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TL1A Inhibition in Systemic Sclerosis-Related Skin Fibrosis and Immunological Alterations: A Proof-of-Concept In Vitro Study (FIBROSTOP) (FIBROSTOP)

4 de junio de 2026 actualizado por: Luca Navarini, Fondazione Policlinico Universitario Campus Bio-Medico

The Potential Pharmacological Role of the TNF-Like Ligand 1A (TL1A) Inhibition in Modulating Systemic Sclerosis (SSc)-Related Skin Fibrosis and Immunological Alterations: A Proof-of-Concept, In Vitro, Study

Systemic Sclerosis (SSc) is a rare autoimmune connective tissue disease characterized by microvascular injury, immune activation, and progressive fibrosis of the skin and internal organs. Diffuse cutaneous SSc (dcSSc), particularly in its early phase, is associated with aggressive fibrotic evolution and high morbidity. Despite advances in immunomodulatory therapy, no treatment has proven capable of consistently halting or reversing fibrosis, highlighting the need for new mechanistic targets.

TL1A (TNF-like ligand 1A) is a cytokine of the TNF superfamily expressed by endothelial and immune cells, which interacts with death receptor 3 (DR3) to regulate immune activation, endothelial dysfunction, and tissue remodeling. Elevated TL1A levels have been observed in SSc patients and correlate with disease activity. TL1A has also been shown to promote lung fibrosis in preclinical models.

The FIBROSTOP study is a proof-of-concept, in vitro, interventional study on biological samples aimed at elucidating the immunological and fibrotic mechanisms regulated by TL1A, and at assessing whether TL1A inhibition can reverse pathogenic processes in SSc.

Ten (n=10) patients with early diffuse cutaneous SSc and ten (n=10) age- and sex-matched healthy controls will be enrolled at a single center (Fondazione Policlinico Universitario Campus Bio-Medico, Rome). Each participant will undergo a single visit (T0) involving peripheral blood sampling and skin biopsy. No follow-up visits are planned.

The study pursues three co-primary objectives: (1) evaluating the role of TL1A and its inhibition in modulating T lymphocyte activity; (2) assessing the effects of TL1A and its inhibition on endothelial cell activation and function; (3) investigating the impact of TL1A and its inhibition on fibrotic remodeling in ex vivo SSc skin cultures using single-cell RNA sequencing.

The findings may inform future targeted antifibrotic interventions in SSc and other fibrotic diseases.

Descripción general del estudio

Descripción detallada

BACKGROUND AND RATIONALE

Systemic sclerosis (SSc) is an immune-mediated connective tissue disease characterized by fibrosis and vasculopathy. SSc is a heterogeneous orphan disease with a broad spectrum of organ involvement and life-threatening manifestations. The hallmark feature is the presence of thickened and hardened skin (scleroderma). The disease is divided into limited cutaneous and diffuse cutaneous SSc subsets based on the extent of skin involvement. Diffuse cutaneous SSc (dcSSc) is associated with a higher risk of interstitial lung disease, renal crisis, and cardiac involvement.

The pathophysiology of SSc involves a progressive self-amplifying process starting with microvascular/endothelial damage, followed by autoimmune response, inflammation, and fibrosis. T lymphocytes, particularly CD4+ T cells with a predominant Th2 cytokine profile, play an essential role in SSc pathogenesis. Regulatory T cells (Tregs) show decreased functional ability to suppress effector T cells.

TL1A (TNF-like cytokine 1A) is a member of the TNF superfamily constitutively expressed in endothelial cells and upregulated in response to TNF-α stimulation. TL1A binds to its receptor death receptor 3 (DR3), activating downstream signaling involved in innate and adaptive immune homeostasis. Elevated TL1A levels have been detected in serum of SSc patients compared to healthy subjects and correlate with disease activity. TL1A has been demonstrated to promote lung fibrosis in bleomycin-induced mouse models. The ATHENA-SSc-ILD study is currently evaluating Tulisokibart, a TL1A inhibitor, for SSc-associated interstitial lung disease.

STUDY DESIGN

FIBROSTOP is a monocentric, non-profit, interventional proof-of-concept in vitro study on biological samples. The study is funded by an unconditional grant from MSD Italia S.r.l. and conducted at the Fondazione Policlinico Universitario Campus Bio-Medico, Rome (Principal Investigator: Prof. Roberto Giacomelli).

