Role of light chain variable region in myeloma with light chain deposition disease: evidence from an experimental model

Blood. 1995 Nov 15;86(10):3655-9.

Abstract

Light chain deposition disease (LCDD) results from a propensity of some human monoclonal L chains to form tissue deposits. We designed an experimental model for in vivo expression of human kappa L chain sequences in mice and compared a somatically mutated LCDD chain with a closely related control kappa chain, both encoded by the unique V kappa IV gene. Mice secreting the LCDD chain but not those producing the control chain showed deposits with a distribution similar to that observed in patients. These data show that discrete changes in V region sequences can play a major role in tissue deposition of human L chains.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Antibodies, Monoclonal / genetics
  • Disease Models, Animal*
  • Genes, Immunoglobulin*
  • Humans
  • Hybridomas / metabolism
  • Hybridomas / transplantation
  • Immunoglobulin Variable Region / genetics*
  • Immunoglobulin kappa-Chains / genetics*
  • Kidney Diseases / etiology*
  • Kidney Diseases / genetics
  • Kidney Diseases / pathology
  • Mice
  • Mice, Inbred BALB C
  • Molecular Sequence Data
  • Multiple Myeloma / genetics*
  • Multiple Myeloma / pathology
  • Myeloma Proteins / genetics*
  • Paraproteinemias / genetics
  • Paraproteinemias / pathology
  • Recombinant Fusion Proteins / biosynthesis
  • Recombinant Fusion Proteins / toxicity
  • Retroperitoneal Neoplasms / genetics
  • Retroperitoneal Neoplasms / pathology
  • Sequence Alignment
  • Sequence Homology, Amino Acid
  • Transfection

Substances

  • Antibodies, Monoclonal
  • Immunoglobulin Variable Region
  • Immunoglobulin kappa-Chains
  • Myeloma Proteins
  • Recombinant Fusion Proteins