Evidence map›Paper›PMID 35812455›Full record

ArticleFrontiers in immunology2022

Galectin-3 Decreases 4-1BBL Bioactivity by Crosslinking Soluble and Membrane Expressed 4-1BB.

Morten Aagaard Nielsen, Kristian Juul-Madsen, John Stegmayr, Chao Gao, Akul Y Mehta, Stinne Ravn Greisen, Tue Wenzel Kragstrup, Malene Hvid, Thomas Vorup-Jensen, Richard D Cummings and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. 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
2.2field-weighted citation impact, top 11% 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, 24 citations in OpenAlex.

  1. Article
  2. Gal-3 blocks the binding between PD-1 and pembrolizumab.Journal for immunotherapy of cancer · 2024
    Article
  3. Surface PD-1 expression in T cells is suppressed by HNRNPK through an exonic splicing silencer on exon 3.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2024
    Article
  4. Article
  5. 4-1BB immunotherapy: advances and hurdles.Experimental & molecular medicine · 2024
    Review
  6. Review
  7. Article
  8. Article
  9. 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

12 authors at 4 institutions in 3 countries.

Morten Aagaard NielsenDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.
Kristian Juul-MadsenDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.
John StegmayrDepartment of Experimental Medical Sciences, Faculty of Medicine, Lund University, Lund, Sweden.
Chao GaoDepartment of Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, National Center for Functional Glycomics, Boston, MA, United States.
Akul Y MehtaDepartment of Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, National Center for Functional Glycomics, Boston, MA, United States.
Stinne Ravn GreisenDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.
Tue Wenzel KragstrupDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.
Malene HvidDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.
Thomas Vorup-JensenDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.
Richard D CummingsDepartment of Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, National Center for Functional Glycomics, Boston, MA, United States.
Hakon LefflerDivision for Microbiology, Immunology and Glycobiology (MIG), Department of Laboratory Medicine, Lund University, Lund, Sweden.
Bent Winding DeleuranDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.
Aarhus University Hospital · DKAarhus University · DKBeth Israel Deaconess Medical Center · USLund University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

4-1BB is a T cell costimulatory receptor and a member of the tumor necrosis factor receptor superfamily. Here, we show that Galectin-3 (Gal-3) decreases the cellular response to its ligand (4-1BBL). Gal-3 binds to both soluble 4-1BB (s4-1BB) and membrane-bound 4-1BB (mem4-1BB), without blocking co-binding of 4-1BBL. In plasma, we detected complexes composed of 4-1BB and Gal-3 larger than 100 nm in size; these complexes were reduced in synovial fluid from rheumatoid arthritis. Both activated 4-1BB

Indexed as

Galectin 3Tumor Necrosis Factor Receptor Superfamily, Member 94-1BB LigandHEK293 CellsHumansReceptors, Antigen, T-CellReceptors, Tumor Necrosis Factor4-1BB LigandGalectin 3Receptors, Antigen, T-CellReceptors, Tumor Necrosis FactorTumor Necrosis Factor Receptor Superfamily, Member 94-1BBcheckpoint receptorGalectin-3inflammationrheumatoid arthritis

Identifiers

PMID35812455
PMCPMC9263355
OpenAlexW4283368630

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.