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Series GSE40223 Query DataSets for GSE40223
Status Public on Oct 22, 2012
Title The blood transcriptional signature of chronic HCV [Illumina data]
Organism Homo sapiens
Experiment type Expression profiling by array
Summary This study characterizes the effects of chronic Hepatitis C virus (HCV) infection on gene expression by analyzing blood samples from 10 treatment-naive HCV patients and 6 healthy volunteers.
Differential expression analysis of microarray data from peripheral blood mononuclear cells (PBMCs) identified a 136 gene signature, including 66 genes elevated in infected individuals. Most of the up-regulated genes were associated with interferon (IFN) activity (including members of the OAS and MX families, ISG15 and IRF7), suggesting an ongoing immune response. This HCV signature was also found to be consistently enriched in many other viral infection and vaccination datasets. Validation of these genes was carried out using a second cohort composed of 5 HCV patients and 5 healthy volunteers, confirming the up-regulation of the IFN signature. In summary, this is the first study to directly compare blood transcriptional profiles from HCV patients with healthy controls. The results show that chronic HCV infection has a pronounced effect on gene expression in PBMCs of infected individuals, and significantly elevates the expression of a subset of interferon-stimulated genes.
 
Overall design Treatment-naïve HCV patients were recruited by hepatologists in the outpatient hepatitis clinic within the Yale Liver Center. Healthy volunteers were recruited from Yale’s PhenoGenetic Cohort of Healthy controls. PBMCs were isolated from whole blood by density gradient centrifugation using Ficoll-Paque (GE Healthcare) centrifugation. Total RNA was isolated from PBMCs using an RNeasy kit (Qiagen, Valencia, CA), and the quality of total RNA was evaluated by A260/A280 ratio and by electrophoresis on an Agilent Bioanalyzer. All subsequent processing, hybridization to the Illumina HumanHT-12 microarray, and quality control analyses were carried out by the Yale Center for Genome Analysis using standard protocols.
 
Contributor(s) Bolen CR, Robek MD, Brodsky L, Schulz V, Lim J, Taylor MW, Kleinstein SH
Citation(s) 23067362
Submission date Aug 20, 2012
Last update date Aug 13, 2018
Contact name Christopher Bolen
E-mail(s) cbolen1@gmail.com
Organization name Yale University
Department Pathology
Lab Steven Kleinstein
Street address 300 George Street, Suite 505
City New Haven
State/province CT
ZIP/Postal code 06511
Country USA
 
Platforms (1)
GPL10558 Illumina HumanHT-12 V4.0 expression beadchip
Samples (10)
GSM988557 Healthy_SK11 [Illumina]
GSM988558 Healthy_SK35 [Illumina]
GSM988559 Healthy_SK59 [Illumina]
This SubSeries is part of SuperSeries:
GSE40224 The blood transcriptional signature of chronic HCV
Relations
BioProject PRJNA173227

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE40223_RAW.tar 26.2 Mb (http)(custom) TAR
GSE40223_non-normalized.txt.gz 3.6 Mb (ftp)(http) TXT
Processed data included within Sample table

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