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Links from GEO DataSets

Items: 20

1.

Effective treatment of psoriasis with etanercept is linked to suppression of IL17 signaling, not immediate response TNF

(Submitter supplied) The success of TNF inhibitors for treatment of psoriasis and other inflammatory diseases was previously attributed to blockade of innate immunity. In a clinical trial using etanercept TNF blocking agent to treat psoriasis vulgaris, we used affymetrix gene arrays to analyze broad gene profiles in lesional skin at multiple timepoints during drug treatment (baseline, and weeks 1, 2, 4 and 12) compared to non-lesional skin. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL571
89 Samples
Download data: CEL
Series
Accession:
GSE11903
ID:
200011903
2.

Shrinking the Psoriasis assessment gap: Early gene-expression profiling accurately predicts response to long-term treatment

(Submitter supplied) Prediction of response to adalimumab and methotrexate treatments based on gene expression profiles at baseline, weeks 1, 2, 4 and 16
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL10558
179 Samples
Download data: TXT
Series
Accession:
GSE85034
ID:
200085034
3.

Pathologic Immune Pathways in Psoriasis are Rapidly Attenuated by Tofacitinib Treatment: A Randomized Phase 2 Study in Patients with Moderate to Severe Psoriasis

(Submitter supplied) Tofacitinib is an oral Janus kinase inhibitor being investigated for psoriasis. We sought to elucidate the molecular mechanisms underlying the clinical efficacy of tofacitinib in patients with psoriasis. Twelve patients with plaque psoriasis were randomized (3:1) to receive 10 mg of tofacitinib or placebo twice daily for 12 weeks. Biopsy specimens were taken from nonlesional (baseline) and lesional (baseline, days 1 and 3, and weeks 1, 2, 4, and 12) skin. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
95 Samples
Download data: CEL
Series
Accession:
GSE69967
ID:
200069967
4.

A Randomized, Placebo-Controlled Study to Evaluate SRT2104, a Selective SIRT1 Activator, in Patients with Moderate to Severe Psoriasis

(Submitter supplied) Activation of Sirtuin (silent mating type information regulation 2 homolog) 1, or SIRT1, is an unexplored therapeutic approach for treatment of inflammatory diseases. The goal of this study was to evaluate the clinical activity and tolerability of multiple doses of SRT2104, a selective activator of SIRT1, in patients with moderate to severe psoriasis after day 84 of treatment. Forty patients were randomized 4:1 to three escalating doses of SRT2104 (250, 500, 1000 mg/d SRT2104 or placebo). more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
22 Samples
Download data: CEL
Series
Accession:
GSE50614
ID:
200050614
5.

Expression data from skin biopsy samples from patients with moderate-to-severe psoriasis

(Submitter supplied) A gene expression profiling sub-study was conducted in which skin biopsy samples were collected from 85 patients with moderate-to-severe psoriasis who were participating in ACCEPT, an IRB-approved Phase 3, multicenter, randomized trial. This analysis identified 4,175 probe-sets as being significantly modulated in psoriasis lesions (LS) compared with matched biopsies of non-lesional (NL) skin.
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4600
Platform:
GPL570
170 Samples
Download data: CEL
Series
Accession:
GSE30999
ID:
200030999
6.
Full record GDS4600

Psoriasis vulgaris ACCEPT cohort: paired lesional and non-lesional skin

Analysis of 85 paired lesional and non-lesional samples from moderate-to-severe psoriasis patients at baseline without active psoriasis therapy. Results provide insight into the molecular mechanisms underlying psoriasis.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 disease state, 33 individual, 82 other, 10 specimen sets
Platform:
GPL570
Series:
GSE30999
170 Samples
Download data: CEL
7.

Early tissue responses to etanercept in psoriasis lesions

(Submitter supplied) Anti-TNF-alpha therapy has made a significant impact on the treatment of psoriasis. Despite being designed to neutralize TNF-alpha activity, the mechanism of action of these agents in the resolution of psoriasis remains unclear. The aim of this study was to better understand the mechanism of action of etanercept by examining very early changes in the lesional skin of psoriasis patients. 20 chronic plaque psoriasis patients were enrolled and received 50mg etanercept twice weekly. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
34 Samples
Download data: CEL
Series
Accession:
GSE47751
ID:
200047751
8.

Integrative responses to IL-17 and TNF-α in human keratinocytes account for key inflammatory pathogenic circuits in psoriasis

(Submitter supplied) We sought to provide a comprehensive evaluation of the effects of TNF-α and IL-17 on the keratinocyte gene profile in order to identify genes that might be co-regulated by these cytokines. We then sought to determine how genes that were synergistically activated by both cytokines relate to the psoriasis transcriptome. Here, we identified 160 unique genes that were synergistically up-regulated by IL-17 and TNF-α and 188 unique genes where the two cytokines had at least an additive effect. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL6947
22 Samples
Download data: TXT
Series
Accession:
GSE24767
ID:
200024767
9.

MoDCs grown with/without Etanercept TNF inhibitor

(Submitter supplied) The process for making monocyte derived DCs (moDCs) has been previously described (46). All analysis was performed on “day 5” immature DCs. Etanercept 10mg/mL was added to experimental wells on days 0, 2, and 4. We chose this concentration of etanercept as it approximates the plasma concentration of drug when given 50mg BIW. Keywords: Inhibition assay
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL571
6 Samples
Download data: CEL, CHP
Series
Accession:
GSE9239
ID:
200009239
10.

