Adenoviral vectors can direct high-level expression of a transgene, but, due to a host immune response to adenoviral antigens, expression is of limited duration, and repetitive administration has generally been unsuccessful. Exposure to foreign proteins beginning in the neonatal period may alter or ablate the immune response. We injected adult and neonatal (immunocompetent) CD-1 mice intravenously with an adenoviral vector expressing human blood coagulation factor IX. In both groups of mice, expression of human factor IX persisted for 12-16 weeks. However, in mice initially injected as adults, repeat administration of the vector resulted in no detectable expression of the transgene, whereas in mice initially injected in the neonatal period,...
The safety of several gene therapy approaches for treatment of the severe, X-linked bleeding disorde...
Following fetal or neonatal gene transfer in mice and other species immune tolerance of the transgen...
Defining immune responses against the secreted transgene product in a gene therapy setting is critic...
Adenoviral vectors can direct high-level expression of a transgene, but, due to a host immune respon...
Inbred immunocompetent C57BL/6 mice have been a favored strain to study transgene expression of huma...
The fundamental hypotheses behind fetal gene therapy are that it may be possible (1) to achieve immu...
Following fetal or neonatal gene transfer in mice and other species immune tolerance of the transgen...
Recombinant adeno-associated virus vectors (AAV) were prepared in high titer (10(12) to 10(13) parti...
We sought to determine whether intramuscular injection of a recombinant adeno-associated virus (rAAV...
Mice with hemophilia B have been engineered using gene targeting techniques. These animals exhibit s...
Copyright © 2015 Megha S. Nivsarkar et al. This is an open access article distributed under the Crea...
The safety of several gene therapy approaches for treatment of the severe, X-linked bleeding disorde...
Following fetal or neonatal gene transfer in mice and other species immune tolerance of the transgen...
Defining immune responses against the secreted transgene product in a gene therapy setting is critic...
Adenoviral vectors can direct high-level expression of a transgene, but, due to a host immune respon...
Inbred immunocompetent C57BL/6 mice have been a favored strain to study transgene expression of huma...
The fundamental hypotheses behind fetal gene therapy are that it may be possible (1) to achieve immu...
Following fetal or neonatal gene transfer in mice and other species immune tolerance of the transgen...
Recombinant adeno-associated virus vectors (AAV) were prepared in high titer (10(12) to 10(13) parti...
We sought to determine whether intramuscular injection of a recombinant adeno-associated virus (rAAV...
Mice with hemophilia B have been engineered using gene targeting techniques. These animals exhibit s...
Copyright © 2015 Megha S. Nivsarkar et al. This is an open access article distributed under the Crea...
The safety of several gene therapy approaches for treatment of the severe, X-linked bleeding disorde...
Following fetal or neonatal gene transfer in mice and other species immune tolerance of the transgen...
Defining immune responses against the secreted transgene product in a gene therapy setting is critic...