Development and Characterization of a Swine Model of Phenylketonuria

Information

  • Research Project
  • 9141707
  • ApplicationId
    9141707
  • Core Project Number
    R43OD021314
  • Full Project Number
    1R43OD021314-01A1
  • Serial Number
    021314
  • FOA Number
    PA-13-092
  • Sub Project Id
  • Project Start Date
    6/1/2016 - 8 years ago
  • Project End Date
    5/31/2017 - 7 years ago
  • Program Officer Name
    CONTRERAS, MIGUEL A.
  • Budget Start Date
    6/1/2016 - 8 years ago
  • Budget End Date
    5/31/2017 - 7 years ago
  • Fiscal Year
    2016
  • Support Year
    01
  • Suffix
    A1
  • Award Notice Date
    5/15/2016 - 8 years ago
Organizations

Development and Characterization of a Swine Model of Phenylketonuria

? DESCRIPTION (provided by applicant): Phenylketonuria (PKU) is one of the most common inborn errors of metabolism. PKU, commonly detected in infants during newborn screening, is due to recessively-inherited phenylalanine hydroxylase (PAH) deficiency. Current treatment strategies rely on restriction of dietary phenylalanine (Phe) intake to prevent the major manifestations of the disease, however, dietary therapy is complicated, unpalatable, and must be sustained throughout life to prevent neurocognitive disability associated with chronic hyperphenylalaninemia. Here, we propose to generate a large animal swine model of PKU to evaluate novel treatments strategies that are difficult to evaluate in murine PKU models due to their small size and physiological and anatomical differences. These novel therapies, including enzyme substitution therapy, hepatocyte transplantation, and gene therapy (liver- directed and muscle-directed gene therapy strategies employing both recombinant adeno-associated virus (rAAV) and non-viral naked DNA vector systems), could be applied to both PKU and many other inherited genetic diseases. A large animal model to evaluate the safety and efficacy of these therapies is critical to bridge the gap between laboratory experiments and the treatment of patients in the clinic. Additionally, a swine model of PKU is critical to understanding the molecular mechanisms through which hyperphenylalaninemia causes harm to the brain and results in physical, neurological and behavioral deficits seen in patients. Further, a model in which physical and molecular phenotypes can be evaluated during Phe-restricted diet treatment, following discontinuation of Phe-restricted diet, and during the implementation of novel treatments such as gene therapy will be critical for better treating patients with PKU. The preclinical experiments we propose to conduct will be vital to understanding the limiting issues in treating patients and will have direct influence upon the design of future human clinical trials

IC Name
OFFICE OF THE DIRECTOR, NATIONAL INSTITUTES OF HEALTH
  • Activity
    R43
  • Administering IC
    OD
  • Application Type
    1
  • Direct Cost Amount
  • Indirect Cost Amount
  • Total Cost
    355198
  • Sub Project Total Cost
  • ARRA Funded
    False
  • CFDA Code
    351
  • Ed Inst. Type
  • Funding ICs
    OD:355198\
  • Funding Mechanism
    SBIR-STTR RPGs
  • Study Section
    ZRG1
  • Study Section Name
    Special Emphasis Panel
  • Organization Name
    RECOMBINETICS, INC.
  • Organization Department
  • Organization DUNS
    829874523
  • Organization City
    SAINT PAUL
  • Organization State
    MN
  • Organization Country
    UNITED STATES
  • Organization Zip Code
    551044125
  • Organization District
    UNITED STATES