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
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Sequence
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Animals
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Antibodies, Monoclonal / genetics
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Disease Models, Animal*
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Genes, Immunoglobulin*
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Humans
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Hybridomas / metabolism
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Hybridomas / transplantation
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Immunoglobulin Variable Region / genetics*
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Immunoglobulin kappa-Chains / genetics*
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Kidney Diseases / etiology*
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Kidney Diseases / genetics
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Kidney Diseases / pathology
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Mice
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Mice, Inbred BALB C
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Molecular Sequence Data
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Multiple Myeloma / genetics*
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Multiple Myeloma / pathology
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Myeloma Proteins / genetics*
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Paraproteinemias / genetics
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Paraproteinemias / pathology
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Recombinant Fusion Proteins / biosynthesis
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Recombinant Fusion Proteins / toxicity
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Retroperitoneal Neoplasms / genetics
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Retroperitoneal Neoplasms / pathology
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Sequence Alignment
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Sequence Homology, Amino Acid
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Transfection
Substances
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Antibodies, Monoclonal
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Immunoglobulin Variable Region
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Immunoglobulin kappa-Chains
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Myeloma Proteins
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Recombinant Fusion Proteins