Autoimmune haemolytic anaemia commonly has a severe course in young childre
n, thus requiring multiple immunosuppressive treatments. Five children with
refractory idiopathic autoimmune haemolytic anaemia, and one child with th
e disease after bone-marrow transplantation, were treated with rituximab-a
monoclonal antibody against CD20. Tolerance of the treatment was good. Howe
ver, circulating B cells were absent and hypogammaglobulinaemia was seen fo
r 9 months after treatment. All patients remained in complete remission 15-
22 months after the start of rituximab therapy. Corticosteroids and immunos
uppressive drugs were stopped or their dose markedly reduced. We suggest th
at rituximab could be a valuable treatment for autoimmune haemolytic anaemi
a, although a long-lasting but transient B-cell deficiency develops.