Evidence map›Paper›PMID 40539032›Full record

ArticleCell surface (Amsterdam, Netherlands)2025

Immunomodulatory function of chitosan is dependent on complement receptor 3.

Jeanette Wagener, Xiaowen Wang, Katharina L Becker, Vishu Aimanianda, Isabel Valsecchi, Mark S Gresnigt, Mihai G Netea, Jean-Paul Latge, Neil A R Gow, Frank L van de Veerdonk

Abstract read
In one paragraph

Article in Cell surface (Amsterdam, Netherlands), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Edible Scaffolds for Cultivated Meat Production.Advances in biochemical engineering/biotechnology · 2026
    Review
  5. Article
  6. 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

10 authors.

Jeanette WagenerJunior Research Group Adaptive Pathogenicity Strategies, Leibniz Institute for Natural Product Research and Infection Biology - Hans Knöll Institute, Jena, Germany.
Xiaowen WangDepartment of Internal Medicine and Radboudumc Center for Infectious Diseases, Nijmegen, the Netherlands.
Katharina L BeckerDepartment of Internal Medicine and Radboudumc Center for Infectious Diseases, Nijmegen, the Netherlands.
Vishu AimaniandaUnité des Aspergillus, Institut Pasteur, Paris, France.Aberdeen Fungal Group, School of Medicine, Medical Sciences & Nutrition, Institute of Medical Sciences, University of Aberdeen, Foresterhill, Aberdeen AB25 2ZD, UK.
Isabel ValsecchiUnité des Aspergillus, Institut Pasteur, Paris, France.Aberdeen Fungal Group, School of Medicine, Medical Sciences & Nutrition, Institute of Medical Sciences, University of Aberdeen, Foresterhill, Aberdeen AB25 2ZD, UK.
Mark S GresnigtDepartment of Internal Medicine and Radboudumc Center for Infectious Diseases, Nijmegen, the Netherlands.
Mihai G NeteaDepartment of Internal Medicine and Radboudumc Center for Infectious Diseases, Nijmegen, the Netherlands.
Jean-Paul LatgeUnité des Aspergillus, Institut Pasteur, Paris, France.Aberdeen Fungal Group, School of Medicine, Medical Sciences & Nutrition, Institute of Medical Sciences, University of Aberdeen, Foresterhill, Aberdeen AB25 2ZD, UK.
Neil A R GowMedical Research Council Centre for Medical Mycology at the University of Exeter University of Exeter, Geoffrey Pope Building, Stocker Road, Exeter EX4 4QD, UK.
Frank L van de VeerdonkDepartment of Internal Medicine and Radboudumc Center for Infectious Diseases, Nijmegen, the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chitosan, the deacetylated product of chitin, is a significant component of the cell walls of nearly all fungi. In contrast with the high level of attention paid to plant immune recognition of chitin and chitosan of plant pathogenic fungi we know much less about the mammalian immune system immune recognition of chitosan during infections by human pathogenic fungal species. Here we show that the mammalian β-integrin CR3 complement scavenger receptor, that is expressed on monocytes and macrophages, recognises chitosan from a range of fungal sources and that this leads to the secretion of IL-6, IL-1β and TNF. The secretion of these pro-inflammatory cytokines was dependent on the phagocytosis of chitosan. The co-provision of chitosan along with a peptide (Aspf2 from

Indexed as

Cell wallChitosanFungal immunologyPattern recognition receptor

Identifiers

PMID40539032
PMCPMC12175732

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.