CYTILDASS: Evaluation of Antigen-specific T Cells in Patients With Antisynthetase Syndrome and Interstitial Lung Disease

Sponsor
Central Hospital, Nancy, France (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05984394
Collaborator
(none)
24
6
24
4
0.2

Study Details

Study Description

Brief Summary

Antisynthetase syndrome (AS) is a rare overlapping myositis characterized by cellular and humoral autoimmune responses directed against aminoacyl-tRNA synthetases. Intesrtitial lung disease (ILD) is a leading cause of mortality in antisynthetase syndrome. Recently, antigen-specific IFN-γ+ CD4+ T cells have been identified in bronchoalveolar fluid (BAL) of patients with antisynthetase syndrome and ILD. Elevated levels of IL1β, IL12, IL18, TNFα, IL17A, IL22 have also been detected in peripheral blood of AS patients, especially those with progressive ILD. Implication of innate lymphoid cells (ILC) and mucosal-associated invariant T cells (MAIT) have not yet been studied in patients with AS. Targeted therapies against Th1 and Th17 cells may represent a promising treatment in patients AS patients with ILD.

Investigators suppose that antigen-specific Th1 and Th17 cells, ILC and MAIT at ILD diagnosis are associated with ILD severity at diagnosis and could predict treatment response at 6 months.

The main objective is to study the correlation between BAL antigen-specific Th1 and Th17 cells at ILD diagnosis and clinical evolution after 6 months of treatment according to initial ILD severity.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: BAL antigen-specific Th1 cells and Th17 cells, ILC and MAIT

Study Design

Study Type:
Observational
Anticipated Enrollment :
24 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Evaluation of Antigen-specific Th1 and T17 Cells, ILC and MAIT in Patients With Antisynthetase Syndrome and Interstitial Lung Disease
Anticipated Study Start Date :
Oct 31, 2023
Anticipated Primary Completion Date :
Oct 31, 2025
Anticipated Study Completion Date :
Oct 31, 2025

Arms and Interventions

Arm Intervention/Treatment
AS patients with ILD

New diagnosis of patients with AS syndrome and ILD

Diagnostic Test: BAL antigen-specific Th1 cells and Th17 cells, ILC and MAIT
BAL antigen-specific Th1 cells and Th17 cells, ILC and MAIT

Outcome Measures

Primary Outcome Measures

  1. BAL antigen-specific Th1 and Th17 cells [baseline (J0)]

    BAL antigen-specific Th1 and Th17 cells percentages among BAL total CD4+ T cells

  2. FVC relative change [within 6 months after diagnosis]

    Relative change of FVC percentage

Secondary Outcome Measures

  1. BAL antigen-specific Th1 and Th17 cells [baseline (J0)]

    BAL antigen-specific Th1 and Th17 cells percentages among total BAL CD4+ T cells

  2. FVC [baseline (J0)]

    FVC percentage at ILD diagnosis

  3. FVC absolute change [within 6 months after diagnosis]

    Absolute change of FVC percentage

  4. Global activity [baseline (J0)]

    MDAAT score

Other Outcome Measures

  1. BAL ILC [baseline (J0)]

    BAL ILC percentage among total BAL lymphoid cells

  2. BAL MAIT [baseline (J0)]

    BAL MAIT percentage among total BAL T cells

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
  • Patient with new diagnosis of AS with ILD
Exclusion Criteria:
  • Patient with ILD differential diagnosis

  • Corticosteroid treatment, immunosuppresive or immunomodulatory drugs in the past 3 months before diagnosis

Contacts and Locations

Locations

Site City State Country Postal Code
1 Bernard Bonnotte Dijon France
2 Julien Campagne Metz France
3 Paul Decker Nancy France
4 Olivier Benveniste Paris France
5 Loïs Bolko Reims France
6 Alain Meyer Strasbourg France

Sponsors and Collaborators

  • Central Hospital, Nancy, France

Investigators

  • Principal Investigator: Paul Decker, MD, CHU Nancy

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Paul DECKER, MD, Principal Investigator, Central Hospital, Nancy, France
ClinicalTrials.gov Identifier:
NCT05984394
Other Study ID Numbers:
  • 2023-A00804-41
First Posted:
Aug 9, 2023
Last Update Posted:
Aug 9, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 9, 2023