| Literature DB >> 12563615 |
Joseph Schwartz1, Javier Pinilla-Ibarz, Rui Rong Yuan, David A Scheinberg.
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). Copyright 2003, Elsevier Science (USA). All rights reserved.Entities:
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Year: 2003 PMID: 12563615 DOI: 10.1053/shem.2003.50007
Source DB: PubMed Journal: Semin Hematol ISSN: 0037-1963 Impact factor: 3.851