Mass cytometry reveals atypical immune profile notably impaired maturation of memory CD4 T with Gb3-related CD27 expression in CD4 T cells in Fabry disease.
| dc.rights.license | open | en_US |
| dc.contributor.author | MAUHIN, Wladimir | |
| dc.contributor.author | DZANGUE-TCHOUPOU, Gaelle | |
| dc.contributor.author | AMELIN, Damien | |
| dc.contributor.author | CORNEAU, Aurélien | |
| dc.contributor.author | LAMARI, Foudil | |
| dc.contributor.author | ALLENBACH, Yves | |
| dc.contributor.author | DUSSOL, Bertrand | |
| dc.contributor.author | LEGUY-SEGUIN, Vanessa | |
| dc.contributor.author | D'HALLUIN, Pauline | |
| dc.contributor.author | MATIGNON, Marie | |
| dc.contributor.author | MAILLOT, François | |
| dc.contributor.author | LY, Kim-Heang | |
| dc.contributor.author | BESSON, Gérard | |
| dc.contributor.author | WILLEMS, Marjolaine | |
| dc.contributor.author | LABOMBARDA, Fabien | |
| dc.contributor.author | MASSEAU, Agathe | |
| dc.contributor.author | LAVIGNE, Christian | |
| hal.structure.identifier | Hôpital Pellegrin | |
| hal.structure.identifier | Service de génétique médicale | |
| hal.structure.identifier | Université de Bordeaux [UB] | |
| hal.structure.identifier | Centre Hospitalier Universitaire de Bordeaux [CHU Bordeaux] | |
| hal.structure.identifier | Laboratoire Maladies Rares: Génétique et Métabolisme (Bordeaux) [U1211 INSERM/MRGM] | |
| dc.contributor.author | LACOMBE, Didier | |
| dc.contributor.author | MAILLARD, Hélène | |
| dc.contributor.author | LIDOVE, Olivier | |
| dc.contributor.author | BENVENISTE, Olivier | |
| dc.date.accessioned | 2024-08-29T14:00:53Z | |
| dc.date.available | 2024-08-29T14:00:53Z | |
| dc.date.issued | 2024-07-01 | |
| dc.identifier.issn | 1573-2665 | en_US |
| dc.identifier.uri | https://oskar-bordeaux.fr/handle/20.500.12278/201356 | |
| dc.description.abstractEn | Fabry disease (FD) is an X-linked disease characterized by an accumulation of glycosphingolipids, notably of globotriaosylceramide (Gb3) and globotriaosylsphingosine (lysoGb3) leading to renal failure, cardiomyopathy, and cerebral strokes. Inflammatory processes are involved in the pathophysiology. We investigated the immunological phenotype of peripheral blood mononuclear cells in Fabry patients depending on the clinical phenotype, treatment, Gb3, and lysoGb3 levels and the presence of anti-drug antibodies (ADA). Leucocytes from 41 male patients and 20 controls were analyzed with mass cytometry using both unsupervised and supervised algorithms. FD patients had an increased expression of CD27 and CD28 in memory CD45- and CD45 + CCR7-CD4 T cells (respectively p < 0.014 and p < 0.02). Percentage of CD45RA-CCR7-CD27 + CD28+ cells in CD4 T cells was correlated with plasma lysoGb3 (r = 0.60; p = 0.0036) and phenotype (p < 0.003). The correlation between Gb3 and CD27 in CD4 T cells almost reached significance (r = 0.33; p = 0.058). There was no immune profile associated with the presence of ADA. Treatment with agalsidase beta was associated with an increased proportion of Natural Killer cells. These findings provide valuable insights for understanding FD, linking Gb3 accumulation to inflammation, and proposing new prognostic biomarkers. | |
| dc.language.iso | EN | en_US |
| dc.subject.en | CD27 | |
| dc.subject.en | Fabry disease | |
| dc.subject.en | Agalsidase | |
| dc.subject.en | Globotriaosylceramide | |
| dc.subject.en | Inflammation | |
| dc.subject.en | Phenotype | |
| dc.title.en | Mass cytometry reveals atypical immune profile notably impaired maturation of memory CD4 T with Gb3-related CD27 expression in CD4 T cells in Fabry disease. | |
| dc.title.alternative | J Inherit Metab Dis | en_US |
| dc.type | Article de revue | en_US |
| dc.identifier.doi | 10.1002/jimd.12727 | en_US |
| dc.subject.hal | Sciences du Vivant [q-bio]/Génétique | en_US |
| dc.identifier.pubmed | 38623626 | en_US |
| bordeaux.journal | Journal of Inherited Metabolic Disease | en_US |
| bordeaux.page | 818-833 | en_US |
| bordeaux.volume | 47 | en_US |
| bordeaux.hal.laboratories | Maladies Rares : Génétique et Métabolisme (MRGM) - UMR 1211 | en_US |
| bordeaux.issue | 4 | en_US |
| bordeaux.institution | Université de Bordeaux | en_US |
| bordeaux.institution | INSERM | en_US |
| bordeaux.peerReviewed | oui | en_US |
| bordeaux.inpress | non | en_US |
| bordeaux.identifier.funderID | Shire Human Genetic Therapies | en_US |
| bordeaux.import.source | pubmed | |
| hal.identifier | hal-04681413 | |
| hal.version | 1 | |
| hal.date.transferred | 2024-08-29T14:00:55Z | |
| hal.popular | non | en_US |
| hal.audience | Internationale | en_US |
| hal.export | true | |
| workflow.import.source | pubmed | |
| dc.rights.cc | Pas de Licence CC | en_US |
| bordeaux.COinS | ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Journal%20of%20Inherited%20Metabolic%20Disease&rft.date=2024-07-01&rft.volume=47&rft.issue=4&rft.spage=818-833&rft.epage=818-833&rft.eissn=1573-2665&rft.issn=1573-2665&rft.au=MAUHIN,%20Wladimir&DZANGUE-TCHOUPOU,%20Gaelle&AMELIN,%20Damien&CORNEAU,%20Aur%C3%A9lien&LAMARI,%20Foudil&rft.genre=article |
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