An interactive web application for exploring systemic lupus erythematosus blood transcriptomic diversity.


Journal

Database : the journal of biological databases and curation
ISSN: 1758-0463
Titre abrégé: Database (Oxford)
Pays: England
ID NLM: 101517697

Informations de publication

Date de publication:
28 May 2024
Historique:
received: 02 10 2023
revised: 07 04 2024
accepted: 22 05 2024
medline: 29 5 2024
pubmed: 29 5 2024
entrez: 28 5 2024
Statut: ppublish

Résumé

In the field of complex autoimmune diseases such as systemic lupus erythematosus (SLE), systems immunology approaches have proven invaluable in translational research settings. Large-scale datasets of transcriptome profiling have been collected and made available to the research community in public repositories, but remain poorly accessible and usable by mainstream researchers. Enabling tools and technologies facilitating investigators' interaction with large-scale datasets such as user-friendly web applications could promote data reuse and foster knowledge discovery. Microarray blood transcriptomic data from the LUPUCE cohort (publicly available on Gene Expression Omnibus, GSE49454), which comprised 157 samples from 62 adult SLE patients, were analyzed with the third-generation (BloodGen3) module repertoire framework, which comprises modules and module aggregates. These well-characterized samples corresponded to different levels of disease activity, different types of flares (including biopsy-proven lupus nephritis), different auto-antibody profiles and different levels of interferon signatures. A web application was deployed to present the aggregate-level, module-level and gene-level analysis results from LUPUCE dataset. Users can explore the similarities and heterogeneity of SLE samples, navigate through different levels of analysis, test hypotheses and generate custom fingerprint grids and heatmaps, which may be used in reports or manuscripts. This resource is available via this link: https://immunology-research.shinyapps.io/LUPUCE/. This web application can be employed as a stand-alone resource to explore changes in blood transcript profiles in SLE, and their relation to clinical and immunological parameters, to generate new research hypotheses.

Identifiants

pubmed: 38805754
pii: 7683726
doi: 10.1093/database/baae045
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : National Institute of Allergy and Infectious Diseases, Autoimmunity Centers of Excellence
ID : U19-AI-082715
Organisme : Association pour le Développement des Recherches Biologiques et Médicales
Organisme : APHM
ID : NCT00920114
Organisme : National Institute of Allergy and Infectious Diseases, Autoimmunity Centers of Excellence
ID : U19-AI-082715
Organisme : Association pour le Développement des Recherches Biologiques et Médicales
Organisme : APHM
ID : NCT00920114

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press.

Auteurs

Eléonore Bettacchioli (E)

B Lymphocytes, Autoimmunity and Immunotherapies, UMR 1227, Univ Brest, Inserm, Brest 29200, France.
Brest University Hospital, Brest 29200, France.

Laurent Chiche (L)

Department of Internal Medicine, Hôpital Européen, Marseille 13003, France.

Damien Chaussabel (D)

Translational Medicine Division, Research Branch, Sidra Medicine, Doha 26999, Qatar.
Computational Sciences Department, The Jackson Laboratory, Farmington, CT 06032, USA.

Divi Cornec (D)

B Lymphocytes, Autoimmunity and Immunotherapies, UMR 1227, Univ Brest, Inserm, Brest 29200, France.
Brest University Hospital, Brest 29200, France.

Noémie Jourde-Chiche (N)

Department of Nephrology, AP-HM, Marseille 13003, France.
C2VN, INSERM, INRAE, Aix-Marseille Universite, Marseille 13003, France.

Darawan Rinchai (D)

Translational Medicine Division, Research Branch, Sidra Medicine, Doha 26999, Qatar.
Department of Infectious Diseases, St Jude's Children Research Hospital, TN, Memphis 38105, USA.

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