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临床试验/NCT06610942
NCT06610942尚未招募不适用

Characterization of the Fungal Immunopeptidome Involved in the Immunopathological Mechanisms of Psoriasis

Assistance Publique - Hôpitaux de Paris1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2025年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
100
试验地点
1
主要终点
Determining the commensal fungi responsible for the immunopathological response in psoriasis.

研究概览

简要总结

Psoriasis is a chronic immune-mediated skin disorder characterized by inflammatory cutaneous plaques and, occasionally, arthritis, affecting 60 million adults and children worldwide. Although a variety of treatments have been developed aimed to relieve the associated symptoms, there is yet no permanent cure for psoriasis. TH17 type immunity, via the production of IL-17A and other pro-inflammatory cytokines, are considered to play a central role in the pathogenesis of this disease. Moreover, experimental evidence obtained in animal models, points to human mycobiota as a trigger for the initiation and/or progression of psoriasis. Therefore, human studies are required to better characterize the major fungi implicated in the local and systemic inflammatory responses, as well as to determine the immunopeptidome that shapes the pathogenic T cell receptor repertoire.

We will explore the hypothesis that commensal fungi could participate in the chronic inflammatory immune response underlying the pathogenesis of human psoriasis via the recognition of cutaneous fungal antigens and/or via a gut-skin mycobiome cross-reactive mechanism

详细描述

The overall aim of the project is :

i) to characterize the nature of human local and systemic inflammatory responses against commensal skin and gut fungal species in psoriatic patients (PsoP) and ii) to determine the fungal immunopeptidome that contributes to the shaping of the T cell receptor (TCR) repertoire of skin-infiltrating T cells. The project is divided into four major scientific objectives:

  1. To determine the mycobiome profiles in healthy donors (HD) and PsoP.
  2. To characterize the contribution of mycobiota to the local cutaneous CD4+ T cell response.
  3. To assess systemic the CD4+ T cell-fungal cross-reactivity.
  4. To establish the immunopeptidome of the major CD4+ T cell-reactive fungus enabling the development of an innovative immunotherapy.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adults with psoriasis failing local treatment. Adults requiring reconstructive plastic surgery (resident skin immunology checks).
  • Adults living in the same household as a patient suffering from psoriasis (intestinal mycobiome checks).

排除标准

  • Minors Individuals under legal protection. Pregnant or breastfeeding women

结局指标

主要结局

Determining the commensal fungi responsible for the immunopathological response in psoriasis.

时间窗: 2 years

Flow cytometry analysis of cytokine secretion profile in healthy and diseased subjects

次要结局

  • Identification of peptides responsible for the immunopathological response in psoriasis.(2 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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