Induction of cytotoxic T-lymphocyte responses to enhanced green and yellow fluorescent proteins after myeloablative conditioning
- 15 January 2004
- journal article
- Published by American Society of Hematology in Blood
- Vol. 103 (2) , 492-499
- https://doi.org/10.1182/blood-2003-07-2324
Abstract
Lentiviral vectors are increasingly being used for transferring genes into hematopoietic stem cells (HSCs) due to their ability to transduce nondividing cells. Whereas results in in vitro studies and the nonobese diabetic/severe combined immunodeficiency (NOD/SCID) model have been highly encourgaging, studies in large animals have not confirmed the superior transduction of HSCs using lentiviral vectors versus oncoretroviral vectors. In contrast to the stable gene marking we have consistently achieved with oncoretroviral vectors in animals that received myeloablative conditioning, we observed the complete disappearance of genetically modified enhanced green or yellow fluorescent protein–expressing cells in 5 baboons that received transplants of HSCs transduced with lentiviral vectors alone or in combination with oncoretroviral vectors. Immune responses to transgene products have been found to be involved in the disappearance of gene-modified cells after nonmyeloablative conditioning. Thus, we examined whether the disappearance of genemodified cells after ablative conditioning may be due to an immune response. In 4 of 5 animals, cytotoxic T lymphocytes specific for the transgene protein were readily detected, demonstrating that immune reactions were responsible for the disappearance of the gene-marked cells in the animals. In summary, we report the induction of transgene-specific immune responses after transplantation of lentivirally transduced repopulating cells in a myeloablative setting.Keywords
This publication has 34 references indexed in Scilit:
- Interleukin-7 improves CD4 T-cell reconstitution after autologous CD34 cell transplantation in monkeysBlood, 2003
- Highly efficient gene transfer into baboon marrow repopulating cells using GALV-pseudotype oncoretroviral vectors produced by human packaging cellsBlood, 2002
- Lentivirus-mediated gene transfer into hematopoietic repopulating cells in baboonsGene Therapy, 2002
- Lentivirus Vector-Mediated Hematopoietic Stem Cell Gene Transfer of Common Gamma-Chain Cytokine Receptor in Rhesus MacaquesJournal of Virology, 2001
- Nonmyeloablative Immunosuppressive Regimen Prolongs In Vivo Persistence of Gene-Modified Autologous T Cells in a Nonhuman Primate ModelJournal of Virology, 2001
- Transduction of Human CD34+CD38- Bone Marrow and Cord Blood-Derived SCID-Repopulating Cells with Third-Generation Lentiviral VectorsMolecular Therapy, 2000
- Introduction of a Xenogeneic Gene via Hematopoietic Stem Cells Leads to Specific Tolerance in a Rhesus Monkey ModelMolecular Therapy, 2000
- Marking and Gene Expression by a Lentivirus Vector in Transplanted Human and Nonhuman Primate CD34+CellsJournal of Virology, 2000
- Immune response to green fluorescent protein: implications for gene therapyGene Therapy, 1999
- Crystal Structure of the Aequorea victoria Green Fluorescent ProteinScience, 1996