Leukemia has been treated with chemotherapy for the past 40 years with
only moderate success. A growing body of evidence suggests that by au
gmenting the immune system more effective results may be obtained. Thi
s is highlighted by T cell reinfusions resulting in durable remissions
in patients with chronic myelogenous leukemia who have relapsed after
an allogeneic transplant. Interleukin-2 is the primary growth factor
for T lymphocytes and is a stimulator of natural killer cell activity.
It has now been shown that a limited number of otherwise refractory l
eukemias can be effectively treated with interleukin-2. However, there
remains a lack of correlation between the biologic and clinical effec
ts of interleukin-4. The clinical activity of interleukin-a appears to
be greatest in myeloid leukemias. A variety of dose schedules and rou
tes of administration make it difficult to determine if interleukin-2
given to patients in clinical remission is of benefit. Large randomize
d studies are necessary to explore the role of interleukin-2 in leukem
ia.