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Induction and Clinical Scoring of Chronic-Relapsing Experimental Autoimmune Encephalomyelitis
Published on: July 4, 2007
Clinical spectrum of contactin-associated protein 2 autoimmune encephalitis in children
Wenjing Hu1, Enhui Wang1, Hongjun Fang1
1Department of Neurology, Hunan Children's Hospital, Changsha, Hunan, China.
Insights
Pediatric anti-contactin-associated protein 2 (CASPR2)-antibody-related autoimmune encephalitis presents with diverse symptoms like movement and consciousness disorders. Most children recover well with immunotherapy, showing a low short-term relapse rate.
Area of Science:
- Neurology
- Immunology
- Pediatrics
Background:
- Anti-contactin-associated protein 2 (CASPR2)-antibody-related autoimmune encephalitis (AE) is increasingly recognized but poorly understood in pediatric populations.
- Limited data exists on the clinical spectrum, diagnosis, and treatment of anti-CASPR2-Ab AE in children, necessitating further investigation.
Purpose of the Study:
- To elucidate the clinical manifestations, diagnostic findings, and treatment outcomes of anti-CASPR2-Ab-related AE in children.
- To enhance the understanding and inform clinical management strategies for pediatric anti-CASPR2-Ab AE.
Main Methods:
- A retrospective study was conducted on pediatric patients diagnosed with anti-CASPR2-Ab-related AE between January 2020 and June 2022.
- Data collected included demographics, clinical symptoms, laboratory results, electroencephalography (EEG), neuroimaging, and treatment responses.
Main Results:
- Thirteen pediatric patients were identified with anti-CASPR2-Ab. Common symptoms included movement disorders (9/13) and consciousness disorders (9/13).
- One patient with co-existing anti-N-methyl-D-aspartate receptor antibodies presented with more severe symptoms. Tumors were not detected. Most patients achieved good recovery with immunotherapy, with no short-term relapses.
- EEG abnormalities were observed in six patients, and neuroimaging revealed abnormalities in ten.
Conclusions:
- Anti-CASPR2-Ab-related AE in children exhibits varied clinical presentations, with higher antibody levels noted in males. Tumors are rare, and immunotherapy is generally effective with a low recurrence rate.
- Overlapping autoimmune encephalitis syndromes present more severe and complex cases requiring prolonged treatment. Long-term prognosis warrants further research.
Objective:
Anti-contactin-associated protein 2 (CASPR2)-related autoimmune encephalitis (AE) is more common in adults than in children. Clinical understanding of anti-CASPR2-antibody (Ab)-related AE, diagnosis and treatment standards are lacking in children. Therefore, this retrospective study on clinical symptoms and treatment outcomes in children with anti-CASPR2-Ab-related AE was conducted, to improve the clinical understanding of the disease, its diagnosis and treatment.
Methods:
This study retrospectively assessed children with anti-CASPR2-Ab-related AE from January 1, 2020, to June 30, 2022, in the Department of Neurology at Hunan Children's Hospital. Data regarding demographics, clinical symptoms, laboratory examinations, electroencephalography (EEG), imaging, and curative were collected.
Results:
Thirteen patients were positive for serum anti-CASPR2-Ab (age at manifestation, 25 months to 13 years old; median, 8.1 years old; male-to-female ratio, 8/5). One patient (P1) had dual Abs, including anti-CASPR2 and anti-N-methyl-D-aspartate receptor Abs; his symptoms were more severe than those of children with anti-CASPR2 Abs alone. The clinical symptoms of the 13 patients with anti-CASPR2 Ab were movement disorders (9/13), consciousness disorders (9/13), abnormal demeanor (8/13), seizures (7/13), language disorders (6/13), fever (6/13), pain (4/13), involuntary exercise (4/13), poor diet (4/13), vomiting (3/13), sleep disorders (3/13), mood disorders (3/13), eczema/itching/redness (2/13), sweating (P8), urinary disorders (P13), and cognitive disorders (P9). No tumors were found in any patient. Additionally, EEG results of six patients were abnormal and imaging findings such as abnormal signals were found in 10 patients. Moreover, all except one patient recovered well after treatment; P1 with overlapping syndrome underwent recovery for more than 2 years. None of the patients who recovered have had a relapse.
Discussion And Conclusion:
Anti-CASPR2-Ab-related AE has several clinical manifestations. Anti-CASPR2-Ab levels were higher in male patients than in female patients. Moreover, related tumors are relatively rare. Most patients benefit from immunotherapy and have a lower chance of recurrence in the short term. Furthermore, different from patients who had anti-CASPR2-Ab AE alone, those with overlapping syndrome had a severe and complex condition requiring lengthy treatment and rehabilitation. Additional studies are needed to evaluate the long-term prognosis of these patients.
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