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Related Concept Videos

Autoimmune Disorders01:29

Autoimmune Disorders

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Autoimmune diseases are a group of disorders in which the body's immune system mistakenly attacks its own cells, tissues, and organs. This results from an overactive immune response against substances and tissues normally present in the body. Let's delve into the concept and mechanism of autoimmune diseases from an immune system point of view, explore different causes and examples of such diseases, and discuss potential solutions.
Concept and Mechanism of Autoimmune Diseases
The immune...
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Myasthenia Gravis: Overview and Treatment01:20

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Myasthenia gravis is a neuromuscular transmission disorder characterized by weakness and increased fatigability of skeletal muscles. It is an autoimmune disease affecting approximately one in 2000 people, where antibodies against the α1 subunit of nicotinic acetylcholine receptors are produced.
These antibodies interfere with the function of the nicotinic receptors in three ways: by binding to the receptor and disrupting acetylcholine binding; by causing cross-linking of receptors which...
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Myasthenia Gravis: Diagnostic Tests01:15

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Myasthenia gravis is an autoimmune condition affecting neuromuscular transmission, causing generalized weakness in skeletal muscles. Initial diagnoses rely on patients' signs, symptoms, and medical history. The challenge lies in distinguishing myasthenia from other muscular dystrophies. An important diagnostic feature is the significant improvement of symptoms after administering anticholinesterase inhibitors.
The edrophonium test is a diagnostic tool for myasthenia gravis. It involves...
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Chemical Synapses01:26

Chemical Synapses

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Chemical synapses are specialized sites between two neurons or between a neuron and a non-neuronal cell like a muscle, glandular or sensory cell.
Because chemical synapses depend on the release of neurotransmitter molecules from synaptic vesicles to pass on their signal, there is an approximately one millisecond delay between when the axon potential reaches the presynaptic terminal and when the neurotransmitter leads to opening of postsynaptic ion channels. Additionally, this signaling is...
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Author Spotlight: Novel Assay for Studying B-Cell Responses in Multiple Sclerosis Research
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Autoimmune myelopathies.

Eoin P Flanagan1

  • 1Department of Neurology, Mayo Clinic, Rochester, MN, USA.

Handbook of Clinical Neurology
|April 27, 2016
PubMed
Summary
This summary is machine-generated.

Autoimmune myelopathies are diverse immune-mediated spinal cord diseases. Novel autoantibodies aid classification, guiding cancer detection, treatment, and prognosis for better patient outcomes.

Keywords:
aquaporin-4-IgGautoimmune myelopathyneuromyelitis opticaparaneoplastic myelopathyspinal cord sarcoidosistransverse myelitis

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Area of Science:

  • Neurology
  • Immunology
  • Oncology

Background:

  • Autoimmune myelopathies represent a complex group of immune-mediated spinal cord disorders.
  • Diagnosis is challenging due to their heterogeneous nature and broad differential diagnosis.
  • Includes conditions like aquaporin-4-IgG (AQP4-IgG) seropositive neuromyelitis optica spectrum disorders (NMOSD), systemic autoimmune disorders, paraneoplastic, and postinfectious causes.

Purpose of the Study:

  • To review the classification and diagnostic approaches for autoimmune myelopathies.
  • To highlight the role of novel neural autoantibodies in diagnosis and management.
  • To discuss the therapeutic goals of immunotherapy and cancer treatment in these conditions.

Main Methods:

  • Review of current literature on autoimmune myelopathies.
  • Emphasis on diagnostic utility of spine magnetic resonance imaging (MRI) findings.
  • Discussion of the significance of identifying neural autoantibodies, such as AQP4-IgG and collapsin response mediator protein-5 (CRMP5)-IgG.

Main Results:

  • Spine MRI characteristics (lesion location, enhancement patterns) are crucial for differential diagnosis.
  • Discovery of novel autoantibodies has significantly improved classification and understanding.
  • Autoantibodies can be pathogenic (e.g., AQP4-IgG) or markers of T-cell responses (e.g., CRMP5-IgG).
  • Antibody presence aids in guiding cancer screening, treatment choices, and predicting outcomes.

Conclusions:

  • Accurate classification of autoimmune myelopathies is enhanced by novel autoantibody discoveries.
  • Management involves targeted immunotherapy to maximize recovery and prevent relapse.
  • For paraneoplastic myelopathies, prompt cancer detection and treatment are paramount.