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Isolation and Quantification of Epstein-Barr Virus from the P3HR1 Cell Line
Published on: September 28, 2022
The role of the Epstein-Barr virus receptor CD21 in multiple sclerosis
Nicole Toepfner1, Sabine Cepok, Verena Grummel
1Department of Neurology, Heinrich Heine University, Moorenstr. 5, 40225 Düsseldorf, Germany.
Abstract:
Multiple Sclerosis (MS) is characterised by a chronic inflammation and demyelination of brain and spinal cord with a yet unknown aetiology. Based on multiple epidemiological and immunological studies, which suggest a role of Epstein-Barr virus (EBV) infection in the pathogenesis of MS, we investigated CD21 (CR2, complement receptor type 2), which serves as the EBV receptor. Serum concentrations of soluble CD21 receptor (sCD21) were determined in MS patients and controls. In accordance with findings in other autoimmune disorders decreased sCD21 levels were found in MS patients. On ß-IFN treatment serum sCD21 concentrations further decreased. To explore the role of the CD21 gene for MS susceptibility and the altered CD21 levels in MS patients we performed exon sequencing of the CD21 gene. While we identified new single nucleotide polymorphism (SNP) and confirmed previously reported SNPs, none of the SNPs was associated with MS. Our findings demonstrate that sCD21 expression is altered in MS patients similar to other autoimmune diseases although no evidence was found for a specific role of the CD21 gene in MS.
Insights
Multiple Sclerosis patients exhibit altered soluble CD21 receptor levels, similar to other autoimmune diseases. However, the CD21 gene itself does not appear to play a specific role in MS susceptibility.
Area of Science:
- Neuroimmunology
- Virology
- Genetics
Background:
- Multiple Sclerosis (MS) involves chronic inflammation and demyelination with unknown causes.
- Epstein-Barr virus (EBV) is implicated in MS pathogenesis.
- CD21 (complement receptor type 2) is the EBV receptor and its soluble form (sCD21) is investigated.
Purpose of the Study:
- To investigate the role of CD21 in Multiple Sclerosis (MS) pathogenesis.
- To analyze serum concentrations of soluble CD21 (sCD21) in MS patients.
- To explore the CD21 gene's association with MS susceptibility and altered sCD21 levels.
Main Methods:
- Serum sCD21 concentrations were measured in MS patients and healthy controls.
- Exon sequencing of the CD21 gene was performed.
- Single nucleotide polymorphisms (SNPs) in the CD21 gene were identified and analyzed.
Main Results:
- MS patients showed decreased serum sCD21 levels compared to controls.
- sCD21 levels further decreased in MS patients undergoing beta-interferon (ß-IFN) treatment.
- New and known SNPs in the CD21 gene were identified, but none were associated with MS.
Conclusions:
- Altered sCD21 expression in MS patients mirrors findings in other autoimmune diseases.
- The CD21 gene does not show a specific association with MS susceptibility.
- The study suggests sCD21 alterations are a feature of MS, but not driven by specific CD21 gene variations.
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