AI Article Synopsis

  • Immune-mediated processes are becoming an important cause of neurological diseases across various neurology fields.
  • Neural autoantibodies are categorized into two types: those targeting intracellular proteins and those targeting cell membrane/synaptic proteins, with the latter being linked to both neurological diseases and cancers.
  • The article reviews various antineural antibodies, their clinical connections, and potential mechanisms through which these antibodies cause disease, noting that creating effective animal models to study these disorders has been challenging.

Article Abstract

Immune-mediated processes represent a rapidly expanding categorical etiology for neurological disease manifestations spanning all subspecialties of neurology. Neural autoantibodies can be grossly divided into two main groups based on localization of the antigen: intracellular and cell membrane/synaptic antibodies. Antibodies reactive with neuronal membrane antigens have been identified in serum and cerebrospinal fluid of patients developing neurological disease either independent of or associated with cancer comorbidity, whereas antibodies directed against intracellular targets have a much higher rate of associated malignancy. Antibodies to neuronal membrane proteins such as the N-methyl-D-aspartate (NMDA) receptor are considered directly pathogenic based on disease models. Similar evidence exists for far fewer autoantibodies directed against intracellular targets. Attempts to produce an antibody-mediated animal model of human paraneoplastic disease have been unsuccessful to date. In this article, we review antineural antibodies and their clinical associations, briefly discuss recently characterized entities, and present proposed mechanisms of antibody pathogenicity.

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Source
http://dx.doi.org/10.1055/s-0038-1660501DOI Listing

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