Evidence map›Paper›PMID 27782331›Full record

ReviewImmunological reviews2016

Properdin: a tightly regulated critical inflammatory modulator.

Adam Z Blatt, Sabina Pathan, Viviana P Ferreira

Open access · hybridAbstract readReview
In one paragraph

Review in Immunological reviews, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
8.4field-weighted citation impact, top 2% 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

61 citing papers in PubMed, 108 citations in OpenAlex.

  1. Article
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  3. Review
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  14. Review
  15. Article
  16. Crosstalk of Inflammation and Coagulation inInternational journal of molecular sciences · 2023
    Review
  17. Single-cell RNAseq provides insight into altered immune cell populations in human fracture nonunions.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2023
    Article
  18. Article
  19. Review
  20. Review

1 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

3 authors at 2 institutions in 1 country.

Adam Z BlattDepartment of Medical Microbiology and Immunology, University of Toledo College of Medicine and Life Sciences, Toledo, OH, USA.
Sabina PathanDepartment of Medical Microbiology and Immunology, University of Toledo College of Medicine and Life Sciences, Toledo, OH, USA.
Viviana P FerreiraDepartment of Medical Microbiology and Immunology, University of Toledo College of Medicine and Life Sciences, Toledo, OH, USA. viviana.ferreira@utoledo.edu.
University of Toledo Medical Center · USUniversity of Toledo · US

Funding

Role of complement regulator properdin in the interaction between platelets and lR01HL112937 · NHLBI · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI FERREIRA, VIVIANA P · 2014 to 2018
$1.9M
The role of complement proteins in cardiovascular diseaseP30HL101317 · NHLBI · UNIVERSITY OF TOLEDO HEALTH SCI CAMPUS · PI TAKASHIMA, AKIRA · 2009 to 2010
$1.2M
NHLBI NIH HHS P30 HL101317NHLBI NIH HHS R01 HL112937
6 · The paper itself

Abstract

The complement alternative pathway is a powerful arm of the innate immune system that enhances diverse inflammatory responses in the human host. Key to the effects of the alternative pathway is properdin, a serum glycoprotein that can both initiate and positively regulate alternative pathway activity. Properdin is produced by many different leukocyte subsets and circulates as cyclic oligomers of monomeric subunits. While the formation of non-physiological aggregates in purified properdin preparations and the presence of potential properdin inhibitors in serum have complicated studies of its function, properdin has, regardless, emerged as a key player in various inflammatory disease models. Here, we review basic properdin biology, emphasizing the major hurdles that have complicated the interpretation of results from properdin-centered studies. In addition, we elaborate on an emerging role for properdin in thromboinflammation and discuss the potential utility of properdin inhibitors as long-term therapeutic options to treat diseases marked by increased formation of platelet/granulocyte aggregates. Finally, we describe the interplay between properdin and the alternative pathway negative regulator, Factor H, and how aiming to understand these interactions can provide scientists with the most effective ways to manipulate alternative pathway activation in complex systems.

Indexed as

Complement Pathway, AlternativeAnimalsComplement Factor HHumansImmunomodulationInflammationMolecular Targeted TherapyPlatelet AggregationProperdinThrombosisComplement Factor HProperdincomplementfactor Hinflammationproperdin

Identifiers

PMID27782331
PMCPMC5096056
OpenAlexW2540306189

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.