Evidence map›Paper›PMID 16269612›Full record

ArticleBlood2006

CD43 is a ligand for E-selectin on CLA+ human T cells.

Robert C Fuhlbrigge, Sandra L King, Robert Sackstein, Thomas S Kupper

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

57 citing papers in PubMed, 109 citations in OpenAlex.

  1. Article
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  7. Article
  8. The biology of E-selectin ligands in leukemogenesis.Advances in cancer research · 2023
    Review
  9. Review
  10. Review
  11. Review
  12. Genome-wide CRISPR screens reveal a specific ligand for the glycan-binding immune checkpoint receptor Siglec-7.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  13. Article
  14. Review
  15. Article
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  18. Article
  19. Review
  20. T-lymphocyte homing: an underappreciated yet critical hurdle for successful cancer immunotherapy.Laboratory investigation; a journal of technical methods and pathology · 2017
    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

4 authors at 1 institution in 1 country.

Robert C FuhlbriggeDepartment of Dermatology, Brigham and Women's Hospital, Harvard Institutes of Medicine, 77 Ave Louis Pasteur, Boston, MA 02115, USA. rfuhlbrigge@partners.org
Sandra L King
Robert Sackstein
Thomas S Kupper
Brigham and Women's Hospital · US

Funding

Skin Homing T CellsR01AR065807 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI KUPPER, THOMAS S. · 2013 to 2022
$6.3M
SKIN HOMING T CELLS--MOLECULAR CHARACTERIZATION OF CLAR01AI041707 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI KUPPER, THOMAS S. · 1997 to 2012
$4.1M
Structure Function Analysis of T Cell E-Selectin LigandsR01AI056084 · NIAID · BRIGHAM AND WOMEN'S HOSPITAL · PI FUHLBRIGGE, ROBERT C · 2003 to 2007
$1.5M
NIAID NIH HHS R01 AI056084NIAID NIH HHS R01 AI-41707NIAMS NIH HHS R01 AR065807
6 · The paper itself

Abstract

The recruitment of memory T cells from blood into tissues is a central element of immune surveillance and adaptive immune responses and a key feature of chronic cutaneous inflammatory diseases such as psoriasis and atopic dermatitis. Human memory T cells that infiltrate skin express the carbohydrate epitope cutaneous lymphocyte-associated antigen (CLA). Expression of the CLA epitope on T cells has been described on P-selectin glycoprotein ligand-1 (PSGL-1) and associated with the acquisition of both E-selectin and P-selectin ligand functions. In this report, we show that CD43, a sialomucin expressed constitutively on T cells, can also be decorated with the CLA epitope and serve as an E-selectin ligand. CLA expressed on CD43 was found exclusively on the high-molecular-weight (125 kDa) glycoform bearing core-2-branched O-linked glycans. CLA+ CD43 purified from human T cells supported tethering and rolling in shear flow via E-selectin but did not support binding of P-selectin. The identification and characterization of CD43 as a T-cell E-selectin ligand distinct from PSGL-1 expands the role of CD43 in the regulation of T-cell trafficking and provides new targets for the modulation of immune functions in skin.

Indexed as

Antibodies, MonoclonalAntigens, Differentiation, T-LymphocyteAntigens, NeoplasmE-SelectinHumansLeukosialinMembrane GlycoproteinsMonocytesT-LymphocytesAntibodies, MonoclonalAntigens, Differentiation, T-LymphocyteAntigens, NeoplasmCTAGE1 protein, humanE-SelectinLeukosialinMembrane GlycoproteinsP-selectin ligand protein

Identifiers

PMID16269612
PMCPMC1895405
OpenAlexW2035724007

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.