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Hepatitis C virus: Quantitation and distribution in liver

The optimal method for viral quantitation and the most appropriate site for determining viral load in patients with chronic hepatitis C virus (HCV) infection are unknown. We developed a method for measuring HCV RNA in the liver with the following features: 1) efficient extraction of RNA from tissue...

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Published in:Journal of medical virology 1997-03, Vol.51 (3), p.217-224
Main Authors: Terrault, Norah A., Dailey, Peter J., Ferrell, Linda, Collins, Mark L., Wilber, Judith C., Urdea, Mickey S., Bhandari, Bhupinder N., Wright, Teresa L.
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container_title Journal of medical virology
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creator Terrault, Norah A.
Dailey, Peter J.
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Bhandari, Bhupinder N.
Wright, Teresa L.
description The optimal method for viral quantitation and the most appropriate site for determining viral load in patients with chronic hepatitis C virus (HCV) infection are unknown. We developed a method for measuring HCV RNA in the liver with the following features: 1) efficient extraction of RNA from tissue (89% of RNA recovered); 2) accurate amplification using branched DNA with strong concordance between a single sample tested on multiple occasions either in the same or in different runs; 3) good sensitivity (95%) and specificity (100%). HCV RNA was detected in as little as 2 mg of tissue, and viral load determined in a needle biopsy was representative of viral load in other parts of the liver. Within individual livers, 68% of the samples quantitated were within 1.5‐fold of the geometric mean, and 95% were within 2.2‐fold of the geometric mean. The mean ratio of virus in the liver and serum was 103, range 17.4–286. A delay of 30 minutes before freezing the liver tissue resulted in a reduction in the measured viral load in some, but not all instances. A sensitive, specific, and reproducible method for quantitating HCV RNA in the liver has been developed. Measurement of viral load at one site was representative of viral load at other sites. While hepatic HCV RNA levels are consistently greater than serum levels, the ratio of liver to serum viral load varies widely. The clinical use of measurement of viral load in the liver remains to be defined. J. Med. Virol. 51:217–224, 1997. © 1997 Wiley‐Liss, Inc.
doi_str_mv 10.1002/(SICI)1096-9071(199703)51:3<217::AID-JMV13>3.0.CO;2-H
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We developed a method for measuring HCV RNA in the liver with the following features: 1) efficient extraction of RNA from tissue (89% of RNA recovered); 2) accurate amplification using branched DNA with strong concordance between a single sample tested on multiple occasions either in the same or in different runs; 3) good sensitivity (95%) and specificity (100%). HCV RNA was detected in as little as 2 mg of tissue, and viral load determined in a needle biopsy was representative of viral load in other parts of the liver. Within individual livers, 68% of the samples quantitated were within 1.5‐fold of the geometric mean, and 95% were within 2.2‐fold of the geometric mean. The mean ratio of virus in the liver and serum was 103, range 17.4–286. A delay of 30 minutes before freezing the liver tissue resulted in a reduction in the measured viral load in some, but not all instances. A sensitive, specific, and reproducible method for quantitating HCV RNA in the liver has been developed. 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identifier ISSN: 0146-6615
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subjects Adult
Aged
Bile Ducts - pathology
Bile Ducts - virology
Biological and medical sciences
Biopsy, Needle
Female
Hepacivirus - isolation & purification
Hepatitis C - blood
Hepatitis C - pathology
Hepatitis C - surgery
hepatitis C virus
Human viral diseases
Humans
Infectious diseases
Inflammation
liver
Liver - pathology
Liver - virology
Liver Transplantation
Male
Medical sciences
Middle Aged
Polymerase Chain Reaction - methods
RNA, Viral - analysis
RNA, Viral - blood
Sensitivity and Specificity
Specimen Handling
Viral diseases
Viral hepatitis
viral quantitation
title Hepatitis C virus: Quantitation and distribution in liver
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