The impressive prolongation of survival has been the most important pr
ogress made in clinical systemic lupus erythematosus (SLE). Quality of
life has also greatly improved, including pregnancy. However, persist
ing disease and therapy-related morbidity outcomes justify new approac
hes, different from the usual long-term palliative immunosuppression.
Haematopoietic stem cells (HSCs) from healthy histocompatible mice are
capable of curing murine SLE after eradication of the original HSCs w
ith total body irradiation. Syngeneic and even autologous HSCs are als
o capable of curing induced experimental autoimmune diseases such as a
djuvant arthritis and experimental allergic encephalomyelitis. In man
allogeneic bone-marrow transplantation (BMT) is becoming progressively
safer, but cannot yet be offered to SLE patients. However, syngeneic
transplants from twins non-concordant for the disease would be justifi
ed. Conditioning with high-dose cyclophosphamide followed by autologou
s HSC rescue, from the marrow and/or from the peripheral blood, may al
ready be regarded as a powerful immunosuppressive procedure for select
ed cases of SLE and other severe autoimmune diseases. Autologous trans
plant procedures are not saddled with the immunologic problems of allo
-BMT. Although eradication of SLE may not be achieved by auto-BMT, min
imal residual immunologic disease can be suppressed or controlled, and
long-term self-maintained remissions may be expected.