Next-generation sequencing of peripheral B-lineage cells pinpoints the circulating clonotypic cell pool in multiple myeloma

Blood. 2014 Jun 5;123(23):3618-21. doi: 10.1182/blood-2014-02-556746. Epub 2014 Apr 21.

Abstract

The identity of the proliferative compartment of myeloma progenitor cells remains a matter of debate. Polymerase chain reaction-based studies suggested pre-switch "clonotypic" B cells sharing the immunoglobulin (Ig) rearrangement of the malignant plasma cell (M-PC), to circulate in the blood and possess stem cell-like properties. Here, we disprove this hypothesis. We screened peripheral blood IgM, IgG, and IgA repertoires of myeloma patients for the clonotypic rearrangement by next-generation sequencing. None of 12 cases showed pre-switch clonotypic transcripts. In the post-switch IgG/IgA repertoires, however, the clonotypic rearrangement was detected at high frequency in 6 of 8 patients with active disease, whereas it was undetectable after treatment, correlating with flow cytometric presence or absence of circulating M-PCs. Minor subclones with alternative post-switch isotypes suggested ongoing switch events and clonal evolution at the M-PC level. Our findings consistently show an absence of pre-switch clonotypic B cells, while M-PCs circulate in the peripheral blood and may contribute to spreading of the disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • B-Lymphocytes / metabolism*
  • Blood Cells / metabolism
  • Cell Lineage / genetics*
  • Clone Cells
  • Cohort Studies
  • Gene Rearrangement, B-Lymphocyte / genetics
  • High-Throughput Nucleotide Sequencing*
  • Humans
  • Immunoglobulin Class Switching
  • Immunoglobulins / genetics
  • Multiple Myeloma / genetics*
  • Multiple Myeloma / pathology*
  • Phenotype
  • Plasma Cells / metabolism
  • Plasma Cells / pathology

Substances

  • Immunoglobulins