Effect of PUVA, narrow-band UVB and cyclosporin on inflammatory cells of the psoriatic plaque

被引:37
作者
Erkin, Gul [1 ]
Ugur, Yesim
Gurer, Cansel Kose
Asan, Esin
Korkusuz, Petek
Sahin, Sedef
Kolemen, Fikret
机构
[1] Hacettepe Univ, Sch Med, Dept Dermatol, TR-06100 Ankara, Turkey
[2] Hacettepe Univ, Sch Med, Dept Histol & Embryol, TR-06100 Ankara, Turkey
关键词
EPIDERMAL LANGERHANS CELLS; ANTIGEN-PRESENTING CELLS; INTRAEPIDERMAL T-CELLS; INCREASED NUMBERS; SKIN; EXPRESSION; VULGARIS; LYMPHOCYTES; MOLECULES; DERMIS;
D O I
10.1111/j.1600-0560.2006.00591.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Because antigen presenting is necessary for T-cell activation, antigen-presenting cells should be involved in the pathogenesis of psoriasis. In this study, our purpose was to evaluate and compare effects of PUVA, cyclosporine A and narrow-band UVB on dendritic cells and activated lymphocytes in the psoriatic lesions. Methods: Forty-five volunteered patients (15 patients in each treatment group as PUVA, cyclosporin A and narrow-band UVB) were enrolled in this study. Lesional skin biopsies were taken from each patient before and after treatments. Fresh frozen biopsies were studied for the expressions of CD1a, CD68, CD86, CD4, CD8 and HLA-DR proteins by immunohistochemistry. Results: There was no correlation between severity of the lesions and expressions of the antigens. Only PUVA significantly decreased CD1a+ epidermal Langerhans cells' (LCs) counts. Treatment modalities decreased expression of costimulator CD86, and most of them decrease antigen-presenting capacity of skin by decreasing HLA class-II expression. Conclusions: All treatment modalities equally reduce lymphocytes, macrophages and dendritic cells. PUVA is the only treatment that decreases epidermal LCs. All treatments effectively diminish expression of CD86 and inhibit this step of inflammation.
引用
收藏
页码:213 / 219
页数:7
相关论文
共 26 条
[1]   Functional diversity of helper T lymphocytes [J].
Abbas, AK ;
Murphy, KM ;
Sher, A .
NATURE, 1996, 383 (6603) :787-793
[2]   A QUANTITATIVE-ANALYSIS OF THE LANGERHANS CELL IN CHRONIC PLAQUE PSORIASIS [J].
ASHWORTH, J ;
MACKIE, RM .
CLINICAL AND EXPERIMENTAL DERMATOLOGY, 1986, 11 (06) :594-599
[3]   PSORIATIC EPIDERMAL-CELLS DEMONSTRATE INCREASED NUMBERS AND FUNCTION OF NON-LANGERHANS ANTIGEN-PRESENTING CELLS [J].
BAADSGAARD, O ;
GUPTA, AK ;
TAYLOR, RS ;
ELLIS, CN ;
VOORHEES, JJ ;
COOPER, KD .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1989, 92 (02) :190-195
[4]   Genetic aspects of psoriasis [J].
Barker, JNWN .
CLINICAL AND EXPERIMENTAL DERMATOLOGY, 2001, 26 (04) :321-325
[5]   IMMUNOCOMPETENT CELLS IN PSORIASIS - INSITU IMMUNOPHENOTYPING BY MONOCLONAL-ANTIBODIES [J].
BOS, JD ;
HULSEBOSCH, HJ ;
KRIEG, SR ;
BAKKER, PM ;
CORMANE, RH .
ARCHIVES OF DERMATOLOGICAL RESEARCH, 1983, 275 (03) :181-189
[6]  
BURGDORF WHC, 2005, SEVERS HISTOPATHOLOG, P681
[7]   Trimethylpsoralen bath PUVA is a remittive treatment for psoriasis vulgaris - Evidence that epidermal immunocytes are direct therapeutic targets [J].
Coven, TR ;
Murphy, FP ;
Gilleaudeau, P ;
Cardinale, I ;
Krueger, JG .
ARCHIVES OF DERMATOLOGY, 1998, 134 (10) :1263-1268
[8]   CD69, HLA-DR and the IL-2R identify persistently activated T cells in psoriasis vulgaris lesional skin: Blood and skin comparisons by flow cytometry [J].
Ferenczi, K ;
Burack, L ;
Pope, M ;
Krueger, JG ;
Austin, LM .
JOURNAL OF AUTOIMMUNITY, 2000, 14 (01) :63-78
[9]  
FREDRIKSSON T, 1978, DERMATOLOGICA, V14, P63
[10]   Immunopathogenic mechanisms in psoriasis [J].
Gudjonsson, JE ;
Johnston, A ;
Sigmundsdottir, H ;
Valdimarsson, H .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2004, 135 (01) :1-8