TREM-1 is a novel therapeutic target in Psoriasis

(Submitter supplied) Our group recently described a population of antigen presenting cells that appear to be critical in psoriasis pathogenesis, termed inflammatory myeloid dendritic cells (CD11c+ BDCA1-). Triggering receptor expressed on myeloid cells type-1 (TREM-1) signaling was a major canonical pathway in the published transcriptome of these cells. TREM-1 is a member of the immunoglobulin superfamily, active through the DAP12 signaling pathway, with an unknown ligand. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4597
Platform:
GPL571
15 Samples
Download data: CEL
Series
Accession:
GSE42305
ID:
200042305
11.
Full record GDS4597

In vitro model for inflammatory dendritic cells

Analysis of an in vitro model of peptidoglycan-activated monocytes as inflammatory myeloid dendritic cells (DCs). DCs are thought to have an important role in the pathogenesis of inflammatory skin lesions such as psoriasis. Results provide insight into molecular basis of psoriasis pathogenesis.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 5 agent sets
Platform:
GPL571
Series:
GSE42305
15 Samples
Download data: CEL
12.

Gene expression profiling in psoriatic lesional and non-lesional skin [brodalumab treatment]

(Submitter supplied) To explore the psoriasis phenotype and pathways involved in psoriasis, we characterized gene expression in lesional and non-lesional skin from psoriasis patients. Furthermore, we explored the effects of various doses of brodalumab on lesional skin over time.
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS5420
Platform:
GPL570
99 Samples
Download data: CEL
Series
Accession:
GSE53552
ID:
200053552
13.
Full record GDS5420

Psoriasis response to brodalumab: dose response and time course

Analysis of non-lesional and lesional psoriatic skins for up to 43 days following treatment with various doses of brodalumab, a human IgG2 mAb that selectively binds and blocks signaling through IL-17RA. Results provide insight into the molecular effect of blocking IL-17 signaling in psoriatic skin.
Organism:
Homo sapiens
Type:
Expression profiling by array, count, 3 agent, 4 dose, 25 individual, 4 time, 2 tissue sets
Platform:
GPL570
Series:
GSE53552
99 Samples
Download data: CEL
DataSet
Accession:
GDS5420
ID:
5420
14.

IL-17A is an essential cytokine to sustain pathogenic cell activation and inflammatory gene circuits in psoriasis vulgaris

(Submitter supplied) In psoriasis, inflammation and epidermal hyperplasia are thought to be controlled by T cell-derived cytokines. Evidence now suggests that Th17 and Th22 cells infiltrate psoriasis lesions and by secreting IL-17 and IL-22, respectively, may drive disease-specific gene or cell responses. While studies in model systems indicate that IL-22 has a dominant pathogenic role, there is evolving evidence that IL-17 contributes to features of psoriasis. more...
Organism:
Homo sapiens
Type:
Expression profiling by array
Dataset:
GDS4458
Platform:
GPL571
30 Samples
Download data: CEL
Series
Accession:
GSE31652
ID:
200031652
15.
Full record GDS4458

Anti-IL-17 monclonal antibody ixekizumab effect on chronic psoriasis

Analysis of psoriatic skin biopsies from patients treated with 150mg of subcutaneous anti-IL-17 mAb ixekizumab (previously LY2439821) at weeks 0 and 2. IL-17 blockade resulted in a high-grade clinical improvement in psoriasis. Results provide insight into the role of IL-17 in disease pathogenesis.
Organism:
Homo sapiens
Type:
Expression profiling by array, transformed count, 2 agent, 17 individual, 2 time sets
Platform:
GPL571
Series:
GSE31652
30 Samples
Download data: CEL
16.

Early quantification of systemic inflammatory (INF) and cardiovascular disease (CVD) proteins predicts long-term treatment response to Tofacitinib and Etanercept

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Other
Platforms:
GPL27152 GPL27151
1020 Samples
Download data
Series
Accession:
GSE136435
ID:
200136435
17.

Early quantification of systemic inflammatory (INF) and cardiovascular disease (CVD) proteins predicts long-term treatment response to Tofacitinib and Etanercept (INF data set)

(Submitter supplied) Proteomic profiles of 92 inflammatory proteins were measured in the blood of psoriasis patients both before and after treatment with tofacitanib or etanercept. These proteomic profiles were used to develop statistical classifiers for predicting PASI75 responses to tofacitinib and etancercept
Organism:
Homo sapiens
Type:
Other
Platform:
GPL27152
528 Samples
Download data: XLSX
Series
Accession:
GSE136434
ID:
200136434
18.

Early quantification of systemic inflammatory (INF) and cardiovascular disease (CVD) proteins predicts long-term treatment response to Tofacitinib and Etanercept (CVD data set)

(Submitter supplied) Proteomic profiles of 91 cardiovascular disease proteins were measured in the blood of psoriasis patients both before and after treatment with tofacitanib or etanercept. These proteomic profiles were used to develop statistical classifiers for predicting PASI75 responses to tofacitinib and etancercept
Organism:
Homo sapiens
Type:
Other
Platform:
GPL27151
492 Samples
Download data: XLSX
Series
Accession:
GSE136431
ID:
200136431
19.

IL-17 and TNF synergistically induce growth-associated cytokines in melanocytes while suppressing melanogenesis

(Submitter supplied) In this study, we sought to determine how IL-17 and TNF influence normal human melanocytes, either alone, or with both cytokines together. We reveal a dichotomous effect of IL-17 and TNF, which not only elicit essential mitogenic cytokines but also suppress melanogenesis by down-regulating genes of melanogenesis pathway
Organism:
Homo sapiens
Type:
Expression profiling by array
Platform:
GPL570
12 Samples
Download data: CEL
Series
Accession:
GSE40413
ID:
200040413
20.

Transcriptomic studies to characterize the gene expression landscape of psoriasis

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Homo sapiens
Type:
Expression profiling by high throughput sequencing
Platform:
GPL9052
216 Samples
Download data
Series
Accession:
GSE63980
ID:
200063980
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