Study of Neonatal IgG Fc Receptor Expression in Natural Killer T Cells Expressing an Invariant T Receptor : Implication in the Pathophysiology of Systemic Lupus
Condition(s) studied
Investigational drug(s) / intervention(s)
Blood sample: Three extra tubes of blood will be taken at each consultation or inpatient visit when routine blood samples are taken as part of lupus monitoring.
Study summary
This study evaluates the variation of expression of the neonatal Fc receptor (FcRn) in Natural Killer T Cells Expressing an Invariant T Receptor (iNKT) and monocytes along with the surface expression of Fc gamma type II receptor (RII) and RIII in active or newly diagnosed lupus patients compared to inactive lupus patients.
Eligibility
Primary outcome measure(s)
- FcRn Expression analysis in Circulating iNKT lymphocytes — through study completion, an average of 3 year
by flow cytometry (mean fluorescence intensity) - FcRn Expression analysis in circulating monocytes — through study completion, an average of 3 year
by flow cytometry (mean fluorescence intensity) - FcgammaRII Expression analysis in Circulating iNKT lymphocytes — through study completion, an average of 3 year
by flow cytometry (mean fluorescence intensity) - FcgammaRII Expression analysis in circulating monocytes — through study completion, an average of 3 year
by flow cytometry (mean fluorescence intensity) - FcgammaRIII Expression analysis in Circulating iNKT lymphocytes — through study completion, an average of 3 year
by flow cytometry (mean fluorescence intensity) - FcgammaRIII Expression analysis in in circulating monocytes — through study completion, an average of 3 year
by flow cytometry (mean fluorescence intensity)
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| University Hospital | Tours | France | Recruiting |
More University Hospital, Tours trials in France
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05859191 on ClinicalTrials.gov ↗ ← All trials in France