| Literature DB >> 31434756 |
Tina Binderup1,2, Raphaël Duivenvoorden1,3, Francois Fay1,4, Mandy M T van Leent1, Joost Malkus1, Samantha Baxter1, Seigo Ishino1, Yiming Zhao1, Brenda Sanchez-Gaytan1, Abraham J P Teunissen1, Yohana C A Frederico1, Jun Tang1,5, Giuseppe Carlucci5,6, Serge Lyashchenko5,7, Claudia Calcagno1, Nicolas Karakatsanis1, Georgios Soultanidis1, Max L Senders1,8, Philip M Robson1, Venkatesh Mani1, Sarayu Ramachandran1, Mark E Lobatto1,9, Barbara A Hutten10, Juan F Granada11, Thomas Reiner5,7, Filip K Swirski12, Matthias Nahrendorf12, Andreas Kjaer2, Edward A Fisher13, Zahi A Fayad14, Carlos Pérez-Medina1,15, Willem J M Mulder14,8,16,17.
Abstract
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.Entities:
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Year: 2019 PMID: 31434756 PMCID: PMC7328283 DOI: 10.1126/scitranslmed.aaw7736
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956