Host Response to Implanted Porcine-Derived Biologic Materials in a Primate Model of Abdominal Wall Repair

被引:132
作者
Sandor, Maryellen [1 ]
Xu, Hui [1 ]
Connor, Jerome [1 ]
Lombardi, Jared [1 ]
Harper, John R. [1 ]
Silverman, Ronald P. [2 ]
McQuillan, David J. [1 ]
机构
[1] LifeCell Corp, Branchburg, NJ 08876 USA
[2] Univ Maryland, Sch Med, Div Plast Surg, Baltimore, MD 21201 USA
关键词
D O I
10.1089/ten.tea.2007.0317
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Three commercially available porcine-derived biologic meshes were implanted in an Old World primate abdominal wall resection repair model to compare biological outcome as a predictor of clinical efficacy. Tissues were explanted over a 6-month period and evaluated for gross pathology, wound healing strength, mesenchymal cellular repopulation, vascularity, and immune response. In vivo functional outcomes were correlated with in vitro profile for each material. Small intestinal submucosa-based implants demonstrated scar tissue formation and contraction, coincident with mesh pleating, and were characterized by immediate and significant cellular and humoral inflammatory responses. Porcine dermal-based grafts demonstrated significant graft pleating, minimal integration, and an absence of cellular repopulation and vascularization. However, a significant cellular immune response surrounded the grafts, coincident with poor initial wound healing strengths. In vivo observations for the three porcine-derived mesh products correlated with individual in vitro profiles, indicating an absence of characteristic biochemical markers and structural integrity. This correlation suggests that in vivo results observed for these mesh products are a direct consequence of specific manufacturing processes that yield modified collagen matrices. The resulting loss of biological and structural integrity elicits a foreign body response while hindering normal healing and tissue integration.
引用
收藏
页码:2021 / 2031
页数:11
相关论文
共 46 条
[1]
Morphologic study of small intestinal submucosa as a body wall repair device [J].
Badylak, S ;
Kokini, K ;
Tullius, B ;
Simmons-Byrd, A ;
Morff, R .
JOURNAL OF SURGICAL RESEARCH, 2002, 103 (02) :190-202
[2]
Immune response to biologic scaffold materials [J].
Badylak, Stephen E. ;
Gilbert, Thomas W. .
SEMINARS IN IMMUNOLOGY, 2008, 20 (02) :109-116
[3]
*BARD COLLAMEND IM, 2006, MMCMSS1 BARD COLLAME
[4]
Contribution of collagen network features to functional properties of engineered cartilage [J].
Bastiaansen-Jenniskens, Y. M. ;
Koevoet, W. ;
de Bart, A. C. W. ;
van der Linden, J. C. ;
Zuurmond, A. M. ;
Weinans, H. ;
Verhaar, J. A. N. ;
van Osch, G. J. V. M. ;
DeGroot, J. .
OSTEOARTHRITIS AND CARTILAGE, 2008, 16 (03) :359-366
[5]
DEPOSITION AND SELECTIVE DEGRADATION OF STRUCTURALLY-ABNORMAL TYPE-1 COLLAGEN IN A COLLAGEN MATRIX PRODUCED BY OSTEOGENESIS IMPERFECTA FIBROBLASTS IN-VITRO [J].
BATEMAN, JF ;
GOLUB, SB .
MATRIX BIOLOGY, 1994, 14 (03) :251-262
[6]
Severely impaired wound healing in the collagenase-resistant mouse [J].
Beare, AHM ;
O'Kane, S ;
Krane, SM ;
Ferguson, MWJ .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2003, 120 (01) :153-163
[7]
The role of bioprosthetics in abdominal wall reconstruction [J].
Butler, CE .
CLINICS IN PLASTIC SURGERY, 2006, 33 (02) :199-+
[8]
*COOK BIOM, 2004, CSAHM604 COOK BIOM
[9]
*COOK SURG, 2006, CEXL1006 COOK SURG
[10]
*COOK SURG, 2008, SCI INF