Myelin Oligodendrocyte Glycoprotein as an Autoantigen in Inflammatory Demyelinating Diseases of the Central Nervous System

• Published in: Biochemistry (Moscow) Vol. 88; no. 4; pp. 551 - 563
• Main Authors: Eliseeva, Daria D., Zakharova, Maria N.
• Format: Journal Article
• Language: English
• Published: Moscow Pleiades Publishing 01-04-2023; Springer; Springer Nature B.V
• Subjects: Alternative splicing; Analysis; Antibodies; Antigens; Aquaporins; Autoantibodies; Autoantigens; Autoimmune diseases; Autoimmunity; Axons; Biochemistry; Biomedical and Life Sciences; Biomedicine; Bioorganic Chemistry; Care and treatment; Central Nervous System; Demyelinating diseases; Demyelinating Diseases - diagnosis; Demyelination; Diagnostic systems; Disease; Encephalitis; Encephalomyelitis; Glycoproteins; Humans; Immunofluorescence; Immunoglobulin G; Immunoglobulins; Immunology; Isoforms; Life Sciences; Lymphocytes; Medical research; Microbiology; Myelin; Myelin proteins; Myelin-Oligodendrocyte Glycoprotein; Neurological disorders; Oligodendrocyte-myelin glycoprotein; Oligodendroglia; Proteins; Review; Spinal cord; Structural integrity; Structural proteins; Russia; antibodies; alternative splicing; myelin oligodendrocyte glycoprotein; demyelinating diseases
• ISSN: 0006-2979; 1608-3040
• DOI: 10.1134/S0006297923040107

Demyelinating diseases of the central nervous system are caused by an autoimmune attack on the myelin sheath surrounding axons. Myelin structural proteins become antigenic, leading to the development of myelin lesions. The use of highly specialized laboratory diagnostic techniques for identification of specific antibodies directed against myelin components can significantly improve diagnostic approaches. Myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease (MOGAD) currently includes demyelinating syndromes with known antigens. Based on the demonstrated pathogenic role of human IgG against MOG, MOGAD was classified as a distinct nosological entity. However, generation of multiple MOG isoforms by alternative splicing hinders antigen detection even with the most advanced immunofluorescence techniques. On the other hand, MOG conformational changes ensure the structural integrity of other myelin proteins and maintain human-specific mechanisms of immune autotolerance.