Evidence map›Paper›PMID 35979531›Full record

ArticlePathology oncology research : POR2022

Immunohistochemical Study of the PD-1/PD-L1 Pathway in Cutaneous Lupus Erythematosus.

Zsófia Király, Ágota Szepesi, Anna Sebestyén, Enikő Kuroli, Fanni Rencz, Béla Tóth, Laura Bokor, József Szakonyi, Márta Medvecz, Bernadett Hidvégi

Open access · goldAbstract read
In one paragraph

Article in Pathology oncology research : POR, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 45% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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 at 3 institutions in 1 country.

Zsófia KirályDepartment of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.
Ágota Szepesi1st Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
Anna Sebestyén1st Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
Enikő KuroliDepartment of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.
Fanni RenczDepartment of Health Economics, Corvinus University of Budapest, Budapest, Hungary.
Béla TóthDepartment of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.
Laura BokorDepartment of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.
József SzakonyiDepartment of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.
Márta MedveczDepartment of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.
Bernadett HidvégiDepartment of Dermatology, Venereology and Dermatooncology, Semmelweis University, Budapest, Hungary.
Semmelweis University · HUHUN-REN Institute of Experimental Medicine · HUCorvinus University of Budapest · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The pathomechanism of various autoimmune diseases is known to be associated with the altered function of programmed cell death 1/programmed cell death ligand 1 (PD-1/PD-L1) axis. We aimed to investigate the role of this pathway and inflammatory cell markers in subtypes of cutaneous lupus erythematosus (CLE): discoid lupus erythematosus (DLE), subacute CLE (SCLE) and toxic epidermal necrolysis (TEN)-like lupus, a hyperacute form of acute CLE (ACLE). Ten skin biopsy samples from 9 patients were analyzed with immunohistochemistry regarding the following markers: CD3, CD4, CD8, Granzyme B, CD123, CD163, PD-1, PD-L1. Our group consisted of 4 SCLE (2 idiopathic (I-SCLE) and 2 PD-1 inhibitor-induced (DI-SCLE)), 4 DLE and 1 TEN-like lupus cases. From the latter patient two consecutive biopsies were obtained 1 week apart. Marker expression patterns were compared through descriptive analysis. Higher median keratinocyte (KC) PD-L1 expression was observed in the SCLE group compared to the DLE group (65% and 5%, respectively). Medians of dermal CD4, Granzyme B (GB), PD-1 positive cell numbers and GB+/CD8

Indexed as

Lupus Erythematosus, CutaneousLupus Erythematosus, DiscoidB7-H1 AntigenGranzymesHumansProgrammed Cell Death 1 ReceptorSkinB7-H1 AntigenGranzymesProgrammed Cell Death 1 Receptordiscoid lupus erythematosusPD-1PD-1 inhibitor-induced SCLEPD-L1subacute cutaneous lupus erythematosusTEN-like lupus

Identifiers

PMID35979531
PMCPMC9377145
OpenAlexW4289333783

What OpenQuestion holds

Textmetadata
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.