R R - American Society of Gene & Cell Therapy
R R - American Society of Gene & Cell Therapy
R R - American Society of Gene & Cell Therapy
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The <strong>American</strong> <strong>Society</strong> <strong>of</strong> <strong>Gene</strong> <strong>Therapy</strong>’s<br />
2004<br />
7th Annual Meeting<br />
final program<br />
Friday, June 4<br />
Poster Session II<br />
4:00 pm – 7:00 pm<br />
Hall D<br />
RNA Virus Vectors II<br />
(Abstracts #396 through #417)<br />
AAV Vectors: Production and Applications<br />
(Abstracts #418 through #439)<br />
Conditionally Replicating Adenovirus Vectors:<br />
Adenovirus Toxicity and Immune Response<br />
(Abstracts #440 through #464)<br />
Lipid Mediated <strong>Gene</strong> Transfer<br />
(Abstracts #465 through #487)<br />
Pulmonary Disease<br />
(Abstracts #488 through #514)<br />
Central Nervous System II<br />
(Abstracts #515 through #541)<br />
Infectious Diseases and Vaccines<br />
(Abstracts #542 through #570)<br />
Tumor Vaccines<br />
(Abstracts #571 through #589)<br />
Cancer Suicide <strong>Gene</strong> <strong>Therapy</strong><br />
(Abstracts #590 through #607)<br />
Targeted Cancer Therapies II<br />
(Abstracts #608 through #629)<br />
<strong>Gene</strong> Regulation: Targets<br />
(Abstracts #630 through #661)<br />
Business Meeting<br />
4:30 pm – 5:15 pm<br />
Room: 213<br />
Corporate Symposium CS340<br />
7:00 pm – 10:00 pm<br />
Room: 200<br />
HIV-Based Lentiviral Vectors<br />
Supported by VIRxSYS<br />
Lentiviral vectors have shown considerable promise as<br />
vectors for efficient and stable gene transfer into human<br />
cells. This lentiviral vector symposium brings together the<br />
leaders in the field from around the world. The objective<br />
<strong>of</strong> the symposium is to present and discuss the advances<br />
in lentivirus-derived vector technology, from the bench<br />
to the bedside. The program will begin with a state-<strong>of</strong>the-art<br />
lecture detailing progress in lentiviral vector<br />
applications in general. The program will follow with a<br />
series <strong>of</strong> four presentations that focus on various aspects<br />
<strong>of</strong> current lentiviral vector applications including stem cell<br />
gene therapy, infectious disease, RNA-based therapies,<br />
and adoptive immunotherapy. The symposium will<br />
conclude with a presentation <strong>of</strong> the most recent data<br />
from the first clinical trial evaluating lentiviral vector gene<br />
therapy in humans. One should walk away from the<br />
symposium with a solid overview <strong>of</strong> lentiviral vector<br />
technology and also with the knowledge <strong>of</strong> the most<br />
recent advances in the field.<br />
Chair<br />
Boro Dropulic, PhD<br />
Speakers<br />
Inder Verma, PhD - Lentiviral Vectors: Old and New Uses<br />
Luigi Naldini, MD, PhD - Stem <strong>Cell</strong> <strong>Gene</strong> Transfer by<br />
Lentiviral Vectors<br />
Didier Trono, MD - Interactions between HIV, Lentiviral<br />
Vectors, and Target <strong>Cell</strong>s<br />
John J. Rossi, PhD - Lentiviral Vector Mediated Delivery<br />
<strong>of</strong> Combinatorial RNA-Based <strong>Gene</strong> <strong>Therapy</strong><br />
Carl H. June, MD - Safety and Feasibility <strong>of</strong> Adoptive<br />
Immunotherapy for HIV Infection With Lentiviral<br />
Engineered T <strong>Cell</strong>s<br />
Boro Dropulic, PhD - Pre-clinical Development <strong>of</strong> HIV-<br />
Based Lentiviral Vectors for a Phase I Clinical Trial for<br />
HIV/AIDS<br />
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