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Autoimmune encephalitis associated with anti-SOX1 autoantibodies in COVID-19: A case report
Peter Sabaka1, Gabriela Timárová2, Mohammad Dababseh1
1Department of Infectology and Geographical Medicine, Faculty of Medicine, Comenius University in Bratislava, Bratislava Slovakia.
Insights
This case study highlights autoimmune encephalitis (AIE) in a COVID-19 patient, identified by anti-SOX1 antibodies. Prompt treatment with steroids and immunoglobulin led to a full recovery, underscoring AIE as a severe COVID-19 complication.
Area of Science:
- Neurology
- Infectious Diseases
- Immunology
Background:
- Coronavirus disease 2019 (COVID-19) can manifest with severe non-respiratory complications, including encephalitis.
- Autoimmune encephalitis (AIE) is a rare but serious cause of encephalopathy in COVID-19 patients, often linked to specific autoantibodies.
- Anti-SOX1 autoantibodies are associated with various neurological conditions, including rare paraneoplastic autoimmune encephalitis.
Observation:
- A 28-year-old female with confirmed COVID-19 presented with fever, headache, disorientation, and new-onset refractory status epilepticus.
- Brain imaging was unremarkable, but cerebrospinal fluid analysis revealed pleocytosis and elevated protein, albumin, and immunoglobulin G.
- Electroencephalography suggested AIE, and serologic testing confirmed the presence of anti-SOX1 autoantibodies.
Findings:
- The patient was diagnosed with anti-SOX1 autoimmune encephalitis secondary to COVID-19.
- Treatment with methylprednisolone and intravenous immunoglobulin resulted in rapid clinical improvement, resolving seizures and neurological/psychiatric symptoms.
- Subsequent oncologic screening excluded a paraneoplastic etiology.
Implications:
- This case underscores the importance of considering AIE in COVID-19 patients presenting with neurological symptoms, particularly status epilepticus.
- Early diagnosis and prompt immunotherapy are crucial for favorable outcomes in anti-SOX1 AIE associated with COVID-19.
- The findings contribute to understanding the diverse neurological manifestations of COVID-19 and the role of specific autoantibodies.
Abstract:
Coronavirus disease 2019 (COVID-19) might be complicated by various non-respiratory conditions, including encephalitis. Encephalitis in COVID-19 represents a heterogenous group of diseases with variable aetiology. Autoimmune encephalitis (AIE) is the least common but one of the most severe causes of encephalopathy in COVID-19. AIE is a rare disease that is associated with different types of autoantibodies mostly directed against various neuronal antigens. Anti-Sry-like high mobility group box (SOX1) autoantibodies have been described in various clinical conditions, including Lambert-Eaton myasthenic syndrome, paraneoplastic cerebellar degeneration and rare cases of paraneoplastic AIE. We present the case of 28-year-old female patient with COVID-19 confirmed by the polymerase chain reaction (PCR) test. She was admitted with fever, headache, disorientation and new-onset refractory status epilepticus. Computed tomography and magnetic resonance imaging of the brain were unremarkable. Cerebrospinal fluid analysis showed pleocytosis, an increased total protein concentration and increased albumin and immunoglobulin G. Electroencephalography revealed findings suggestive of AIE. Serologic examination of antineuronal antibodies showed anti-SOX1 autoantibodies. A course of parenteral methylprednisolone and intravenous immunoglobulin led to rapid clinical improvement. The patient was discharged free of seizures as well as neurologic and psychiatric symptoms. After discharge, an oncologic screening was performed and ruled out a paraneoplastic aetiology.
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