Evidence map›Paper›PMID 16634804›Full record

ArticleClinical and experimental immunology2006

Cerebral leucocyte infiltration in lupus-prone MRL/MpJ-fas lpr mice--roles of intercellular adhesion molecule-1 and P-selectin.

W G James, P Hutchinson, D C Bullard, M J Hickey

Open access · greenAbstract read
In one paragraph

Article in Clinical and experimental immunology, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

20 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Non-pathogenic tissue-resident CD8Scientific reports · 2017
    Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. C5a alters blood-brain barrier integrity in experimental lupus.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2010
    Article
  17. Article
  18. Article
  19. Article
  20. 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

4 authors at 2 institutions in 2 countries.

W G JamesCentre for Inflammatory Diseases, Monash University Department of Medicine, Monash Medical Centre, 246 Clayton Road, Victoria 3168, Australia.
P Hutchinson
D C Bullard
M J Hickey
Monash University · AUUniversity of Alabama at Birmingham · US

Funding

GENETIC MOUSE MODELS FOR CHRONIC INFLAMMATORY DISEASER01RR017009 · NCRR · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BULLARD, DANIEL C · 2002 to 2006
$1.6M
Roles of MIF and iNOS in SLE-associate inflammationR01AR051807 · NIAMS · MONASH UNIVERSITY · PI HICKEY, MICHAEL J · 2004 to 2007
$964k
NCRR NIH HHS R01 RR017009NCRR NIH HHS RR 017009NIAMS NIH HHS AR 51807-01NIAMS NIH HHS R01 AR051807
6 · The paper itself

Abstract

The autoimmune disease which affects MRL/MpJ-fas(lpr) mice results in cerebral leucocyte recruitment and cognitive dysfunction. We have previously observed increased leucocyte trafficking in the cerebral microcirculation of these mice; however, the types of leucocytes recruited have not been analysed thoroughly, and the roles of key endothelial adhesion molecules in recruitment of these leucocytes have not been investigated. Therefore the aim of this study was to classify the phenotypes of leucocytes present in inflamed brains of MRL/MpJ-fas(lpr) mice, and dissect the roles of endothelial adhesion molecules in their accumulation in the brain. Immunohistochemical analysis revealed significant leucocyte infiltration in the brains of 16- and 20-week-old MRL/MpJ-fas(lpr) mice, affecting predominantly the choroid plexus. Isolation of brain-infiltrating leucocytes revealed that lymphocytes and neutrophils were the main populations present. The CD3(+) lymphocytes in the brain consisted of similar proportions of CD4(+), CD8(+) and CD4(-)/CD8(-)[double negative (DN)] populations. Assessment of MRL/MpJ-fas(lpr) mice deficient in endothelial adhesion molecules intercellular adhesion molecule-1 (ICAM-1) or P-selectin indicated that cerebral leucocyte recruitment persisted in the absence of these molecules, with only minor changes in the phenotypes of infiltrating cells. Together these data indicate that the brains of MRL/MpJ-fas(lpr) mice are affected by a mixed leucocyte infiltrate, of which the unusual DN lymphocyte phenotype contributes a substantial proportion. In addition, endothelial adhesion molecules ICAM-1 and P-selectin, which modulate survival of MRL/MpJ-fas(lpr) mice, do not markedly inhibit leucocyte entry into the central nervous system.

Indexed as

AnimalsAntigens, CDBrainChoroid PlexusImmunohistochemistryImmunophenotypingIntercellular Adhesion Molecule-1LeukocytesLupus Erythematosus, SystemicMiceMice, Inbred MRL lprNeutrophilsP-SelectinT-LymphocytesAntigens, CDIntercellular Adhesion Molecule-1P-Selectin

Identifiers

PMID16634804
PMCPMC1809650
OpenAlexW2003759043

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.