C1q deficiency promotes the production of transgenic-derived IgM and IgG3 autoantibodies in anti-DNA knock-in transgenic mice

Mol Immunol. 2008 Feb;45(3):787-95. doi: 10.1016/j.molimm.2007.06.162. Epub 2007 Aug 1.


C1q-deficient mice have been shown to develop a lupus-like disease and to display an impaired clearance of apoptotic cells that are enriched in lupus autoantigens. However, the role of C1q in the regulation of autoreactive B cells remains debatable. To explore this we crossed MRL/Mp C1q-deficient mice with knock-in transgenic (Tg) mice expressing an anti-ssDNA antibody (VH3H9R and VH3H9R/VLkappa8R). Analysis of the VH3H9R mice showed that in the absence of C1q higher titres of Tg-derived IgM and IgG3 anti-ssDNA antibodies were detectable. In contrast, in the VH3H9R/VLkappa8R C1q-deficient animals no increase in Tg antibody levels was observed. In both models the lack of C1q induced a marked reduction of marginal zone B cells and this was paralleled by a significant increase in the percentage of plasmocytes. Thus, one could postulate that in the absence of C1q the failure to clear efficiently dying cells provides an additional stimulus to the autoreactive Tg B cells resulting in their emigration from the marginal zone B cell compartment with subsequent increase in plasmocytes. However, the lack of C1q led to an increased production of Tg IgM and IgG3 antibodies only in VH3H9R mice indicating that additional genetic susceptibility factors are required to break self-tolerance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Antinuclear / genetics
  • Antibodies, Antinuclear / immunology*
  • Cell Death / genetics
  • Cell Death / immunology
  • Complement C1q / deficiency*
  • Germinal Center / immunology
  • Germinal Center / pathology
  • Immunoglobulin G / genetics
  • Immunoglobulin G / immunology*
  • Immunoglobulin M / genetics
  • Immunoglobulin M / immunology*
  • Lupus Erythematosus, Systemic / genetics
  • Lupus Erythematosus, Systemic / immunology
  • Lupus Erythematosus, Systemic / pathology
  • Mice
  • Mice, Transgenic
  • Models, Immunological*
  • Plasma Cells / immunology
  • Plasma Cells / pathology
  • Self Tolerance* / genetics
  • Transgenes / immunology*


  • Antibodies, Antinuclear
  • Immunoglobulin G
  • Immunoglobulin M
  • Complement C1q