Evidence map›Paper›PMID 11438456›Full record

ArticleThe American journal of pathology2001

HLA-G and NK receptor are expressed in psoriatic skin: a possible pathway for regulating infiltrating T cells?

S Aractingi, N Briand, C Le Danff, M Viguier, H Bachelez, L Michel, L Dubertret, E D Carosella

Open access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

39 citing papers in PubMed, 154 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. HLA-G Neo-Expression on Tumors.Frontiers in immunology · 2020
    Review
  12. Article
  13. Stem Cells as Potential Candidates for Psoriasis Cell-Replacement Therapy.International journal of molecular sciences · 2017
    Review
  14. Immunoregulatory Role of HLA-G in Allergic Diseases.Journal of immunology research · 2016
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Synthetic HLA-G proteins for therapeutic use in transplantation.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2013
    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

8 authors at 3 institutions in 1 country.

S AractingiSRHI (CEA,DSV-DRM), Commissariat à l'Energie Atomique,Unité de Dermatologie, Paris, France. selim.aractingi@tnn.ap-hop-paris.fr
N Briand
C Le Danff
M Viguier
H Bachelez
L Michel
L Dubertret
E D Carosella
Hôpital Saint-Louis · FRCommissariat à l'Énergie Atomique et aux Énergies Alternatives · FRSorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent data have suggested that in psoriasis, the T-infiltrating cells could be submitted to regulatory pathways, possibly through natural killer receptors. HLA-G binds to different natural killer receptors and is able to inhibit T-cell functions. Because this molecule is induced by interferon-gamma, a major cytokine in psoriasis, we asked whether HLA-G and its receptor might be expressed in this disease. Specific RNAs for HLA-G1 and HLA-G5 were consistently found in lesional skin specimens, soluble HLA-G5 transcripts being found only in psoriasis. HLA-G protein was found in all psoriatic sections, but never in normal skin controls. Double labeling demonstrated that HLA-G-positive cells were CD68(+), CD11c(+) macrophages. The NKR ILT2 was also present in psoriatic skin, the T CD4(+)-infiltrating cells expressing indeed ILT2. The demonstration of HLA-G and ILT2 expression in psoriatic skin suggests that this pathway may act as an inhibitory feed back aimed to down-regulate the deleterious effects of T-cell infiltrate in this disease.

Indexed as

Alternative SplicingAntigens, CDAntigens, Differentiation, MyelomonocyticCD4-Positive T-LymphocytesCD68 MoleculeFemaleHistocompatibility Antigens Class IHLA AntigensHLA-G AntigensHumansIntegrin alphaXbeta2Leukocyte Immunoglobulin-like Receptor B1Lymphocytes, Tumor-InfiltratingMacrophagesPsoriasisReceptors, ImmunologicAntigens, CDAntigens, Differentiation, MyelomonocyticCD68 antigen, humanCD68 MoleculeHistocompatibility Antigens Class IHLA AntigensHLA-G AntigensIntegrin alphaXbeta2Leukocyte Immunoglobulin-like Receptor B1LILRB1 protein, humanNKTR protein, humanReceptors, ImmunologicRNA, Messenger

Identifiers

PMID11438456
PMCPMC1850403
OpenAlexW1532423969

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.