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Interleukin-2 binding proteins in sera from normal subjects and multiple sclerosis patients
J L Trotter1, C A Damico, A L Trotter
1Washington University School of Medicine, Department of Neurology and Neurosurgery, St. Louis, MO 63110, USA.
Neurology
|November 1, 1995
Summary
Elevated interleukin 2 (IL-2) in multiple sclerosis (MS) is bound by serum proteins, including antibodies and soluble receptors. This binding may inhibit IL-2 activity, suggesting a novel immunomodulatory mechanism in MS.
Area of Science:
- Immunology
- Neuroscience
- Biochemistry
Background:
- Elevated serum levels of interleukin 2 (IL-2) have been previously observed in patients with chronic progressive multiple sclerosis (MS).
- Interleukin 2 plays a crucial role in immune regulation and T-cell activation, making its modulation a potential factor in MS pathogenesis.
Purpose of the Study:
- To investigate the binding of IL-2 to serum proteins in patients with MS.
- To identify the specific serum proteins interacting with IL-2.
- To assess the functional impact of IL-2 binding on its biological activity.
Main Methods:
- Gel chromatography and protein A sepharose affinity chromatography were employed to isolate and purify serum proteins.
- Enzyme-linked immunosorbent assays (ELISAs) were used to quantify IL-2 and its soluble receptor (sIL-2R).
- A CTLL cell assay was utilized to measure the bioactivity of IL-2 in the presence of serum fractions.
Main Results:
- Interleukin 2 in MS patient serum was found to be complexed with various serum proteins.
- Identified binding proteins include antibodies to IL-2, soluble IL-2 receptors, and high-molecular-weight proteins.
- A specific serum fraction containing IgG antibodies to IL-2 demonstrated inhibition of IL-2 activity in a cell-based assay.
Conclusions:
- Serum proteins, including specific antibodies and soluble receptors, bind to IL-2 in patients with MS.
- This binding potentially leads to the immunomodulation of IL-2 activity.
- These findings suggest a novel mechanism of cytokine regulation contributing to the immunopathology of MS.