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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 />

43

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