Systemic Lupus Erythematosus
Conditions
Keywords
Systemic lupus erythematosus, autoimmunity, O-GlcNAcylation
Brief summary
This study aims at defining the role of O-GlcNAcylation is in the physiopathology of systemic lupus erythematosus (SLE). O-GlcNAcylation is a metabolic pathway potentially implicated in SLE with potential for the discovery of new therapeutic strategies.
Detailed description
Systemic lupus erythematosus (SLE) is a rare and potentially life-threatening auto-immune systemic disease. There is an urgent need for better comprehension of the physiopathology of the disease and to discover new therapeutic pathways. The hexosamine biosynthesis pathway, or HBP, is an important regulator of immunity and results in a post-transductional modification of proteins called O-GlcNAcylation and involved in inflammation and immunity. There is a very unbalanced sex ratio in favor of women in SLE suggesting a role of the X chromosome in the physiopathology of the disease. The human OGT gene (a key O-GlcNAcylation enzyme) is localized on the X chromosome, near the XIST gene responsible for the inactivation of one X chromosome by methylation. Moreover, genes encoding CD40L, CXCR3 and OGT have been shown to be demethylated and overexpressed in T cells of women with systemic systemic lupus erythematosus compared to men with the same pathology. The investigators hypothesize that O-GlcNAcylation is increased in the effector lymphocytes of SLE patients and involved in the pathophysiology of the disease. Therefore, inhibiting O-GlcNAcylation may be a promising therapeutic option in SLE. This study will recruit 100 patients with SLE followed in Bordeaux University Hospital. Among classical disease activity information, blood samples will be collected at study visit to study O-GlcNAcylation levels in immune cells. Fundamental research will be realized on patients' sample. Clinical and biological disease activity, treatment and outcomes will be studied in correlation with O-GlcNAcylation levels. Patients will be included within their usual follow-up. No extra visit will be needed and blood samples will be drawn at the same times as those drawn for clinical purposes.
Interventions
BIOLOGICALblood sample
30 ml whole blood for Peripheral blood mononuclear cell (PBMC) and monocytes isolation
Sponsors
University Hospital, Bordeaux
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Adult patient aged over 18 years old * Diagnosis of systemic lupus erythematosus * Affiliated person or beneficiary of a social security scheme. * Having signed an informed consent (at the latest on the day of inclusion and before any examination required by research).
Exclusion criteria
* Pregnant or breastfeeding women, * Patient concerned by articles L 1121-5 to L 1121-8 (persons deprived of their liberty by a judicial or administrative decision, minors, persons of legal age who are the object of a legal protection measure or unable to express their consent)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Quantification of O-GlcNAcylation level in the blood samples of SLE | At baseline (Day 0) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Disease activity according to Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) | At baseline (Day 0) | score (Min value: 0 - Max value: 105), with higher values mean higher disease activity. |
| Disease activity according to British Lupus Assessment Group Index 2004 (BILAG-2004) | At baseline (Day 0) | (Min value : 0 - Max value : 4), with higher values mean more severe symptoms |
| Quantification of OGT biallelic expression in the blood samples of SLE | At baseline (Day 0) | — |
Countries
France
Outcome results
None listed