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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1989 Jan;86(1):312–316. doi: 10.1073/pnas.86.1.312

Detection of serum hepatitis B virus DNA in patients with chronic hepatitis using the polymerase chain reaction assay.

S Kaneko 1, R H Miller 1, S M Feinstone 1, M Unoura 1, K Kobayashi 1, N Hattori 1, R H Purcell 1
PMCID: PMC286454  PMID: 2643103

Abstract

We compared the sensitivity of the polymerase chain-reaction (PCR) assay to that of slot-blot hybridization for detecting hepatitis B virus (HBV) DNA in the serum of 31 patients with chronic hepatitis. Of 14 chronic hepatitis patients positive for both HBV surface and HBV e antigens, 9 were positive for HBV DNA by slot-blot hybridization and all 14 by PCR. Also, of 9 patients positive for HBV surface antigen and antibody against HBV e antigen, 2 were positive for HBV DNA by slot-blot analysis and 8 by PCR. Finally, in 8 patients positive for HBV DNA by slot-blot hybridization, but 4 were positive by PCR. We find that analysis by the PCR technique provides a greater than 10(4)-fold increase in sensitivity over the slot-blot hybridization assay. This result represents an important breakthrough in sensitivity because it is now possible to detect as few as three HBV DNA genomes per sample of serum.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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