Prevention of immunosuppression by sunscreens in humans is unrelated to protection from erythema and dependent on protection from ultraviolet A in the face of constant ultraviolet B protection

被引:59
作者
Poon, TSC [1 ]
Barnetson, RS [1 ]
Halliday, GM [1 ]
机构
[1] Univ Sydney, Royal Prince Alfred Hosp, Sydney Canc Ctr, Melanoma & Skin Canc Res Inst,Dept Med Dermatol, Sydney, NSW 2006, Australia
基金
英国医学研究理事会;
关键词
sunscreening agents; ultraviolet rays;
D O I
10.1046/j.1523-1747.2003.12317.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Sunscreens have been advocated as an important means of preventing skin cancer. Ultraviolet radiation induced immunosuppression is recognized as an important event in skin cancer development, yet the effectiveness of sunscreens in protecting the human immune system from ultraviolet radiation (i.e. ultraviolet radiation) is still unclear. The only currently accepted method of sunscreen rating is the sun protection factor system based on the prevention of erythema. We determined immune protection factors for six commercially available sunscreens using a nickel contact hypersensitivity model in humans. Both sun protection factor and immune protection factor testing was performed using the same solar simulated ultraviolet radiation source and dose-responses were used to determine endpoints both with and without sunscreens. We found that the immune protection factor did not correlate with the sun protection factor; however, immune protection factor was significantly correlated to the ultraviolet A protective capability of the sunscreens, indicating that sunscreen protection from ultraviolet A is important for the prevention of ultraviolet immunosuppression, when there is constant ultraviolet B protection. We recommend that sunscreens should be rated against their immune protective capability to provide a better indication of their ability to protect against skin cancer.
引用
收藏
页码:184 / 190
页数:7
相关论文
共 53 条
[1]   SKIN-CANCER [J].
ARMSTRONG, BK ;
KRICKER, A .
DERMATOLOGIC CLINICS, 1995, 13 (03) :583-594
[2]   Mechanisms involved in ultraviolet light-induced immunosuppression [J].
Beissert, S ;
Schwarz, T .
JOURNAL OF INVESTIGATIVE DERMATOLOGY SYMPOSIUM PROCEEDINGS, 1999, 4 (01) :61-64
[3]   Chronic low-dose UVA irradiation induces local suppression of contact hypersensitivity, Langerhans cell depletion and suppressor cell activation in C3H/HeJ mice [J].
Bestak, R ;
Halliday, GM .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1996, 64 (06) :969-974
[4]  
BESTAK R, 1995, J INVEST DERMATOL, V105, P345, DOI 10.1111/1523-1747.ep12320580
[5]   Sunscreens protect from UV-promoted squamous cell carcinoma in mice chronically irradiated with doses of UV radiation insufficient to cause edema [J].
Bestak, R ;
Halliday, GM .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1996, 64 (01) :188-193
[6]   Ultraviolet A irradiation of C57BL/6 mice suppresses systemic contact hypersensitivity or enhances secondary immunity depending on dose [J].
Byrne, SN ;
Spinks, N ;
Halliday, GM .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2002, 119 (04) :858-864
[7]  
Chardon A., 1997, SUNSCREENS DEV EVALU, P559
[8]  
*COLIPA, 1994, COLIPA SUN PROT FACT
[9]   Measurement of ultraviolet radiation-induced suppression of recall contact and delayed-type hypersensitivity in humans [J].
Damian, DL ;
Halliday, GM .
METHODS, 2002, 28 (01) :34-45
[10]   Measurement of in vivo sunscreen immune protection factors in humans [J].
Damian, DL ;
Barnetson, RS ;
Halliday, GM .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1999, 70 (06) :910-915