Evidence map›Paper›PMID 37509608›Full record

ArticleBiomedicines2023

A Dual Role of Osteopontin in Modifying B Cell Responses.

Rittika Chunder, Verena Schropp, Manuel Marzin, Sandra Amor, Stefanie Kuerten

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.7field-weighted citation impact, top 9% 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

11 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Osteopontin: Its Properties, Recent Studies, and Potential Applications.International journal of molecular sciences · 2025
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Overexpression ofAging · 2024
    Article
  10. Review
  11. 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

5 authors at 2 institutions in 2 countries.

Rittika ChunderFaculty of Medicine, Institute of Neuroanatomy, University of Bonn, 53115 Bonn, Germany.
Verena SchroppFaculty of Medicine, Institute of Neuroanatomy, University of Bonn, 53115 Bonn, Germany.
Manuel MarzinDepartment of Pathology, Amsterdam University Medical Center, 1007 MB Amsterdam, The Netherlands.
Sandra AmorDepartment of Pathology, Amsterdam University Medical Center, 1007 MB Amsterdam, The Netherlands.
Stefanie KuertenFaculty of Medicine, Institute of Neuroanatomy, University of Bonn, 53115 Bonn, Germany.ORCID 0000-0001-6119-605X
University of Bonn · DEAmsterdam University Medical Centers · NL

Funding

Deutsche Forschungsgemeinschaft KU2760/4-1
6 · The paper itself

Abstract

The occurrence of B cell aggregates within the central nervous system (CNS) has prompted the investigation of the potential sources of pathogenic B cell and T cell responses in a subgroup of secondary progressive multiple sclerosis (MS) patients. Nevertheless, the expression profile of molecules associated with these aggregates and their role in aggregate development and persistence is poorly described. Here, we focused on the expression pattern of osteopontin (OPN), which is a well-described cytokine, in MS brain tissue. Autopsied brain sections from MS cases with and without B cell pathology were screened for the presence of CD20

Indexed as

aggregationB cellscentral nervous systemmultiple sclerosisosteopontin

Identifiers

PMID37509608
PMCPMC10377065
OpenAlexW4384201823

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.