Gallarda J L, Dragon E
Roche Molecular Systems, Inc, Pleasanton, CA 94588, USA.
Mol Diagn. 2000 Mar;5(1):11-22. doi: 10.1007/BF03262018.
Nucleic acid amplification technology (NAT) is presently being evaluated in US clinical trials to determine the safety and efficacy of mini-pool testing for human immunodeficiency virus (HIV) and hepatitis C virus (HCV) RNA in the blood-donor population. Although the risk for transfusion-transmitted HIV and HCV infection is extremely low, there is still a small chance that blood donated by infected individuals before seroconversion can escape detection by current antibody-based assays.
This report describes the amplification technologies being used and reviews several issues surrounding NAT-based blood screening. The performance features of NAT and current enzyme immunoassay technologies are compared, and the benefits of NAT in reducing transfusion-transmitted infections are discussed.
The current US clinical trials of mini-pool NAT testing for HIV and HCV RNA have successfully identified preseroconversion infectious blood units. Although the current NAT-based screening systems are semiautomated, mini-pool testing represents an unprecedented innovation among government and nongovernment agencies in the highly regulated blood transfusion industry. Despite cost-effectiveness issues, based on the public perception of infectious diseases acquired through blood transfusion, NAT-based screening of the blood supply is expected to become a standard in transfusion medicine.
目前美国正在进行临床试验,评估核酸扩增技术(NAT)用于检测献血人群中人类免疫缺陷病毒(HIV)和丙型肝炎病毒(HCV)RNA的微池检测法的安全性和有效性。尽管输血传播HIV和HCV感染的风险极低,但感染个体在血清转化前捐献的血液仍有小概率无法被目前基于抗体的检测方法检测出来。
本报告描述了所使用的扩增技术,并回顾了围绕基于NAT的血液筛查的几个问题。比较了NAT和当前酶免疫测定技术的性能特点,并讨论了NAT在减少输血传播感染方面的益处。
目前美国针对HIV和HCV RNA的微池NAT检测临床试验已成功识别出血清转化前的感染性血液单位。尽管目前基于NAT的筛查系统是半自动的,但微池检测在高度规范的输血行业中代表了政府和非政府机构前所未有的创新。尽管存在成本效益问题,但基于公众对通过输血获得传染病的认知,基于NAT的血液供应筛查有望成为输血医学的标准。