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Antibody Structure01:10

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Antibodies, also known as immunoglobulins (Ig), are essential players of the adaptive immune system. These antigen-binding proteins are produced by B cells and make up 20 percent of the total blood plasma by weight. In mammals, antibodies fall into five different classes, which each elicits a different biological response upon antigen binding.
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Antibodies, or immunoglobulins, are critical players in the immune system's arsenal against invading pathogens. Produced by B cells and plasma cells, their primary role is to detect and bind to specific antigens, molecules found on the surface of pathogens like bacteria or viruses. Beyond antigen recognition, antibodies perform several vital functions that contribute to immune defense.
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Antibodies, also known as immunoglobulins, are produced by B cells in response to foreign substances, such as bacteria and viruses. These proteins are critical for recognizing and neutralizing these substances, protecting the body from potential harm.
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Related Experiment Video

Updated: Jan 27, 2026

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MOG antibody-associated encephalomyelitis/encephalitis.

Sara Salama1, Majid Khan2, Santiago Pardo3

  • 1Department of Neurology, Johns Hopkins University, Baltimore, MD, USA/Department of Neurology, University of Alexandria, Alexandria, Egypt.

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Summary
This summary is machine-generated.

Myelin oligodendrocyte glycoprotein antibody disease is a rare autoimmune condition. This review focuses on MOG antibody disease presenting as encephalitis or ADEM-like conditions in the brain.

Keywords:
MOG antibody diseaseMOG encephalomyelitisMOG-EManti-MOGmyelin oligodendrocyte glycoproteinoptic neuritistransverse myelitis

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Area of Science:

  • Neurology
  • Immunology
  • Neuroimmunology

Background:

  • Myelin oligodendrocyte glycoprotein (MOG) antibody disease is a rare autoimmune disorder.
  • Antibodies target MOG, primarily affecting the optic nerve and spinal cord, causing vision loss and paralysis.
  • Brain involvement can mimic acute disseminated encephalomyelitis (ADEM).

Purpose of the Study:

  • To review MOG antibody disease cases with central nervous system presentations.
  • To discuss MOG-positive encephalitis, encephalopathy, and ADEM-like phenotypes.
  • To synthesize findings from recently published case series.

Main Methods:

  • Literature review of recent MOG antibody disease case series.
  • Analysis of clinical presentations, including encephalitis, encephalopathy, and ADEM-like symptoms.
  • Focus on MOG-positive cases involving the brain.

Main Results:

  • MOG antibody disease can present with neurological symptoms beyond opticospinal presentations.
  • Encephalitic and ADEM-like presentations are observed in MOG antibody disease.
  • Recent series highlight the spectrum of MOG antibody disease in the brain.

Conclusions:

  • MOG antibody disease is a significant cause of acquired CNS demyelination.
  • Recognition of MOG antibody disease is crucial for accurate diagnosis and management.
  • Further research is needed to fully understand MOG antibody disease phenotypes.