Evidence map›Paper›PMID 11737079›Full record

ArticleClinical and experimental immunology2001

Differential roles of osteopontin/Eta-1 in early and late lpr disease.

G F Weber, H Cantor

Open access · greenAbstract read
In one paragraph

Article in Clinical and experimental immunology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

16 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  8. Review
  9. Article
  10. Role of osteopontin in systemic lupus erythematosus.Archivum immunologiae et therapiae experimentalis · 2014
    Review
  11. Article
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  14. Review
  15. Article
  16. T-bet-dependent expression of osteopontin contributes to T cell polarization.Proceedings of the National Academy of Sciences of the United States of America · 2005
    Article
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

2 authors at 2 institutions in 1 country.

G F WeberDepartment of Cancer Immunology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA. gweber@lifespan.org
H Cantor
Dana-Farber Cancer Institute · USHarvard University · US

Funding

SYNERGISM BETWEEN CD44 AND OSTEOPONTIN IN METASTASISR29CA076176 · NCI · TUFTS MEDICAL CENTER · PI WEBER, GEORG F · 1998 to 2002
$342k
NCI NIH HHS CA76176NCI NIH HHS R29 CA076176PHS HHS A137833
6 · The paper itself

Abstract

The cytokine osteopontin (Eta-1) leads to macrophage-dependent polyclonal B-cell activation and is induced early in autoimmune prone mice with the lpr mutation, suggesting a significant pathogenic role for this molecule. Indeed, C57BL/6-Fas(lpr/lpr) mice crossed with osteopontin(-/-) mice display delayed onset of polyclonal B-cell activation, as judged by serum immunoglobulin levels. In contrast, they are subject to normal onset, but late exacerbation of lymphoproliferation and evidence of kidney disease. These observations define two stages of Fas(lpr/lpr) disease with respect to osteopontin-dependent pathogenesis that should be taken into account in the design of therapeutic approaches to the clinical disease.

Indexed as

AnimalsAutoimmune DiseasesB-Lymphocytesfas ReceptorFemaleLupus Erythematosus, SystemicLupus NephritisLymphocyte ActivationMaleMiceMice, Inbred C57BLMice, Inbred MRL lprMice, KnockoutMutationOsteopontinSialoglycoproteinsfas ReceptorOsteopontinSialoglycoproteinsSpp1 protein, mouse

Identifiers

PMID11737079
PMCPMC1906233
OpenAlexW2055327883

What OpenQuestion holds

Textmetadata
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.