Matt Beatty
Graduate Student
Division of Human Gene Therapy

572 Biomedical Research Building II
901 19th Street South
Birmingham, AL 35294

Email: Beattym@uab.edu

Phone: (205) 975-8768
DHGT phone: (205)-934-8627
DHGT fax: (205) 975-7476

Mentor: David T. Curiel

Undergraduate Institution: University of Florida
Entered DHGT: August 2006


Research Interests

The recruitment of regulatory T cells to ovarian cancer tumors has been negatively correlated with patient survival outcome. To this end we are developing a novel adenoviral vector targeted to these regulatory T cells. Allowing the patients immune system to better recognize and kill the tumor cells.

Il-18, an inflammatory cytokine, has been associated with many inflammatory diseases such as 4rheumatoid arthritis and atherosclerosis. A native down regulator of IL-18, IL-18 binding protein may be a possible therapeutic target for treatment of inflammatory disease. We are currently developing a gutless adenovirus to deliver long term expression of secreted IL-18 binding protein to the pulmonary vasculature for treatment of rheumatoid arthritis.

Novel locations for the incorporation of heterlogous peptides may help to further expand the adenovirus vectors uses. We are currently exploring minor capsid protein IIIa for peptide as a site for targeting ligands to expand the ability of pIIIa to infect low CAR cells.

About Matt Beatty

After graduating from the University of Florida with a bachelors of science in microbiology and minors in chemistry and classics I came to University of Alabama at Birmingham through the IBS program. In 2006 I joined the department of pathology and started my research in gene therapy. I am now under the mentorship of Dr. Curiel in the Division of Human Gene Therapy.