Polyclonal B cell activation and antigen-specific stimulation in mice with chronic graft-versus-host reaction

Clin Immunol Immunopathol. 1993 Mar;66(3):254-9. doi: 10.1006/clin.1993.1033.

Abstract

Primary chronic graft-versus-host reaction (GVHR) was induced in (C57BL/10 x DBA/2)F1 (BDF1) mice via the transfer of parental DBA/2 derived lymphocytes. A significant increase in the absolute number of IgM- and IgG-secreting cells was found in recipient BDF1 mice at 3 weeks post-transfer. The increase included B cells reactive with both self- and non-self-antigens, without being skewed toward the production of autoantibodies. Later in the disease process (approximately 6-8 weeks post-transfer), we detected an increased number of B cells that secreted antibodies reactive with a select subset of autoantigens in about 30% of BDF1 recipients (3 of 9 mice). These findings suggest that not only antigen-specific stimulation, which was detected in a late stage, but also initial polyclonal activation may account for chronic GVHR.

MeSH terms

  • Animals
  • Antibody-Producing Cells / immunology
  • B-Lymphocytes / immunology*
  • Chronic Disease
  • Epitopes
  • Female
  • Graft vs Host Disease / immunology
  • Graft vs Host Reaction / immunology*
  • Immunoglobulin G / biosynthesis
  • Immunoglobulin M / biosynthesis
  • Lymphocyte Activation
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred DBA

Substances

  • Epitopes
  • Immunoglobulin G
  • Immunoglobulin M