J Virol Methods. 1999 Jun;80(1):33-44. Unique Identifier : AIDSLINE
This study was undertaken in order to determine whether screening of
viremic blood donations by testing of pooled donor samples could
constitute a technically feasible transfusional safety measure. A pilot
study of real-time simulation, on a day-to-day basis, of screening of
three viral genomes (hepatitis B virus (HBV), hepatitis C virus (HCV)
and human immunodeficiency virus (HIV)) was conducted by five French
Blood Centers on plasma samples collected from blood donors and studied
within undiluted samples and within sample pools of various sizes. This
study was carried out within time conditions compatible with the release
of platelets. For the detection of HCV and HIV genomes, the five
laboratories achieved a sensitivity that decreased with the size of the
sample pool. Four were successful in detecting all undiluted samples. In
the 1/10 diluted samples, four failed to detect one HIV or HCV sample.
In the 1/100 diluted samples, all laboratories failed to detect one or
more HIV or HCV samples. For HBV genome, no participating laboratories
detected all of the samples of the panel, even undiluted samples, and
the sample pooling considerably affected sensitivity. The improvement
and standardization of assays needs to be attained, and training of
laboratories appears to be a step crucial for routine screening of viral
genomes in blood donations.
JOURNAL ARTICLE MULTICENTER STUDY Blood/VIROLOGY *Blood Donors
*Genome, Viral Hepatitis B Virus/GENETICS/*ISOLATION & PURIF Hepatitis
C-Like Viruses/GENETICS/*ISOLATION & PURIF Human
HIV/GENETICS/*ISOLATION & PURIF Mass Screening/METHODS Pilot Projects
Polymerase Chain Reaction Sensitivity and Specificity Time Factors
Viral Load