Efficacy of different UV-emitting light sources in the induction of T-cell apoptosis

被引:38
作者
Novák, Z
Bérces, A
Rontó, G
Pállinger, E
Dobozy, A
Kemény, L
机构
[1] Univ Szeged, Dept Dermatol, H-6701 Szeged, Hungary
[2] Hungarian Acad Sci, MTA SE Res Grp Biophys, Budapest, Hungary
[3] Semmelweis Univ, Inst Biophys, H-1085 Budapest, Hungary
[4] Hungarian Acad Sci, Mol Immunol Res Grp, Budapest, Hungary
关键词
D O I
10.1562/RA-003R.1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ultraviolet B (UV-B) radiation is a modality widely used for the treatment of different skin diseases. One of the major mechanisms of UV-B inummosuppression in this treatment modality is thought to be an apoptosis-inducing effect on T cells infiltrating the skin. We examined the T-cell apoptosis-induction capacities of four different UV light sources, with and without UV filters. The xenon chloride (XeCl) laser proved to be the strongest apoptosis inducer. The use of a phtalic acid filter eliminated UV radiation almost completely below 300 nm, which resulted in a severe decrease in the apoptosis-inducing capacity of different UV-B sources. Using the results of the measurements with polychromatic UV light sources, the wavelength dependence of UV-B light for the induction of T-cell apoptosis was also determined. The regression line of the action spectrum demonstrated a continuous decrease from 290 to 311 nm. The apoptosis-inducing capacity of the XeCl laser was almost four times higher than the calculated value according to the action spectrum, which might be attributed to the high irradiance of the laser as compared with nonlaser light sources.
引用
收藏
页码:434 / 439
页数:6
相关论文
共 30 条
[21]   Xenon chloride ultraviolet B laser is more effective in treating psoriasis and in inducing T cell apoptosis than narrow-band ultraviolet B [J].
Novák, Z ;
Bónis, B ;
Baltás, E ;
Ocsovszki, I ;
Ignácz, F ;
Dobozy, A ;
Kemény, L .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 2002, 67 (01) :32-38
[22]   312-nanometer ultraviolet B light (narrow-band UVB) induces apoptosis of T cells within psoriatic lesions [J].
Ozawa, M ;
Ferenczi, K ;
Kikuchi, T ;
Cardinale, I ;
Austin, LM ;
Coven, TR ;
Burack, LH ;
Krueger, JG .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 189 (04) :711-718
[23]   ACTION SPECTRUM FOR PHOTOTHERAPY OF PSORIASIS [J].
PARRISH, JA ;
JAENICKE, KF .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1981, 76 (05) :359-362
[24]   ACTION SPECTRA FOR THE INDUCTION OF PYRIMIDINE(6-4)PYRIMIDONE PHOTOPRODUCTS AND CYCLOBUTANE PYRIMIDINE DIMERS IN NORMAL HUMAN-SKIN FIBROBLASTS [J].
ROSENSTEIN, BS ;
MITCHELL, DL .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1987, 45 (06) :775-780
[25]   WAVELENGTHS IN SUNLIGHT EFFECTIVE IN PRODUCING SKIN CANCER - THEORETICAL ANALYSIS [J].
SETLOW, RB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1974, 71 (09) :3363-3366
[26]  
Spann CT, 2001, CUTIS, V68, P351
[27]   High-dose 308-nm excimer laser for the treatment of psoriasis [J].
Trehan, M ;
Taylor, CR .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2002, 46 (05) :732-737
[28]   The effects of UVA-I (340-400 nm), UVA-II (320-340 nm) and UVA-I+II on the photoisomerization of urocanic acid in vivo [J].
Webber, LJ ;
Whang, E ;
DeFabo, EC .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1997, 66 (04) :484-492
[29]  
World Health Organization, 1994, Environmental Health Criteria, V160
[30]   APOPTOSIS - DEATH GETS A BRAKE [J].
WYLLIE, AH .
NATURE, 1994, 369 (6478) :272-273