Multiple sclerosis (MS) is an autoimmune demyelinating disease exhibiting g
reat clinical variability. For control of its primary and secondary progres
sive variants, treatment has met with limited success. In recent years, inc
reasing experience has been gained with the administration of high dose che
motherapy supported by the autologous infusion of hematopoietic progenitor
cells (HPC), in some instances depleted of T cells. The European and Intern
ational Registry of Hematopoietic Cell Transplantation for Autoimmune Disea
ses include 43 MS patients. BEAM was the most frequently used conditionatin
g therapy. Treatment related mortality was 7%. The actuarial disease free s
urvival and the overall projected survival at 38 months were 85% and 90% re
spectively. The inclusion of an increasing number of MS patients into these
treatment programs and the growing submission of cases to the Registries w
ill provide useful information to determine if the initial enthusiasm gener
ated by this approach for the control of primary and secondary progressive
forms of MS is justified.