| Literature DB >> 27967655 |
Pedro Alvarez-Urena1, Eleanor Davis1, Corinne Sonnet1, Gabrielle Henslee1, Zbigniew Gugala2, Edward V Strecker2, Laura J Linscheid2, Maude Cuchiara3, Jennifer West3, Alan Davis1,4,5, Elizabeth Olmsted-Davis1,4,5.
Abstract
Gene therapy approaches have been difficult to implement due to pre-existing immunity against the virus used for delivery. To circumvent this problem, a cell-based approach was developed that avoided the use of free virus within the animal. However, even cells transduced in vitro with E1- to E3-deleted adenovirus encoding bone morphogenetic protein 2 (AdBMP2) resulted in the production of virus-neutralizing antibodies in mice. Furthermore, when mice received an intramuscular injection of nonencoding adenovirus (AdEmpty)-transduced cells, AdBMP2-transduced cells were unable to launch bone formation when an intramuscular injection of these BMP2-producing cells was delivered 1 week later. This phenomenon was not observed in NOD/SCID mice, and could be overcome in C57BL/6 mice by encapsulating the adenovirus-transduced cells in a nondegradable hydrogel poly(ethylene glycol) diacrylate (PEGDA). Data collectively suggest that PEGDA hydrogel encapsulation of AdBMP2-transduced cells prevents pre-existing immunity from suppressing BMP2-induced bone formation.Entities:
Keywords: bone formation; cell therapy; in vivo delivery system; priming
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Year: 2017 PMID: 27967655 PMCID: PMC6016100 DOI: 10.1089/ten.TEA.2016.0277
Source DB: PubMed Journal: Tissue Eng Part A ISSN: 1937-3341 Impact factor: 3.845