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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 |
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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. 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.</description><identifier>ISSN: 0146-6615</identifier><identifier>EISSN: 1096-9071</identifier><identifier>DOI: 10.1002/(SICI)1096-9071(199703)51:3<217::AID-JMV13>3.0.CO;2-H</identifier><identifier>PMID: 9139087</identifier><identifier>CODEN: JMVIDB</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>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</subject><ispartof>Journal of medical virology, 1997-03, Vol.51 (3), p.217-224</ispartof><rights>Copyright © 1997 Wiley‐Liss, Inc.</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c4613-fe7c8f73203d4300366b86f487e1a105b68779102e6ab6771ac4c2772d26b42b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2590012$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9139087$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Terrault, Norah A.</creatorcontrib><creatorcontrib>Dailey, Peter J.</creatorcontrib><creatorcontrib>Ferrell, Linda</creatorcontrib><creatorcontrib>Collins, Mark L.</creatorcontrib><creatorcontrib>Wilber, Judith C.</creatorcontrib><creatorcontrib>Urdea, Mickey S.</creatorcontrib><creatorcontrib>Bhandari, Bhupinder N.</creatorcontrib><creatorcontrib>Wright, Teresa L.</creatorcontrib><title>Hepatitis C virus: Quantitation and distribution in liver</title><title>Journal of medical virology</title><addtitle>J. Med. Virol</addtitle><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.</description><subject>Adult</subject><subject>Aged</subject><subject>Bile Ducts - pathology</subject><subject>Bile Ducts - virology</subject><subject>Biological and medical sciences</subject><subject>Biopsy, Needle</subject><subject>Female</subject><subject>Hepacivirus - isolation & purification</subject><subject>Hepatitis C - blood</subject><subject>Hepatitis C - pathology</subject><subject>Hepatitis C - surgery</subject><subject>hepatitis C virus</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Inflammation</subject><subject>liver</subject><subject>Liver - pathology</subject><subject>Liver - virology</subject><subject>Liver Transplantation</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Polymerase Chain Reaction - methods</subject><subject>RNA, Viral - analysis</subject><subject>RNA, Viral - blood</subject><subject>Sensitivity and Specificity</subject><subject>Specimen Handling</subject><subject>Viral diseases</subject><subject>Viral hepatitis</subject><subject>viral quantitation</subject><issn>0146-6615</issn><issn>1096-9071</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><recordid>eNqFkVFv0zAUhSMEGt3gJyDlAaHtIeVeO7HjApOmwNZOK9XEGI9XTuJIZmla7Gawf0-yRH0BaU-Wjo8_HX0Ogk8IUwRg74-_LbLFCYISkQKJx6iUBH6S4Ix_ZChns7PF5-hyeYv8lE9hmq0-sGj-LJjsXzwPJoCxiITA5GVw6P1PAEgVYwfBgUKuIJWTQM3NVu_szvowC--ta_0svG5100VdvGlC3ZRhaf3O2bx9DGwT1vbeuFfBi0rX3rwez6Pg-_mXm2weXa0uFtnZVVTEAnlUGVmkleQMeBlzAC5EnooqTqVBjZDkIpVSITAjdC6kRF3EBZOSlUzkMcv5UfBu4G7d5ldr_I7W1hemrnVjNq0nmaZprIR6soiJSpBhXxyXFm7jvTMVbZ1da_dACNS7J-rdU2-SepM0uKcEiVPnnqhzT4_uuwAoWxGjecd9Mw5o87Up99RRdnf_drzXvtB15XRTWL-vsUQBIOtqt0Ptt63Nwz_bnpj2v2VD0IGjAdx9p_mzB2t3R0JymdCPrxd0c80ul8jPacn_AlqeuGU</recordid><startdate>199703</startdate><enddate>199703</enddate><creator>Terrault, Norah A.</creator><creator>Dailey, Peter J.</creator><creator>Ferrell, Linda</creator><creator>Collins, Mark L.</creator><creator>Wilber, Judith C.</creator><creator>Urdea, Mickey S.</creator><creator>Bhandari, Bhupinder N.</creator><creator>Wright, Teresa L.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>199703</creationdate><title>Hepatitis C virus: Quantitation and distribution in liver</title><author>Terrault, Norah A. ; Dailey, Peter J. ; Ferrell, Linda ; Collins, Mark L. ; Wilber, Judith C. ; Urdea, Mickey S. ; Bhandari, Bhupinder N. ; Wright, Teresa L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4613-fe7c8f73203d4300366b86f487e1a105b68779102e6ab6771ac4c2772d26b42b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Bile Ducts - pathology</topic><topic>Bile Ducts - virology</topic><topic>Biological and medical sciences</topic><topic>Biopsy, Needle</topic><topic>Female</topic><topic>Hepacivirus - isolation & purification</topic><topic>Hepatitis C - blood</topic><topic>Hepatitis C - pathology</topic><topic>Hepatitis C - surgery</topic><topic>hepatitis C virus</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Inflammation</topic><topic>liver</topic><topic>Liver - pathology</topic><topic>Liver - virology</topic><topic>Liver Transplantation</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Polymerase Chain Reaction - methods</topic><topic>RNA, Viral - analysis</topic><topic>RNA, Viral - blood</topic><topic>Sensitivity and Specificity</topic><topic>Specimen Handling</topic><topic>Viral diseases</topic><topic>Viral hepatitis</topic><topic>viral quantitation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Terrault, Norah A.</creatorcontrib><creatorcontrib>Dailey, Peter J.</creatorcontrib><creatorcontrib>Ferrell, Linda</creatorcontrib><creatorcontrib>Collins, Mark L.</creatorcontrib><creatorcontrib>Wilber, Judith C.</creatorcontrib><creatorcontrib>Urdea, Mickey S.</creatorcontrib><creatorcontrib>Bhandari, Bhupinder N.</creatorcontrib><creatorcontrib>Wright, Teresa L.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of medical virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Terrault, Norah A.</au><au>Dailey, Peter J.</au><au>Ferrell, Linda</au><au>Collins, Mark L.</au><au>Wilber, Judith C.</au><au>Urdea, Mickey S.</au><au>Bhandari, Bhupinder N.</au><au>Wright, Teresa L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hepatitis C virus: Quantitation and distribution in liver</atitle><jtitle>Journal of medical virology</jtitle><addtitle>J. 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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. 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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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