Systemic lupus erythematosus as a genetic disease.

Clin Immunol

Division of Rheumatology, Department of Pediatrics, University of Pittsburgh School of Medicine, UPMC Children's Hospital of Pittsburgh, Pittsburgh, PA, USA; Division of Rheumatology and Clinical Immunology, Department of Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA; Department of Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA; Lupus Center of Excellence, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA. Electronic address:

Published: March 2022

AI Article Synopsis

  • Systemic lupus erythematosus (SLE) is a complex autoimmune disease characterized by wide-ranging symptoms and the presence of autoantibodies targeting nuclear components.
  • Modern genetic studies reveal that SLE typically occurs when genetic risk factors align with environmental triggers, challenging previous assumptions about its genetic basis.
  • Research efforts focus on understanding the genetic structure of SLE, how it affects disease processes, illustrating the disease's multifaceted nature, and effectively communicating these findings to patients.

Article Abstract

Systemic lupus erythematosus is the prototypical systemic autoimmune disease, as it is characterized both by protean multi-organ system manifestations and by the uniform presence of pathogenic autoantibodies directed against components of the nucleus. Prior to the modern genetic era, the diverse clinical manifestations of SLE suggested to many that SLE patients were unlikely to share a common genetic risk basis. However, modern genetic studies have revealed that SLE usually arises when an environmental exposure occurs in an individual with a collection of genetic risk variants passing a liability threshold. Here, we summarize the current state of the field aimed at: (1) understanding the genetic architecture of this complex disease, (2) synthesizing how this genetic risk architecture impacts cellular and molecular disease pathophysiology, (3) providing illustrative examples that highlight the rich complexity of the pathobiology of this prototypical autoimmune disease and (4) communicating this complex etiopathogenesis to patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9167620PMC
http://dx.doi.org/10.1016/j.clim.2022.108953DOI Listing

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