W. Schwinger et al., TREATMENT OF APLASTIC-ANEMIA WITH A MONOCLONAL-ANTIBODY DIRECTED AGAINST THE INTERLEUKIN-2 RECEPTOR, Annals of hematology, 66(4), 1993, pp. 181-184
Severe aplastic anemia (SAA) has been related in most cases to underly
ing autoimmune conditions. Various immunosuppressive regimens have bee
n recommended in the absence of an HLA-identical bone marrow donor. Pr
ednisolone, antithymocyte globulin, and cyclosporin A have been shown
to be effective. This report describes the successful treatment of a 2
3-year-old woman suffering from severe aplastic anemia who had become
multiresistant against previously administered immunosuppressive agent
s, using a monoclonal IL-2-receptor blocking antibody. The patient res
ponded within 4 weeks. The time to the next relapse was 8 months; howe
ver, another remission with a second course of horse-antithymocyte glo
bulin was achieved and has been maintained for 27 months to date with
low doses of cyclosporin A. Although this is an anecdotical report, IL
-2-receptor blockade using a monoclonal antibody might be considered a
s a further alternative in multi-resistant SAA, perhaps increasing the
susceptibility to further immunosuppressive trials.