Determining the Cause of Discrepant Results in HCV NAT Comparative Tests.
- Author:
Hyun Jin CHO
1
;
Jae Sook LEE
;
Myung Han KIM
;
Kwang HUH
;
Quehn PARK
;
Nam Sun CHO
Author Information
1. Central Blood Laboratory Center, The Republic of Korean Red Cross, Seoul, Korea. bs510@redcross.or.kr
- Publication Type:Original Article
- Keywords:
NAT;
HCV;
Comparative test
- MeSH:
Blood Donors;
Genotype;
Humans;
Mass Screening;
Plasma;
Red Cross;
RNA;
Uronic Acids;
Viral Load
- From:Korean Journal of Blood Transfusion
2010;21(1):36-42
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
BACKGROUND: The Korean Red Cross blood laboratory centers have been performing comparative tests for NAT reactive specimens since February 2005. However, five discrepant specimens were found in HCV-diluted specimens between 2007 and 2008 and the reasons for this has been investigated. METHODS: For the five discrepant specimens, the HCV RNA concentration was measured in 5 tubes for each speciment. Subsequently, in order to compare the sensitivity of the low titer specimens measured by RT-PCR and TMA, comparative tests of diluted samples were examined six times per sample. Finally, the genotype was tested in order to determine the characteristics of the discrepant samples. RESULTS: Result of the quantitative tests for HCV RNA demonstrated that aliquots of the plasma bag were homogenous in term of viral load quantitation. As a result of the comparative test, all samples were found to contain over 1.0x10(1) IU/mL as detected by the two analytical systems. In contrast, those less than 1.0x10(1) IU/mL were not entirely detected by the two systems. CONCLUSION: It was impossible to completely detect using the two NAT system and the detection rates for both systems were equivalent for the samples examined. In particular, with respect to HCV, it may be undetectable on the NAT test because viral load decreases rapidly before and after sero-conversion. This result indicates that anti-HCV and NAT should be performed together as an HCV screening test prior to blood donation.
