The contribution of HERV-E clone 4-1 and other HERV-E members to the pathogenesis of rheumatic autoimmune diseases

APMIS. 2020 May;128(5):367-377. doi: 10.1111/apm.13039. Epub 2020 Apr 30.

Abstract

Human endogenous retroviruses (HERV)-E consist of a family of more than 1300 elements, stably integrated in the human genome. Some of them are full-length proviruses able to synthesize the viral proteins gag, pol and env. The reactivation of HERV-E elements has been associated to placentation, cancer and autoimmunity. In this narrative review, we aimed to report the status of the art concerning the involvement of HERV-E in rheumatic autoimmune diseases. Following a research on PubMed database, a total of 87 articles were selected. The highest amount of evidence derives from studies on systemic lupus erythematosus (SLE), whereas a few to no data are available on other immune-mediated diseases. In SLE, the hyper-expression of HERV-E clone 4-1 in peripheral blood mononuclear cells or differentiated lymphocytes has been associated with disease activity and autoantibody production. It is likely that HERV-E take part to the pathogenesis of rheumatic autoimmune diseases but additional research is needed.

Keywords: HERV-E; HERV-E clone 4-1; Rheumatic autoimmune diseases; human endogenous retroviruses; immunology; pathogenesis; virology.

Publication types

  • Review

MeSH terms

  • DNA Methylation
  • Endogenous Retroviruses / genetics*
  • Humans
  • Leukocytes, Mononuclear / virology*
  • Lupus Erythematosus, Systemic / genetics*
  • Lupus Erythematosus, Systemic / immunology
  • Lupus Erythematosus, Systemic / virology
  • Rheumatic Diseases / genetics*
  • Rheumatic Diseases / immunology
  • Rheumatic Diseases / virology