Progress and prospects: graft-versus-host disease
Gene Ther. 2010 May 27. [Epub ahead of print]
Mastaglio S, Stanghellini MT, Bordignon C, Bondanza A, Ciceri F, Bonini C.
[1] Hematology and BMT Unit, Department of Oncology, San Raffaele Scientific Institute, Milano, Italy [2] Experimental Hematology Unit Cancer Immunotherapy and Gene Therapy Program, Division of Regenerative Medicine, Stem Cell and Gene Therapy, San Raffaele Scientific Institute, Milano, Italy [3] University Vita-Salute, Milano, Italy [4] MolMed SpA, Milano, Italy.
Abstract
Graft-versus-host disease (GvHD) is one of the major complications of allogeneic hematopoietic stem cell transplantation, an otherwise highly effective therapeutic modality for patients affected by hematological diseases. The main inducers of GvHD are alloreactive donor T cells, which recognize host antigens presented by recipient cells. The critical role of lymphocytes in GvHD is well documented by the observation that T-cell depletion from the graft prevents GvHD. Unfortunately, the removal of donor lymphocytes from the graft increases the incidence of disease relapse and life-threatening infectious complications. Gene transfer technologies are promising tools to manipulate donor T-cell immunity to enforce graft-versus-tumor/graft-versus-infection while preventing or controlling GvHD. For this purpose, several cell and gene transfer approaches have been investigated at the preclinical level and implemented in clinical trials.Gene Therapy advance online publication, 27 May 2010; doi:10.1038/gt.2010.83.
PMID: 20508597 [PubMed - as supplied by publisher]

