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Links from GEO DataSets

Items: 18

1.

The blood transcriptional signature of chronic HCV [Illumina data]

(Submitter supplied) 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. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
10 Samples
Download data: TXT
Series
Accession:
GSE40223
ID:
200040223
2.

The blood transcriptional signature of chronic HCV

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by array
Platforms:
GPL10558 GPL96
28 Samples
Download data: CEL
Series
Accession:
GSE40224
ID:
200040224
3.

The blood transcriptional signature of chronic HCV [Affymetrix data]

(Submitter supplied) 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. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL96
18 Samples
Download data: CEL
Series
Accession:
GSE40184
ID:
200040184
4.

Expression profiling of peripheral blood of chronic HCV infection

(Submitter supplied) In the present study, we studied chronic HCV patients who responded to IFN-based therapy as evidenced by absence of HCV RNA at the end of treatment, and focused on two issues that have not received much attention. Firstly, we evaluated whether specific genes or gene expression patterns in blood were able to distinguish responder patients with a viral relapse from responder patients who remained virus-negative after cessation of treatment. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
79 Samples
Download data: CEL
Series
Accession:
GSE59312
ID:
200059312
5.

Impaired TLR3-mediated immune responses from macrophages of patients chronically infected with Hepatitis C virus

(Submitter supplied) Hepatitis C virus (HCV) is the most common chronic blood-borne infection in the United States with the majority of patients becoming chronically infected and a subset (20%) progressing to cirrhosis and hepatocellular carcinoma. Individual variations in immune responses may help define successful resistance to infection with HCV. We have examined the immune response in primary macrophages from patients who have spontaneously cleared HCV (viral load negative, VL-, n = 37) compared to HCV genotype 1 chronically infected (VL+) subjects (n=32) and found that macrophages from VL- subjects have an elevated baseline expression of Toll-like receptor 3 (TLR3). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
80 Samples
Download data: TXT
Series
Accession:
GSE40812
ID:
200040812
6.

Longitudinal transcriptomic characterization of the immune response to acute hepatitis C virus infection

(Submitter supplied) Most individuals exposed to hepatitis C virus (HCV) become persistently infected while a minority spontaneously eliminate the virus. Although early immune events influence infection outcome, the cellular composition, molecular effectors, and timeframe of the host response active shortly after viral exposure remain incompletely understood. Employing specimens collected from people who inject drugs (PWID) with high risk of HCV exposure, we utilized RNA-Seq to characterize immune function in peripheral blood before, during, and after acute HCV infection resulting in spontaneous resolution. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL16791
53 Samples
Download data: TXT
7.

Single-cell transcriptomic analyses of T cells in chronic HCV-infected patients dominated by DAA-induced interferon signaling changes

(Submitter supplied) Chronic infection with HCV is manifested by dysregulation of innate immune responses and impaired T cell function at multiple levels. These changes may impact susceptibility to other infections, responsiveness to antiviral therapies, vaccine responsiveness, and development of complications such as hepatocellular carcinoma. Highly effective direct-acting antiviral (DAA) therapy has revolutionized the management of chronic HCV, with expected cure rates exceeding 95%. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
21 Samples
Download data: MTX, TSV
Series
Accession:
GSE178756
ID:
200178756
8.

Interferon alfa regulated gene expression in patients initiating interferon treatment for chronic hepatitis C

(Submitter supplied) Interferon alfa (IFN-alpha) is an approved therapeutic agent for chronic hepatitis C. To directly characterize the effects of IFN-alpha in humans, we used microarrays to profile gene expression in peripheral blood mononuclear cells (PBMCs) from hepatitis C patients treated with IFN-alpha. Seven patients were studied using two strategies: (1) in vivo: PBMCs were collected immediately before the first dose of IFN-alpha, and 3 and 6 hours after the dose; (2) ex vivo: PBMCs that were collected before the first IFN-alpha dose were incubated with IFN-alpha for 3 and 6 hours. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
4 related Platforms
46 Samples
Download data
Series
Accession:
GSE4134
ID:
200004134
9.

IFN alpha-induced gene expression in human NK cells

(Submitter supplied) NK cells are believed to contribute to the control of hepatitis C virus infection and pathogenesis of liver disease. Standard treatment of both acute and chronic hepatitis C is based on the administration of interferon alpha, however, the effects of type I interferons on human NK cells have not been studied in the context of hepatitis C. We therefore first performed a microarray screen for genes differentially regulated in human NK cells after stimulation of PBMC with recombinant interferon alpha-2b. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4163
Platform:
GPL570
4 Samples
Download data: CEL
Series
Accession:
GSE15743
ID:
200015743
10.
Full record GDS4163

Recombinant Interferon α effect on natural killer cells in vitro

Analysis of natural killer (NK) cells sorted from healthy donor peripheral blood mononuclear cells (PBMCs) stimulated for 6h in media containing 1 or 100 ng/ml recombinant interferon (IFN)-alpha-2b. Results provide insight into the effects of type I IFNs on NK cells.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 2 agent, 3 dose, 2 growth protocol sets
Platform:
GPL570
Series:
GSE15743
4 Samples
Download data: CEL
DataSet
Accession:
GDS4163
ID:
4163
11.

