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Neuron-specific Humoral and Cellular Immune Correlates of Structural and Functional Brain Connectomics in Neuropsychiatric Lupus (INLES)

S

San Donato Group (GSD)

Status

Enrolling

Conditions

Systemic Lupus Erythematosus

Treatments

Diagnostic Test: MRI

Study type

Observational

Funder types

Other

Identifiers

NCT05880121
GR-2021-12372172

Details and patient eligibility

About

Systemic lupus erythematosus (SLE) is the prototype systemic autoimmune disease. Neuropsychiatric SLE (NPSLE) is a major cause of morbidity. Its pathophysiology remains unclear and target autoantigens have not yet been identified. Site- specific autoantigen expression might correlate with imaging abnormalities. Based on existing expertise on the use of peptide/protein arrays and on antigen-specific T cell tracking, we plan to identify new fingerprints and targets for NPSLE. SLE patients +/- NPSLE and healthy subjects will undergo advanced magnetic resonance imaging. Three-dimensional data on structural or functional brain architecture will be integrated with brain transcriptome atlases and candidate antigens for autoreactive autoantibodies and T lymphocytes identified and validated. The evidence will add to current knowledge on NPSLE pathophysiology, provide new multimodal diagnostic tools for better patient care and a platform for innovative, personalized treatments.

Enrollment

200 estimated patients

Sex

All

Ages

15+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients with SLE

  • Diagnosis of SLE according to the ACR 1997, SLICC 2012 or EULAR/ACR 2019 criteria
  • age ≥ 18 years (reference centre)
  • age 15-17 years (affiliated centre)

Healthy subjects

  • Charlson's Comorbidity Index=0 and no chronic treatment
  • age ≥ 18 years (reference centre)
  • age 15-17 years (affiliated centre)

Exclusion criteria

  • History of T-cell neoplasia
  • Active B-cell neoplasia or history of B-cell neoplasia of less than five years
  • Contraindications to MRI
  • Pregnancy
  • Ongoing or past treatment with T-depleting agents
  • History of brain cancer
  • History of congenital brain disorders
  • Cerebral disorders secondary to trauma, toxins or other metabolic or environmental factors unrelated to SLE according to the Investigator's evaluation
  • Any other condition conferring excessive physical and psychological risk to the subject according to the Investigator's opinion

Trial design

200 participants in 2 patient groups

systemic lupus erythematosus
Description:
Patients with SLE according to the 1997 ACR, 2012 SLICC or 2019 EULAR/ACR criteria will undergo MRI along with neuropsychological tests, rheumatological evaluation and blood sample collection at baseline and after at least 12 months or during a new neuropsychiatric manifestation. In case of existing MRI with compatible features, they will be used as baseline studies.
Treatment:
Diagnostic Test: MRI
healthy controls
Description:
Subjects with Charlson's Comorbidity Index=0 with no ongoing chronic therapy and no history of immune-mediated disease will undergo a single MRI study, along with neuropsychological tests and blood sample collection. In case of existing MRI with compatible features, no additional studies will be performed in this cohort.
Treatment:
Diagnostic Test: MRI

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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