Evidence map›Paper›PMID 29669994›Full record

ReviewInternational journal of molecular sciences2018

Mechanisms of ATP Release by Inflammatory Cells.

Michel Dosch, Joël Gerber, Fadi Jebbawi, Guido Beldi

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04790240 (The Trial Uses Medicinal Herbs to Direct T Cells to Engulf the COVID-19 Virus and Protect the Organs Well), which is not on this map. Cited by 161 papers.

0numbers the graph read from it
0cells of the map it votes in
161citing papers in PubMed
18.6field-weighted citation impact, top 1% 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.

NCT04790240 phase1 / phase2recruitingnot on this mapstarted 2025, after this paper: background citation

The Trial Uses Medicinal Herbs to Direct T Cells to Engulf the COVID-19 Virus and Protect the Organs Well

TypeinterventionalSponsorAll Natural Medicine Clinic, LLCRan2025 to 2027Enrolled100ConditionsCovid19 Virus InfectionArmsInflammation (I), Inflammation (II), Inflammation (III), Standard of care
3 · Its place in the literature

Who cites it

161 citing papers in PubMed, 264 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
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  6. Review
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  10. Article
  11. AMetabolites · 2026
    Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Cellular signaling pathway of Shiga toxin-induced ATP release.Frontiers in cellular and infection microbiology · 2026
    Article
  17. Review
  18. Review
  19. Review
  20. Article

101 more citing papers are in PubMed but not listed here.

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

4 authors at 1 institution in 1 country.

Michel DoschDepartment for Visceral Surgery and Medicine, Bern University Hospital, University of Bern, CH-3010 Bern, Switzerland. michel.dosch@dbmr.unibe.ch.ORCID 0000-0002-4087-4293
Joël GerberDepartment for Visceral Surgery and Medicine, Bern University Hospital, University of Bern, CH-3010 Bern, Switzerland. joel.gerber@students.unibe.ch.
Fadi JebbawiDepartment for Visceral Surgery and Medicine, Bern University Hospital, University of Bern, CH-3010 Bern, Switzerland. fadi.febbawi@dbmr.unibe.ch.
Guido BeldiDepartment for Visceral Surgery and Medicine, Bern University Hospital, University of Bern, CH-3010 Bern, Switzerland. guido.beldi@insel.ch.ORCID 0000-0002-9914-3807
University of Bern · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extracellular nucleotides (e.g., ATP, ADP, UTP, UDP) released by inflammatory cells interact with specific purinergic P2 type receptors to modulate their recruitment and activation. The focus of this review is on stimuli and mechanisms of extracellular nucleotide release and its consequences during inflammation. Necrosis leads to non-specific release of nucleotides, whereas specific release mechanisms include vesicular exocytosis and channel-mediated release via connexin or pannexin hemichannels. These release mechanisms allow stimulated inflammatory cells such as macrophages, neutrophils, and endothelial cells to fine-tune autocrine/paracrine responses during acute and chronic inflammation. Key effector functions of inflammatory cells are therefore regulated by purinergic signaling in acute and chronic diseases, making extracellular nucleotide release a promising target for the development of new therapies.

Indexed as

Adenosine TriphosphateAnimalsExocytosisHumansInflammationIon ChannelsModels, BiologicalSecretory VesiclesAdenosine TriphosphateIon ChannelsATP releaseconnexinsendothelial cellsextracellular nucleotidesinflammationmonocytes/macrophagesneutrophilsnon-specific nucleotide releasepannexinspurinergic signalingvesicular exocytosis

Identifiers

PMID29669994
PMCPMC5979498
OpenAlexW2801022696

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.