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.
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. No additional visits are planned for research purposes.
Study Type
OBSERVATIONAL
Enrollment
50
Hôpital Bichat
Paris, France
RECRUITINGLevels 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)
Time frame: at 3 and/or 6 month
level of antibodies specific to the VZV gE glycoprotein after stimulation with peptides contained in the vaccine (in SFC/106 PBMC)
Time frame: at 3 and/or 6 month
Frequency of specific T cells
Time frame: before vaccination, at 3 and/or 6 month
Tolerance of the VZV vaccine
occurrence of non-serious adverse events
Time frame: at 3 and/or 6 month
Safety of the VZV vaccine
occurrence of serious adverse events
Time frame: at 3 and/or 6 month
measuring change in IMID (Immune mediated inflammatory disease) activity. The data collected will be aggregated into a composite score.
The measures used depend on the scale specific to each IMID. The parameters collected will be the scales (SLEDAI for SLE, ESSDAI for Sjögren's syndrome, mRSS for systemic sclerosis, BSAS for Behcet's disease and BVAS for vasculitis), the physiological parameters collected by the referring doctor and, where appropriate, certain biological activity parameters (C-reactive protein, anti-DNA, ANCA, etc.). The data collected will be aggregated into a composite score.
Time frame: at 3 and/or 6 month
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