HSV-TK Gene Transfer into Donor Lymphocytes for Control of Allogeneic Graft-Versus-Leukemia

Author:

Bonini Chiara123,Ferrari Giuliana123,Verzeletti Simona123,Servida Paolo123,Zappone Elisabetta123,Ruggieri Luciano123,Ponzoni Maurilio123,Rossini Silvano123,Mavilio Fulvio123,Traversari Catia123,Bordignon Claudio123

Affiliation:

1. C. Bonini, G. Ferrari, P. Servida, E. Zappone, L. Ruggieri, S. Rossini, F. Mavilio, C. Traversari, C. Bordignon, Telethon Institute for Gene Therapy (TIGET), Istituto Scientifico H. S. Raffaele, 20132 Milan, Italy.

2. S. Verzeletti, Molmed S.p.A., 20132 Milan, Italy.

3. M. Ponzoni, Department of Pathology, Istituto Scientifico H. S. Raffaele, 20132 Milan, Italy.

Abstract

In allogeneic bone marrow transplantation (allo-BMT), donor lymphocytes play a central therapeutic role in both graft-versus-leukemia (GvL) and immune reconstitution. However, their use is limited by the risk of severe graft-versus-host disease (GvHD). Eight patients who relapsed or developed Epstein-Barr virus–induced lymphoma after T cell–depleted BMT were then treated with donor lymphocytes transduced with the herpes simplex virus thymidine kinase (HSV-TK) suicide gene. The transduced lymphocytes survived for up to 12 months, resulting in antitumor activity in five patients. Three patients developed GvHD, which could be effectively controlled by ganciclovir-induced elimination of the transduced cells. These data show that genetic manipulation of donor lymphocytes may increase the efficacy and safety of allo-BMT and expand its application to a larger number of patients.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference45 articles.

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