A high incidence of oligoclonal serum M-components is observed in multiple
myeloma (MM) patients treated with autologous Stem cell transplantation (AS
CT). To determine whether these hi-components are produced by myeloma clona
lly related cells or caused by an aberrant B-cell regeneration we analysed
by semi-nested ASO-RT-PCR and DNA sequencing the immunoglobulin (Ig) variab
le genes (VH) obtained from bone marrow samples obtained before and after t
ransplantation and peripheral blood stern cell (PBSC) samples from seven pa
tients.
Myeloma clonally related cells are identifiable by the expression of varian
t Ig heavy chain isotypes and were detected in two patients at presentation
. No myeloma clonally related cells were found in post-transplantation samp
les (n = 7) in spite of the appearance of new serum M-components, However,
in two cases we amplified sequences from post-transplantation bone marrow c
ells that were able to bind to the B-cell clone-specific CDR3 oligonucleoti
des but showed no further similarity regarding the VDT rearrangement,
These data indicate that serum oligoclonality posttransplantation is not ca
used by myeloma clonally related B cells but rather by the regenerating B-c
ell compartment.