Novel targeted and immunotherapeutic strategies in chronic myeloid leukemia☆☆☆
Abstract
The advanced understanding of the molecular biology and immunology of chronic myeloid leukemia (CML) has led to novel therapeutic strategies unique to this disease. CML responds to immune-mediated therapies, including stem cell transplantation, donor lymphocyte infusion (DLI), and interferon alfa. T cells and other immune effectors are implicated in the mechanisms of action of these immune therapies. Recently, clinical observations supported by laboratory data have demonstrated the presence of CML-specific T cells in patients. Several proteins may potentially act as leukemia-specific antigens for major histocompatibility complex (MHC)-restricted cytotoxicity in CML, and active specific therapies (vaccines) are in development. Antigens under investigation include bcr-abl, PR1, Wilms tumor protein (WT1), minor histocompatibility antigens (mH), CML-66, CML-28, and survivin. Other strategies target vascular endothelial growth factor (VEGF) and heat shock protein 90 (Hsp90) inhibitors or make use of CML-derived dendritic cells (DC). Semin Hematol 40:87-96. Copyright 2003, Elsevier Science (USA). All rights reserved.
☆ D.A.S. is a Doris Duke Distinguished Clinical Scientist. J.S. is a Lauri Strauss Leukemia Foundation Fellow.
☆☆ Address reprint requests to David A. Scheinberg, MD, PhD, Department of Medicine, Memorial Sloan Kettering Cancer Center, 1275 York Ave, Box 531, New York, NY 10021.
PII: S0037-1963(03)70046-8
© 2003 Published by Elsevier Inc.
