Evidence map›Paper›PMID 27438772›Full record

ArticleImmunity2016

CD95-Mediated Calcium Signaling Promotes T Helper 17 Trafficking to Inflamed Organs in Lupus-Prone Mice.

Amanda Poissonnier, Doriane Sanséau, Matthieu Le Gallo, Marine Malleter, Nicolas Levoin, Roselyne Viel, Lucie Morere, Aubin Penna, Patrick Blanco, Alain Dupuy and 14 more

Open access · hybridAbstract read
In one paragraph

Article in Immunity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
5.6field-weighted citation impact, top 4% 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

42 citing papers in PubMed, 80 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. CD95/Fas stoichiometry in future precision medicine.Cell death and differentiation · 2025
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. A Contemporary Update on the Diagnosis of Systemic Lupus Erythematosus.Clinical reviews in allergy & immunology · 2022
    Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. miR-216b-5p Inhibited the Progression of Experimental Optic Neuritis via Downregulating FAS.Evidence-based complementary and alternative medicine : eCAM · 2022
    Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 8 institutions in 3 countries.

Amanda PoissonnierCentre Eugène Marquis, Rue Bataille Flandres Dunkerque, 35042 Rennes, France; INSERM ERL440-OSS, Equipe Labellisée, Ligue Contre Le Cancer, 35042 Rennes, France; Université de Rennes 1, 2 Ave. du Prof. Léon Bernard, 35043 Rennes, France.
Doriane SanséauCentre Eugène Marquis, Rue Bataille Flandres Dunkerque, 35042 Rennes, France; INSERM ERL440-OSS, Equipe Labellisée, Ligue Contre Le Cancer, 35042 Rennes, France; Université de Rennes 1, 2 Ave. du Prof. Léon Bernard, 35043 Rennes, France.
Matthieu Le GalloCentre Eugène Marquis, Rue Bataille Flandres Dunkerque, 35042 Rennes, France; INSERM ERL440-OSS, Equipe Labellisée, Ligue Contre Le Cancer, 35042 Rennes, France; Université de Rennes 1, 2 Ave. du Prof. Léon Bernard, 35043 Rennes, France.
Marine MalleterCentre Eugène Marquis, Rue Bataille Flandres Dunkerque, 35042 Rennes, France; INSERM ERL440-OSS, Equipe Labellisée, Ligue Contre Le Cancer, 35042 Rennes, France; Université de Rennes 1, 2 Ave. du Prof. Léon Bernard, 35043 Rennes, France; Biosit, Plateforme H2P2, Biogenouest, 2 Ave. du Prof. Léon Bernard, 35043 Rennes, France.
Nicolas LevoinBioprojet Biotech, Rue du Chesnay Beauregard, 35760 Saint-Grégoire, France.
Roselyne VielUniversité de Rennes 1, 2 Ave. du Prof. Léon Bernard, 35043 Rennes, France; Biosit, Plateforme H2P2, Biogenouest, 2 Ave. du Prof. Léon Bernard, 35043 Rennes, France.
Lucie MorereCentre Eugène Marquis, Rue Bataille Flandres Dunkerque, 35042 Rennes, France; INSERM ERL440-OSS, Equipe Labellisée, Ligue Contre Le Cancer, 35042 Rennes, France; Université de Rennes 1, 2 Ave. du Prof. Léon Bernard, 35043 Rennes, France.
Aubin PennaUniversité de Rennes 1, 2 Ave. du Prof. Léon Bernard, 35043 Rennes, France; INSERM U1085, 2 Ave. du Prof. Léon Bernard, 35043 Rennes, France.
Patrick BlancoUniversité de Bordeaux, CHU Bordeaux, 146 Rue Léo Saignat, 33076 Bordeaux, France; CNRS UMR 5164, 146 Rue Léo Saignat, 33076 Bordeaux, France.
Alain DupuyUniversité de Rennes 1, 2 Ave. du Prof. Léon Bernard, 35043 Rennes, France; Centre Hospitalier Universitaire Rennes, 2 Rue Henri Le Guilloux, 35022 Rennes, France.
Florence PoizeauCentre Eugène Marquis, Rue Bataille Flandres Dunkerque, 35042 Rennes, France; INSERM ERL440-OSS, Equipe Labellisée, Ligue Contre Le Cancer, 35042 Rennes, France; Centre Hospitalier Universitaire Rennes, 2 Rue Henri Le Guilloux, 35022 Rennes, France.
Alain FautrelUniversité de Rennes 1, 2 Ave. du Prof. Léon Bernard, 35043 Rennes, France; Biosit, Plateforme H2P2, Biogenouest, 2 Ave. du Prof. Léon Bernard, 35043 Rennes, France.
Julien SeneschalUniversité de Bordeaux, CHU Bordeaux, 146 Rue Léo Saignat, 33076 Bordeaux, France; INSERM U1035, 146 rue Léo Saignat, 33076 Bordeaux, France.
Florence JouanCentre Eugène Marquis, Rue Bataille Flandres Dunkerque, 35042 Rennes, France; INSERM ERL440-OSS, Equipe Labellisée, Ligue Contre Le Cancer, 35042 Rennes, France; Université de Rennes 1, 2 Ave. du Prof. Léon Bernard, 35043 Rennes, France.
Jerome RitzDivision of Hematologic Malignancies and Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, United States.
Edouard ForcadeUniversité de Bordeaux, CHU Bordeaux, 146 Rue Léo Saignat, 33076 Bordeaux, France; CNRS UMR 5164, 146 Rue Léo Saignat, 33076 Bordeaux, France; Division of Hematologic Malignancies and Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, United States.
Nathalie RiouxUniversité de Rennes 1, 2 Ave. du Prof. Léon Bernard, 35043 Rennes, France; INSERM U1085, 2 Ave. du Prof. Léon Bernard, 35043 Rennes, France; INSERM U1035, 146 rue Léo Saignat, 33076 Bordeaux, France.
Cécile Contin-BordesUniversité de Bordeaux, CHU Bordeaux, 146 Rue Léo Saignat, 33076 Bordeaux, France; CNRS UMR 5164, 146 Rue Léo Saignat, 33076 Bordeaux, France.
Thomas DucretUniversité de Bordeaux, CHU Bordeaux, 146 Rue Léo Saignat, 33076 Bordeaux, France; INSERM U1045, 146 rue Léo Saignat, 33076 Bordeaux, France.
Anne-Marie VacherUniversité de Bordeaux, CHU Bordeaux, 146 Rue Léo Saignat, 33076 Bordeaux, France; INSERM U1218, Institut Bergonié, 33076 Bordeaux, France.
Paul A BarrowSchool of Veterinary Medicine and Science, University of Nottingham, Leicestershire LE12 5RD, United Kingdom.
Robin J FlynnSchool of Veterinary Medicine and Science, University of Nottingham, Leicestershire LE12 5RD, United Kingdom.
Pierre VacherUniversité de Bordeaux, CHU Bordeaux, 146 Rue Léo Saignat, 33076 Bordeaux, France; INSERM U1218, Institut Bergonié, 33076 Bordeaux, France.
Patrick LegembreCentre Eugène Marquis, Rue Bataille Flandres Dunkerque, 35042 Rennes, France; INSERM ERL440-OSS, Equipe Labellisée, Ligue Contre Le Cancer, 35042 Rennes, France; Université de Rennes 1, 2 Ave. du Prof. Léon Bernard, 35043 Rennes, France; Biosit, Plateforme H2P2, Biogenouest, 2 Ave. du Prof. Léon Bernard, 35043 Rennes, France. Electronic address: patrick.legembre@inserm.fr.
Inserm · FRUniversité de Bordeaux · FRCentre National de la Recherche Scientifique · FRStructure Fédérative de Recherche en Biologie et Santé de Rennes · FRUniversity of Nottingham · GBBioprojet (France) · FRCentre Hospitalier Universitaire de Rennes · FRDana-Farber Cancer Institute · US

