As previously described,9 to define HCV infection status, we first tested for HCV antibody by the HCV version 3.0 enzyme-linked immunosorbent assay Test System (Ortho-Clinical Diagnostics,

Raritan, NJ). Participants who were positive by HCV enzyme immunoassay were considered to have been infected with HCV and those with sufficient archived plasma (n = 2,073) were tested for HCV viremia by a branched-chain DNA assay (bDNA) (VERSANT HCV RNA 3.0 Assay, analytic sensitivity 2.5 × 103 copies/mL; Bayer-Diagnostics, Tarrytown, NY). Those positive for HCV RNA were considered to have chronic HCV infection and those with a negative result were considered to have resolved HCV infection. Methods of testing for HIV-1 and HBV infection status in these subjects have been described.9 Total nucleic acid was isolated from 500 μL of serum (Roche MagNa EPZ-6438 mw Pure LC Total Nucleic Acid Isolation Kit-Large Volume; Roche Diagnostics Corporation, Indianapolis, IN), and reverse transcription (RT) was performed. Polymerase chain reaction (PCR)

was carried out in a reaction mixture containing 3 μL of complementary DNA, 10 μL of HotStar Taq Master Mix Tamoxifen supplier (Qiagen, Valencia, CA), and 1 μL of each of the following primers: forward 5′- TGGGGTTCTCGTATGATACCC-3′ and reverse 5′-CCTGGTCATAGCCTCCGTGAA-3′, to amplify the 5′-NS5B (nonstructural 5B protein) region. PCR product was purified with Exosap-IT (USB Corporation, Cleveland, OH) and combined with 2.0 μL of Big MCE公司 Dye terminator (ABI Prism Big Dye Terminator Cycle Sequencing Ready Reaction Kit v3.1; Applied Biosystems, Foster City, CA) and 100 pmol of primer forward (5′-NC or 5′-NS5B). The sequencing reaction was carried out for 30 cycles, and electrophoresis was performed on an ABI Prism 3730 XL instrument (Genewiz, South Plainfield, NJ). Raw sequence data were analyzed by Sequencher 4.8 Gene codes to trim ambiguous sequences. To query HCV genotype, sequences were compared to an HCV database operated by the Los Alamos National Laboratory (available at: http://hcv.lanl.gov/content/sequence/BASIC_BLAST/basic_blast.html) using BLAST. Viral genotype

call was based on the highest score and lowest e-value, using the NS5B sequence, unless those results were negative or missing, in which case genotype was based on the 5′NC region. DNA was extracted from cryopreserved lymphocytes using a modified salt precipitation-extraction method (Gentra Systems, Minneapolis, MN) or from granulocytes using a silica membrane-binding method using Qiagen DNA purification columns (Qiagen). The NCI Core Genotyping Facility performed genotyping for IL28B rs12979860 using an optimized TaqMan assay (available at: http://variantgps.nci.nih.gov/cgfseq/pages/snp500.do). All analyses were cross-sectional and based on a single study visit. We determined median HCV RNA levels (log10 copies/mL) overall and among subgroups.