Alter Harvey J
Department of Transfusion Medicine, Warren Grant Magnuson Clinical Center, National Institutes of Health, Bethesda, MD 20892, USA.
Transfus Med Rev. 2008 Apr;22(2):97-102. doi: 10.1016/j.tmrv.2008.01.001.
Although remarkable advances have been made in the prevention of the major transfusion-transmitted diseases, long intervals have transpired between the first recognition of transfusion risk and the implementation of a preventive strategy. For hepatitis B virus, that interval was 30 years; for non-A, non-B/hepatitis C virus, 15 years; and for human immunodeficiency virus, West Nile virus, Trypanosoma cruzi, and bacteria, 3, 4, 5, and 18 years, respectively. In our existing reactive approach, there is a fundamental and inevitable delay before we can react; and thus, infections are destined to occur. The continued emergence or reemergence of transfusion-transmitted infections calls for a new paradigm of preemptive pathogen reduction (PR). Two PR systems, psoralen/UV-A and riboflavin/UV-A, have shown efficacy and safety for platelets and plasma; and psoralen/UV-A technology has been successfully implemented for platelets in Europe. Pathogen reduction can eliminate or reduce the risk for any nucleic acid containing agent, including bacteria, and thus will be effective for all but prion diseases. It is possible to introduce PR for platelets and plasma now and to concentrate resources on developing PR for red cells. This will require an intellectual and financial commitment from the National Institutes of Health, the Food and Drug Administration, industry, and the blood bank establishment, just as occurred for nucleic acid testing (NAT) technology. This can be done if there is sufficient will to do it.
尽管在预防主要的输血传播疾病方面已取得显著进展,但从首次认识到输血风险到实施预防策略之间仍间隔了很长时间。对于乙型肝炎病毒,这一间隔为30年;对于非甲非乙型/丙型肝炎病毒,为15年;而对于人类免疫缺陷病毒、西尼罗河病毒、克氏锥虫和细菌,分别为3年、4年、5年和18年。在我们现有的应对方法中,在我们能够做出反应之前存在根本性且不可避免的延迟;因此,感染注定会发生。输血传播感染的持续出现或再次出现需要一种新的预防性病原体灭活(PR)模式。两种PR系统,补骨脂素/紫外线A和核黄素/紫外线A,已在血小板和血浆方面显示出有效性和安全性;并且补骨脂素/紫外线A技术已在欧洲成功应用于血小板。病原体灭活可以消除或降低任何含核酸病原体的风险,包括细菌,因此除朊病毒疾病外对所有疾病均有效。现在有可能对血小板和血浆引入PR,并将资源集中用于开发红细胞的PR。这将需要美国国立卫生研究院、食品药品监督管理局、行业以及血库机构在智力和资金上的投入,就如同核酸检测(NAT)技术那样。如果有足够的意愿去做,这是可以实现的。