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临床试验/NCT07047053
NCT07047053招募中不适用

Evaluation of the Anti-VZV Vaccine Response of Patients With Immune-mediated Systemic Inflammatory Diseases Vaccinated in the Care Setting

Assistance Publique - Hôpitaux de Paris1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年6月10日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
50
试验地点
1
主要终点
level of antibodies specific to the VZV gE glycoprotein after stimulation with peptides contained in the vaccine (in SFC/106 PBMC)

研究概览

简要总结

Patients with immune-mediated systemic inflammatory diseases (IMID) are at increased risk of shingles due to treatment-induced immunosuppression. In line with international recommendations, the French National Authority for Health (HAS) updated the varicella-zoster virus (VZV) vaccination strategy in March 2024. The HAS now recommends that immunocompromised people aged 18 and over be vaccinated with the recombinant VZV vaccine. However, due to the immunosuppressive treatment received, the vaccine response in MIMI patients is often suboptimal, and the protection induced by the herpes zoster vaccine in this context is unknown.

The aim of our study is to determine the rate of anti-VZV seroconversion after vaccination with recombinant anti-VZV vaccine, in patients followed up for MIMI.

详细描述

Vaccination with the recombinant anti-VZV vaccine (Shingrix) is carried out as part of treatment in all immunocompromised patients over 18 years of age, in accordance with HAS recommendations (the vaccination schedule requires 2 doses 2 months apart).

The vaccine response will be measured during hospitalisation and/or follow-up consultations, using the same sample as that used to monitor MIMI in the same laboratory (Immunology Laboratory, CHU Bichat).

Clinical and biological data will be collected to study factors associated with vaccine response, vaccine tolerance and MIMI activity.

Information relating to diagnosis, examinations and follow-up will be collated in the patient's medical file.

Patients are systematically seen every 6 months for follow-up consultations as part of their MIMI.

研究设计

研究类型
Observational
观察模型
Cohort
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
否

入选标准

  • •Patient over 18 years of age being managed for MIMI, including
  • •Systemic lupus
  • •Gougerot-Sjögren's syndrome
  • •Systemic scleroderma
  • •Mixed connectivitis
  • •Inflammatory myositis
  • •Systemic sarcoidosis
  • •Systemic vasculitis (necrotizing vasculitis and giant cell arteritis)
  • •Behçet's disease
  • •Adult Still's disease
  • •IgG4-associated disease
  • •Autoimmune cytopenias (autoimmune hemolytic anemia, immunological thrombocytopenic purpura, Evans syndrome)
  • •Susac syndrome
  • •Followed in the internal medicine department of Hôpital Bichat, Paris
  • •Justifying VZV vaccination due to immunosuppression or age over
  • •Vaccinated as part of care between June 2025 and June 2026
  • •Regardless of history of shingles
  • •With a serum sample available for analysis
  • •Having received at least the first dose of the vaccine regimen (in hospital or in the community)

排除标准

  • •Evolving cancer, with or without treatment (chemotherapy, immunotherapy, etc.)
  • •History of VZV vaccination (live or recombinant)
  • •Patient who has had an allergic reaction to a vaccine
  • •Pregnancy
  • •Patient under legal protection, guardianship or trusteeship
  • •Not affiliated to a social security scheme (general or CMU)
  • •Patient unable to understand research information
  • •Absence of non-opposition

结局指标

主要结局

level of antibodies specific to the VZV gE glycoprotein after stimulation with peptides contained in the vaccine (in SFC/106 PBMC)

时间窗: at 3 and/or 6 month

Levels of antibodies specific to VZV gE glycoprotein and levels of specific T lymphocytes after stimulation with peptides contained in the vaccine (in SFC/106 PBMC)

时间窗: at 3 and/or 6 month

次要结局

  • measuring change in IMID (Immune mediated inflammatory disease) activity. The data collected will be aggregated into a composite score.(at 3 and/or 6 month)
  • Frequency of specific T cells(before vaccination, at 3 and/or 6 month)
  • Tolerance of the VZV vaccine(at 3 and/or 6 month)
  • Safety of the VZV vaccine(at 3 and/or 6 month)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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