Evidence map›Paper›PMID 25467802›Full record

ArticleMolecular immunology2015

Alternative complement pathway component Factor D contributes to efficient clearance of tissue debris following acute CCl₄-induced injury.

Gail A Cresci, Daniela Allende, Megan R McMullen, Laura E Nagy

Open access · greenAbstract read
In one paragraph

Article in Molecular immunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
0.1field-weighted citation impact, top 48% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Role of Complement in Liver Diseases.Seminars in liver disease · 2024
    Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Complement Factor D protects mice from ethanol-induced inflammation and liver injury.American journal of physiology. Gastrointestinal and liver physiology · 2018
    Article
  10. 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

4 authors at 1 institution in 1 country.

Gail A CresciDepartment of Gastroenterology, Cleveland Clinic, Cleveland, OH 44195, USA; Department of Pathobiology, Cleveland Clinic, Cleveland, OH 44195, USA.
Daniela AllendeDepartment of Pathology Cleveland Clinic, Cleveland, OH 44195, USA.
Megan R McMullenDepartment of Pathobiology, Cleveland Clinic, Cleveland, OH 44195, USA.
Laura E NagyDepartment of Gastroenterology, Cleveland Clinic, Cleveland, OH 44195, USA; Department of Pathobiology, Cleveland Clinic, Cleveland, OH 44195, USA. Electronic address: nagyL3@ccf.org.
Cleveland Clinic · US

Funding

CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR024989 · NCRR · CASE WESTERN RESERVE UNIVERSITY · PI DAVIS, PAMELA B · 2007 to 2011
$53.7M
Clinical and Translational Science Collaborative of ClevelandUL1TR000439 · NCATS · CASE WESTERN RESERVE UNIVERSITY · PI KONSTAN, MICHAEL W. · 2012 to 2016
$50.0M
Role of Adipose in Ethanol-Induced Tissue InjuryR37AA011876 · NIAAA · CLEVELAND CLINIC LERNER COM-CWRU · PI NAGY, LAURA E. · 2009 to 2018
$4.0M
INSULIN MEDIATED GLUCOSE TRANSPORT DISRUPT BY ETHANOLR01AA011876 · NIAAA · CLEVELAND CLINIC LERNER COM-CWRU · PI NAGY, LAURA E · 1998 to 2007
$2.4M
Complement and ethanol-induced liver injury.R01AA016399 · NIAAA · CLEVELAND CLINIC LERNER COM-CWRU · PI NAGY, LAURA E. · 2006 to 2010
$1.7M
Role of Butyrate in the Gut-Liver Interaction of Ethanol Induced Liver InjuryF32AA021044 · NIAAA · CLEVELAND CLINIC LERNER COM-CWRU · PI CRESCI, GAIL ANN · 2011 to 2013
$155k
NCATS NIH HHS UL1 TR000439NCRR NIH HHS UL1 RR024989NCRR NIH HHS UL1RR024989NIAAA NIH HHS F32 AA021044NIAAA NIH HHS F32AA021044NIAAA NIH HHS R01 AA011876NIAAA NIH HHS R01 AA016399NIAAA NIH HHS R37 AA011876
6 · The paper itself

Abstract

Complement, part of the innate immune system, is involved with immune protection against invading pathogens as well as cell survival and tissue regeneration. It is known that complement activation is required for timely hepatocyte recovery following an acute toxic injury, but which pathway of complement activation is involved in response to hepatocyte injury has not been identified. In these studies we utilize mice deficient in C1qa, C4 and Factor D, lacking the classical, classical/MBL, and alternative pathways of complement activation, respectively, to identify an essential role for Factor D in the ability of the liver to recover from acute toxic injury. Here we demonstrate that following an acute CCl4-induced injury, the involvement of the alternative complement pathway is essential for efficient liver recovery.

Indexed as

AnimalsCarbon TetrachlorideCell ProliferationChemical and Drug Induced Liver InjuryComplement C1qComplement C3Complement Factor DComplement Pathway, AlternativeFemaleHepatocytesInflammationInterleukin-6LiverMice, Inbred C57BLNecrosisNeutrophil InfiltrationCarbon TetrachlorideComplement C1qComplement C3Complement Factor DInterleukin-6STAT3 Transcription FactorAcute liver injuryAlternative pathwayComplementFactor DNecrosis

Identifiers

PMID25467802
PMCPMC4282836
OpenAlexW2052869957

What OpenQuestion holds

Textmetadata
LicenceTDM
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.