STUDY DESIGN: Prospective, randomized, controlled preclinical trial. OBJECTIVE: This study seeks to characterize the localized and systemic host response to recombinant human bone morphogenetic protein-2 (rhBMP-2) in a well established rodent spine arthrodesis model utilizing cytokine analysis and magnetic resonance imaging (MRI). SUMMARY OF BACKGROUND DATA: Although high fusion rates are achieved with rhBMP-2 in the spine, several complications have also been reported, including a localized response leading to radiculitis and seroma formation. The mechanism in which this occurs clinically is yet unknown. METHODS: One hundred female Fischer rats underwent a posterolateral intertransverse lumbar spinal fusion, with paraspinal muscle tissue resection, using iliac crest autograft, type I absorbable collagen sponge (ACS), 10- or 100-μg rhBMP-2/ACS. The animals underwent magnetic resonance imaging evaluation, serum cytokine analysis, manual palpation, and gross tissue inspection at 2, 4, 7, 10, and 21 days, postoperatively. RESULTS: Qualitative evaluation of MR images demonstrated a transient fluid collection at the surgery site in the rhBMP-2 animals as early as 4 and 7 days that was greater than the autograft or ACS groups. Quantitative analysis on T2-weighted axial images demonstrated greater signal intensity in the rhBMP-2 animals compared with the ACS and autograft groups in a time-dependent fashion. Higher concentrations of several cytokines were also detected at 2, 4, and 7 days, including interleukin 1β, interleukin 18, tumor necrosis factor α, macrophage inflammatory protein 1α, and monocyte chemotactic protein 1 in animals treated with rhBMP-2/ACS relative to ACS alone. CONCLUSION: Our data suggest that the in vivo host response to rhBMP-2 in an animal model may be associated with circulating proinflammatory and osteoclastic cytokines.
STUDY DESIGN: Prospective, randomized, controlled preclinical trial. OBJECTIVE: This study seeks to characterize the localized and systemic host response to recombinant humanbone morphogenetic protein-2 (rhBMP-2) in a well established rodent spine arthrodesis model utilizing cytokine analysis and magnetic resonance imaging (MRI). SUMMARY OF BACKGROUND DATA: Although high fusion rates are achieved with rhBMP-2 in the spine, several complications have also been reported, including a localized response leading to radiculitis and seroma formation. The mechanism in which this occurs clinically is yet unknown. METHODS: One hundred female Fischer rats underwent a posterolateral intertransverse lumbar spinal fusion, with paraspinal muscle tissue resection, using iliac crest autograft, type I absorbable collagen sponge (ACS), 10- or 100-μg rhBMP-2/ACS. The animals underwent magnetic resonance imaging evaluation, serum cytokine analysis, manual palpation, and gross tissue inspection at 2, 4, 7, 10, and 21 days, postoperatively. RESULTS: Qualitative evaluation of MR images demonstrated a transient fluid collection at the surgery site in the rhBMP-2 animals as early as 4 and 7 days that was greater than the autograft or ACS groups. Quantitative analysis on T2-weighted axial images demonstrated greater signal intensity in the rhBMP-2 animals compared with the ACS and autograft groups in a time-dependent fashion. Higher concentrations of several cytokines were also detected at 2, 4, and 7 days, including interleukin 1β, interleukin 18, tumor necrosis factor α, macrophage inflammatory protein 1α, and monocyte chemotactic protein 1 in animals treated with rhBMP-2/ACS relative to ACS alone. CONCLUSION: Our data suggest that the in vivo host response to rhBMP-2 in an animal model may be associated with circulating proinflammatory and osteoclastic cytokines.
Authors: Sungsoo S Lee; Erin L Hsu; Marco Mendoza; Jason Ghodasra; Michael S Nickoli; Amruta Ashtekar; Mahesh Polavarapu; Jacob Babu; Rehan M Riaz; Joseph D Nicolas; David Nelson; Sohaib Z Hashmi; Start R Kaltz; Jeffrey S Earhart; Bradley R Merk; Jeff S McKee; Shawn F Bairstow; Ramille N Shah; Wellington K Hsu; Samuel I Stupp Journal: Adv Healthc Mater Date: 2014-04-22 Impact factor: 9.933
Authors: Juliane D Glaeser; Khosrowdad Salehi; Linda E A Kanim; Dmitriy Sheyn; Zachary NaPier; Phillip H Behrens; Leslie Garcia; Jason M Cuéllar; Hyun W Bae Journal: Tissue Eng Part A Date: 2018-07-03 Impact factor: 3.845
Authors: Mark A Plantz; Silvia Minardi; Joseph G Lyons; Allison C Greene; David J Ellenbogen; Mitchell Hallman; Jonathan T Yamaguchi; Soyeon Jeong; Chawon Yun; Adam E Jakus; Kenneth R Blank; Robert M Havey; Muturi Muriuki; Avinash G Patwardhan; Ramille N Shah; Wellington K Hsu; Stuart R Stock; Erin L Hsu Journal: Acta Biomater Date: 2021-04-06 Impact factor: 10.633
Authors: Kendall Mitchell; Jill P Shah; Clifton L Dalgard; Lyubov V Tsytsikova; Ashley C Tipton; Anton E Dmitriev; Aviva J Symes Journal: BMC Neurosci Date: 2016-12-01 Impact factor: 3.288
Authors: Mark Plantz; Joseph Lyons; Jonathan T Yamaguchi; Allison C Greene; David J Ellenbogen; Mitchell J Hallman; Vivek Shah; Chawon Yun; Adam E Jakus; Daniele Procissi; Silvia Minardi; Ramille N Shah; Wellington K Hsu; Erin L Hsu Journal: Spine (Phila Pa 1976) Date: 2022-01-01 Impact factor: 3.468
Authors: Jason H Ghodasra; Michael S Nickoli; Sohaib Z Hashmi; John T Nelson; Marco Mendoza; Joseph D Nicolas; Sharath S Bellary; Kevin Sonn; Amruta Ashtekar; Christian J Park; Jacob Babu; Chawon Yun; Anjan Ghosh; Abhishek Kannan; Stuart R Stock; Wellington K Hsu; Erin L Hsu Journal: Global Spine J Date: 2015-06-24
Authors: Mitchell Hallman; J Adam Driscoll; Ryan Lubbe; Soyeon Jeong; Kevin Chang; Meraaj Haleem; Adam Jakus; Richard Pahapill; Chawon Yun; Ramille Shah; Wellington K Hsu; Stuart R Stock; Erin L Hsu Journal: Tissue Eng Part A Date: 2020-03-26 Impact factor: 3.845