Evidence map›Paper›PMID 39686536›Full record

ArticleJournal of leukocyte biology2024

Mertk signaling and immune regulation in T cells.

Christopher Varsanyi, Raymond B Birge

Abstract readEditorialComment
In one paragraph

Article in Journal of leukocyte biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Christopher VarsanyiDepartment of Microbiology, Biochemistry and Molecular Genetics, Center for Cell Signaling, Rutgers New Jersey Medical School, 205 South Orange Ave, Newark, NJ 07103, United States.
Raymond B BirgeDepartment of Microbiology, Biochemistry and Molecular Genetics, Center for Cell Signaling, Rutgers New Jersey Medical School, 205 South Orange Ave, Newark, NJ 07103, United States.ORCID 0009-0004-0104-8978

Funding

Targeting a phosphatidylserine/TAM receptor/PD-L1 axis as a vulnerability in cancerR01CA260137 · NCI · RUTGERS BIOMEDICAL AND HEALTH SCIENCES · PI Raymond B. Birge, SERGEI V KOTENKO · 2022 to 2026
$2.4M
NCI NIH HHS R01 CA260137
6 · The paper itself

Abstract

While widely viewed as inhibitory receptors that drive efferocytosis and immune resolution on myeloid cells, TAM family members, particularly Mertk, have emerged as promising targets in immune-oncology to help stimulate host antitumor immunity. A recent study shows that Mertk expressed on human T cells, including CD8+ T cells and differentiated central memory T cells, has a co-stimulatory function for the T Cell Receptor. These new findings reveal the complexity and diversification of Mertk in immune regulation and its implications to cancer therapeutics.

Indexed as

c-Mer Tyrosine KinaseSignal TransductionAnimalsHumansNeoplasmsT-Lymphocytesc-Mer Tyrosine KinaseMERTK protein, humancancercentral memoryco-stimulationMertkT cells

Identifiers

PMID39686536
PMCPMC12797865

What OpenQuestion holds

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LicenceTDM
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.