INFLAMAST: Are Mast Cells Involved in Autoinflammatory Diseases

Sponsor
Assistance Publique - Hôpitaux de Paris (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05292768
Collaborator
Institut Imagine (Other)
590
1
55
10.7

Study Details

Study Description

Brief Summary

Autoinflammatory diseases (AID) are caused by innate immunity dysregulation. AID pathophysiology is only partly understood, especially in the case of unclassified AID. Mast cells (MC) are innate immune cells associated with a spectrum of disease between systemic mastocytosis and mast cell activation syndrome. The implication of MC has been shown in cryopyrin associated periodic syndrome (CAPS).Our aim is to evaluate the involvement of MC in AID by assessing clinical and biological signs of MC activation and studying cutaneous and digestive biopsies.

Detailed Description

Autoinflammatory diseases (AID) are caused by innate immunity dysregulation and characterized by recurrent bouts of fever, frequently associated with digestive, articular or cutaneous symptoms, and sometimes ocular, auricular or neurologic inflammation. The most frequent monogenic AID is Familial Mediterranean fever (FMF).

Despite recent genetic progress AID pathophysiology is only partly understood, especially in the case of unclassified AID.

Mast cells (MC) are innate immune cells associated with a spectrum of disease between systemic mastocytosis and mast cell activation syndrome (MCAS). In MCAS, patients have various symptoms including abdominal pain, bloating, pruritus, flush, anxiety, fatigue, among which some are similar to those seen in patients with AID. The implication of MC has been shown in cryopyrin associated periodic syndrome (CAPS).

Our hypothesis is that MC could be involved in AID pathophysiology,

In order to test this hypothesis, we plan to study :
  • clinical MC activation symptoms via a standardized clinical score

  • biological MC mediators : by measuring total serum tryptase and histamine in total blood, plasma and urine

  • MC infiltration on gastro-intestinal (GI) tract and cutaneous biopsies We will compare clinical MC activation score in AID patients to patients with mastocytosis, with other inflammatory diseases, and with healthy controls.

Study Design

Study Type:
Observational
Anticipated Enrollment :
590 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Are Mast Cells Involved in Autoinflammatory Diseases
Anticipated Study Start Date :
Mar 1, 2022
Anticipated Primary Completion Date :
Oct 1, 2026
Anticipated Study Completion Date :
Oct 1, 2026

Arms and Interventions

Arm Intervention/Treatment
Patients with AID

Control patients with mastocytosis

Control patients with normal digestive biopsy

Control patients with renal biopsy

Control patients with inflammatory disease

Healthy control from healthcare workers

Outcome Measures

Primary Outcome Measures

  1. : presence of MCAS [at inclusion]

    presence of clinical and biological markers of MCAS

Secondary Outcome Measures

  1. comparison of clinical symptoms of MC activation between groups [at inclusion]

    we will compare clinical symptoms of MC activation between AID patients and other groups

  2. MC mediators associated to AID [at inclusion]

    determine which MC mediators are elevated in AID and if they correlate with inflammation

  3. MC infiltration in biopsies from AID patients [at inclusion, retrospectively]

    we will study MC infiltration in digestive, renale and cutaneous biopsies from patients with AID and compare them with biopsies from the other groups from subgroups of patients who had a biopsy performed.

  4. basophilic polynuclear activation in AID patients [at inclusion, retrospectively]

    we will study basophilic polynuclear activation from blood samples of AID patients

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
  • Patients >18 years old with Auto-inflammatory diseases already followed up at the CeRéMAIA (french national reference center for autoinflamamtory diseases and AA amyloidosis) of Tenon hospital and included in the JIRcohorte

  • Healthy adult controls, age- and sex-matched with MAI patients, and controls with mastocytosis, an immuno-inflammatory disease.

  • Subject affiliated to or entitled to a social security scheme

  • Collection of the patient's or healthy control's non-opposition

Exclusion Criteria:
  • Subjects unable to answer questions or express themselves

  • Subjects who do not speak French

  • Subject deprived of liberty or under legal protection.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Service de Médecine Interne Paris France 75020

Sponsors and Collaborators

  • Assistance Publique - Hôpitaux de Paris
  • Institut Imagine

Investigators

  • Principal Investigator: Sophie GEORGIN-LAVIALLE, PU-PH, Assistance Publique - Hôpitaux de Paris

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Assistance Publique - Hôpitaux de Paris
ClinicalTrials.gov Identifier:
NCT05292768
Other Study ID Numbers:
  • APHP210126
First Posted:
Mar 23, 2022
Last Update Posted:
Mar 23, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Assistance Publique - Hôpitaux de Paris
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 23, 2022