Immunohistochemical characterization of the cellular infiltrate in localized scleroderma

被引:17
作者
Xie, Yong [1 ]
Zhang, Xiaoyong [1 ]
Wakasugi, Shoji [1 ]
Makino, Takamitsu [1 ]
Inoue, Yuji [1 ]
Ihn, Hironobu [1 ]
机构
[1] Kumamoto Univ, Grad Sch Med & Pharmaceut Sci, Dept Dermatol & Plast & Reconstruct Surg, Kumamoto 8608556, Japan
关键词
D O I
10.1111/j.1365-4632.2008.03615.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 [皮肤病与性病学];
摘要
Background Localized scleroderma is a connective tissue disorder with hardening of the skin and fibrosis of the affected tissue as the most prominent features. The etiology of localized scleroderma is still unknown, but immunologic factors may play an important role in the pathogenesis. This study was performed to determine the immunohistochemical features of the cellular infiltrate in localized scleroderma. Methods Skin samples were obtained from six patients by 6-mm punch biopsy. The samples were stained with monoclonal antibodies against CD1a, CD3, CD4, CD8, CD20, CD25, CD30, and CD57. The number of cells stained with each monoclonal antibody was calculated. Results There were more CD1a+, CD3+, CD4+, CD8+, CD20+, CD25+, and CD57+ cells in the dermal infiltrate in localized scleroderma relative to those in normal controls. The numbers of CD1a+, CD3+, CD4+, CD8+, and CD57+ cells in localized scleroderma were significantly greater than those in normal skin (P < 0.05). The number of CD30+ cells in localized scleroderma was almost the same as that in normal skin. Conclusions This study reveals that T lymphocytes, Langerhans cells, and natural killer cells may play important roles in the pathogenesis of localized scleroderma.
引用
收藏
页码:438 / 442
页数:5
相关论文
共 18 条
[1]
PREFERENTIAL EXPRESSION OF CD30 BY HUMAN CD4(+) T-CELLS PRODUCING TH2-TYPE CYTOKINES [J].
DELPRETE, G ;
DECARLI, M ;
ALMERIGOGNA, F ;
DANIEL, CK ;
DELIOS, MM ;
ZANCUOGHI, G ;
VINANTE, F ;
PIZZOLO, G ;
ROMAGNANI, S .
FASEB JOURNAL, 1995, 9 (01) :81-86
[2]
Ercole LP, 2003, J INVEST ALLERG CLIN, V13, P87
[3]
ANTINUCLEAR AND ANTI-SINGLE-STRANDED DNA ANTIBODIES IN MORPHEA AND GENERALIZED MORPHEA [J].
FALANGA, V ;
MEDSGER, TA ;
REICHLIN, M .
ARCHIVES OF DERMATOLOGY, 1987, 123 (03) :350-353
[4]
LINEAR SCLERODERMA - CLINICAL SPECTRUM, PROGNOSIS, AND LABORATORY ABNORMALITIES [J].
FALANGA, V ;
MEDSGER, TA ;
REICHLIN, M ;
RODNAN, GP .
ANNALS OF INTERNAL MEDICINE, 1986, 104 (06) :849-857
[5]
HIGH TITERS OF ANTIBODIES TO SINGLE-STRANDED-DNA IN LINEAR SCLERODERMA [J].
FALANGA, V ;
MEDSGER, TA ;
REICHLIN, M .
ARCHIVES OF DERMATOLOGY, 1985, 121 (03) :345-347
[6]
FITZPATRICK TB, 2003, DERMATOLOGY GEN MED
[7]
Ihn H, 1996, BRIT J DERMATOL, V134, P843
[8]
Immunological activation of dermal Langerhans cells in contact with lymphocytes in a model of human inflamed skin [J].
Katou, F ;
Ohtani, H ;
Saaristo, A ;
Nagura, H ;
Motegi, K .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 156 (02) :519-527
[9]
ANTINUCLEAR ANTIBODIES IN LOCALIZED SCLERODERMA - UNIQUE STAINING IN CHROMOSOME SPREADS [J].
KIKUCHI, K ;
TAKEHARA, K ;
ISHIBASHI, Y .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1989, 21 (06) :1301-1303
[10]
MODULATION OF ONGOING HUMAN-IMMUNOGLOBULIN SYNTHESIS BY NATURAL-KILLER-CELLS [J].
KIMATA, H ;
SHANAHAN, F ;
BROGAN, M ;
TARGAN, S ;
SAXON, A .
CELLULAR IMMUNOLOGY, 1987, 107 (01) :74-88