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Immunotherapy. 2010 Jul;2(4):521-37. doi: 10.2217/imt.10.19.

Suicide gene therapy for graft-versus-host disease.

Author information

1
Karolinska University Hospital Huddinge, Stockholm, Sweden.

Abstract

In allogeneic hematopoietic stem cell transplantation, donor-derived T cells are key players for early immune reconstitution and efficient engraftment, as well as the graft-versus-leukemia and graft-versus-infection effects. However, a severe and quite common life-threatening complication is the development of graft-versus-host disease, during which the alloreactive donor T cells attack the host. Controlling graft-versus-host disease while preserving the benefits of graft-versus-leukemia still constitutes a challenge. A promising approach for the control of graft-versus-host disease is suicide gene therapy, which involves the ex vivo genetic modification of donor T cells with a suicide gene that allows for the selective elimination of the cells in vivo if graft-versus-host disease occurs. This article presents an overview of such approaches with special reference to lessons learned from previous clinical experiences, as well as a discussion of critical factors in suicide gene therapy.

PMID:
20636006
DOI:
10.2217/imt.10.19
[Indexed for MEDLINE]

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