Evidence map›Paper›PMID 38631843›Full record

ArticleMolecular pain

The regulation of the PD-1/PD-L1 pathway in imiquimod-induced chronic psoriasis itch and itch sensitization in mouse.

Zhehao Xu, Yue Wang, Changcheng Jiang, Zhengwei Wang, YongFeng Cheng, Manli Fan

Open access · goldAbstract read
In one paragraph

Article in Molecular pain. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. Review
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

6 authors at 1 institution in 1 country.

Zhehao XuDepartment of Pharmacology, Clinic Medical College, Anhui Medical University, Hefei, China.ORCID 0000-0002-2252-9058
Yue WangDepartment of Pharmacology, Clinic Medical College, Anhui Medical University, Hefei, China.
Changcheng JiangDepartment of Pharmacology, Clinic Medical College, Anhui Medical University, Hefei, China.
Zhengwei WangDepartment of Pharmacology, Clinic Medical College, Anhui Medical University, Hefei, China.
YongFeng ChengDepartment of Pharmacology, Clinic Medical College, Anhui Medical University, Hefei, China.
Manli FanDepartment of Pharmacy, Fuyang Hospital, Anhui Medical University, Fuyang, China.ORCID 0009-0001-1132-097X
Anhui Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PD-1/PD-L1 inhibitors have been demonstrated to induce itch in both humans and experimental animals. However, whether the PD-1/PD-L1 pathway is involved in the regulation of chronic psoriatic itch remains unclear. This study aimed to investigate the role of the PD-1/PD-L1 pathway in imiquimod-induced chronic psoriatic itch. The intradermal injection of PD-L1 in the nape of neck significantly alleviated chronic psoriatic itch in imiquimod-treated skin. Additionally, we observed that spontaneous scratching behavior induced by imiquimod disappeared on day 21. Still, intradermal injection of PD-1/PD-L1 inhibitors could induce more spontaneous scratching for over a month, indicating that imiquimod-treated skin remained in an itch sensitization state after the spontaneous scratching behavior disappeared. During this period, there was a significant increase in PD-1 receptor expression in both the imiquimod-treated skin and the spinal dorsal horn in mice, accompanied by significant activation of microglia in the spinal dorsal horn. These findings suggest the potential involvement of the peripheral and central PD-1/PD-L1 pathways in regulating chronic itch and itch sensitization induced by imiquimod.

Indexed as

B7-H1 AntigenImiquimodProgrammed Cell Death 1 ReceptorPruritusPsoriasisAnimalsChronic DiseaseMaleMiceMice, Inbred C57BLSignal TransductionSkinB7-H1 AntigenImiquimodPdcd1 protein, mouseProgrammed Cell Death 1 ReceptorImiquimoditchitch sensitizationPD-1/PD-L1 inhibitor

Identifiers

PMID38631843
PMCPMC11069332
OpenAlexW4394921056

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.