The site and stage of anti-DNA B-cell deletion

Nature. 1995 Jan 19;373(6511):252-5. doi: 10.1038/373252a0.

Abstract

Antibodies to DNA and nucleoproteins are found in sera of individuals with systemic autoimmune disease. In the population (and in the autoimmune mouse strain MRL/lpr) there is a great variety of such antinuclear antibodies, but individuals with systemic lupus erythematosus or single MRL mice express a subset only of the antinuclear specificities found in the population. These observations have been interpreted to mean that these antibodies arise by immunization. The oligoclonal nature of the autoantibody response and the evidence of selection acting on somatically mutated autoantibodies favour this interpretation. Specific activation of autoantibodies in disease implies either that autoantibodies are regulated in non-diseased individuals or that autoantigen availability is variable. The former has been demonstrated in anti-DNA transgenic mice. In normal mice, transgene-encoded antibodies against double-stranded (ds) DNA are not expressed in serum or on B cells. Here we describe modified anti-dsDNA transgenic mice which allow us to study the site and developmental stage at which such B-cell regulation occurs. This model shows that in normal mice B cells expressing anti-DNA specificity are deleted in the bone marrow at a pre-B to immature B transitional stage.

Publication types

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

MeSH terms

  • Animals
  • Autoantibodies / biosynthesis
  • Autoantibodies / genetics
  • Autoantibodies / immunology*
  • B-Lymphocytes / cytology
  • B-Lymphocytes / immunology*
  • Base Sequence
  • Bone Marrow Cells
  • Cell Differentiation
  • DNA / immunology*
  • DNA Primers
  • Flow Cytometry
  • Immunoglobulin Heavy Chains / genetics
  • Immunoglobulin Heavy Chains / immunology
  • Mice
  • Mice, Inbred BALB C
  • Mice, Mutant Strains
  • Mice, Transgenic
  • Molecular Sequence Data
  • Spleen / cytology

Substances

  • Autoantibodies
  • DNA Primers
  • Immunoglobulin Heavy Chains
  • DNA