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本文引用的文献

1
Prevalence of platelet transfusion reactions before and after implementation of leukocyte-depleted platelet concentrates by filtration.采用过滤法制备白细胞去除血小板浓缩物前后血小板输血反应的发生率
Vox Sang. 1993;65(2):103-7. doi: 10.1111/j.1423-0410.1993.tb02124.x.
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Rise of cytomegalovirus antibodies in an infectious-mononucleosis-like syndrome after transfusion.输血后传染性单核细胞增多症样综合征中巨细胞病毒抗体的升高。
Br Med J. 1966 May 21;1(5498):1270-2. doi: 10.1136/bmj.1.5498.1270.
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Prevention of HLA immunization with leukocyte-poor packed red cells and platelet concentrates obtained by filtration.
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Prevention of refractoriness and HLA-alloimmunization using filtered blood products.使用过滤血液制品预防难治性和HLA同种免疫。
Blood. 1988 May;71(5):1402-7.
5
Detection of cytomegalovirus antibody in stored blood products using latex agglutination.采用乳胶凝集法检测储存血液制品中的巨细胞病毒抗体。
Transfusion. 1988 Nov-Dec;28(6):563-5. doi: 10.1046/j.1537-2995.1988.28689059032.x.
6
Successful strategy for prevention of cytomegalovirus interstitial pneumonia after human leukocyte antigen-identical bone marrow transplantation.人类白细胞抗原相合骨髓移植后预防巨细胞病毒间质性肺炎的成功策略。
Rev Infect Dis. 1990 Sep-Oct;12 Suppl 7:S805-10. doi: 10.1093/clinids/12.supplement_7.s805.
7
Cytomegalovirus infections after allogeneic bone marrow transplantation.异基因骨髓移植后的巨细胞病毒感染
Rev Infect Dis. 1990 Sep-Oct;12 Suppl 7:S776-92. doi: 10.1093/clinids/12.supplement_7.s776.
8
The risk of cytomegalovirus infection in solid organ and bone marrow transplant recipients: transfusion of blood products.实体器官和骨髓移植受者巨细胞病毒感染的风险:血液制品的输注
Transfusion. 1990 Sep;30(7):659-66. doi: 10.1046/j.1537-2995.1990.30790385528.x.
9
Limited efficacy of leukopoor platelets for prevention of febrile transfusion reactions.
Am J Clin Pathol. 1991 May;95(5):733-8. doi: 10.1093/ajcp/95.5.733.
10
Detection of cytomegalovirus antibody in platelet concentrates by fluorescence immunoassay and latex agglutination.
Transfusion. 1991 Mar-Apr;31(3):245-8. doi: 10.1046/j.1537-2995.1991.31391165174.x.

血液成分长期储存期间血浆中巨细胞病毒抗体的稳定性。

Stability of cytomegalovirus antibodies in plasma during prolonged storage of blood components.

作者信息

Pappin A, Grissom M, Mackay W, Huang Y, Yomtovian R

机构信息

Department of Pathology, Case Western Reserve University, Cleveland, Ohio.

出版信息

Clin Diagn Lab Immunol. 1995 Jan;2(1):25-9. doi: 10.1128/cdli.2.1.25-29.1995.

DOI:10.1128/cdli.2.1.25-29.1995
PMID:7719908
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC170095/
Abstract

Cytomegalovirus (CMV) antibody testing is currently limited by manufacturers' guidelines to specimens stored for 7 days or less. We examined the stability of CMV antibodies in plasma from platelets and whole-blood units during storage using a rapid, automated, recombinant protein-based immunoassay which qualitatively detects total antibody to human CMV. Testing of single-donor apheresis platelets was performed on baseline serum and platelet-free plasma and on platelet-free plasma 8 days later. Indeterminate, positive, and negative CMV antibody results were maintained over time for 97% (75 of 77) of the platelet specimens. For whole-blood units, initial testing of donor serum and plasma obtained from erythrocyte segments took place within 7 days of phlebotomy. Indeterminate, positive, and negative CMV antibody results were maintained on subsequent analyses performed on erythrocyte segments at 2, 4, 6, and 8 weeks for 100% of whole-blood specimens. An important potential benefit of CMV antibody testing of stored platelets and blood is the elimination of a costly, dedicated, CMV-negative inventory. The study suggests that CMV antibody testing can be conveniently and reliably performed on blood components over the entire storage period.

摘要

目前,根据制造商的指南,巨细胞病毒(CMV)抗体检测仅限于储存7天或更短时间的标本。我们使用一种快速、自动化的基于重组蛋白的免疫测定法,对血小板和全血单位血浆中CMV抗体在储存期间的稳定性进行了检测,该方法可定性检测人CMV总抗体。对单采血小板供者的基线血清和无血小板血浆以及8天后的无血小板血浆进行检测。97%(77份中的75份)血小板标本的CMV抗体结果在一段时间内保持不确定、阳性和阴性。对于全血单位,在采血后7天内对从红细胞段获得的供者血清和血浆进行初始检测。对于100%的全血标本,在第2、4、6和8周对红细胞段进行的后续分析中,CMV抗体结果保持不确定、阳性和阴性。对储存的血小板和血液进行CMV抗体检测的一个重要潜在好处是无需保留昂贵的专用CMV阴性库存。该研究表明,在整个储存期内都可以方便、可靠地对血液成分进行CMV抗体检测。