| Literature DB >> 33495503 |
Hiroyasu Muramatsu1, Taichi Kuramochi2, Hitoshi Katada1, Atsunori Ueyama1, Yoshinao Ruike1, Ken Ohmine1, Meiri Shida-Kawazoe1, Rie Miyano-Nishizawa1, Yuichiro Shimizu1, Momoko Okuda2, Yuji Hori1, Madoka Hayashi1, Kenta Haraya1, Nobuhiro Ban1, Tatsuya Nonaka1, Masaki Honda1, Hidetomo Kitamura1, Kunihiro Hattori1, Takehisa Kitazawa1, Tomoyuki Igawa2, Yoshiki Kawabe1, Junichi Nezu3.
Abstract
Myostatin, a member of the transforming growth factor-β superfamily, is an attractive target for muscle disease therapy because of its role as a negative regulator of muscle growth and strength. Here, we describe a novel antibody therapeutic approach that maximizes the potential of myostatin-targeted therapy. We generated an antibody, GYM329, that specifically binds the latent form of myostatin and inhibits its activation. Additionally, via "sweeping antibody technology", GYM329 reduces or "sweeps" myostatin in the muscle and plasma. Compared with conventional anti-myostatin agents, GYM329 and its surrogate antibody exhibit superior muscle strength-improvement effects in three different mouse disease models. We also demonstrate that the superior efficacy of GYM329 is due to its myostatin specificity and sweeping capability. Furthermore, we show that a GYM329 surrogate increases muscle mass in normal cynomolgus monkeys without any obvious toxicity. Our findings indicate the potential of GYM329 to improve muscle strength in patients with muscular disorders.Entities:
Year: 2021 PMID: 33495503 PMCID: PMC7835227 DOI: 10.1038/s41598-021-81669-8
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379