Evidence map›Paper›PMID 28824882›Full record

ReviewFrontiers in cellular and infection microbiology2017

Purinergic Signaling: A Common Path in the Macrophage Response against

Laetitia Petit-Jentreau, Ludovic Tailleux, Janine L Coombes

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in cellular and infection microbiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

  1. The authors respond to feedback onFrontiers in oncology · 2026
    Article
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  3. Adenosine AFrontiers in pharmacology · 2024
    Article
  4. TZD-Based Hybrid Molecules Act as Dual Anti-International journal of molecular sciences · 2023
    Article
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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

3 authors at 2 institutions in 2 countries.

Laetitia Petit-JentreauInstitute of Infection and Global Health, Department of Infection Biology, University of LiverpoolLiverpool, United Kingdom.
Ludovic TailleuxMycobacterial Genetics Unit, Institut PasteurParis, France.
Janine L CoombesInstitute of Infection and Global Health, Department of Infection Biology, University of LiverpoolLiverpool, United Kingdom.
University of Liverpool · GBInstitut Pasteur · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune responses are essential for the protection of the host against external dangers or infections and are normally efficient in the clearance of invading microbes. However, some intracellular pathogens have developed strategies to replicate and survive within host cells resulting in latent infection associated with strong inflammation. This excessive response can cause cell and tissue damage and lead to the release of the intracellular content, in particular the nucleotide pool, into the extracellular space. Over the last decade, new studies have implicated metabolites from the purinergic pathway in shaping the host immune response against intracellular pathogens and proved their importance in the outcome of the infection. This review aims to summarize how the immune system employs the purinergic system either to fight the pathogen, or to control collateral tissue damage. This will be achieved by focusing on the macrophage response against two intracellular pathogens, the human etiologic agent of tuberculosis,

Indexed as

Signal TransductionAdenosine TriphosphateAnimalsHumansImmunity, InnateMacrophagesMycobacterium tuberculosisPurinergic AgentsToxoplasmaToxoplasmosisTuberculosisAdenosine TriphosphatePurinergic AgentsATPinnate immunitymacrophagesMycobacterium tuberculosisnucleotidespurinergic agentsToxoplasma gondii

Identifiers

PMID28824882
PMCPMC5545599
OpenAlexW2744905302

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.