Evidence map›Paper›PMID 32354869›Full record

ArticleHaematologica2021

Fibrinogen interaction with complement C3: a potential therapeutic target to reduce thrombosis risk.

Rhodri J King, Katharina Schuett, Christian Tiede, Vera Jankowski, Vicky John, Abhi Trehan, Katie Simmons, Sreenivasan Ponnambalam, Robert F Storey, Colin W G Fishwick and 3 more

Open access · goldAbstract read
In one paragraph

Article in Haematologica, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 16% 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, 23 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Increased MAP-1 and lectin complement activation capacity in Klinefelter syndrome.The Journal of clinical endocrinology and metabolism · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Complement C3b contributes toFrontiers in immunology · 2022
    Article
  10. Review
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

13 authors at 3 institutions in 2 countries.

Rhodri J KingLeeds Institute for Cardiovascular and Metabolic Medicine, Leeds, UK.
Katharina SchuettDepartment of Internal Medicine I, University Hospital RWTH Aachen, Germany.
Christian TiedeBioscreening Technology Group,School of Molecular and Cellular Biology, University of Leeds, UK.
Vera JankowskiInstitute for Molecular and Cardiovascular Research, Aachen University, Germany.
Vicky JohnLeeds Institute for Cardiovascular and Metabolic Medicine, Leeds, UK.
Abhi TrehanLeeds Institute for Cardiovascular and Metabolic Medicine, Leeds, UK.
Katie SimmonsSchool of Chemistry, University of Leeds, Leeds, UK.
Sreenivasan PonnambalamSchool of Molecular and Cellular Biology, University of Leeds, Leeds, UK.
Robert F StoreySchool of Medicine, University of Sheffield, Sheffield, UK.
Colin W G FishwickSchool of Chemistry, University of Leeds, Leeds, UK.
Michael J McPhersonBioscreening Technology Group, School of Molecular and Cellular Biology, University of Leeds, UK.
Darren C TomlinsonBioscreening Technology Group, School of Molecular and Cellular Biology, University of Leeds, UK.
Ramzi A AjjanLeeds Institute for Cardiovascular and Metabolic Medicine, Leeds, UK.
University of Leeds · GBRWTH Aachen University · DEUniversity of Sheffield · GB

Funding

British Heart Foundation FS/10/020/28242British Heart Foundation FS/15/40/31536British Heart Foundation FS/16/24/32133British Heart Foundation FS/17/30/32832
6 · The paper itself

Abstract

Complement C3 binds fibrinogen and compromises fibrin clot lysis thereby enhancing thrombosis risk. We investigated the role of fibrinogen-C3 interaction as a novel therapeutic target to reduce thrombosis risk by analysing: i) consistency in the fibrinolytic properties of C3, ii) binding sites between fibrinogen and C3 and iii) modulation of fibrin clot lysis by manipulating fibrinogen-C3 interactions. Purified fibrinogen and C3 from the same individuals (n=24) were used to assess inter-individual variability in the anti-fibrinolytic effects of C3. Microarray screening and molecular modelling evaluated C3 and fibrinogen interaction sites. Novel synthetic conformational proteins, termed Affimers, were used to modulate C3-fibrinogen interaction and fibrinolysis. C3 purified from patients with type 1 diabetes showed enhanced prolongation of fibrinolysis compared with healthy control protein [195±105 and 522±166 seconds, respectively (p=0.04)], with consistent effects but a wider range (5-51% and 5-18% lysis prolongation, respectively). Peptide microarray screening identified 2 potential C3-fibrinogen interactions sites within fibrinogen β chain (residues 424-433, 435-445). One fibrinogen-binding Affimer was isolated that displayed sequence identity with C3 in an exposed area of the protein. This Affimer abolished C3-induced prolongation of fibrinolysis (728±25.1 seconds to 632±23.7 seconds, p=0.005) and showed binding to fibrinogen in the same region that is involved in C3-fibrinogen interactions. Moreover, it shortened plasma clot lysis of patients with diabetes, cardiovascular disease or controls by 7-11%. C3 binds fibrinogen β-chain and disruption of fibrinogen-C3 interaction using Affimer proteins enhances fibrinolysis, which represents a potential novel target tool to reduce thrombosis in high risk individuals.

Indexed as

FibrinogenThrombosisComplement C3FibrinFibrinolysisHumansComplement C3FibrinFibrinogen

Identifiers

PMID32354869
PMCPMC8168514
OpenAlexW3022504201

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.