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High-throughput Flow Cytometry Cell-based Assay to Detect Antibodies to N-Methyl-D-aspartate Receptor or Dopamine-2 Receptor in Human Serum
Published on: November 23, 2013
Serum complement levels in anti-N-methyl-d-aspartate receptor encephalitis
1Department of Neurology, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.
Serum C4 levels were elevated in patients with anti-N-methyl-d-aspartate receptor (NMDAR) encephalitis, correlating with disease severity and other complement factors. These findings offer insights into NMDAR encephalitis pathogenesis and potential biomarkers.
Area of Science:
- Neuroimmunology
- Clinical Immunology
Background:
- Anti-N-methyl-d-aspartate receptor (NMDAR) encephalitis is a severe autoimmune neurological disorder.
- The role of serum complement system activation in NMDAR encephalitis pathogenesis requires further elucidation.
Purpose of the Study:
- To investigate the relationship between serum complement levels and anti-NMDAR encephalitis.
- To explore correlations between complement factors, disease severity, and treatment response.
Main Methods:
- Serum levels of complement components (C3, C4, CH50), immunoglobulins, and C-reactive protein were measured in 40 anti-NMDAR encephalitis patients and 40 controls.
- Clinical data, including Modified Rankin Scale (mRS) scores, and cerebrospinal fluid parameters were assessed.
- Follow-up evaluations were performed on 11 patients after 6 months.
Main Results:
- Serum C4 levels were significantly elevated in anti-NMDAR encephalitis patients compared to controls, particularly in females and those with severe impairment (mRS ≥ 4).
- Elevated serum CH50 levels were associated with severe impairment and limited treatment response.
- Serum C4 positively correlated with C3, CH50, and mRS scores, while C3 correlated with CH50 and CSF white blood cells. CH50 correlated with age, mRS, and CRP.
- Follow-up showed improved mRS scores, with a negative correlation between changes in C3 and mRS.
Conclusions:
- Serum C4 is elevated in anti-NMDAR encephalitis and is associated with disease severity and other complement factors.
- These findings suggest a potential role for complement system dysregulation in the pathophysiology of anti-NMDAR encephalitis.
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