Evidence map›Paper›PMID 31413105›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2019

Complement Component C5 and TLR Molecule CD14 Mediate Heme-Induced Thromboinflammation in Human Blood.

Anub M Thomas, Alexandra Gerogianni, Martin B McAdam, Yngvar Fløisand, Corinna Lau, Terje Espevik, Per H Nilsson, Tom Eirik Mollnes, Andreas Barratt-Due

Open access · bronzeAbstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

28 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Acute Incompatible Red Blood Cell Transfusion in Mice.Methods in molecular biology (Clifton, N.J.) · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Circulating free heme induces cytokine storm and pulmonary hypertension through the MKK3/p38 axis.American journal of physiology. Lung cellular and molecular physiology · 2024
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. [Anti-endothelial cell antibodies in predicting early miscarriage].Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2023
    Article
  14. Review
  15. Article
  16. Review
  17. Management of hemolytic transfusion reactions.Hematology. American Society of Hematology. Education Program · 2021
    Review
  18. Article
  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

9 authors at 4 institutions in 3 countries.

Anub M ThomasDepartment of Immunology, Oslo University Hospital and K.G. Jebsen Inflammation Research Centre, University of Oslo, 0318 Oslo, Norway.
Alexandra GerogianniLinnaeus Centre for Biomaterials Chemistry, Linnaeus University, 391 82 Kalmar, Sweden.ORCID 0000-0002-6194-6903
Martin B McAdamDepartment of Immunology, Oslo University Hospital and K.G. Jebsen Inflammation Research Centre, University of Oslo, 0318 Oslo, Norway.
Yngvar FløisandDepartment of Haematology, Oslo University Hospital, Rikshospitalet, 0424 Oslo, Norway.
Corinna LauResearch Laboratory, Nordland Hospital, 8092 Bodo, Norway.ORCID 0000-0003-1750-8065
Terje EspevikCentre of Molecular Inflammation Research, Norwegian University of Science and Technology, 7491 Trondheim, Norway.ORCID 0000-0003-0354-5068
Per H NilssonDepartment of Immunology, Oslo University Hospital and K.G. Jebsen Inflammation Research Centre, University of Oslo, 0318 Oslo, Norway.
Tom Eirik MollnesDepartment of Immunology, Oslo University Hospital and K.G. Jebsen Inflammation Research Centre, University of Oslo, 0318 Oslo, Norway.ORCID 0000-0002-5785-802X
Andreas Barratt-DueDepartment of Immunology, Oslo University Hospital and K.G. Jebsen Inflammation Research Centre, University of Oslo, 0318 Oslo, Norway; andreas.barrattdue@gmail.com.ORCID 0000-0001-5408-7162
Oslo University Hospital · NOLinnaeus University · SENordland Hospital · NONorwegian University of Science and Technology · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heme is a critical danger molecule liberated from hemeproteins in various conditions, including from hemoglobin in hemolytic diseases. Heme may cause thromboinflammatory damage by activating inflammatory and hemostatic pathways, such as complement, the TLRs, coagulation, and platelets. In this study, we explored the effect of single and dual inhibition of complement component C5 and TLR coreceptor CD14 on heme-induced thromboinflammation in an ex vivo human whole blood model. Heme induced a dose-dependent activation of complement via the alternative pathway. Single inhibition of C5 by eculizumab attenuated the release of IL-6, IL-8, TNF, MCP-1, MIP-1α, IFN-γ, LTB-4, MMP-8 and -9, and IL-1Ra with more than 60% (

Indexed as

AdultAnemia, Sickle CellAnimalsBlood CoagulationComplement ActivationComplement C5CytokinesGranulocytesHemeHemolysisHumansInflammationLipopolysaccharide ReceptorsMaleMonocytesSwineCD14 protein, humanComplement C5CytokinesHemeLipopolysaccharide ReceptorsThromboplastin

Identifiers

PMID31413105
PMCPMC6731449
OpenAlexW2967174867

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.