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Innate immunity in the Guillain-Barré syndrome

Innate immunity in the Guillain-Barré syndrome - Innate immunity in GBS (iGBS)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON45725
Enrollment
124
Registered
2017-08-21
Start date
2017-11-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

acute inflammatory demyelinating polyneuropathy no lay-term

Interventions

Guillain-Barré syndrome
Innate immunity
Leukocytes
Viruses

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: Healthy controls: - Age 18 years or older - Written informed consent given by the subject Former GBS patients: - Fulfilling the diagnostic criteria for GBS (Asbury, 1990), or its variant Miller Fisher syndrome (MFS). - Current age 18 years or older - Written informed consent given by the patient;Recurrent GBS patients: - Occurrence of at least two episodes of GBS, as determined by the diagnostic criteria for GBS (Asbury, 1990), or its variant Miller Fisher syndrome (MFS). - Age 18 years - Written informed consent given by the patient

Exclusion criteria

Exclusion criteria: Healthy controls: - No serological evidence for exposure to a virus, as determined by IgG serology for EBV, CMV, HEV or influenza antigens.;All groups: Additional diseases or disorders at time of blood sampling that may influence the endpoints: - autoimmune diseases (like multiple sclerosis, psoriasis, Crohn*s disease, ulcerative colitis, rheumatoid arthritis, SLE and other systemic diseases) - acute and chronic infectious diseases (like infectious mononucleosis, HIV/AIDS) - malignancies (not in remission) Medicines at time of blood sampling that may affect endpoints (i.e. inflammatory processes): - NSAIDs, oral corticosteroids, cyclosporine - Cytostatic compounds - Cytokines (analogues) and biologicals - Intravenous immunoglobulins.

Design outcomes

Primary

MeasureTime frame
The primary study parameter is the innate response of leukocytes to microbial triggers as determined by the type I interferon production in response to stimulation of Toll-like receptor 3, 7 or 9.

Secondary

MeasureTime frame
The production of other cytokines and the expression of maturation/activation markers will be determined at the cell surface of leukocytes. Additionally, genetic variants that influence the innate response of leukocytes to microbial triggers will be determined.

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)