Intravenouse immunoglobuline in dysautonomia

Clin Immunol. 2022 Jul:240:109039. doi: 10.1016/j.clim.2022.109039. Epub 2022 May 13.

Abstract

Nowadays intravenous immunoglobulin (IVIg) treatment is considered to play a promising role in the autoimmune disease therapy. Despite its significant beneficial effects, the precise mechanism of action needs further studies, as well as recommended dosage in the treatment of autoimmune dysautonomia. In some diseases, like Guillain-Barre syndrome (GBS) and chronic inflammatory demyelinating neuropathy (CIDP), IVIg has a strong evidence that allows to recommend and prescribe the medication, while in other diseases only single case studies are available that requires further research. The review summarizes the currently available information on the effectiveness of IVIg in primary autoimmune neuropathies and neurological complications of systemic diseases, as well as side effects, features of clinical use with an emphasis on doses and treatment protocols in dysautonomia. Being safe and effective therapy, immunologic treatment is one of the most promising tools to achieve clinical remission of dysautonomia and good quality of life in autoimmune patients.

Keywords: Autoimmune autonomic gangliopathy (AAG); Chronic inflammatory demyelinating neuropathy (CIDP); Guillain-Barre syndrome (GBS); Intravenous immunoglobulins; Neuropathy; Small fiber neuropathy.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Guillain-Barre Syndrome*
  • Humans
  • Immunoglobulins, Intravenous
  • Polyradiculoneuropathy, Chronic Inflammatory Demyelinating* / chemically induced
  • Polyradiculoneuropathy, Chronic Inflammatory Demyelinating* / drug therapy
  • Primary Dysautonomias* / drug therapy
  • Quality of Life

Substances

  • Immunoglobulins, Intravenous