Funding

Biotechnology and Biological Sciences Research Council BB/M018369/1
6 · The paper itself

Abstract

CD95 ligand (CD95L) is expressed by immune cells and triggers apoptotic death. Metalloprotease-cleaved CD95L (cl-CD95L) is released into the bloodstream but does not trigger apoptotic signaling. Hence, the pathophysiological role of cl-CD95L remains unclear. We observed that skin-derived endothelial cells from systemic lupus erythematosus (SLE) patients expressed CD95L and that after cleavage, cl-CD95L promoted T helper 17 (Th17) lymphocyte transmigration across the endothelial barrier at the expense of T regulatory cells. T cell migration relied on a direct interaction between the CD95 domain called calcium-inducing domain (CID) and the Src homology 3 domain of phospholipase Cγ1. Th17 cells stimulated with cl-CD95L produced sphingosine-1-phosphate (S1P), which promoted endothelial transmigration by activating the S1P receptor 3. We generated a cell-penetrating CID peptide that prevented Th17 cell transmigration and alleviated clinical symptoms in lupus mice. Therefore, neutralizing the CD95 non-apoptotic signaling pathway could be an attractive therapeutic approach for SLE treatment.

Indexed as

Calcium SignalingAnimalsCells, CulturedDisease Models, Animalfas ReceptorFemaleHumansInflammationInterferon-gammaInterleukin-17Lupus Erythematosus, SystemicLysophospholipidsMiceMice, Inbred MRL lprPeptide FragmentsPhospholipase C gammafas ReceptorInterferon-gammaInterleukin-17LysophospholipidsPeptide FragmentsPhospholipase C gammaPlcg1 protein, mouseSphingosinesphingosine 1-phosphateCalciumCD95inflammationlupussphingosine-1 phosphateTh17 cell

Identifiers

PMID27438772
PMCPMC4961226
OpenAlexW2479818795

What OpenQuestion holds

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LicenceCC BY
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.