OBJECTIVES AND ENDPOINTS

Co-Primary Objectives:

  • OBJ1: To evaluate the role of TL1A and its inhibition in modulating T lymphocyte activity in SSc. Peripheral blood T-cell subsets (CD4+, CD8+, and Tregs) will be isolated from SSc patients and controls, and cultured with TL1A ± DR3 silencing. Effects on cytokine production, cellular activation, autophagy, apoptosis, and necroptosis will be analyzed through multiplex assays, flow cytometry, and Western blot.
  • OBJ2: To assess the effects of TL1A and its inhibition on endothelial cell activation and function. Human Umbilical Vein Endothelial Cells (HUVEC) cultured with SSc serum will be treated with TL1A ± DR3 silencing to evaluate adhesion molecule expression, angiogenic capacity, and cell death/autophagy pathways. Bulk RNA sequencing will profile TL1A-regulated transcriptional signatures.
  • OBJ3: To investigate the impact of TL1A and its inhibition on cellular interactions and fibrotic remodeling in SSc skin. Ex vivo skin biopsies from SSc patients and controls will be cultured with TL1A ± neutralizing antibody, and single-cell RNA sequencing (scRNA-seq) will identify transcriptional reprogramming in fibroblasts, lymphocytes, and endothelial cells.

Co-Primary Endpoints:

  • EP1: Changes in cytokine production (IFN-gamma, IL-1beta, IL-6, IL-10, IL-17A, IL-35, TNF-alpha, TGF-beta), cellular activation, autophagy, apoptosis, and necroptosis in T-cell subsets following TL1A stimulation and inhibition.
  • EP2: Endothelial sprouting and angiogenic capacity; changes in expression of P-selectin, E-selectin, ICAM-1, VCAM-1, and Matrigel tube formation, as well as bulk RNA-seq profiles in HUVECs following TL1A stimulation and inhibition.
  • EP3: Expression of fibrotic and inflammatory markers (Col-1, alphaSMA) in ex vivo SSc skin cultures following TL1A stimulation and inhibition.

STUDY POPULATION AND PROCEDURES

Ten (n=10) patients with SSc (ACR/EULAR 2013 criteria, diffuse cutaneous subset per LeRoy et al. 1988, disease onset ≤5 years from first non-Raynaud symptom) and ten (n=10) age- and sex-matched healthy controls will be enrolled consecutively over approximately 12 months.

Each participant undergoes a single study visit (T0) involving:

  • Peripheral blood sampling: PBMCs will be isolated by Ficoll-Paque density gradient centrifugation; CD4+, CD8+, and Treg subsets purified using MACS separation kits and cultured under four experimental conditions (untreated, TL1A stimulation, DR3 silencing by siRNA, TL1A + DR3 silencing).
  • Skin biopsy: A 3×3 mm punch biopsy from the forearm of the most affected side (SSc patients) or from residual surgical tissue/voluntary donation (controls). Ex vivo cultures will be treated with TL1A ± neutralizing antibody and analyzed by scRNA-seq.
  • Endothelial cell assays: HUVECs cultured with SSc serum under five experimental conditions will be assessed for activation markers, angiogenic function, and bulk RNA sequencing.

STATISTICAL CONSIDERATIONS

The FIBROSTOP study is exploratory in nature; no formal sample size calculation is required. Statistical analyses will include Student's t-test or Mann-Whitney U test for two-group comparisons, one-way/two-way ANOVA or Kruskal-Wallis test for multiple-group comparisons, and Spearman's rank correlation for continuous variables. Transcriptomic data will be analyzed using DESeq2 (bulk RNA-seq) and Seurat (scRNA-seq) pipelines. Pathway enrichment analyses will use Reactome, Gene Ontology (GO), and KEGG databases.

DURATION

Total study duration: 24 months (12 months enrollment + 12 months data generation and analysis). Each participant takes part in a single visit only.

Tipo de estudio

De observación

Inscripción (Estimado)

20

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Estudio Contacto

Ubicaciones de estudio

    • Italy
      • Rome, Italy, Italia, 00128
        • Immunorheumatology Unit, Fondazione Policlinico Universitario Campus Bio-Medico
        • Contacto:
        • Contacto:
        • Sub-Investigador:
          • Antonio Orlando, MD

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

  • Adulto
  • Adulto Mayor

Acepta Voluntarios Saludables

Sí

Método de muestreo

Muestra no probabilística

Población de estudio

Ten patients with early diffuse cutaneous Systemic Sclerosis (dcSSc) fulfilling the 2013 ACR/EULAR classification criteria and the LeRoy subset definition, with disease onset ≤5 years from the first non-Raynaud symptom, consecutively recruited from the Scleroderma Unit of Fondazione Policlinico Universitario Campus Bio-Medico, Rome. Ten age- and sex-matched healthy controls without SSc diagnosis, donating peripheral blood and residual skin tissue from elective surgical procedures or voluntary donation.

