Fiscal Year:
2001
Title:
TREATMENT OF ANEMIA USING AAV VECTORS
Agency:
HHS
Contract:
N/A
Award Amount:
$256,725.00
Abstract:
DESCRIPTION (applicant's abstract): The innovative use of AAV vector technology
is proposed to develop milestones essential for the safe treatment of anemia
secondary to chronic renal failure in cats. An A.AV-FeEPO vector has been
constructed. The initial, in vitro, study will determine whether this vector
can achieve FeEPO expression, and will also validate a HuEPO ELISA kit to
measure FeEPO. This vector will then be administered IM to cats to investigate
gene expression, in vivo. The transduced skeletal muscle will then be
surgically excised to determine whether FeEPO expression is abolished.
Transduction of tissues distant to the injection site will be determined by
using PCR. Two studies will be performed to find the optimum method of FeEPO
expression in feline patients with anemia. Firstly, AAV-FeEPO will be
repeatedly administered at low doses to determine if this results in
predictable incremental FeEPO expression. Finally, an AAV-FeEPO vector
controlled by the Tet-On system will be constructed. Oral doxycycline will be
administered at different doses (to demonstrate dose-dependent FeEPO
expression) intermittently (to ascertain whether FeEPO expression can be
"turned-on and off"). Cell mediated, and humoral immune responses against the
vector will be measured in these cats.
PROPOSED COMMERCIAL APPLICATION:
Feline erythropoietin cDNA will be incorporated in an adeno-associated virus vector
(AAV-FeEPO) and administered to cats with chronic renal failure and other types of
erythropoietin responsive anemia. Expression of the feline erythropoietin cDNA will
be controlled by a tetracycline regulatory element. This vector construct may be sold
as a veterinary only pharmaceutical.
Principal Investigator:
Mark C. Walker
Business Contact:
9044260880
Small Business Information at Submission:
APPLIED GENETIC TECHNOLOGIES CRP
12085 RESEARCH DR ALACHUA, FL 32615
EIN/Tax ID:
593553710
DUNS:
N/A
Number of Employees:
N/A
Woman-Owned:
No
Minority-Owned:
No
HUBZone-Owned:
No