Evidence map›Paper›PMID 19895991›Full record

Trial reportThe Journal of allergy and clinical immunology2009

Effective treatment of psoriasis with etanercept is linked to suppression of IL-17 signaling, not immediate response TNF genes.

Lisa C Zaba, Mayte Suárez-Fariñas, Judilyn Fuentes-Duculan, Kristine E Nograles, Emma Guttman-Yassky, Irma Cardinale, Michelle A Lowes, James G Krueger

Open access · greenAbstract readClinical Trial
In one paragraph

Trial report in The Journal of allergy and clinical immunology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 126 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
126citing papers in PubMed, 4 pooled it
8.0field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

126 citing papers in PubMed, 4 syntheses or guidelines pooled it, 300 citations in OpenAlex.

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66 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Lisa C ZabaLaboratory for Investigative Dermatology, Rockefeller University, New York, NY 10065, USA.
Mayte Suárez-Fariñas
Judilyn Fuentes-Duculan
Kristine E Nograles
Emma Guttman-Yassky
Irma Cardinale
Michelle A Lowes
James G Krueger
Rockefeller University · US

Funding

Weill Cornell/Rockefeller/Sloan-Kettering MST ProgramT32GM007739 · NIGMS · WEILL MEDICAL COLL OF CORNELL UNIV · PI HSU, KATHARINE C · 1985 to 2023
$51.1M
TRANSFORMING TRANSLATIONAL SCIENCE AND EDUCATION TO BENEFIT HUMAN HEALTHUL1RR024143 · NCRR · ROCKEFELLER UNIVERSITY · PI COLLER, BARRY · 2006 to 2011
$49.1M
WOUND HEALING IN INDIVIDUALS OF DIFFERENT AGE AND GENETIC BACKGROUNDM01RR000102 · NCRR · ROCKEFELLER UNIVERSITY · PI COLLER, BARRY · 1985 to 2006
$32.8M
Dendritic cells in psoriasis and effects of efalizumabK23AR052404 · NIAMS · ROCKEFELLER UNIVERSITY · PI LOWES, MICHELLE A · 2006 to 2010
$731k
NCRR NIH HHS M01 RR000102NCRR NIH HHS UL1 RR024143NCRR NIH HHS UL1RR024143NIAMS NIH HHS K23 AR052404NIAMS NIH HHS K23 AR052404-01A1NIGMS NIH HHS GM07739NIGMS NIH HHS T32 GM007739
6 · The paper itself

Abstract

backgroundTNF inhibitors have revolutionized the treatment of psoriasis vulgaris as well as psoriatic and rheumatoid arthritis and Crohn disease. Despite our understanding that these agents block TNF, their complex mechanism of action in disease resolution is still unclear.

objectiveTo analyze globally the genomic effects of TNF inhibition in patients with psoriasis, and to compare genomic profiles of patients who responded or did not respond to treatment.

methodsIn a clinical trial using etanercept TNF inhibitor to treat psoriasis vulgaris (n = 15), Affymetrix gene arrays were used to analyze gene profiles in lesional skin at multiple time points during drug treatment (baseline and weeks 1, 2, 4, and 12) compared with nonlesional skin. Patients were stratified as responders (n = 11) or nonresponders (n = 4) on the basis of histologic disease resolution. Cluster analysis was used to define gene sets that were modulated with similar magnitude and velocity over time.

resultsIn responders, 4 clusters of downregulated genes and 3 clusters of upregulated genes were identified. Genes downmodulated most rapidly reflected direct inhibition of myeloid lineage immune genes. Upregulated genes included the stable dendritic cell population genes CD1c and CD207 (langerin). Comparison of responders and nonresponders revealed rapid downmodulation of innate IL-1beta and IL-8 sepsis cascade cytokines in both groups, but only responders downregulated IL-17 pathway genes to baseline levels.

conclusionAlthough both responders and nonresponders to etanercept inactivated sepsis cascade cytokines, response to etanercept is dependent on inactivation of myeloid dendritic cell genes and inactivation of the T(H)17 immune response.

Indexed as

Anti-Inflammatory Agents, Non-SteroidalDendritic CellsDown-RegulationEtanerceptGene ExpressionGene Expression ProfilingHumansImmunoglobulin GInterferon-gammaInterleukin-17Interleukin-1betaInterleukin-8Myeloid CellsOligonucleotide Array Sequence AnalysisPsoriasisReceptors, Tumor Necrosis FactorAnti-Inflammatory Agents, Non-SteroidalEtanerceptImmunoglobulin GInterferon-gammaInterleukin-17Interleukin-1betaInterleukin-8Receptors, Tumor Necrosis FactorTumor Necrosis Factor-alpha

Identifiers

PMID19895991
PMCPMC2852188
OpenAlexW2151991135

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.