CD11b+ cells and ultraviolet-B-resistant CD1a+ cells in skin of patients with polymorphous light eruption

被引:66
作者
Kölgen, W [1 ]
Van Weelden, H [1 ]
Den Hengst, S [1 ]
Guikers, KLH [1 ]
Kiekens, RCM [1 ]
Knol, EF [1 ]
Bruijnzeel-Koomen, CAFM [1 ]
van Vloten, WA [1 ]
de Gruijl, FR [1 ]
机构
[1] Univ Utrecht Hosp, Dept Dermatol HP G02124, AZU, NL-3584 CX Utrecht, Netherlands
关键词
Langerhans cell; macrophages; photodermatoses; ultraviolet immunosuppression;
D O I
10.1046/j.1523-1747.1999.00625.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
After ultraviolet exposure Langerhans cells (epidermal CD1a(+) cells) disappear from the healthy skin, and CD11b(+) macrophage-like cells, which are reported to produce interleukin-10, appear in a matter of days. These phenomena are related to the ultraviolet-induced local suppression of contact hypersensitivity reactions. A defect in this suppression might allow inadvertent immune reactions to develop after ultraviolet (over)exposure; i.e., it could cause ultraviolet-B-induced polymorphous light eruption. In order to test this we first exposed buttock skin of eight healthy volunteers to six minimal erythema doses from Philips TL12 lamps, and indeed observed a dramatic disappearance of CD1a(+) cells 48 and 72 h later, at which time the number of CD11b(+) cells increased in the dermis, and some occurred in the epidermis, The epidermis thickened and showed large defects, filled by CD11b(+) cells, just below the stratum corneum, In 10 patients with polymorphous light eruption (five with a normal minimal erythema dose and five with a low minimal erythema dose) CD1a(+) cells were present in the epidermis as well as in the dermis before exposure. Strikingly, these cells were still present in considerable number at 48 and 72 h after exposure to six minimal erythema doses. CD11b(+) cells already present in the dermis before ultraviolet exposure, increased after ultraviolet exposure, and subsequently also invaded the epidermis, Despite the six minimal erythema doses, there were no apparent defects in the epidermis of the polymorphous light eruption patients. This deviant early response to ultraviolet radiation is likely to be of direct relevance to the polymorphous light eruption and is perhaps useful as a diagnostic criterion.
引用
收藏
页码:4 / 10
页数:7
相关论文
共 41 条
[1]   ULTRAVIOLET-LIGHT DEPLETES SURFACE-MARKERS OF LANGERHANS CELLS [J].
ABERER, W ;
SCHULER, G ;
STINGL, G ;
HONIGSMANN, H ;
WOLFF, K .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1981, 76 (03) :202-210
[2]   Distribution of myocardial macrophages in the normal human heart [J].
Azzawi, M ;
Hasleton, PS ;
Kan, SW ;
Hillier, VF ;
Quigley, A ;
Hutchinson, IV .
JOURNAL OF ANATOMY, 1997, 191 :417-423
[3]   Failed antigen presentation after UVB radiation correlates with modifications of Langerhans cell cytoskeleton [J].
Bacci, S ;
Nakamura, T ;
Streilein, JW .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1996, 107 (06) :838-843
[4]   UV-induced cutaneous photobiology [J].
Beissert, S ;
Granstein, RD .
CRITICAL REVIEWS IN BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1996, 31 (5-6) :381-404
[5]  
Boonstra A, 1997, EUR CYTOKINE NETW, V8, P117
[6]   Cell-mediated immunosuppressive mechanisms induced by UV radiation [J].
Cooper, KD .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1996, 63 (04) :400-406
[7]   ANTIGEN-PRESENTING OKM5+ MELANOPHAGES APPEAR IN HUMAN-EPIDERMIS AFTER ULTRAVIOLET-RADIATION [J].
COOPER, KD ;
NEISES, GR ;
KATZ, SI .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1986, 86 (04) :363-370
[8]   UV EXPOSURE REDUCES IMMUNIZATION RATES AND PROMOTES TOLERANCE TO EPICUTANEOUS ANTIGENS IN HUMANS - RELATIONSHIP TO DOSE, CD1A-DR+ EPIDERMAL MACROPHAGE INDUCTION, AND LANGERHANS CELL DEPLETION [J].
COOPER, KD ;
OBERHELMAN, L ;
HAMILTON, TA ;
BAADSGAARD, O ;
TERHUNE, M ;
LEVEE, G ;
ANDERSON, T ;
KOREN, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (18) :8497-8501
[9]  
CUMBERBATCH M, 1992, IMMUNOLOGY, V75, P257
[10]   Inflammatory response in cervical intraepithelial neoplasia and squamous cell carcinoma of the uterine cervix [J].
Davidson, B ;
Goldberg, I ;
Kopolovic, J .
PATHOLOGY RESEARCH AND PRACTICE, 1997, 193 (07) :491-495