TY - JOUR
T1 - Imaging-assisted nanoimmunotherapy for atherosclerosis in multiple species
AU - Binderup, Tina
AU - Duivenvoorden, Raphaël
AU - Fay, Francois
AU - Van Leent, Mandy M.T.
AU - Malkus, Joost
AU - Baxter, Samantha
AU - Ishino, Seigo
AU - Zhao, Yiming
AU - Sanchez-Gaytan, Brenda
AU - Teunissen, Abraham J.P.
AU - Frederico, Yohana C.A.
AU - Tang, Jun
AU - Carlucci, Giuseppe
AU - Lyashchenko, Serge
AU - Calcagno, Claudia
AU - Karakatsanis, Nicolas
AU - Soultanidis, Georgios
AU - Senders, Max L.
AU - Robson, Philip M.
AU - Mani, Venkatesh
AU - Ramachandran, Sarayu
AU - Lobatto, Mark E.
AU - Hutten, Barbara A.
AU - Granada, Juan F.
AU - Reiner, Thomas
AU - Swirski, Filip K.
AU - Nahrendorf, Matthias
AU - Kjaer, Andreas
AU - Fisher, Edward A.
AU - Fayad, Zahi A.
AU - Pérez-Medina, Carlos
AU - Mulder, Willem J.M.
PY - 2019/8
Y1 - 2019/8
N2 - Nanomedicine research produces hundreds of studies every year, yet very few formulations have been approved for clinical use. This is due in part to a reliance on murine studies, which have limited value in accurately predicting translational efficacy in larger animal models and humans. Here, we report the scale-up of a nanoimmunotherapy from mouse to large rabbit and porcine atherosclerosis models, with an emphasis on the solutions we implemented to overcome production and evaluation challenges. Specifically, we integrated translational imaging readouts within our workflow to both analyze the nanoimmunotherapeutic's in vivo behavior and assess treatment response in larger animals. We observed our nanoimmunotherapeutic's anti-inflammatory efficacy in mice, as well as rabbits and pigs. Nanoimmunotherapy-mediated reduction of inflammation in the large animal models halted plaque progression, supporting the approach's translatability and potential to acutely treat atherosclerosis.
AB - Nanomedicine research produces hundreds of studies every year, yet very few formulations have been approved for clinical use. This is due in part to a reliance on murine studies, which have limited value in accurately predicting translational efficacy in larger animal models and humans. Here, we report the scale-up of a nanoimmunotherapy from mouse to large rabbit and porcine atherosclerosis models, with an emphasis on the solutions we implemented to overcome production and evaluation challenges. Specifically, we integrated translational imaging readouts within our workflow to both analyze the nanoimmunotherapeutic's in vivo behavior and assess treatment response in larger animals. We observed our nanoimmunotherapeutic's anti-inflammatory efficacy in mice, as well as rabbits and pigs. Nanoimmunotherapy-mediated reduction of inflammation in the large animal models halted plaque progression, supporting the approach's translatability and potential to acutely treat atherosclerosis.
U2 - 10.1126/scitranslmed.aaw7736
DO - 10.1126/scitranslmed.aaw7736
M3 - Journal article
C2 - 31434756
AN - SCOPUS:85071299820
VL - 11
JO - Science Translational Medicine
JF - Science Translational Medicine
SN - 1946-6234
IS - 506
M1 - eaaw7736
ER -