第94回日本細菌学会総会

講演情報

オンデマンド口頭発表(ODP)

5 病原体と感染症(疫学を含む)

[ODP5E] e. その他

[ODP-112] 創傷浸出液の222 nm-UVCに対する干渉作用は皮膚損傷部線維芽細胞を防御する

○成田 浩司1,2,森本 幸裕3,4,5,大橋 広行4,五十嵐 龍志4,浅野 クリスナ2,3,中根 明夫3 (1弘前大・院医・動物実験施設,2弘前大・院医・感染生体防御,3弘前大・院医・生体高分子健康科学,4ウシオ電機株式会社,5阪大・産業科学研究所)

Ultraviolet C (UVC) elicits anti-microbial property. 254 nm-UVC generating lamp is used as germicidal devices. However, 254 nm-UVC is carcinogenic and cataractogenic through DNA damage in dermal keratinocytes. We recently reported that 222 nm-UVC has the same level of germicidal effect as 254 nm-UVC against pathogenic bacteria, fungi and viruses. Different from 254 nm-UVC, 222 nm-UVC is harmless to keratinocytes because penetration of the light into the skin is blocked in stratum corneum. Therefore, 222 nm-UVC is harmless to dermis. However, impact of 222 nm-UVC to fibroblasts exposed to body surface in dermal defect site is not clarified. 222 nm- and 254 nm-UVC irradiation induced cytopathic effect to primary normal human dermal fibroblast cells, but fibroblasts covered with thin layer of 10% fetal calf serum were protected from 222 nm-UVC but not 254 nm-UVC. Irradiation with 254 nm-UVC induces cyclobutane pyrimidine dimer (CPD) in dermal damaged sites of the fibroblast, but 222 nm-UVC did not induce the CPD in fibroblasts. However, when 222 nm-UVC irradiation was performed under flow of PBS to eliminate wound exudate, CPD was detected in fibroblasts in wound. These results indicate that the 222 nm-UVC light irradiation is harmless to skin wound because the light is interfered by wound exudates.