Published February 2011 | Version v1
Journal article

Evaluation of the tissue reaction to a new bilayered collagen matrix in vivo and its translation to the clinic

  • 1. REPAIR-Lab, Institute of Pathology, Johannes Gutenberg University, Mainz (Germany)
  • 2. Bayreuther Strasse 39, D-91301, Forchheim (Germany)
  • 3. Department of Biomedical Engineering, Northwestern University, Evanston, IL 60208 (United States)
  • 4. Institute for Dental Material Sciences and Technology, University Medical Center of the Johannes Gutenberg University, Mainz (Germany)
  • 5. Geistlich Pharma AG, Wolhusen (Switzerland)
  • 6. Department of Materials Science and Engineering, Chemistry, and Medicine, Northwestern University, Evanston, IL 60208 (United States)
  • 7. Clinic for Maxillofacial and Plastic Surgery, Johann Wolfgang Goethe University, Frankfurt Am Main (Germany)

Description

This study evaluates a new collagen matrix that is designed with a bilayered structure in order to promote guided tissue regeneration and integration within the host tissue. This material induced a mild tissue reaction when assessed in a murine model and was well integrated within the host tissue, persisting in the implantation bed throughout the in vivo study. A more porous layer was rapidly infiltrated by host mesenchymal cells, while a layer designed to be a barrier allowed cell attachment and host tissue integration, but at the same time remained impermeable to invading cells for the first 30 days of the study. The tissue reaction was favorable, and unlike a typical foreign body response, did not include the presence of multinucleated giant cells, lymphocytes, or granulation tissue. In the context of translation, we show preliminary results from the clinical use of this biomaterial applied to soft tissue regeneration in the treatment of gingival tissue recession and exposed roots of human teeth. Such a condition would greatly benefit from guided tissue regeneration strategies. Our findings demonstrate that this material successfully promoted the ingrowth of gingival tissue and reversed gingival tissue recession. Of particular importance is the fact that the histological evidence from these human studies corroborates our findings in the murine model, with the barrier layer preventing unspecific tissue ingrowth, as the scaffold becomes infiltrated by mesenchymal cells from adjacent tissue into the porous layer. Also in the clinical situation no multinucleated giant cells, no granulation tissue and no evidence of a marked inflammatory response were observed. In conclusion, this bilayered matrix elicits a favorable tissue reaction, demonstrates potential as a barrier for preferential tissue ingrowth, and achieves a desirable therapeutic result when applied in humans for soft tissue regeneration.

Availability note (English)

Available from http://dx.doi.org/10.1088/1748-6041/6/1/015010

Additional details

Identifiers

DOI
10.1088/1748-6041/6/1/015010;
PII
S1748-6041(11)66726-5;

Publishing Information

Journal Title
Biomedical Materials (Bristol. Online)
Journal Volume
6
Journal Issue
1
Journal Page Range
[12 p.]
ISSN
1748-605X

INIS

Country of Publication
United Kingdom
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
43015743
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
COLLAGEN; EVALUATION; GRANULATION; HOST; HUMAN POPULATIONS; IN VIVO; LAYERS; LYMPHOCYTES; POROUS MATERIALS; REGENERATION; TUMOR CELLS
Descriptors DEC
ANIMAL CELLS; BIOLOGICAL MATERIALS; BLOOD; BLOOD CELLS; BODY FLUIDS; CONNECTIVE TISSUE CELLS; FABRICATION; LEUKOCYTES; MATERIALS; ORGANIC COMPOUNDS; POPULATIONS; PROTEINS; SCLEROPROTEINS; SOMATIC CELLS