17.01.2015 Views

Final Program - American Society of Gene & Cell Therapy

Final Program - American Society of Gene & Cell Therapy

Final Program - American Society of Gene & Cell Therapy

SHOW MORE
SHOW LESS

You also want an ePaper? Increase the reach of your titles

YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.

<strong>Program</strong> Schedule, Wednesday, May 15, 2013<br />

Manfred Schmidt, PhD<br />

Clonality and Biosafety Aspects <strong>of</strong> Illegitimate Integration<br />

Integrating retroviral vectors have been used successfully in clinical applications. With the occurrence <strong>of</strong> integration associated<br />

severe side effects, enhanced efforts have been set for the clinical translation <strong>of</strong> integrase deicient viral vectors to guarantee<br />

improved biosafety. In this presentation, the focus is set on studies performed for assessing frequency, proile and mechanisms <strong>of</strong><br />

(illegitimate) integration.<br />

Scott H. Robbins, PhD<br />

Development <strong>of</strong> an ID-LV as a <strong>Gene</strong> Delivery Platform for Immunotherapy Applications<br />

One <strong>of</strong> the most fundamental challenges for the design <strong>of</strong> next generation vaccines is the generation <strong>of</strong> antigen-speciic CD8 T<br />

cell responses. The direct administration <strong>of</strong> lentivector-based vaccines genetically encoding antigen is proving to be an effective<br />

approach to elicit CD8 T cell responses in pre-clinical animal models. The ability to alter the tropism <strong>of</strong> lentiviral vectors via<br />

pseudotyping and other mechanisms makes them attractive as a platform technology on which to base product candidates for<br />

clinical applications such as antigen-directed immunotherapy and vaccines. Examples <strong>of</strong> the functionality <strong>of</strong> integration-competent<br />

and -deicient lentiviral vectors as antigen delivery vehicles in pre-clinical settings will be provided as well as an example <strong>of</strong> the<br />

design <strong>of</strong> a dendritic cell-directed integration-deicient lentiviral vector that is currently under development as an antigen-directed<br />

cancer immunotherapy (a “cancer vaccine”).<br />

Wednesday, May 15, 2013<br />

Oral Abstract Session 130<br />

3:15 pm - 5:15 pm<br />

ROOM: BALLROOM A<br />

AAV Vector Development & Application<br />

CO-CHAIRS: Mavis Agbandje-McKenna, PhD and Hiroyuki Nakai, MD, PhD<br />

(Abstracts 1 through 8; see page 87)<br />

Oral Abstract Session 131<br />

3:15 pm - 5:15 pm<br />

ROOM: BALLROOM B<br />

Cancer - Immunotherapy I<br />

CO-CHAIRS: Malcolm K. Brenner, MD, PhD and John J. Nemunaitis, MD<br />

(Abstracts 9 through 16; see pages 87-88)<br />

Oral Abstract Session 132<br />

3:15 pm - 5:15 pm<br />

ROOM: 150 DEFG<br />

Cancer - Oncolytic Viruses<br />

CO-CHAIRS: David Kirn, MD and Stephen J. Russell, MD, PhD<br />

(Abstracts 17 through 24; see page 88)<br />

Oral Abstract Session 133<br />

3:15 pm - 5:15 pm<br />

ROOM: BALLROOM C<br />

Advancing the Science <strong>of</strong> <strong>Gene</strong> <strong>Therapy</strong> for Hematologic Diseases<br />

CO-CHAIRS: Arnab Ghosh, MD, PhD and Donald B. Kohn, MD<br />

(Abstracts 25 through 32; see pages 88-89)<br />

<strong>Final</strong> <strong>Program</strong> SALT LAKE CITY, UTAH May 15–18, 2013<br />

43

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!