Evidence map›Paper›PMID 27597829›Full record

ReviewFrontiers in pharmacology2016

CB2 and GPR55 Receptors as Therapeutic Targets for Systemic Immune Dysregulation.

Juan Zhou, Ian Burkovskiy, Hyewon Yang, Joel Sardinha, Christian Lehmann

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in pharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
4.0field-weighted citation impact, top 7% 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

24 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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  6. Review
  7. Article
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  9. Article
  10. Article
  11. Review
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  13. Article
  14. The Roles of Orphan G Protein-Coupled Receptors in Autoimmune Diseases.Clinical reviews in allergy & immunology · 2021
    Review
  15. Article
  16. Review
  17. Viruses · 2019
    Article
  18. Review
  19. Review
  20. Article
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 1 institution in 1 country.

Juan ZhouDepartment of Anesthesia, Dalhousie UniversityHalifax, NS, Canada; Department of Microbiology and Immunology, Dalhousie UniversityHalifax, NS, Canada.
Ian BurkovskiyDepartment of Anesthesia, Dalhousie UniversityHalifax, NS, Canada; Department of Pharmacology, Dalhousie UniversityHalifax, NS, Canada.
Hyewon YangDepartment of Anesthesia, Dalhousie UniversityHalifax, NS, Canada; Department of Microbiology and Immunology, Dalhousie UniversityHalifax, NS, Canada.
Joel SardinhaDepartment of Anesthesia, Dalhousie University Halifax, NS, Canada.
Christian LehmannDepartment of Anesthesia, Dalhousie UniversityHalifax, NS, Canada; Department of Microbiology and Immunology, Dalhousie UniversityHalifax, NS, Canada; Department of Pharmacology, Dalhousie UniversityHalifax, NS, Canada.
Dalhousie University · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The endocannabinoid system (ECS) is involved in many physiological processes and has been suggested to play a critical role in the immune response and the central nervous system (CNS). Therefore, ECS modulation has potential therapeutic effects on immune dysfunctional disorders, such as sepsis and CNS injury-induced immunodeficiency syndrome (CIDS). In sepsis, excessive release of pro- and anti-inflammatory mediators results in multi-organ dysfunction, failure, and death. In CIDS, an acute CNS injury dysregulates a normally well-balanced interplay between CNS and the immune system, leading to increased patients' susceptibility to infections. In this review, we will discuss potential therapeutic modulation of the immune response in sepsis and CNS injury by manipulation of the ECS representing a novel target for immunotherapy.

Indexed as

central nervous system injuryCNS injury-induced immunodeficiency syndromeendocannabinoid systemGPR55immune dysfunctionimmunosuppressionsepsis

Identifiers

PMID27597829
PMCPMC4992728
OpenAlexW2517414714

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.