Clinical performance of a new multiplex assay for the detection of HIV-1, HIV-2, HCV, HBV, and HEV in blood donations in Catalonia (Spain)

被引:4
|
作者
Sauleda, Silvia [1 ,2 ,3 ]
Bes, Marta [1 ,2 ,3 ]
Piron, Maria [1 ,2 ,3 ]
Ong, Edgar [4 ]
Coco, Sonia Bakkour [5 ]
Carrio, Jaume [6 ]
Linnen, Jeffrey M. [4 ,7 ]
机构
[1] Banc Sang & Teixits Catalunya Blood & Tissue Bank, Transfus Safety Lab, Barcelona, Spain
[2] Inst Salud Carlos III, Ctr Invest Biomed Red Enfermedades Hepat & Digest, Madrid, Spain
[3] Vall Hebron Inst Recerca VHIR, Transfus Med Grp, Barcelona, Spain
[4] Grifols Diagnost Solut Inc, San Diego, CA USA
[5] Grifols Diagnost Solut Inc, Emeryville, CA USA
[6] Grifols SA, Sant Cugat Del Valles, Spain
[7] Grifols Diagnost Solut Inc, 10804 Willow Court, San Diego, CA 92127 USA
关键词
HEPATITIS-E VIRUS; INFECTION;
D O I
10.1111/trf.17518
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Commercial multiplex nucleic acid tests (NATs) for HIV-1/HIV-2/HCV/HBV are widely used in developed countries to screen blood donations. HEV NAT screening has been implemented in some blood banks but is tested with a different assay.Study Design and Methods: This study describes the clinical sensitivity and specificity of the Procleix (R) UltrioPlex E (UPxE) assay on the automated Procleix Panther (R) system for the simultaneous detection of HIV-1/HIV-2/HCV/HBV/HEV. To evaluate routine performance, 10,138 donations were tested in parallel with UPxE (in ID-NAT) and current assays (Procleix Ultrio Elite [UE] assay in ID-NAT and Procleix HEV assay in pool of 16). To assess clinical sensitivity, archived donations positive for HCV, HIV-1, HBV, HEV, or occult HBV infection (OBI) were tested (n = 104-186).Results: Five donations were initially reactive (IR) with UPxE; none of them were reactive with current assays. Two of the three samples IR for HIV-1/HIV-2/HCV/HBV were confirmed positive for HBV (HBV NAT and/or anti-HBV core positive) and classified as OBI. The two samples IR for HEV were confirmed positive (Procleix HEV assay in ID-NAT and in-house RT-PCR HEV assay). One sample IR for HIV-1/HIV-2/HCV/HBV with UPxE and another with UE were not confirmed. UPxE showed a specificity of 99.99% for HIV-1/HIV-2/HCV/HBV and 100% for HEV. Comparable sensitivities were observed for HIV-1, HCV, HBV, OBI, and HEV samples tested in the UPxE, UE, and Procleix HEV assays.Discussion: UPxE may provide an efficient solution for the simultaneous detection of HIV-1, HIV-2, HCV, HBV, and HEV in blood donations in a single test.
引用
收藏
页码:2098 / 2105
页数:8
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