High-dose therapy with subsequent allogeneic or autologous transplantation
of haemopoietic progenitor cells has proved to be an important therapy for
patients with haematological malignancies, certain non-haematological cance
rs and several nonmalignant disorders such as severe aplastic anaemia. Allo
geneic and autologous transplantation are associated with specific complica
tions. One major problem after allotransplantation is the graft versus host
disease with jaundice, diarrhoea and erythema. The major problem of autolo
gous stem cell transplantation is a potential reinfusion of contaminating t
umor cells. Allogeneic transplantation has been refined, and an approach to
modulate graft versus host disease is a partial or complete lymphocyte dep
letion. Especially in the allogeneic setting, the field of cell therapy for
modulation of graft versus host disease and treatment of transplant-relate
d complications is expanding. For autologous transplantation different tech
niques to purge autografts from malignant contaminants have been developed.
These cell selection techniques consist of immunological, biological, cult
ural, chemotherapeutical and physical techniques. This article reviews tech
niques currently used for graft engineering in bone marrow and blood stem c
ell transplantation.