An injectable method for noninvasive spine fusion.

Journal Article (Journal Article)

Background context

Bone morphogenetic proteins (BMPs) induce bone formation but are difficult to localize, and subsequent diffusion from the site of interest and short half-life reduce the efficacy of the protein. Currently, spine fusion requires stripping, decortications of the transverse processes, and an autograft harvest procedure. Even in combination with BMPs, clinical spinal fusion has a high failure rate, presumably because of difficulties in localizing sufficient levels of BMP.


The goal was to achieve reliable spine fusion through a single injection of a cell-based gene therapy system without the need for any surgical intervention.

Study design

Eighty-seven immunodeficient (n=44) and immune-competent (n=43) mice were injected along the paraspinous musculature to achieve rapid induction of heterotopic ossification (HO) and ultimately spinal arthrodesis.


Immunodeficient and immune-competent mice were injected with fibroblasts, transduced with an adenoviral vector to express BMP2, along the paraspinous musculature. Bone formation was evaluated via radiographs, microcomputed tomography, and biomechanical analysis.


ew bridging bone between the vertebrae and the fusion to adjacent skeletal bone was obtained as early as 2 weeks. Reduction in spine flexion-extension also occurred as early as 2 weeks after injection of the gene therapy system, with greater than 90% fusion by 4 weeks in all animals regardless of their genetic background.


Injection of our cell-based system into the paraspinous musculature induces spinal fusion that is dependent neither on the cell type nor on the immune status. These studies are the first to harness HO in an immune-competent model as a noninvasive injectable system for clinically relevant spinal fusion and may one day impact human spinal arthrodesis.

Full Text

Duke Authors

Cited Authors

  • Olabisi, RM; Lazard, Z; Heggeness, MH; Moran, KM; Hipp, JA; Dewan, AK; Davis, AR; West, JL; Olmsted-Davis, EA

Published Date

  • June 2011

Published In

Volume / Issue

  • 11 / 6

Start / End Page

  • 545 - 556

PubMed ID

  • 21292563

Pubmed Central ID

  • PMC3327508

Electronic International Standard Serial Number (EISSN)

  • 1878-1632

International Standard Serial Number (ISSN)

  • 1529-9430

Digital Object Identifier (DOI)

  • 10.1016/j.spinee.2010.12.011


  • eng