Evidence map›Paper›PMID 36609665›Full record

ArticleScientific reports2023

Purified complement C3b triggers phagocytosis and activation of human neutrophils via complement receptor 1.

Elena Boero, Ronald D Gorham, Emmet A Francis, Jonathan Brand, Lay Heng Teng, Dennis J Doorduijn, Maartje Ruyken, Remy M Muts, Christian Lehmann, Admar Verschoor and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. 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
5.3field-weighted citation impact, top 4% 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, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. mSphere · 2026
    Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. The Alzheimer's disease-associated complement receptor 1 variant confers risk by impacting glial phagocytosis.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  16. Article
  17. Article
  18. Article
  19. The battle within: cell death by phagocytosis in cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Review
  20. Pathogenic and Protective Roles of Neutrophils inPathogens (Basel, Switzerland) · 2025
    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 6 institutions in 3 countries.

Elena Boero *Department of Medical Microbiology, University Medical Center Utrecht, Utrecht University, Heidelberglaan 100, 3584 CX, Utrecht, The Netherlands.
Ronald D Gorham *Department of Medical Microbiology, University Medical Center Utrecht, Utrecht University, Heidelberglaan 100, 3584 CX, Utrecht, The Netherlands.
Emmet A FrancisDepartment of Biomedical Engineering, University of California Davis, Davis, CA, 95616, USA.
Jonathan BrandDepartment of Biomedical Engineering, University of California Davis, Davis, CA, 95616, USA.
Lay Heng TengDepartment of Biomedical Engineering, University of California Davis, Davis, CA, 95616, USA.
Dennis J DoorduijnDepartment of Medical Microbiology, University Medical Center Utrecht, Utrecht University, Heidelberglaan 100, 3584 CX, Utrecht, The Netherlands.
Maartje RuykenDepartment of Medical Microbiology, University Medical Center Utrecht, Utrecht University, Heidelberglaan 100, 3584 CX, Utrecht, The Netherlands.
Remy M MutsDepartment of Medical Microbiology, University Medical Center Utrecht, Utrecht University, Heidelberglaan 100, 3584 CX, Utrecht, The Netherlands.
Christian LehmannLaboratory of Dendritic Cell Biology, Department of Dermatology, University Hospital of Erlangen, Friedrich-Alexander-Universität (FAU) Erlangen-Nürnberg, 91052, Erlangen, Germany.
Admar VerschoorDepartment of Otorhinolaryngology, Technische Universität München and Klinikum Rechts der Isar, 81675, Munich, Germany.
Kok P M van KesselDepartment of Medical Microbiology, University Medical Center Utrecht, Utrecht University, Heidelberglaan 100, 3584 CX, Utrecht, The Netherlands.
Volkmar HeinrichDepartment of Biomedical Engineering, University of California Davis, Davis, CA, 95616, USA.
Suzan H M RooijakkersDepartment of Medical Microbiology, University Medical Center Utrecht, Utrecht University, Heidelberglaan 100, 3584 CX, Utrecht, The Netherlands. s.h.m.rooijakkers@umcutrecht.nl.
University of California, Davis · USUniversity Hospital Heidelberg · DEUniversity Medical Center Utrecht · NLFriedrich-Alexander-Universität Erlangen-Nürnberg · DEHeidelberg University · DEKlinikum rechts der Isar · DE

Funding

Cytoskeletal Membrane Anchors: Key Switchboards for Cellular Communication, MechaR01GM098060 · NIGMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI HEINRICH, VOLKMAR · 2012 to 2015
$1.1M
NIGMS NIH HHS R01 GM098060
6 · The paper itself

Abstract

The complement system provides vital immune protection against infectious agents by labeling them with complement fragments that enhance phagocytosis by immune cells. Many details of complement-mediated phagocytosis remain elusive, partly because it is difficult to study the role of individual complement proteins on target surfaces. Here, we employ serum-free methods to couple purified complement C3b onto E. coli bacteria and beads and then expose human neutrophils to these C3b-coated targets. We examine the neutrophil response using a combination of flow cytometry, confocal microscopy, luminometry, single-live-cell/single-target manipulation, and dynamic analysis of neutrophil spreading on opsonin-coated surfaces. We show that purified C3b can potently trigger phagocytosis and killing of bacterial cells via Complement receptor 1. Comparison of neutrophil phagocytosis of C3b- versus antibody-coated beads with single-bead/single-target analysis exposes a similar cell morphology during engulfment. However, bulk phagocytosis assays of C3b-beads combined with DNA-based quenching reveal that these are poorly internalized compared to their IgG1 counterparts. Similarly, neutrophils spread slower on C3b-coated compared to IgG-coated surfaces. These observations support the requirement of multiple stimulations for efficient C3b-mediated uptake. Together, our results establish the existence of a direct pathway of phagocytic uptake of C3b-coated targets and present methodologies to study this process.

Indexed as

Complement C3bNeutrophilsComplement System ProteinsEscherichia coliHumansImmunoglobulin GPhagocytosisReceptors, ComplementReceptors, Complement 3bComplement C3bComplement System ProteinsImmunoglobulin GReceptors, ComplementReceptors, Complement 3b

Identifiers

PMID36609665
PMCPMC9822988
OpenAlexW4313575504

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.