Galel Susan A
Medical Affairs - Donor Screening, Roche Diagnostics Solutions, Pleasanton, California, USA.
Department of Pathology, Stanford University School of Medicine, Stanford, California, USA.
Transfusion. 2024 Dec;64(12):2325-2331. doi: 10.1111/trf.18061. Epub 2024 Nov 6.
Transfusion-transmitted malaria (TTM) is rare in non-endemic areas (non-EAs) but can potentially be fatal. This review analyzes the laboratory results of donors causing TTM in non-EAs, to assess the detectability of their Plasmodium infection by molecular or antibody tests.
TTM cases in the United States, Canada, and Europe since 2010 were identified through a literature review. Authors and laboratories were contacted for missing details about sample types and laboratory methods. Results of Plasmodium polymerase chain reaction (PCR) and antibody tests were summarized.
Twelve cases of TTM and one bone marrow transplant transmission were identified. Of the 13 source donors, 12 were tested by PCR, 10 were positive on at least one sample; the 2 negative donors were tested only on retained segments of blood refrigerated for several weeks. All donors were PCR positive on a fresh sample except one who was positive on a retained but not a fresh sample. These PCRs targeted Plasmodium DNA with sensitivities in the range of 1000-10,000 parasites/mL. Antibody EIA was positive in only three of seven donors tested.
This review found that antibody EIAs failed to detect four of the seven TTM donors tested. DNA-based PCRs were able to detect Plasmodium infection in all donors tested except for two tested only on samples likely to have deteriorated from prolonged storage. Recently developed ribosomal RNA-based molecular donor screening assays are approximately 1000 fold more sensitive than these DNA-based PCRs, holding promise as a potential method to further reduce TTM.
输血传播疟疾(TTM)在非流行地区(非EA)很少见,但可能致命。本综述分析了导致非EA地区TTM的献血者的实验室检测结果,以评估通过分子或抗体检测对其疟原虫感染的可检测性。
通过文献综述确定了2010年以来美国、加拿大和欧洲的TTM病例。与作者和实验室联系,获取有关样本类型和实验室方法的缺失细节。总结了疟原虫聚合酶链反应(PCR)和抗体检测的结果。
确定了12例TTM病例和1例骨髓移植传播病例。在13名源头献血者中,12人接受了PCR检测,10人至少有一个样本呈阳性;2名检测结果为阴性的献血者仅对冷藏数周的留存血液片段进行了检测。除1名在留存样本而非新鲜样本上呈阳性的献血者外,所有献血者的新鲜样本PCR检测均为阳性。这些PCR检测针对疟原虫DNA,灵敏度范围为每毫升1000 - 10000个寄生虫。在接受检测的7名献血者中,只有3人的抗体酶联免疫吸附测定(EIA)呈阳性。
本综述发现,抗体EIA未能检测出接受检测的7名TTM献血者中的4人。基于DNA的PCR能够检测出所有接受检测的献血者中的疟原虫感染,但有两名献血者仅对可能因长期储存而变质的样本进行了检测。最近开发的基于核糖体RNA的分子献血者筛查检测方法比这些基于DNA的PCR灵敏度高约1000倍,有望成为进一步减少TTM的潜在方法。