Molecular mimicry: its evolution from concept to mechanism as a cause of autoimmune diseases

Monoclon Antib Immunodiagn Immunother. 2014 Jun;33(3):158-65. doi: 10.1089/mab.2013.0090. Epub 2014 Apr 2.


On a clonal level, certain antibodies and T cells can interact with dissimilar antigens found in microbes and in host cells. More than 5% of over 800 monoclonal antibodies derived from multiple RNA and DNA viruses, as well as from a large number of T cell clones, engage in such interactions. Several of these cross-reactions, which we termed molecular mimicry, are against unique host proteins involved in autoimmune responses and diseases. Thus, molecular mimicry initiated as a host response to a virus or a microbial infection, but alternatively cross-reacting with an appropriate host-antigen, can be a mechanism for instigating an autoimmune disease. Molecular mimicry provides an explanation for the genetic observation that identical twins rarely manifest the same autoimmune disease and the documented epidemiologic evidence that microbial and/or viral infections often precede autoimmune disorders.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Antibodies, Monoclonal / immunology*
  • Antibodies, Monoclonal / metabolism
  • Antigens / immunology*
  • Antigens / metabolism
  • Autoimmune Diseases / immunology*
  • Humans
  • Infections / immunology*
  • Infections / microbiology
  • Infections / virology
  • Molecular Mimicry / immunology*
  • T-Lymphocytes / immunology*


  • Antibodies, Monoclonal
  • Antigens