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.

PubMed

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.
Abstract

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