Influence of narrow-band UVB phototherapy on cutaneous microbiota of children with atopic dermatitis

被引:59
作者
Silva, S. H.
Guedes, A. C. M.
Gontijo, B.
Ramos, A. M. C.
Carmo, L. S.
Farias, L. M.
Nicoli, J. R.
机构
[1] Univ Fed Minas Gerais, Inst Ciencias Biol, Dept Microbiol, Belo Horizonte, MG, Brazil
[2] Univ Fed Minas Gerais, Fac Med, Serv Dermatol, Ambulatorio Fototerapia Hosp Clin, Belo Horizonte, MG, Brazil
关键词
atopic dermatitis; cutaneous microbiota; narrow-band UVB; Staphylococcus aureus; superantigen exotoxins;
D O I
10.1111/j.1468-3083.2006.01748.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Objective In the present work, the effect of narrow-band ultraviolet B (UVB) phototherapy on a cutaneous microbial population was evaluated in patients with atopic dermatitis (AD) and compared with control patients (vitiligo). Methods Count, isolation and identification of cutaneous microbiota from anticubital fossa were performed in 10 controls and 10 AD patients, both submitted to similar levels (P > 0.05) of UVB phototherapy (4.3 +/- 0.9 and 4.3 +/- 0.8 accumulated joules, respectively). Additionally, Staphylococcus aureus isolates were screened for the production of exotoxins. Results The total and staphylococcal cutaneous microbial population levels were higher (P < 0.05) in AD patients than in the controls. All these population levels decreased (P < 0.05) for both AD and control patients after UVB phototherapy, which also decreased the SCORAD for AD patients. All patients with AD and 50% of controls were carriers of S. aureus, and harboured the bacteria simultaneously on skin and anterior nares. All of the S. aureus strains recovered from AD patient skin produced toxin and the B type was the most frequently detected (70%), followed by C (20%) and A (10%) toxins. Only 40% of the S. aureus isolates from control patients produced toxin. After UVB treatment, microbial population levels of AD patients were similar (P > 0.05) to the ones found in control patients before phototherapy, and toxin production ability of S. aureus isolates decreased drastically. Conclusion The results of the present study show the beneficial effect of UVB phototherapy on AD and suggest that this may be attributable not only to reduction of skin surface bacteria but also to the suppression of superantigen production from S. aureus.
引用
收藏
页码:1114 / 1120
页数:7
相关论文
共 24 条
[1]   Prevalence of producers of enterotoxins and toxic shock syndrome toxin-1 among Staphylococcus aureus strains isolated from atopic dermatitis lesions [J].
Akiyama, H ;
Toi, Y ;
Kanzaki, H ;
Tada, J ;
Arata, J .
ARCHIVES OF DERMATOLOGICAL RESEARCH, 1996, 288 (07) :418-420
[2]  
[Anonymous], ACTA DERM VENERE S92, DOI [10.2340/00015555924447, DOI 10.2340/00015555924447]
[3]   Suppressed alloantigen presentation, increased TNF-α, IL-1, IL-1Ra, IL-10, and modulation of TNF-R in UV-irradiated human skin [J].
Barr, RM ;
Walker, SL ;
Tsang, WL ;
Harrison, GI ;
Ettehadi, P ;
Greaves, MW ;
Young, AR .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1999, 112 (05) :692-698
[4]  
Bergdoll M.S., 1984, COMPENDIUM METHODS M, P428
[5]   Staphylococcus aureus:: colonizing features and influence of an antibacterial treatment in adults with atopic dermatitis [J].
Breuer, K ;
Häussler, S ;
Kapp, A ;
Werfel, T .
BRITISH JOURNAL OF DERMATOLOGY, 2002, 147 (01) :55-61
[6]   Severe atopic dermatitis is associated with sensitization to staphylococcal enterotoxin B (SEB) [J].
Breuer, K ;
Wittmann, M ;
Bösche, B ;
Kapp, A ;
Werfel, T .
ALLERGY, 2000, 55 (06) :551-555
[7]   Evidence for a disease-promoting effect of Staphylococcus aureus-derived exotoxins in atopic dermatitis [J].
Bunikowski, R ;
Mielke, MEA ;
Skarabis, H ;
Worm, M ;
Anagnostopoulos, I ;
Kolde, G ;
Wahn, U ;
Renz, H .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2000, 105 (04) :814-819
[8]  
CASMAN EP, 1969, HEALTH LAB SCI, V6, P185
[9]   THE ADHERENCE OF STAPHYLOCOCCUS-AUREUS TO HUMAN CORNEOCYTES [J].
COLE, GW ;
SILVERBERG, NL .
ARCHIVES OF DERMATOLOGY, 1986, 122 (02) :166-169
[10]   STAPHYLOCOCCAL SKIN COLONIZATION IN CHILDREN WITH ATOPIC-DERMATITIS - PREVALENCE, PERSISTENCE, AND TRANSMISSION OF TOXIGENIC AND NONTOXIGENIC STRAINS [J].
HOEGER, PH ;
LENZ, W ;
BOUTONNIER, A ;
FOURNIER, JM .
JOURNAL OF INFECTIOUS DISEASES, 1992, 165 (06) :1064-1068