The Increasing use of haematopoietic stem and progenitor cells from the per
ipheral blood (PBPC) to restore haematopoiesis following high-dose chemothe
rapy has widely propagated the development of techniques for the ex vivo ma
nipulation of haematopoietic cells. In particular, protocols for the ex viv
o expansion of PBPC have been developed for different clinical purposes. Qu
antitative expansion of PBPC may provide a successful strategy for tumour c
ell purging of autologous grafts, or may generate sufficient cell numbers f
or sequential transplantation protocols. Furthermore, allogeneic transplant
ation of megadoses of PBPC may enable us to overcome immunological barriers
, and may substantially increase the number of suitable donors for an indiv
idual patient. Clinical applications also include the use of ex vivo genera
ted, partially differentiated, post-progenitor cells, antigen presenting ce
lls for immunotherapy of minimal residual disease, and ex vivo transduced h
aematopoietic cells as attractive vehicles for genetic therapy.