Evidence map›Paper›PMID 35223897›Full record

ArticleFrontiers in medicine2022

Expression of the Immune Checkpoint Protein VISTA Is Differentially Regulated by the TGF-β1 - Smad3 Signaling Pathway in Rapidly Proliferating Human Cells and T Lymphocytes.

Stephanie Schlichtner, Inna M Yasinska, Sabrina Ruggiero, Steffen M Berger, Nijas Aliu, Mateja Prunk, Janko Kos, N Helge Meyer, Bernhard F Gibbs, Elizaveta Fasler-Kan and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.5field-weighted citation impact, top 9% 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

26 citing papers in PubMed, 26 citations in OpenAlex.

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  8. Emerging new immune checkpoint inhibitors in solid tumor immunotherapy.Naunyn-Schmiedeberg's archives of pharmacology · 2025
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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

11 authors at 5 institutions in 4 countries.

Stephanie SchlichtnerMedway School of Pharmacy, Universities of Kent and Greenwich, Chatham Maritime, United Kingdom.
Inna M YasinskaMedway School of Pharmacy, Universities of Kent and Greenwich, Chatham Maritime, United Kingdom.
Sabrina RuggieroDepartment of Pediatric Surgery, Children's Hospital, Inselspital Bern, University of Bern, Bern, Switzerland.
Steffen M BergerDepartment of Pediatric Surgery, Children's Hospital, Inselspital Bern, University of Bern, Bern, Switzerland.
Nijas AliuDepartment of Human Genetics, Inselspital Bern, University of Bern, Bern, Switzerland.
Mateja PrunkDepartment of Biotechnology, JoŽef Stefan Institute, Ljubljana, Slovenia.
Janko KosDepartment of Biotechnology, JoŽef Stefan Institute, Ljubljana, Slovenia.
N Helge MeyerDivision of Experimental Allergology and Immunodermatology, Department of Human Medicine, University of Oldenburg, Oldenburg, Germany.
Bernhard F GibbsDivision of Experimental Allergology and Immunodermatology, Department of Human Medicine, University of Oldenburg, Oldenburg, Germany.
Elizaveta Fasler-KanDepartment of Pediatric Surgery, Children's Hospital, Inselspital Bern, University of Bern, Bern, Switzerland.
Vadim V SumbayevMedway School of Pharmacy, Universities of Kent and Greenwich, Chatham Maritime, United Kingdom.
Medway School of Pharmacy · GBUniversity Hospital of Bern · CHCarl von Ossietzky Universität Oldenburg · DEJožef Stefan Institute · SIUniversity of Bern · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoint proteins play crucial roles in human embryonic development but are also used by cancer cells to escape immune surveillance. These proteins and biochemical pathways associated with them form a complex machinery capable of blocking the ability of cytotoxic immune lymphoid cells to attack cancer cells and, ultimately, to fully suppress anti-tumor immunity. One of the more recently discovered immune checkpoint proteins is V-domain Ig-containing suppressor of T cell activation (VISTA), which plays a crucial role in anti-cancer immune evasion pathways. The biochemical mechanisms underlying regulation of VISTA expression remain unknown. Here, we report for the first time that VISTA expression is controlled by the transforming growth factor beta type 1 (TGF-β)-Smad3 signaling pathway. However, in T lymphocytes, we found that VISTA expression was differentially regulated by TGF-β depending on their immune profile. Taken together, our results demonstrate the differential biochemical control of VISTA expression in human T cells and various types of rapidly proliferating cells, including cancer cells, fetal cells and keratinocytes.

Indexed as

anti-cancer immunitygalectin-9immune checkpointT lymphocytesVISTA

Identifiers

PMID35223897
PMCPMC8866318
OpenAlexW4211078614

What Socratic 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 Socratic graph.