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Regenerative Stromal Cell Therapy in Allogeneic Hematopoietic Stem Cell Transplantation: Current Impact and Future Directions

Journal

BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION
Volume 16, Issue 7, Pages 891-906

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.bbmt.2009.12.005

Keywords

Graft-versus-host disease; Hematopoietic stem cell transplantation; Immunomodulation; Mesenchymal stem cell; Microenvironment; Multipotent adult progenitor cell; Rgenerative stromal cell therapy

Funding

  1. National Institutes of Health [AI57801]
  2. Center for Stem Cell and Regenerative Medicine at Case Western Reserve University
  3. Ohio Third Frontier Biomedical Research and Commercialization Program (BRCP)
  4. Burroughs Wellcome Fund

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Regenerative stromal cell therapy (RSCT) has the potential to become a novel therapy for preventing and treating acute graft-versus-host disease (GVHD) in the allogeneic hematopoietic stem cell transplant (HSCT) recipient. However, enthusiasm for using RSCT in allogeneic HSCT has been tempered by limited clinical data and poorly defined in vivo mechanisms of action. As a result, the full clinical potential of RSCT in supporting hematopoietic reconstitution and as treatment for GVHD remains to be determined. This manuscript reviews the immunomodulatory activity of regenerative stromal cells in preclinical models of allogeneic HSCT, and emphasizes an emerging literature suggesting that microenvironment influences RSC activation and function. Understanding this key finding may ultimately define the proper niche for RSCT in allogeneic HSCT. In particular, mechanistic studies are needed to delineate the in vivo effects of RSCT in response to inflammation and injury associated with allogeneic HSCT, and to define the relevant sites of RSC interaction with immune cells in the transplant recipient. Furthermore, development of in vivo imaging technology to correlate biodistribution patterns, desired RSC effect, and clinical outcome will be crucial to establishing dose-response effects and minimal biologic dose thresholds needed to advance translational treatment strategies for complications like GVHD. Biol Blood Marrow Transplant 16: 891-906 (2010) (C) 2010 American Society for Blood and Marrow Transplantation

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