In Silico Risk Assessment of HLA-A*02:06-Associated Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis Caused by Cold Medicine Ingredients

被引:15
作者
Isogai, Hideto [1 ]
Miyadera, Hiroko [2 ]
Ueta, Mayumi [3 ]
Sotozono, Chie [3 ]
Kinoshita, Shigeru [3 ]
Tokunaga, Katsushi [2 ]
Hirayama, Noriaki [1 ]
机构
[1] Tokai Univ, Sch Med, Bas Med Sci & Mol Med, 147 Shimokasuya, Isehara, Kanagawa 2591143, Japan
[2] Univ Tokyo, Sch Int Hlth, Grad Sch Med, Dept Human Genet,Bunkyo Ku, Tokyo 1130033, Japan
[3] Kyoto Prefectural Univ Med, Dept Ophthalmol, Kamigyo Ku, Kyoto 6020841, Japan
关键词
D O I
10.1155/2013/514068
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are severe drug hypersensitivities with high mortality. Typical over-the-counter drugs of cold medicines are suggested to be causative. As multiple ingredients are generally contained in cold medicines, it is of particular interest to investigate which ingredients are responsible for SJS/TEN. However, experimental examination of causal relationships between SJS/TEN and a particular drug molecule is not straightforward. Significant association between HLA-A*02:06 and SJS/TEN with severe ocular surface complications has been observed in the Japanese. In the present study, we have undertaken in silico docking simulations between various ingredients contained in cold medicines available in Japan and the HLA-A*02:06 molecule. We use the composite risk index (CRI) that is the absolute value of the binding affinity multiplied by the daily dose to assess the potential risk of the adverse reactions. The drugs which have been recognized as causative drugs of SJS/TEN in Japan have revealed relatively high CRI, and the association between SJS/TEN and HLA-A * 02: 06 has been qualitatively verified. The results have also shown that some drugs whose links to SJS/TEN have not been clinically recognized in Japan show the high CRI and suggested that attention should be paid to their adverse drug reactions.
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页数:6
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