Author/Authors :
Manske، نويسنده , , Michelle K. and Zuckerman، نويسنده , , Neta S. and Timm، نويسنده , , Michael M. and Maiden، نويسنده , , Stephanie and Edelman، نويسنده , , Hanna and Shahaf، نويسنده , , Gitit and Barak، نويسنده , , Michal and Dispenzieri، نويسنده , , Angela and Gertz، نويسنده , , Morie A. and Mehr، نويسنده , , Ramit and Abraham، نويسنده , , Roshini S.، نويسنده ,
Abstract :
Light chain amyloidosis (AL) is a bone marrow (BM) plasma cell neoplasia with systemic deposition of Ig light chain amyloid fibrils. Here, we report the identification of clonal CD19 B cells in the BM and the use of a novel mathematical algorithm to generate B cell lineage trees of the clonal CD19 B cells and CD138 plasma cells from the BM of AL patients to delineate the relationship between these two clonal populations. The CD19+ clonal B cells in the BM of AL patients related to the clonal plasma cells represent a pre-plasma cell precursor population. The B cell lineage trees from AL patients also show significant differences in clonal diversification and antigenic selection compared to clones from normal, healthy controls. These data provide a robust example of the use of graphical quantification methods in delineating the role of neoplastic precursors in the pathogenesis of hematopoietic malignancies.
Keywords :
human , Immunoglobulin light chain amyloidosis , B cells , Plasma cell dyscrasia , monoclonal gammopathy , Clone