ontario, Canada).
Statistical analysis
Data collected were tabulated and analyzed using the Statistical Package for Social Science (version 16; SPSS Inc., Chicago, Illinois, USA). Presentation and analysis of the present study was conducted using the mean and SD, the χ2 -test, and the Pearson correlation.
Results | |  |
Clinical results
This study was conducted as a case-control study that included 30 patients with psoriasis vulgaris involving at least 20% of their total body surface area. They included 16 female and 14 male patients, with their age ranging from 15-60 years, with a mean of 34.43 ± 17.7 years. The control group included 14 female and six male participants with their age ranging from 18 to 51 years, with a mean of 35.1 ± 9.65 years. There was no statistically significant difference between the patient and the control groups regarding their age and sex (P = 0.879 and 0.239, respectively). Of the patients involved in the study, two patients achieved nearly complete clearance with PASI score of 4 or less and mean number of sessions 17.5 ± 0.71, whereas 28 patients achieved variable degrees of improvement, with mean number of sessions 30.64 ± 6.6. There was a statistically significant difference in the PASI scores before and after NB-UVB phototherapy (P = 0.001; [Table 1] and [Figure 1] and [Figure 2]). | Table 1: A comparison of PASI scores before and after NB-UVB phototherapy in the patient group
Click here to view |
Lab results
There was a statistically significant difference between the patient group before treatment and the control group regarding sICAM-1 and sE-selectin serum levels (P = 0.001 for both) [Table 2]. | Table 2: A comparison between the patient and the control groups regarding sICAM-1 and sE-selectin serum levels before treatment
Click here to view |
Regarding the patient group, there was a statistically significant difference in sICAM-1 and sE-selectin serum levels before and after NB-UVB phototherapy (P = 0.001 for both) [Table 3]. | Table 3: A comparison of sICAM-1 and sE-selectin serum levels before and after NB-UVB phototherapy in the patient group
Click here to view |
A significant positive correlation was found between PASI scores, sICAM-1, and sE-selectin serum levels before and after NB-UVB phototherapy [Table 4] and [Table 5]. | Table 4: The correlation between PASI scores and sICAM-1 serum levels before and after NB-UVB phototherapy in the patient group
Click here to view |
 | Table 5: The correlation between PASI scores and sE-selectin serum levels before and after NB-UVB treatment in the patient group
Click here to view |
Discussion | |  |
Before the onset of therapy, there was a statistically significant difference between patients and controls regarding sICAM-1 serum levels (P = 0.001). These results agreed with Schopf et al. [16], Krasowska et al. [17], Gangemi et al. [18], Borskà et al. [19], and Batycka-Baran et al. [20]. The same result was obtained with regard to sE-selectin serum levels (P = 0.001), which agreed with studies that focused on the endothelial activity [19],[20],[21],[22],[23],[24],[25],[26],[27]. In contrast, Ghalamkarpour et al. [28] found elevated serum levels of sE-selectin in psoriatic patients compared with controls, but with no statistical significance (P = 0.240). This difference may be due to the fact that in their study the average age of the control group was 15 years higher than that of the patients.
With regard to the patient group, there was a statistically significant difference regarding sE-selectin serum levels before and after NB-UVB phototherapy (P = 0.001). These results were consistent with those of Bonifati et al. [22], Carducci et al. [23], D'Auria et al. [25], Szepietowski et al. [26], Borskà et al. [19], and Long et al. [3]. However, Krasowska et al. [27], Kowalzick et al. [21], and Czech et al. [23] did not find a significant difference in sE-selectin serum levels before and after treatment with dithranol and combined dithranol and UVB. The reasons for these conflicting study outcomes might be related to differences in the study regimens, study designs, or patient population characteristics.
Also, there was a statistically significant difference regarding sICAM-1 serum levels before and after NB-UVB phototherapy (P=0.001), which is in agreement with Batycka-Baran et al. [20]. In contrast, Borskà et al. [19], Kowalzick et al. [21], and Long et al. [3] found no statistically significant difference in serum levels of sICAM-1 before and after treatment with Goeckerman's therapy, topical dithranol + UVB, and NB-UVB phototherapy, respectively.
Serum levels of sE-selectin after NB-UVB phototherapy, although lower than the pretreatment level in the present study, were still higher than that found in healthy controls, as was also found by Borskà et al. [19], Long et al. [3], and Krasowska et al. [27]. The reason for the increased serum sE-selectin levels remains unknown, although it is indicative of an altered endothelial function in psoriasis.
