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Hepatitis B NAT virus‐positive blood donors in the early and late stages of HBV infection: analyses of the window period and kinetics of HBV DNA
Author(s) -
Yoshikawa Akira,
Gotanda Yuhko,
Itabashi Masako,
Minegishi Kiyoshi,
Kanemitsu Kimihiro,
Nishioka Kusuya
Publication year - 2005
Publication title -
vox sanguinis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.68
H-Index - 83
eISSN - 1423-0410
pISSN - 0042-9007
DOI - 10.1111/j.1423-0410.2005.00602.x
Subject(s) - nat , window period , virology , hbsag , hepatitis b virus , viral load , immunoassay , hepatitis b , medicine , multiplex , virus , biology , immunology , serology , antibody , genetics , computer network , computer science
Background and Objectives The Japanese Red Cross (JRC) carries out nucleic acid amplification testing (NAT) for hepatitis B virus (HBV), hepatitis C virus (HCV) and human immunodeficiency virus‐1 (HIV‐1) by using a multiplex (MPX) reagent. Screening is undertaken on serologically negative units. In this study we characterized HBV NAT‐positive donations individually and analysed the window period and kinetics of HBV DNA, during acute infection, in follow‐up studies. Materials and Methods Two hundred and seventy‐seven HBV DNA‐positive donations have been identified in Japan since the introduction of NAT screening of 50‐donation minipools. The viral loads and genotypes of these HBV DNA‐positive donations were characterized. The doubling time and half‐life of HBV was estimated from the data of 123 follow‐up donors. The sensitivity of the NAT system (based on 50‐donation minipools) was compared with the sensitivities of the enzyme immunoassay (EIA) and the chemiluminescence immunoassay (CLIA). Samples that were CLIA negative, but with > 10 4 copies/ml of HBV DNA, were analysed by sequencing the hepatitis B surface antigen (HBsAg) region. Results Out of 277 HBV NAT‐positive samples, 125 (45%) were found to have an increasing viral load and 45 (16%) a decreasing viral load. Forty per cent of HBV NAT‐positive samples with an increasing viral load, and 33% of those with a decreasing viral load, were negative when tested by using the CLIA. No mutations related to escape mutants were found in the samples that were CLIA negative but with HBV DNA loads of > 10 4 copies/ml. The median HBV doubling time was 2·6 days ( n = 93, 1·3–15·2 days) and the half‐life was 1·6 days ( n = 55, 0·9–6·3 days). Some kinetic difference was observed between genotypes A and B. Conclusions HBV NAT screening detected HBV DNA in both early (the so‐called serological window period) and late stages of acute HBV infection.