Haematological recovery following autologous peripheral blood stem cell tre
atment is very rapid. Immune recovery is a more prolonged process requiring
a year or more for full reconstitution. Because high-dose chemotherapy fol
lowed by autologous peripheral blood stem cell treatment results in (or is
presumed to result in) minimal burden of residual malignant disease it prov
ides a potentially ideal setting for immune-mediated anti-tumour therapy. T
he slow immune reconstitution following transplantation may however hamper
the development of effective immunotherapy. Among different approaches prop
osed, we focus on the potential use of tumour antigens in conjunction with
cellular therapy in an attempt to eliminate residual tumour following autol
ogous transplantation.