Evidence map›Paper›PMID 14523038›Full record

ArticleThe Journal of clinical investigation2003

Prevention of leukocyte migration to inflamed skin with a novel fluorosugar modifier of cutaneous lymphocyte-associated antigen.

Charles J Dimitroff, Thomas S Kupper, Robert Sackstein

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.5field-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

33 citing papers in PubMed, 71 citations in OpenAlex.

  1. Article
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  11. A common sugar-nucleotide-mediated mechanism of inhibition of (glycosamino)glycan biosynthesis, as evidenced by 6F-GalNAc (Ac3).FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2015
    Article
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  15. Article
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  18. Therapeutic perspectives in atopic dermatitis.Clinical reviews in allergy & immunology · 2011
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Charles J DimitroffHarvard Skin Disease Research Center, Department of Dermatology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA. cdimitroff@rics.bwh.harvard.edu
Thomas S Kupper
Robert Sackstein
Harvard University · USBrigham and Women's Hospital · US

Funding

Virus discovery in cutaneous T cell lymphomaP30AR042689 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI KUPPER, THOMAS S. · 1994 to 2010
$6.8M
Structure &Biology of Hematopoietic E-/L-SelectinR01HL060528 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI SACKSTEIN, ROBERT · 1997 to 2006
$2.4M
ADHESION MOLECULES MEDIATING SKIN TROPISM IN ACUTE GVHDR01CA084156 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI SACKSTEIN, ROBERT · 2000 to 2003
$1.4M
Identity and Structural Biology of CLA in LeukemiasF32CA091780 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI DIMITROFF, CHARLES J · 2001 to 2002
$86k
NCI NIH HHS CA91780-01NCI NIH HHS F32 CA091780NCI NIH HHS R01 CA084156NCI NIH HHS R01 CA84156NHLBI NIH HHS R01 HL060528NHLBI NIH HHS R01 HL60528NIAMS NIH HHS P30 AR042689NIAMS NIH HHS P30 AR42689
6 · The paper itself

Abstract

E-selectin and P-selectin on dermal postcapillary venules play critical roles in the migration of effector T cells into inflamed skin. P-selectin glycoprotein ligand-1 (PSGL-1) modified by alpha1,3-fucosyltransferase is the principal selectin ligand on skin-homing T cells and is required for effector T cell entry into inflamed skin. We have previously shown that a fluorinated analog of N-acetylglucosamine peracetylated-4-fluorinated-d-glucosamine (4-F-GlcNAc), inhibits selectin ligand expression on human T cell PSGL-1. To analyze 4-F-GlcNAc efficacy in dampening effector T cell migration to inflamed skin, we elicited allergic contact hypersensitivity (CHS) reactions in mice treated with 4-F-GlcNAc. We also investigated 4-F-GlcNAc efficacy on lymphocyte E-selectin ligand expression in LNs draining antigen-sensitized skin and on other immunological processes requisite for CHS responses. Our results showed that 4-F-GlcNAc treatment attenuated lymphocyte E-selectin ligand expression in skin-draining LNs and prevented CHS reactions. Significant reductions in inflammatory lymphocytic infiltrate were observed, while pathways related to antigenic processing and presentation and naive T cell recognition within skin-draining LNs were unaffected. These data indicate that 4-F-GlcNAc prevents CHS by inhibiting selectin ligand activity and the capacity of effector T cells to enter antigen-challenged skin without affecting the afferent phase of CHS.

Indexed as

AcetylglucosamineAnimalsAntigen PresentationAntigens, Differentiation, T-LymphocyteAntigens, NeoplasmCell MovementDermatitis, ContactE-SelectinMembrane GlycoproteinsMiceP-SelectinSkinT-Lymphocytes2-acetamido-1,3,6-tri-O-acetyl-4-deoxy-4-fluoroglucopyranoseAcetylglucosamineAntigens, Differentiation, T-LymphocyteAntigens, NeoplasmCTAGE1 protein, humanE-SelectinMembrane GlycoproteinsP-SelectinP-selectin ligand protein

Identifiers

PMID14523038
PMCPMC198531
OpenAlexW2095376774

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.