Perforin protects against autoimmunity in lupus-prone mice

J Immunol. 1998 Jan 15;160(2):652-60.

Abstract

The roles of cytolytic regulatory mechanisms in the immune system of lupus-prone mice were examined in perforin-deficient animals bearing functional or defective (lpr) Fas Ag (CD95). Perforin-deficient Fas+ animals developed accelerated autoimmunity, characterized by increased hypergammaglobulinemia, autoantibody production, and immune deposit-related end-organ disease compared with perforin-intact counterparts. In comparison, perforin-deficient lpr animals had accelerated mortality compared with perforin-intact lpr mice, associated with the abnormal accumulation of CD3+CD4-CD8- alphabeta T cells in conjunction with unaltered hypergammaglobulinemia, autoantibody production, and immune complex renal disease. These results indicate that cytolytic lymphoid regulation plays critical roles in the immune homeostasis of lupus-prone animals, and identify perforin-mediated cytotoxicity as a specific mechanism in the regulation of systemic autoimmunity.

Publication types

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

MeSH terms

  • Animals
  • Autoimmune Diseases / genetics
  • Autoimmune Diseases / mortality
  • Autoimmune Diseases / pathology
  • Autoimmune Diseases / prevention & control*
  • Cell Movement / genetics
  • Cell Movement / immunology
  • Crosses, Genetic
  • Disease Susceptibility
  • Lupus Nephritis / genetics*
  • Lupus Nephritis / immunology
  • Lupus Nephritis / mortality
  • Lupus Nephritis / pathology
  • Lymphocytes / pathology
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / immunology
  • Membrane Glycoproteins / physiology*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred MRL lpr
  • Mice, Knockout
  • Perforin
  • Pore Forming Cytotoxic Proteins
  • Survival Analysis
  • fas Receptor / genetics

Substances

  • Membrane Glycoproteins
  • Pore Forming Cytotoxic Proteins
  • fas Receptor
  • Perforin