Proteasome Inhibition and Allogeneic Hematopoietic Stem Cell Transplantation: A Review
Received 15 June 2009; accepted 16 July 2009. published online 25 September 2009.
The proteasome and its associated ubiquitin protein modification system have proved to be an important therapeutic target in the treatment of multiple myeloma and other cancers. In addition to direct antitumor effects, proteasome inhibition also exerts strong effects on nonneoplastic immune cells. This indicates that proteasome inhibition, through the use of agents like bortezomib, could be used therapeutically to modulate immune responses. In this review we explore the emerging data, both preclinical and clinical, highlighting the importance of proteasome targeting of immunologic responses, primarily in the context of allogeneic hematopoietic stem cell transplantation (HSCT), both for the control of transplant-related toxicities like acute and chronic graft-versus-host disease (aGVHD, cGHVHD), and for improved malignant disease control after allogeneic HSCT.
1Division of Hematologic Malignancies, Dana-Farber Cancer Institute, Boston, Massachustts
2Department of Dermatology, UC Davis School of Medicine, Sacramento, California
Correspondence and reprint requests: William J. Murphy, MD, PhD, Department of Dermatology, University of California, Davis School of Medicine, Research III, Room 3300, 4645 2nd Avenue, Sacramento, CA 95818.
Financial disclosure: See Acknowledgments on page 1509.