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Cytokines and soluble IL-4 in patients with acute optic neuritis and multiple sclerosis
F Sellebjerg1, K Bendtzen, M Christiansen
1Department of Neurology, University of Copenhagen, Glostrup Hospital, 57 Norder Ringvej, DK-2600 GlostrupInstitute for Inflammation Research, RHIMA Center, National University HospitalDepartment of Clinical Biochemistry, Statens Seruminstitut, Copenhagen, Denmark.
Insights
Cytokine profiles in cerebrospinal fluid (CSF) and plasma reveal distinct immune responses in multiple sclerosis (MS) subtypes. Patients with non-optic neuritis (ON) MS attacks show heightened pro-inflammatory markers, suggesting autoimmune activation.
Area of Science:
- Neuroimmunology
- Inflammatory Diseases
- Autoimmune Disorders
Background:
- Multiple Sclerosis (MS) is a complex autoimmune disease affecting the central nervous system.
- Optic Neuritis (ON) can be an initial presentation of MS or occur independently.
- Understanding the immunological differences between MS subtypes is crucial for diagnosis and treatment.
Purpose of the Study:
- To compare cerebrospinal fluid (CSF) and plasma cytokine profiles in patients with different forms of MS and optic neuritis.
- To investigate the role of specific cytokines and receptors in the pathogenesis of MS and ON.
- To differentiate immunological characteristics between idiopathic ON, ON in MS, and other MS attack forms.
Main Methods:
- Enzyme-linked immunosorbent assay (ELISA) was used to measure CSF and plasma concentrations of various cytokines and receptors.
- Analyzed 12 patients each in four groups: acute idiopathic ON, ON with MS, other MS attacks, and neurological controls.
- Included measurements for interleukins (IL)-1α, IL-1β, IL-2, IL-4, IL-6, IL-10, tumor necrosis factor (TNF)-α, TNF-β, interferon (IFN)-γ, IL-1 receptor antagonist, and soluble IL-4 receptor (sIL-4r).
Main Results:
- CSF concentrations of IL-1β, IL-2, and IFN-γ were significantly different across patient groups, highest in non-ON MS attacks.
- TNF-β was exclusively detected in CSF of neurological control subjects.
- Elevated plasma sIL-4r was observed in patients with non-ON MS attacks.
Conclusions:
- Increased CSF IL-1β, IL-2, IFN-γ, and plasma sIL-4r in non-ON MS attacks support an autoimmune basis with T-helper type 1-like cell activation.
- Immunological profiles suggest that idiopathic ON and ON associated with MS may differ from other MS attack forms.
- These findings highlight distinct inflammatory pathways in different MS presentations.
Abstract:
We measured the cerebrospinal fluid (CSF) and plasma concentrations of interleukin (IL)-1α, IL-1β, IL-2, IL-4, IL-6, IL-10, tumor necrosis factor (TNF)-α, TNF-β, interferon (IFN)-γ, the IL-1 receptor antagonist, and soluble IL-4 receptor (sIL-4r) by ELISA in 12 patients each with acute, monosymptomatic, idiopathic optic neuritis (ON), ON as part of MS, other attack forms of MS, and in neurological control subjects. CSF concentrations of IL-1β, IL-2 and IFN-γ differed significantly between the different patient groups and were detected most commonly at the highest concentrations in patients with non-ON attacks of MS. TNF-β was detected exclusively in CSF from neurological control patients. The patients with non-ON attacks of MS also had significantly elevated concentrations of sIL-4r in plasma. Increased CSF concentrations of IL-1β, IL-2 and IFN-γ together with increased plasma concentrations of sIL-4r support the concept of MS as an autoimmune disease with preferential activation of proinflammatory or T-helper type 1-like cells. Patients with idiopathic ON or ON as part of MS may, however, differ immunologically from patients with other attack forms of MS.
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