Functional Tissue Engineering for Cartilage Repair

Award Information
Agency:
Department of Health and Human Services
Branch
n/a
Amount:
$1,303,192.00
Award Year:
2013
Program:
STTR
Phase:
Phase II
Contract:
2R42AR055042-02
Award Id:
n/a
Agency Tracking Number:
R42AR055042
Solicitation Year:
2013
Solicitation Topic Code:
NIAMS
Solicitation Number:
PA12-089
Small Business Information
2608 ERWIN ROAD, DURHAM, NC, 27715-1317
Hubzone Owned:
N
Minority Owned:
N
Woman Owned:
N
Duns:
783502466
Principal Investigator:
FARSHID GUILAK
(919) 684-2521
cytex.therapeutics@gmail.com
Business Contact:
BRADLEY ESTES
(919) 912-9839
bradley.estes@cytextherapeutics.com
Research Institution:
DUKE UNIVERSITY

DUKE UNIVERSITY
2200 W Main St., Suite 820
DURHAM, NC, 27705-
() -
Nonprofit college or university
Abstract
DESCRIPTION (provided by applicant): The overall goal of this study is to develop a tissue-engineered total joint replacement from an engineered biomaterial scaffold combined with adult bone marrow-derived mesenchymal stem cells (MSCs) for regeneration ofthe entire femoral surface of the hip joint. We have developed a novel three-dimensionally (3D) woven scaffold that mimics the biomechanical properties of native articular cartilage at the initial time of cell seeding. This anatomically formed scaffold isseeded with MSCs and pre-cultured ex vivo to create a hemispherical layer of living cartilage that can be used to completely replace a damaged joint surface. In the present study, we propose to perform in vivo studies in our canine osteoarthritis model toexamine the potential of completely replacing the cartilage surface of the femoral head of the hip. The following two groups will be tested: 1) cartilage denuded from femoral head with implantation of fixation devices (i.e., anchors and suture) only (positive osteoarthritis control group), and 2) preformed 3D woven scaffold precultured with autologous MSCs (2 week ex vivo culture). All groups will be tested in vivo for 6 months. Primary outcomes will be based on joint function and comfort as measured by static and dynamic kinetic analysis, and validated semi-quantitative pain scales. Sequential radiographs of the hip (baseline and every month) will also be taken to monitor any joint morphological changes. At sacrifice, the histological and biomechanical properties of the joint tissues will be compared to radiograph-based measurements. Serum, synovial fluid, synovium, and lymph nodes will be analyzed for biomarkers of osteoarthritis, as well as for adverse inflammatory reactions and to test for wear debris inthe joint. Acetabular wear and labral damage will also be assessed histologically. PUBLIC HEALTH RELEVANCE PUBLIC HEALTH RELEVANCE: The goal of this study is to develop a technology for total bioartificial joint resurfacing as a treatment for hip osteoarthritis. The technologic basis involvs a combination of adult stem cells, retrieved from bone marrow, and a novel three-dimensionally woven scaffold that is designed to withstand joint loading and induce differentiation of the stem cells. The ultimate goal of this study is to develop tissue-engineering technologies that can eventually be used to treat osteoarthritis and other joint diseases.

* information listed above is at the time of submission.

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