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Myelin Oligodendrocyte Glycoprotein MOG35-55 Induced Experimental Autoimmune Encephalomyelitis EAE in C57BL/6 Mice
Published on: April 15, 2014
[Cerebral cortical encephalitis with anti-myelin oligodendrocyte glycoprotein (MOG) antibody]
Hiroshi Adachi1, Yukiko Ide1, Toshiyuki Takahashi2,3
1Department of Neurology, Hyogo Prefectural Amagasaki General Medical Center.
Abstract:
A 27-year-old man developed acute encephalitis with headache, fever, seizures, and aphasia. Analysis of cerebrospinal fluid showed elevated levels of cell counts and protein. A brain MRI demonstrated increased FLAIR signals in the left cerebral cortex with cortical swelling. An MRA also showed mild vasodilatation of the left middle cerebral artery branches. After admission, severe psychomotor excitement developed. Immunotherapy with intravenous high-dose steroid and subsequent oral steroid was successful, and the patient returned to premorbid working position. Repeated MRI study showed complete resolution. Serum anti-myelin oligodendrocyte glycoprotein (MOG) antibody was positive, while anti-aquaporin-4 antibody, anti-N-methyl-D-aspartate (NMDA) receptor antibody, and other autoimmune antibodies were all negative. There were no relapses at final follow-up of 8 months after onset. Cerebral cortical encephalitis with unknown etiology can occur associated with anti-MOG antibody, and anti-MOG antibody may play certain role in the pathogenesis.
Insights
A young man experienced acute encephalitis, successfully treated with steroids. Myelin oligodendrocyte glycoprotein (MOG) antibody was identified as a potential cause, highlighting its role in cerebral cortical encephalitis.
Area of Science:
- Neuroscience
- Immunology
- Neurology
Background:
- Encephalitis presents with diverse neurological symptoms.
- Cerebral cortical encephalitis often has an unknown etiology.
- Autoimmune antibodies are implicated in some encephalitis cases.
Observation:
- A 27-year-old man presented with acute encephalitis, including seizures and aphasia.
- Cerebrospinal fluid analysis revealed elevated cells and protein.
- Brain MRI showed left cerebral cortex FLAIR hyperintensities and swelling, with MRA revealing mild vasodilatation.
Findings:
- The patient developed psychomotor excitement, responsive to high-dose steroid immunotherapy.
- Serum testing confirmed positive anti-myelin oligodendrocyte glycoprotein (MOG) antibody.
- Other autoimmune antibodies, including anti-aquaporin-4 and anti-NMDA receptor antibodies, were negative.
Implications:
- This case suggests a potential role for anti-MOG antibodies in cerebral cortical encephalitis.
- MOG antibody-associated encephalitis may present with symptoms mimicking other forms of encephalitis.
- Prompt immunotherapy can lead to complete resolution and recovery.
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10:47Simple and Efficient Production and Purification of Mouse Myelin Oligodendrocyte Glycoprotein for Experimental Autoimmune Encephalomyelitis Studies
Published on: October 27, 2016
18:17Derivation of Enriched Oligodendrocyte Cultures and Oligodendrocyte/Neuron Myelinating Co-cultures from Post-natal Murine Tissues
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