Descripción

Inclusion Criteria:

For both SSc and healthy control populations:

  • Signed written informed consent
  • Age ≥18 years at the time of consent

For SSc population only:

  • Diagnosis of SSc according to ACR/EULAR 2013 classification criteria
  • Diffuse cutaneous SSc subtype (LeRoy et al., 1988)
  • Disease onset (defined as the first non-Raynaud symptom) within 5 years prior to recruitment
  • No new initiation of immunosuppressive therapy (including methotrexate, mycophenolate mofetil, cyclophosphamide, rituximab, tocilizumab, or prednisone >20 mg/day) within the 2 months preceding recruitment
  • Ongoing immunosuppressive therapy must be at a stable dose for at least 1 month prior to enrollment

Exclusion Criteria:

  • Coexisting active or treated skin diseases (e.g., atopic dermatitis), except for SSc
  • Diagnosis of other systemic autoimmune rheumatic diseases, including overlap syndromes (e.g., SSc + dermatomyositis)
  • History or current signs/symptoms of severe or uncontrolled non-rheumatic diseases
  • Active malignancy or history of malignancy within the previous 5 years (except adequately treated non-melanoma skin cancer or in situ cervical carcinoma)
  • Chronic or recurrent infections, including viral hepatitis B/C, HIV, or untreated tuberculosis
  • Severe active infection or major surgery within 8 weeks before enrollment
  • Non-serious skin infections within 8 weeks before enrollment
  • Limited cutaneous SSc or SSc sine scleroderma
  • SSc patients unable to undergo therapeutic stabilization due to severe organ complications
  • Pregnancy or lactation
  • Inability to provide informed consent

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

Cohortes e Intervenciones

Grupo / Cohorte
Intervención / Tratamiento
SSc Patients
Ten patients with early diffuse cutaneous Systemic Sclerosis (dcSSc) fulfilling the 2013 ACR/EULAR classification criteria and the LeRoy subset definition, with disease onset ≤5 years from the first non-Raynaud symptom, on stable immunosuppressive therapy. Each participant undergoes a single visit (T0) for peripheral blood sampling and skin punch biopsy (3x3 mm).
Biological samples (T-cell subsets, HUVECs, and ex vivo skin cultures) are treated in vitro under experimental conditions including TL1A stimulation, DR3 silencing by siRNA, and TL1A neutralizing antibody. No intervention is administered to study participants.
Healthy Controls
Ten age- and sex-matched donors not affected by SSc. Peripheral blood samples are collected for research purposes. Skin samples are derived from residual tissue of minor elective surgical procedures or voluntary skin donation.
Biological samples (T-cell subsets, HUVECs, and ex vivo skin cultures) are treated in vitro under experimental conditions including TL1A stimulation, DR3 silencing by siRNA, and TL1A neutralizing antibody. No intervention is administered to study participants.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
T-cell cytokine production and activation following TL1A stimulation and inhibition
Periodo de tiempo: Within 12 months from biological sample collection (single visit at T0)
Changes in cytokine production (IFN-gamma, IL-1beta, IL-6, IL-10, IL-17A, IL-35, TNF-alpha, TGF-beta), cellular activation, autophagy, apoptosis, and necroptosis in CD4+, CD8+, and Treg subsets isolated from SSc patients and healthy controls, following TL1A stimulation and DR3 silencing by siRNA, assessed by multiplex assays, flow cytometry, and Western blot.
Within 12 months from biological sample collection (single visit at T0)
Endothelial cell activation and angiogenic capacity following TL1A stimulation and inhibition
Periodo de tiempo: Within 12 months from biological sample collection (single visit at T0)
Changes in expression of P-selectin, E-selectin, ICAM-1, VCAM-1, and Matrigel tube formation capacity in HUVECs cultured with SSc serum and treated with TL1A stimulation and DR3 silencing by siRNA, assessed by Western blot, Matrigel assay, and bulk RNA sequencing.
Within 12 months from biological sample collection (single visit at T0)
Fibrotic and inflammatory marker expression in ex vivo skin cultures following TL1A modulation
Periodo de tiempo: Within 12 months from biological sample collection (single visit at T0)
Expression of fibrotic markers (Col-1, alphaSMA) and transcriptional reprogramming in fibroblasts, lymphocytes, and endothelial cells in ex vivo skin cultures treated with TL1A and TL1A neutralizing antibody, assessed by single-cell RNA sequencing (scRNA-seq).
Within 12 months from biological sample collection (single visit at T0)

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Publicaciones y enlaces útiles

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Publicaciones Generales

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Estimado)

1 de septiembre de 2026

Finalización primaria (Estimado)

1 de septiembre de 2027

Finalización del estudio (Estimado)

1 de septiembre de 2028

Fechas de registro del estudio

Enviado por primera vez

4 de junio de 2026

Primero enviado que cumplió con los criterios de control de calidad

4 de junio de 2026

Publicado por primera vez (Actual)

11 de junio de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

11 de junio de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

4 de junio de 2026

Última verificación

1 de junio de 2026

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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