Evidence map›Paper›PMID 34852377›Full record

ArticleThrombosis and haemostasis2022

Anti-Galectin-2 Antibody Treatment Reduces Atherosclerotic Plaque Size and Alters Macrophage Polarity.

Jamie Kane, Matthijs Jansen, Sebastian Hendrix, Laura A Bosmans, Linda Beckers, Claudia van Tiel, Marion Gijbels, Noam Zelcer, Carlie J de Vries, Philipp von Hundelshausen and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Thrombosis and haemostasis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Galectin-2 in Health and Diseases.International journal of molecular sciences · 2022
    Review
  8. 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

15 authors at 4 institutions in 3 countries.

Jamie KaneDepartment of Nephrology, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Centre, Amsterdam, The Netherlands.
Matthijs JansenDepartment of Medical Biochemistry, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Centre, Amsterdam, The Netherlands.
Sebastian HendrixDepartment of Medical Biochemistry, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Centre, Amsterdam, The Netherlands.
Laura A BosmansDepartment of Medical Biochemistry, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Centre, Amsterdam, The Netherlands.
Linda BeckersDepartment of Medical Biochemistry, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Centre, Amsterdam, The Netherlands.
Claudia van TielDepartment of Medical Biochemistry, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Centre, Amsterdam, The Netherlands.
Marion GijbelsDepartment of Medical Biochemistry, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Centre, Amsterdam, The Netherlands.
Noam ZelcerDepartment of Medical Biochemistry, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Centre, Amsterdam, The Netherlands.
Carlie J de VriesDepartment of Medical Biochemistry, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Centre, Amsterdam, The Netherlands.
Philipp von HundelshausenInstitute for Cardiovascular Prevention (IPEK), Ludwig-Maximillian's University, Munich, Germany.ORCID 0000-0001-7474-9370
Marc VervloetDepartment of Nephrology, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Centre, Amsterdam, The Netherlands.
Ed EringaDepartment of Physiology, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Centre, Amsterdam, The Netherlands.
Anton J HorrevoetsDepartment of Molecular Cell Biology and Immunology, Amsterdam University Medical Centre, Amsterdam, The Netherlands.
Niels van RoyenDepartment of Cardiology, Radboud University Medical Centre, Nijmegen, The Netherlands.
Esther LutgensDepartment of Medical Biochemistry, Amsterdam Cardiovascular Sciences, Amsterdam University Medical Centre, Amsterdam, The Netherlands.
Maastricht University · NLMayo Clinic · USRadboud University Nijmegen · NLUniversity of Amsterdam · NL

Funding

812699 Marie Skłodowska-Curie ActionsCRC 1123 Deutsche ForschungsgemeinschaftCVON2017-22 Development and the Royal Netherlands Academy of Sciences for the GENIUS-II project 'Generating the best evidence-based pharmaceutical targets for atherosclerosis
6 · The paper itself

Abstract

backgroundGalectins have numerous cellular functions in immunity and inflammation. Short-term galectin-2 (Gal-2) blockade in ischemia-induced arteriogenesis shifts macrophages to an anti-inflammatory phenotype and improves perfusion. Gal-2 may also affect other macrophage-related cardiovascular diseases.

objectivesThis study aims to elucidate the effects of Gal-2 inhibition in atherosclerosis.

methods

resultsGal-2 inhibition reduced the progression of existing atherosclerosis. Atherosclerotic plaque area in the aortic root was decreased, especially so in mice treated with 2C10 nanobodies. This clone showed reduced atherosclerosis severity as reflected by a decrease in fibrous cap atheromas in addition to decreases in plaque size.The number of plaque resident macrophages was unchanged; however, there was a significant increase in the fraction of CD206

conclusionProlonged and frequent treatment with anti-Gal-2 nanobodies reduced plaque size, slowed plaque progression, and modified the phenotype of plaque macrophages toward an anti-inflammatory profile. These results hold promise for future macrophage modulating therapeutic interventions that promote arteriogenesis and reduce atherosclerosis.

Indexed as

AtherosclerosisHyperlipidemiasPlaque, AtheroscleroticSingle-Domain AntibodiesAnimalsAnti-Inflammatory AgentsApolipoproteins ECholesterolDisease Models, AnimalGalectin 2MacrophagesMiceMice, Inbred C57BLMice, KnockoutMice, Knockout, ApoEAnti-Inflammatory AgentsApolipoproteins ECholesterolGalectin 2Single-Domain Antibodies

Identifiers

PMID34852377
PMCPMC9251707
OpenAlexW3215069767

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.