A hierarchical role for classical pathway complement proteins in the clearance of apoptotic cells in vivo

J Exp Med. 2000 Aug 7;192(3):359-66. doi: 10.1084/jem.192.3.359.


The strongest susceptibility genes for the development of systemic lupus erythematosus (SLE) in humans are null mutants of classical pathway complement proteins. There is a hierarchy of disease susceptibility and severity according to the position of the missing protein in the activation pathway, with the severest disease associated with C1q deficiency. Here we demonstrate, using novel in vivo models of apoptotic cell clearance during sterile peritonitis, a similar hierarchical role for classical pathway complement proteins in vivo in the clearance of apoptotic cells by macrophages. Our results constitute the first demonstration of an impairment in the phagocytosis of apoptotic cells by macrophages in vivo in a mammalian system. Apoptotic cells are thought to be a major source of the autoantigens of SLE, and impairment of their removal by complement may explain the link between hereditary complement deficiency and the development of SLE.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / immunology*
  • Apoptosis / radiation effects
  • Cells, Cultured
  • Complement C1q / genetics
  • Complement C1q / immunology*
  • Complement Pathway, Classical*
  • Female
  • Humans
  • Jurkat Cells
  • Macrophages, Peritoneal / immunology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Monocytes / immunology
  • Peritonitis / immunology
  • Phagocytosis / immunology
  • Thymus Gland / cytology


  • Complement C1q