Evidence map›Paper›PMID 35898500›Full record

ReviewFrontiers in immunology2022

GARP as a Therapeutic Target for the Modulation of Regulatory T Cells in Cancer and Autoimmunity.

Niklas Zimmer, Emily R Trzeciak, Barbara Graefen, Kazuki Satoh, Andrea Tuettenberg

Open access · goldAbstract readReview
In one paragraph

Review 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 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

23 citing papers in PubMed, 24 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

5 authors at 3 institutions in 2 countries.

Niklas ZimmerDepartment of Dermatology, University Medical Center Mainz, Johannes Gutenberg University Mainz, Mainz, Germany.
Emily R TrzeciakDepartment of Dermatology, University Medical Center Mainz, Johannes Gutenberg University Mainz, Mainz, Germany.
Barbara GraefenDepartment of Dermatology, University Medical Center Mainz, Johannes Gutenberg University Mainz, Mainz, Germany.
Kazuki SatohEarly Clinical Development Department, Daiichi Sankyo Co., Ltd., Tokyo, Japan.
Andrea TuettenbergDepartment of Dermatology, University Medical Center Mainz, Johannes Gutenberg University Mainz, Mainz, Germany.
Johannes Gutenberg University Mainz · DEUniversity Medical Center of the Johannes Gutenberg University Mainz · DEDaiichi-Sankyo (Japan) · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Regulatory T cells (Treg) play a critical role in immune homeostasis by suppressing several aspects of the immune response. Herein, Glycoprotein A repetitions predominant (GARP), the docking receptor for latent transforming growth factor (LTGF-β), which promotes its activation, plays a crucial role in maintaining Treg mediated immune tolerance. After activation, Treg uniquely express GARP on their surfaces. Due to its location and function, GARP may represent an important target for immunotherapeutic approaches, including the inhibition of Treg suppression in cancer or the enhancement of suppression in autoimmunity. In the present review, we will clarify the cellular and molecular regulation of GARP expression not only in human Treg but also in other cells present in the tumor microenvironment. We will also examine the overall roles of GARP in the regulation of the immune system. Furthermore, we will explore potential applications of GARP as a predictive and therapeutic biomarker as well as the targeting of GARP itself in immunotherapeutic approaches.

Indexed as

NeoplasmsT-Lymphocytes, RegulatoryAutoimmunityGlycoproteinsHumansMembrane ProteinsTumor MicroenvironmentGlycoproteinsMembrane ProteinsbiomarkerGARP mRNAGlycoprotein A repetitions predominant (GARP)LRRC32Soluble GARP or soluble Glycoprotein A repetitions predominant (sGARP)therapyTreg

Identifiers

PMID35898500
PMCPMC9309211
OpenAlexW4284962583

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.