Evidence map›Paper›PMID 33023856›Full record

ArticleTrends in immunology2020

The Complement C5a-C5aR1 GPCR Axis in COVID-19 Therapeutics.

Trent M Woodruff, Arun K Shukla

Open access · bronzeAbstract read
In one paragraph

Article in Trends in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
1.3field-weighted citation impact, top 11% 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

33 citing papers in PubMed, 53 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Host-Based Treatments for Severe COVID-19.Current issues in molecular biology · 2023
    Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  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

2 authors at 2 institutions in 2 countries.

Trent M WoodruffThe School of Biomedical Sciences, Faculty of Medicine, The University of Queensland, Brisbane 4072, Australia; Queensland Brain Institute, The University of Queensland, Brisbane 4072, Australia. Electronic address: t.woodruff@uq.edu.au.
Arun K ShuklaDepartment of Biological Sciences and Bioengineering, Indian Institute of Technology, Kanpur 208016, India. Electronic address: arshukla@iitk.ac.in.
Indian Institute of Technology Kanpur · INUniversity of Queensland · AU

Funding

Wellcome Trust
6 · The paper itself

Abstract

The current pandemic of coronavirus disease (COVID-19) caused by SARS-CoV-2 is a significant global health challenge. A recent study by Carvelli and colleagues now demonstrates the involvement of complement C5a and its receptor C5aR1 in disease progression and suggests that blockade of the C5a-C5aR1 axis may represent a potential therapeutic strategy against COVID-19.

Indexed as

AnimalsAntibodies, MonoclonalBetacoronavirusComplement C5aCoronavirus InfectionsCOVID-19Disease Models, AnimalHumansPandemicsPneumonia, ViralReceptor, Anaphylatoxin C5aReceptors, G-Protein-CoupledSARS-CoV-2Signal TransductionAntibodies, MonoclonalC5AR1 protein, humanComplement C5aReceptor, Anaphylatoxin C5aReceptors, G-Protein-Coupledcellular signalingcomplement systemCOVID-19drug discoveryGPCRsSARS-CoV-2

Identifiers

PMID33023856
PMCPMC7510552
OpenAlexW3088132250

What OpenQuestion holds

Textmetadata
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.