Evidence map›Paper›PMID 39240039›Full record

ReviewEuropean journal of immunology2024

Key actors in neuropathophysiology: The role of γδ T cells.

Deniz Bulgur, Raquel Macedo Moura, Julie C Ribot

Abstract readReview
In one paragraph

Review in European journal of immunology, 2024. 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
–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

2 citing papers in PubMed.

  1. Article
  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

3 authors.

Deniz Bulgur *Instituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa Avenida Professor Egas Moniz, Lisbon, 1649-028, Portugal.
Raquel Macedo Moura *Instituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa Avenida Professor Egas Moniz, Lisbon, 1649-028, Portugal.
Julie C RibotInstituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa Avenida Professor Egas Moniz, Lisbon, 1649-028, Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The neuroimmune axis has been the focus of many studies, with special emphasis on the interactions between the central nervous system and the different immune cell subsets. T cells are namely recognized to play a critical role due to their interaction with nerves, by secreting cytokines and neurotrophins, which regulate the development, function, and survival of neurons. In this context, γδ T cells are particularly relevant, as they colonize specific tissues, namely the meninges, and have a wide variety of complex functions that balance physiological systems. Notably, γδ T cells are not only key components for maintaining brain homeostasis but are also responsible for triggering or preventing inflammatory responses in various pathologies, including neurodegenerative diseases as well as neuropsychiatric and developmental disorders. Here, we provide an overview of the current state of the art on the contribution of γδ T cells in neuropathophysiology and delve into the molecular mechanisms behind it. We aim to shed light on γδ T cell functions in the central nervous system while highlighting upcoming challenges in the field and providing new clues for potential therapeutic strategies.

Indexed as

Central Nervous SystemReceptors, Antigen, T-Cell, gamma-deltaAnimalsBrainCytokinesHumansIntraepithelial LymphocytesNeurodegenerative DiseasesNeuroimmunomodulationT-LymphocytesT-Lymphocyte SubsetsCytokinesReceptors, Antigen, T-Cell, gamma-deltaBehaviourBrain functionsInflammationNeuroimmune axis

Identifiers

PMID39240039
PMCPMC11628923

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.