A significant positive correlation was found between sE-selectin serum levels and PASI scores before and after NB-UVB phototherapy, which was in agreement [28], Kowalzick et al. [21], Carducci et al. [23], Bonifati et al. [22], and Krasowska et al. [27], although this finding was against Czech et al. [24] and Long et al. [3]. This may be due to the use of different method for treatment (topical steroid) [24] and different number of patients in their studies (n = 16 and 58 respectively).
Significant positive correlation was found between sICAM-1 serum levels and PASI scores before and after NB-UVB. These results were in agreement with Gangemi et al. [18], Ameglio et al. [29], Borskà et al. [19], Θabrijan and Lipozenθiζ [5], and Long et al. [3]. On the contrary, Krasowska et al. [30] had not found any correlation between plasma levels of sICAM-1 and PASI scores.
Conclusion | |  |
The study emphasizes the complex nature of the roles played by sCAMs in the immunopathogenesis of psoriasis and the effect of NB-UVB on their values in relation to PASI score. Also results of this study provide rationale for possible application of sE-selectin and sICAM-1 serum measurement as biomarkers of psoriasis activity. Adhesion molecules are currently considered as possible targets of future psoriasis therapies but still needs further studies.
Acknowledgements | |  |
Conflicts of interest
None declared.
References | |  |
1. | Nakajima K. Critical role of the interleukin-23/T-helper 17 cell axis in the pathogenesis of psoriasis. J Dermatol 2012; 39 :219-224.  [PUBMED] |
2. | Dunphy S, Gardiner CM. NK cells and psoriasis. J Biomed Biotechnol 2011; 2011:248317. Available at: http://dx.doi.org/10.1155/2011/248317. [Accessed 15 January 2014]  |
3. | Long JW, Tao J, Pi XM. Effect of narrow-band UVB phototherapy on soluble cell adhesion molecules in patients with psoriasis vulgaris. J Int Med Res 2010; 38 :1507-1512.  |
4. | Kohka H, Yoshino T, Iwagaki H, Sakuma I, Tanimoto T, Matsuo Y, et al. Interleukin-18/interferon gamma-inducing factor, a novel cytokin, up-regulates ICAM-1(CD54) expression in KG-1 cells. J Leukoc Biol 1998; 64 :519-527.  |
5. | Èabrijan L, Lipozenèiæ J. Adhesion molecules in keratinocytes. Clin Dermatol 2011; 29 :427-431.  |
6. | Lee RT, Briggs WH, Cheng GC, Rossiter HB, Libby P, Kupper T. Mechanical deformation promotes secretion of IL-1 alpha and IL-1 receptor antagonist. J Immunol 1997; 159 :5084-5088.  |
7. | Pober JS, Bevilacqua MP, Mendrick DL, Cotran RS, Gimbrone MAJr. Two distinct monokines, interleukin 1 and tumor necrosis factor, each independently induce biosynthesis and transient expression of the same antigen on the surface of cultured human vascular endothelial cells. J Immunol 1986; 136 :1680-1687.  |
8. | Gho YS, Kleinman HK, Sosne G. Angiogenic activity of human soluble intercellular adhesion molecule-1. Cancer Res 1999; 59 :5128-5132.  |
9. | Constans J, Conri C. Circulating markers of endothelial function in cardiovascular disease. Clin Chim Acta 2006; 368 :33-47.  |
10. | 1Tsakadze NL, Sithu SD, Sen U, English WR, Murphy G, D′Souza SE. Tumor necrosis factor-α-converting enzyme (TACE/ ADAM-17) mediates the ectodomain cleavage of intercellular adhesion molecule-1 (ICAM-1). J Biol Chem 2006; 281 :3157-3164.  |
11. | 1Ruchaud-Sparagano MH, Drost EM, Donnelly SC, Bird MI, Haslett C, Dransfield I. Potential pro-inflammatory effects of soluble E-selectin upon neutrophil function. Eur J Immunol 1998; 28 :80-89.  |
12. | 1Carrascosa JM, López-Estebaranz JL, Carretero G. Narrowband UV-B, monochromatic excimer laser, and photodynamic therapy in psoriasis: a consensus statement of the Spanish Psoriasis Group. Actas Dermosifiliogr 2011; 102 :175-186.  |
