Evidence map›Paper›PMID 36483564›Full record

ArticleFrontiers in immunology2022

IL-17A and TNF-α inhibitors induce multiple molecular changes in psoriasis.

Qiang Dong, Dan Li, Bi Bo Xie, Li Hua Hu, Jia Huang, Xiao Xiao Jia, Yan Li Tang, Gan Hong Liu, Ning Ning Shen, Xiao Bing Yu

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

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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

10 authors.

Qiang DongDepartment of Dermatology, Dermatology Hospital of Zhejiang Province, Huzhou, Zhejiang, China.
Dan LiDepartment of Dermatology, Dermatology Hospital of Zhejiang Province, Huzhou, Zhejiang, China.
Bi Bo XieDepartment of Dermatology, Dermatology Hospital of Zhejiang Province, Huzhou, Zhejiang, China.
Li Hua HuDepartment of Dermatology, Dermatology Hospital of Zhejiang Province, Huzhou, Zhejiang, China.
Jia HuangDepartment of Dermatology, Dermatology Hospital of Zhejiang Province, Huzhou, Zhejiang, China.
Xiao Xiao JiaDepartment of Dermatology, Dermatology Hospital of Zhejiang Province, Huzhou, Zhejiang, China.
Yan Li TangDepartment of Dermatology, Dermatology Hospital of Zhejiang Province, Huzhou, Zhejiang, China.
Gan Hong LiuDepartment of Dermatology, Dermatology Hospital of Zhejiang Province, Huzhou, Zhejiang, China.
Ning Ning ShenDepartment of Dermatology, Dermatology Hospital of Zhejiang Province, Huzhou, Zhejiang, China.
Xiao Bing YuDepartment of Dermatology, Dermatology Hospital of Zhejiang Province, Huzhou, Zhejiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adalimumab and secukinumab are commonly used for moderate to severe psoriasis vulgaris (PV). Although distinct individual responses to and impaired effectiveness of these biological agents occur occasionally, little is known about the underlying reasons. Here, we report a proteomic analysis of psoriatic lesions from patients treated with these drugs using data-independent acquisition mass spectrometry (DIA-MS). Thousands of differentially expressed proteins (DEPs) changed over 12 weeks of treatment. Network analysis showed that DEPs could interact and induce transformation in matrix components, metabolic regulation, and immune response. The results of parallel reaction monitoring (PRM) analysis suggested that S100s, STAT1, KRT2, TYMP, SOD2, HSP90AB1, TFRC, and COL5A1 were the most significantly changed proteins in both groups. There was a positive association between the Psoriasis Area and Severity Index (PASI) score and three proteins (TFRC, IMPDH2, KRT2). Our study findings suggest that inhibition of IL-17A and TNF-α can induce changes in multiple molecules in psoriatic lesions and have an overlapping influence on the immune response and process through direct or indirect effects.

Indexed as

Interleukin-17Tumor Necrosis Factor InhibitorsHumansProteomicsTumor Necrosis Factor-alphaInterleukin-17Tumor Necrosis Factor-alphaTumor Necrosis Factor Inhibitorsadalimumabbiological agentdata-independent acquisition mass spectrometryingenuity pathway analysisparallel reaction monitoringproteomicspsoriasissecukinumab

Identifiers

PMID36483564
PMCPMC9723344
OpenAlexW4309542996

What OpenQuestion holds

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LicenceCC BY
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.