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病原体灭活方法:优势与局限

Pathogen-reduction methods: advantages and limits.

作者信息

Klein H G, Bryant B J

机构信息

Department of Transfusion Medicine, Clinical Center, National Institutes of Health, Bethesda, MD 20892, USA.

Blood Bank division, Department of Pathology, University of Texas at Galveston, Galveston, TX, USA.

出版信息

ISBT Sci Ser. 2009 Mar;4(1):154-160. doi: 10.1111/j.1751-2824.2009.01224.x. Epub 2009 Feb 13.

DOI:10.1111/j.1751-2824.2009.01224.x
PMID:32328162
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7169281/
Abstract

Pathogen-reduction (inactivation) provides a proactive approach to reducing transfusion-transmitted infection. Pathogen-reduction technologies have been successfully implemented by plasma fractionators resulting in no transmission of human immunodeficiency, hepatitis C, or hepatitis B viruses by US-licensed plasma derivatives since 1987. Fractionation technologies cannot be used to treat cellular blood components. Although blood donor screening, deferral and disease testing have drastically reduced the incidence of transfusion-transmitted diseases, the threat of new or re-emerging pathogens remains. Of particular concern is the silent emergence of a new agent with a prolonged latent period in which asymptomatic infected carriers would donate and spread infection. The ultimate goal of pathogen-inactivation is to reduce transmission of potential pathogens without significantly compromising the therapeutic efficacy of the cellular and protein constituents of blood. The acceptable technology must not introduce toxicities into the blood supply nor result in neoantigen formation and subsequent antibody production. Several promising pathogen-inactivation technologies are being developed and tested, and others are currently in use, but all of them have limits. Pathogen-reduction promises an additional 'layer of protection' from infectious agents and has the potential to impact the safety of blood transfusions worldwide.

摘要

病原体灭活(失活)为减少输血传播感染提供了一种积极主动的方法。自1987年以来,病原体灭活技术已被血浆分馏商成功应用,美国获批的血浆衍生物未出现人类免疫缺陷病毒、丙型肝炎病毒或乙型肝炎病毒的传播。分馏技术不能用于处理细胞血液成分。尽管对献血者的筛查、延期献血和疾病检测已大幅降低了输血传播疾病的发生率,但新出现或再次出现的病原体的威胁依然存在。特别令人担忧的是,一种潜伏期延长的新型病原体悄然出现,无症状感染携带者会献血并传播感染。病原体灭活的最终目标是减少潜在病原体的传播,同时又不会显著损害血液中细胞和蛋白质成分的治疗效果。可接受的技术不得将毒性引入血液供应中,也不得导致新抗原形成及随后的抗体产生。目前正在研发和测试几种有前景的病原体灭活技术,其他一些技术也正在使用,但它们都有局限性。病原体灭活有望为防范感染因子提供额外的“一层保护”,并有可能影响全球输血的安全性。

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本文引用的文献

1
Pathogen inactivation: making decisions about new technologies. Report of a consensus conference.病原体灭活:关于新技术的决策。共识会议报告。
Transfusion. 2007 Dec;47(12):2338-47. doi: 10.1111/j.1537-2995.2007.01512.x.
2
A process for solvent/detergent treatment of plasma for transfusion at blood centers that use a disposable-bag system.一种在使用一次性袋系统的血库中对用于输血的血浆进行溶剂/去污剂处理的方法。
Transfusion. 2006 Dec;46(12):2100-8. doi: 10.1111/j.1537-2995.2006.01035.x.
3
Photochemically treated fresh frozen plasma for transfusion of patients with acquired coagulopathy of liver disease.光化学处理的新鲜冰冻血浆用于肝病获得性凝血病患者的输血。
Blood. 2006 May 1;107(9):3753-60. doi: 10.1182/blood-2004-03-0930. Epub 2006 Jan 12.
4
Clearance of prions during plasma protein manufacture.血浆蛋白制造过程中朊病毒的清除
Transfus Med Rev. 2006 Jan;20(1):57-62. doi: 10.1016/j.tmrv.2005.08.005.
5
Clinical safety of platelets photochemically treated with amotosalen HCl and ultraviolet A light for pathogen inactivation: the SPRINT trial.用盐酸氨甲环酸和紫外线A光进行光化学处理的血小板用于病原体灭活的临床安全性:SPRINT试验
Transfusion. 2005 Dec;45(12):1864-75. doi: 10.1111/j.1537-2995.2005.00639.x.
6
Removal of exogenous (spiked) and endogenous prion infectivity from red cells with a new prototype of leukoreduction filter.使用新型白细胞滤除过滤器原型从红细胞中去除外源性(添加的)和内源性朊病毒感染性。
Transfusion. 2005 Dec;45(12):1839-44. doi: 10.1111/j.1537-2995.2005.00640.x.
7
Therapeutic efficacy and safety of red blood cells treated with a chemical process (S-303) for pathogen inactivation: a Phase III clinical trial in cardiac surgery patients.经化学处理(S-303)进行病原体灭活的红细胞的治疗效果及安全性:一项针对心脏手术患者的III期临床试验
Transfusion. 2005 Nov;45(11):1739-49. doi: 10.1111/j.1537-2995.2005.00583.x.
8
Meeting transfusion safety expectations.满足输血安全期望。
Ann Intern Med. 2005 Oct 4;143(7):537-8. doi: 10.7326/0003-4819-143-7-200510040-00012.
9
Fresh frozen plasma prepared with amotosalen HCl (S-59) photochemical pathogen inactivation: transfusion of patients with congenital coagulation factor deficiencies.用盐酸氨甲环酸(S-59)光化学病原体灭活法制备的新鲜冰冻血浆:用于先天性凝血因子缺乏患者的输血治疗
Transfusion. 2005 Aug;45(8):1362-72. doi: 10.1111/j.1537-2995.2005.00216.x.
10
Blood supply and demand.血液供应与需求。
Lancet. 2005;365(9478):2151.