Why the study?
Does the second-generation C200/C22 ELISA improve early detection of HCV antibodies compared to the first-generation C100 ELISA in post-transfusion HCV-infected patients?
Does the second-generation C200/C22 ELISA improve early detection of HCV antibodies compared to the first-generation C100 ELISA in post-transfusion HCV-infected patients?
The second-generation C200/C22 ELISA is more sensitive and detects antibodies earlier than the C100 ELISA during early HCV infection.
May support earlier post-transfusion HCV detection with C200/C22 ELISA; hypothesis-generating and should not yet change practice.
Detection of early antibody to hepatitis C virus (HCV) by a new second- generation C200/C22 anti-HCV enzyme-linked immunosorbent assay (ELISA) and a four-antigen recombinant immunoblot assay (4-RIBA) was compared with the first-generation anti-HCV C100 ELISA using sequential serum samples of 9 recipients who were infected with HCV, as detected by polymerase chain reaction after transfusion of blood products. Within 26 weeks after transfusion, 9/9 (100%) recipients seroconverted with C200/22 ELISA, and 6/9 (67%) seroconverted with C100 ELISA. Compared with C100 ELISA, C200/ C22 ELISA seroconversion occurred simultaneously in 3 cases, 5-6 weeks earlier in 3 other cases, and 20 weeks earlier in 1 case. Seven of 9 (78%) recipients became positive, and 2/9 (22%) became indeterminate with 4-RIBA. In 8 cases with clinical posttransfusion hepatitis non-A, non-B (PTH- NANB), anti-HCV C200/C22 ELISA seroconversion occurred 2-17 (mean 6) weeks after the onset of hepatitis. In 6 cases of PTH-NANB, anti-HCV C100 ELISA seroconversion occurred 2-26 (mean 9) weeks after the onset of hepatitis. It is concluded that the second-generation C200/C22 ELISA is more sensitive than the C100 ELISA for the detection of antibody during early HCV infection. Indeterminate 4-RIBA results are found in the early phase of HCV infection.
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Poel et al. (1992) studied this question.
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