Role of Immunoglobulins in Muscular Dystrophies and Inflammatory Myopathies

Front Immunol. 2021 Jul 14:12:666879. doi: 10.3389/fimmu.2021.666879. eCollection 2021.

Abstract

Muscular dystrophies and inflammatory myopathies are heterogeneous muscular disorders characterized by progressive muscle weakness and mass loss. Despite the high variability of etiology, inflammation and involvement of both innate and adaptive immune response are shared features. The best understood immune mechanisms involved in these pathologies include complement cascade activation, auto-antibodies directed against muscular proteins or de-novo expressed antigens in myofibers, MHC-I overexpression in myofibers, and lymphocytes-mediated cytotoxicity. Intravenous immunoglobulins (IVIGs) administration could represent a suitable immunomodulator with this respect. Here we focus on mechanisms of action of immunoglobulins in muscular dystrophies and inflammatory myopathies highlighting results of IVIGs from pre-clinical and case reports evidences.

Keywords: autoantibodies; autoimmunity; immunoglobulins; inflammatory myopathies; muscle inflammation; muscular dystrophies.

Publication types

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

MeSH terms

  • Autoantibodies / immunology
  • Autoimmunity*
  • Humans
  • Immunoglobulins / immunology*
  • Immunoglobulins / metabolism
  • Muscle Proteins / metabolism
  • Muscular Dystrophies / immunology*
  • Muscular Dystrophies / metabolism
  • Muscular Dystrophies / pathology
  • Myositis / immunology*
  • Myositis / metabolism
  • Myositis / pathology

Substances

  • Autoantibodies
  • Immunoglobulins
  • Muscle Proteins