Interferon Pathway Activation in Monogenic and Nonmonogenic Forms of Pediatric SLE
- Conditions
- Systemic Lupus Erythematosus of Childhood
- Interventions
- Other: Assessment activation of interferon pathway
- Registration Number
- NCT06586710
- Lead Sponsor
- Meyer Children's Hospital IRCCS
- Brief Summary
Pediatric SLE includes monogenic forms, some of which involve the interferon type I (IFN-I) pathway. The IFN-I pathway is renally active in adult SLE and correlates with the extent of renal damage. In pediatric SLE, and particularly in lupus nephritis, activation of the IFN-I pathway has never been studied, nor is it known whether monogenic forms underlie more pronounced interferon activation.
- Detailed Description
Pediatric systemic lupus erythematosus (SLE) (cSLE), compared with adult SLE, is characterized by a more severe phenotype, with more marked hematologic, neuropsychiatric, and renal changes. Lupus nephritis is a pivotal manifestation of pediatric SLE and an important prognostic factor. It is hypothesized that activation of the interferon pathway is more pronounced in monogenic forms, in which the response to IFN-I represents the primary alteration and likely the main pathogenic mechanism.
This finding may also be relevant in light of the availability of new drugs that selectively target the IFN-I pathway.
Demonstration of IFN-I pathway activation could be used as a diagnostic algorithm in aggressive pediatric forms resistant to immunosuppressive therapy and represent a therapeutic target.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 60
- Diagnosis of SLE arising before the age of majority (until the age of 18 years) according to SLICC and/or EULAR criteria 2019;
- Clinical, laboratory and/or histologic evidence of renal involvement manifested before the age of 18 years;
- Signature of informed consent.
- Onset of renal disease after the age of 18 years;
- SLE secondary to drugs or associated with other diseases such as systemic sclerosis, rheumatoid arthritis, Sjögren's syndrome, and other connectivities.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Activation of interferon pathway Assessment activation of interferon pathway Assessment activation of interferon pathway on biological samples (blood and kidney biopsy) in cSLE patients
- Primary Outcome Measures
Name Time Method Difference between monogenic and non-monogenic forms of cSLE At the enrollment, in case of renal flare, in case of disease remission Quantification of the IFN-I target genes distinguishing between monogenic and non-monogenic forms.
Evaluation of expression of MXA protein in renal biopsy Biopsy available at enrollment Evaluation of expression of MXA protein in renal biopsy (by fluorescence microscopy), distinguishing between genetic and non-genetic forms
Evaluation of the proportions of the various WHO histological classes of renal biopsy At the end of the study (24 months after enrollment) Evaluation of the proportions of the various WHO histological classes of renal biopsy in patients with monogenic and non-monogenic lupus nephritis.
Histological diagnosis at renal biopsy: WHO histological pattern, activity index, chronicity index, renal TMA
- Secondary Outcome Measures
Name Time Method Phenotype characterization of cSLE At the onset of the disease, 3, 6, 12, 24 months from the kidney biopsy, Description of clinical parameters, as SLEDAI-2K, in patients with cSLE and renal involvement, distinguishing between monogenic and non-monogenic forms.
Description of laboratory parameters as renal function (eGFR CKiD 25) in patients with cSLE and renal involvement, distinguishing between monogenic and non-monogenic formsCorrelation between the clinical phenotype, response to treatment and amplification of the interferon pathway At the onset of the disease, 3, 6, 12, 24 months from the kidney biopsy, Correlation between the clinical phenotype (laboratory parameters and during renal flare), response to treatment and amplification of the interferon pathway, distinguishing between monogenic and non-monogenic forms.
Clinical, laboratory and histological data relating to any renal flare: number of flares, date of the flare, months from the first biopsy diagnosis of lupus nephritis, clinical manifestations, data from the biopsy performed during the flare, WHO histological pattern compared with the first biopsy, activity index, chronicity index, induction therapy, maintenance therapy
Trial Locations
- Locations (3)
Meyer Children's Hospital IRCCS
🇮🇹Firenze, Italy
IRCCS Gianna Gaslini
🇮🇹Genova, Italy
IRCCS Humanitas Research Hospital
🇮🇹Rozzano, Italy