Comparison of Huh6 and Huh7 cells under IFNgamma treatment

(Submitter supplied) All major types of interferon (IFN) efficiently inhibit hepatitis C virus (HCV) replication in vitro and in vivo. Remarkably, HCV replication is not sensitive to IFNγ in the hepatoma cell line Huh6, despite an intact signaling pathway. We performed transcriptome analyses between Huh6 and Huh-7 to identify effector genes of the IFNγ response and thereby identified the DExD/H box helicase DDX60L as a restriction factor of HCV replication. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
7 Samples
Download data: CEL
Series
Accession:
GSE68927
ID:
200068927
12.

Gene expression programs in PBMCs elicited by 6 major mediators of the immune response.

(Submitter supplied) Abstract: Background Interferons are key modulators of the immune system, and are central to the control of many diseases. The response of immune cells to stimuli in complex populations is the product of direct and indirect effects, homotypic and heterotypic cell interactions. Dissecting the global transcriptional profiles of immune cell populations may provide insights into this regulatory interplay. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL8601
151 Samples
Download data
Series
Accession:
GSE17762
ID:
200017762
13.

PBMC Cell Subset Stimulation

(Submitter supplied) PBMC cell subsets were treated with 0.6 pM IFNg for 0-24h and compared to mock-treated time series. Abstract: Background Interferons are key modulators of the immune system, and are central to the control of many diseases. The response of immune cells to stimuli in complex populations is the product of direct and indirect effects, homotypic and heterotypic cell interactions. Dissecting the global transcriptional profiles of immune cell populations may provide insights into this regulatory interplay. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL8601
76 Samples
Download data
Series
Accession:
GSE16253
ID:
200016253
14.

PBMC IFNg Dose Reponse

(Submitter supplied) PBMC response to three concentrations of IFNg (0.006, 0.6 and 60 pM) from 0-12h. Abstract: Background Interferons are key modulators of the immune system, and are central to the control of many diseases. The response of immune cells to stimuli in complex populations is the product of direct and indirect effects, homotypic and heterotypic cell interactions. Dissecting the global transcriptional profiles of immune cell populations may provide insights into this regulatory interplay. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL8601
28 Samples
Download data
Series
Accession:
GSE16252
ID:
200016252
15.

PBMC Cytokine Comparison

(Submitter supplied) Treatment of PBMC with 0.6 pM cytokine from 0-24h Abstract: Background Interferons are key modulators of the immune system, and are central to the control of many diseases. The response of immune cells to stimuli in complex populations is the product of direct and indirect effects, homotypic and heterotypic cell interactions. Dissecting the global transcriptional profiles of immune cell populations may provide insights into this regulatory interplay. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL8601
47 Samples
Download data
Series
Accession:
GSE16251
ID:
200016251
16.

Blood gene expression profiles following vaccination in 2-month old infants

(Submitter supplied) Analyzed the gene expression changes in infant of 2 month old after vaccination of HepB, DTaP, Hib, IPV, PCV13, and RV vaccines in 7 days and 30 days
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
68 Samples
Download data: TXT
Series
Accession:
GSE237318
ID:
200237318
17.

Young infants display heterogeneous serological responses and extensive but reversible transcriptional changes following initial immunizations

(Submitter supplied) Infants necessitate vaccinations to prevent life-threatening infections. Our understanding of the infant immune responses to routine vaccines remains limited. We analyzed two cohorts of 2-month-old infants before vaccination, one week, and one-month post-vaccination. We report remarkable heterogeneity but limited antibody responses to the different antigens. Whole-blood transcriptome analysis in an initial cohort showed marked overexpression of interferon-stimulated genes (ISGs) and to a lesser extent of inflammation-genes at day 7, which normalized one month post-vaccination. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL24676
18 Samples
Download data: MTX, TSV
Series
Accession:
GSE204716
ID:
200204716
18.

Inflammatory and interferon gene expression signatures in patients with mitochondrial disease

(Submitter supplied) People with mitochondrial disease are susceptible to metabolic decompensation and neurological symptom progression in response to an infection. Increasing evidence suggests that mitochondrial dysfunction may cause chronic inflammation, which may promote hyperresponsiveness to pathogens and neurodegeneration. We collected whole blood and isolated peripheral blood mononuclear cells from mitochondrial disease patients and healthy controls and examined transcriptional changes to identify common gene signatures of immune dysfunction in mitochondrial disease. more...
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21290
81 Samples
Download data: TXT
Series
Accession:
GSE233883
ID:
200233883
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