Self-organized criticality theory of autoimmunity

PLoS One. 2009 Dec 31;4(12):e8382. doi: 10.1371/journal.pone.0008382.

Abstract

Background: The cause of autoimmunity, which is unknown, is investigated from a different angle, i.e., the defect in immune 'system', to explain the cause of autoimmunity.

Methodology/principal findings: Repeated immunization with antigen causes systemic autoimmunity in mice otherwise not prone to spontaneous autoimmune diseases. Overstimulation of CD4(+) T cells led to the development of autoantibody-inducing CD4(+) T (aiCD4(+) T) cell which had undergone T cell receptor (TCR) revision and was capable of inducing autoantibodies. The aiCD4(+) T cell was induced by de novo TCR revision but not by cross-reaction, and subsequently overstimulated CD8(+) T cells, driving them to become antigen-specific cytotoxic T lymphocytes (CTL). These CTLs could be further matured by antigen cross-presentation, after which they caused autoimmune tissue injury akin to systemic lupus erythematosus (SLE).

Conclusions/significance: Systemic autoimmunity appears to be the inevitable consequence of over-stimulating the host's immune 'system' by repeated immunization with antigen, to the levels that surpass system's self-organized criticality.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigen Presentation / immunology
  • Autoantibodies / immunology
  • Autoimmunity / immunology*
  • CD8-Positive T-Lymphocytes / cytology
  • CD8-Positive T-Lymphocytes / immunology
  • Cell Proliferation
  • Cross-Priming / immunology
  • Female
  • Immunization
  • Mice
  • Mice, Inbred BALB C
  • Models, Immunological*
  • Organ Specificity / immunology
  • Proteinuria / immunology
  • Receptors, Antigen, T-Cell / immunology

Substances

  • Autoantibodies
  • Receptors, Antigen, T-Cell