Drug Discovery, Center for Research and Development, Kexing Biopharm Co. Ltd, Shenzhen, China.
MAbs. 2024 Jan-Dec;16(1):2416453. doi: 10.1080/19420862.2024.2416453. Epub 2024 Oct 14.
Cachexia is a complicated metabolic syndrome mainly associated with cancers, characterized by extreme weight loss and muscle wasting. It is a debilitating condition that negatively affects prognosis and survival. However, there is currently no effective pharmacological intervention that can reverse body weight loss and improve physical performance in patients with cachexia. Growth differentiation factor 15 (GDF15) can suppress appetite and regulate energy balance through binding to glial cell-derived neurotrophic factor receptor alpha-like (GFRAL). In order to develop a novel, effective treatment for cachexia, we generated a GDF15-targeting VHH nanobody, GB18-06, that was able to bind GDF15 with high affinity. , GB18-06 potently inhibited the GDF15-GFRAL signaling pathway, leading to a reduction of downstream ERK and AKT phosphorylation levels; , GB18-06 alleviated weight loss (>20%) in cancer and chemotherapy-induced cachexia models in mice. Compared with the control (phosphate-buffered saline) group, the ambulatory activity of mice in the GB18-06-treated group also increased 77%. Furthermore, GB18-06 exhibited desirable pharmacokinetic properties and an excellent developability profile. Our study has demonstrated a means of developing targeted treatment for cachexia with high efficacy, potentially leading to improved clinical outcomes and quality of life for patients with cachexia.
恶病质是一种复杂的代谢综合征,主要与癌症有关,其特征是极度消瘦和肌肉消耗。它是一种使人虚弱的疾病,会对预后和生存产生负面影响。然而,目前没有有效的药物干预措施可以逆转恶病质患者的体重下降并改善其身体机能。生长分化因子 15(GDF15)可以通过与神经胶质细胞衍生的神经营养因子受体α样(GFRAL)结合来抑制食欲和调节能量平衡。为了开发治疗恶病质的新方法,我们生成了一种靶向 GDF15 的 VHH 纳米抗体 GB18-06,它能够与 GDF15 高亲和力结合。GB18-06 强烈抑制 GDF15-GFRAL 信号通路,导致下游 ERK 和 AKT 磷酸化水平降低;GB18-06 减轻了癌症和化疗引起的恶病质模型中小鼠的体重减轻(超过 20%)。与对照组(磷酸盐缓冲液)相比,GB18-06 治疗组小鼠的活动能力增加了 77%。此外,GB18-06 表现出理想的药代动力学特性和出色的开发性。我们的研究表明,有可能开发出针对恶病质的高效靶向治疗方法,从而可能改善恶病质患者的临床结局和生活质量。