da Cruz A D, Curry J, Curado M P, Glickman B W
Centre for Environmental Health, University of Victoria, British Columbia, Canada.
Environ Mol Mutagen. 1996;27(3):165-75. doi: 10.1002/(SICI)1098-2280(1996)27:3<165::AID-EM1>3.0.CO;2-E.
Modern technologies have provided the opportunity to monitor mutations in people in vivo. The subjects of this study were accidentally exposed to 137Cesium in a radiological accident that occurred in September 1987 in Goiânia, Brazil, during which more than 150 people received doses greater than 0.1 Gy and as high as 7 Gy. The objective of this study was to determine how long the hprt mutant T-cells in the peripheral blood contribute to mutant frequency by examining the time-course of the T-lymphocyte response to ionizing radiation. This report describes the results obtained over a period of 2.3 to 4.5 years subsequent to the accident, from 11 subjects with doses ranging from 1 to 7 Gy, and from nine control subjects selected from the same population. The mean In MF (+/- SE) of the control group was 2.5 (+/- 0.2) + In10(-6). The exposed group had a significantly increased mutant frequency; the mean In MF (+/- SE) were 3.3 (+/- 0.3) + In10(-6), 2.8 (+/- 0.2) + In10(-6), and 2.3 (+/- 0.2) + In10(-6), in the years 1990-1992 respectively. Based on the decline of mutant frequency and using Buckton's models [Buckton et al. (1967): Nature 214:470-473], we demonstrated that mutant T-cells have a short-term memory with a half-life of 2.1 years. This relatively short half-life limits the effective use of the hprt assay as the method of choice to monitor past exposure. The data also demonstrate a positive correlation with age, and an inverse correlation with plating efficiency.
现代技术为在人体内监测突变提供了机会。本研究的对象在1987年9月发生于巴西戈亚尼亚的一起放射性事故中意外接触了铯 - 137,在此期间,超过150人接受的剂量大于0.1 Gy,最高达7 Gy。本研究的目的是通过检查T淋巴细胞对电离辐射的反应时间进程,确定外周血中hprt突变T细胞对突变频率的影响持续多久。本报告描述了事故发生后2.3至4.5年期间,对11名受照剂量在1至7 Gy之间的受试者以及从同一人群中选取的9名对照受试者所获得的结果。对照组的平均ln MF(±SE)为2.5(±0.2)+ ln10⁻⁶。受照组的突变频率显著增加;在1990 - 1992年期间,平均ln MF(±SE)分别为3.3(±0.3)+ ln10⁻⁶、2.8(±0.2)+ ln10⁻⁶和2.3(±0.2)+ ln10⁻⁶。基于突变频率的下降并使用Buckton模型[Buckton等人(1967年):《自然》214:470 - 473],我们证明突变T细胞具有半衰期为2.1年的短期记忆。这种相对较短的半衰期限制了将hprt检测作为监测既往暴露首选方法的有效应用。数据还显示与年龄呈正相关,与接种效率呈负相关。