13. | 1Menter A, Korman NJ, Elmets CA. Guidelines of care for the management of psoriasis and psoriatic arthritis: Section 5. Guidelines of care for the treatment of psoriasis with phototherapy and photochemotherapy. J Am Acad Dermatol 2010; 62 :114-135.  |
14. | 1de Rie MR, Goedkoop AY, Bos JD. Overview of psoriasis. Dermatol Ther 2004; 17 :341-349.  |
15. | 1Berth-Jones J, Grotzinger K, Rainville C. A study examining inter-and intrarater reliability of three scales for measuring severity of psoriasis: Psoriasis Area and Severity Index, Physician′s Global Assessment and Lattice System physician′s Global Assessment. Br J Dermatol 2006; 155 :707-713.  |
16. | 1Schopf RE, Naumann S, Rehder M. Soluble intercellular adhesion molecule-1 levels in patients with psoriasis. Br J Dermatol 1993; 128 :34-37.  |
17. | 1Krasowska D, Chodorowska G, Kozio³ M. Plasma levels of sICAM-1 in patients affected by psoriasis: no relation to disease severity. Med Sci Monit 2000; 6 :353-355.  |
18. | 1Gangemi S, Merendino RA, Guarneri F. Serum levels of interleukin-18 and s-ICAM-1 in patients affected by psoriasis: preliminary considerations. J Eur Acad Dermatol Venereol 2003; 17 :42-46.  |
19. | 1Borskà L, Fiala Z, Krejsek J. Selected immunological changes in patients with Goeckerman′s therapy TNF-alpha, sE-selectin, sP-selectin, sICAM-1 and IL-8. Physiol Res 2006; 55 :699-706.  |
20. | 2Batycka-Baran A, Paprocka M, Krawczenko A. Increased number of circulating endothelial cells (CECs) in patients with psoriasis - preliminary report. J Eur Acad Dermatol Venereol 2014; 28 :116-119.  |
21. | 2Kowalzick L, Neuber K, Weichenthal M. Elevated serum-soluble ELAM-1 levels in patients with severe plaque-type psoriasis. Arch Dermatol Res 1994; 286 :414-416.  |
22. | 2Bonifati C, Trento E, Carducci M. Soluble E-selectin and soluble tumour necrosis factor receptor (60 kD) serum levels in patients with psoriasis. Dermatology 1995; 190 :128-131.  |
23. | 2Carducci M, Mussi A, Bonifati C. Correlation of lesional skin corneometry values with serum E-selectin levels and disease severity in patients affected by plaque-type psoriasis: recovery after effective therapy. J Dermatol 1995; 22 :475-479.  |
24. | 2Czech W, Schöpf E, Kapp A. Soluble E-selectin in sera of patients with atopic dermatitis and psoriasis-correlation with disease activity. Br J Dermatol 1996; 134 :17.  |
25. | 2D′Auria L, Bonifati C, Mussi A, Ameglio F. Monitoring of sE-selectin levels in three different dermatoses. Clin Ter 1998; 149 :49-52.  |
26. | 2Szepietowski J, Wasik F, Bielicka E, Nockowski P, Noworolska A. Soluble E-selectin serum levels correlate with disease activity in psoriatic patients. Clin Exp Dermatol 1999; 24 :33-36.  |
27. | 2Krasowska D, Pietrzak A, Lecewicz-Torun B. Serum level of sELAM-1 in psoriatic patients correlates with disease activity. J Eur Acad Dermatol Venereol 1999; 12 :140-142.  |
28. | 2Ghalamkarpour F, Saeedi M, Hedayati M. Soluble E-selectin and P-selectin serum levels in patients with psoriasis compared to healthy controls. Iran J Dermatol 2010; 13 :9-11.  |
29. | 2Ameglio F, Bonifati C, Carducci M, Sacerdoti G, Fazio F. Soluble intercellular adhesion molecule-1 and procollagen III peptide are reliable markers of disease severity in psoriasis. Acta Derm Venereol Suppl (Stockh) 1994; 186 :19-20.  |
30. | 3Kowalzick L, Bildau H, Neuber K, Kohler I, Ring J. Clinical improvement in psoriasis during dithranol/UVB therapy does not correspond with a decrease in elevated serum soluble ICAM-1 levels. Arch Dermatol Res 1993; 285 :233-235.  |
[Figure 1], [Figure 2]
[Table 1], [Table 2], [Table 3], [Table 4], [Table 5]
|