Liu Xiaolei, Li Li, Wang Qian, Jiang Fengchao, Zhang Pei, Guo Fei, Liu Hongjun, Huang Jian
Department of Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, United States.
IPHASE Therapeutic Ltd., Philadelphia, PA, United States.
Front Immunol. 2022 Jan 19;12:816646. doi: 10.3389/fimmu.2021.816646. eCollection 2021.
Interleukin-6 (IL-6), a pleiotropic cytokine that regulates immune responses and inflammatory reactions, plays a pivotal role in the development of rheumatoid arthritis (RA). Blockade of IL-6 signaling with the monoclonal antibody (mAb) represents an important advancement in RA treatment. Although two IL-6 receptor antibodies are already available in the clinic, there is no mAb specifically targeting the human IL-6 to block IL-6 signaling for RA treatment. In this study, we have developed a novel humanized anti-IL-6 mAb HZ-0408b with potent binding and neutralizing activity to human IL-6. We demonstrated that HZ-0408b has a high species specificity and low cross-reactivity. Moreover, HZ-0408b showed a more potent inhibitory effect on IL-6 signaling than Siltuximab, an FDA-approved anti-IL-6 chimeric mAb. HZ-0408b is comparable to Olokizumab, a humanized mAb against IL-6 that is already in phase III studies. We observed that HZ-0408b is well tolerated at doses that can achieve therapeutic serum levels in cynomolgus monkey. Most importantly, we proved that HZ-0408b treatment significantly ameliorated joint swelling after the onset of arthritis and dramatically reduced plasma C-reactive protein (CRP) levels in a monkey collagen-induced arthritis (CIA) model. Collectively, our findings using non-human primates indicate that humanized anti-IL-6 mAb HZ-0408b has excellent safety and efficacy profiles for RA therapy.
白细胞介素-6(IL-6)是一种调节免疫反应和炎症反应的多效性细胞因子,在类风湿性关节炎(RA)的发展中起关键作用。用单克隆抗体(mAb)阻断IL-6信号通路是RA治疗的一项重要进展。尽管临床上已经有两种IL-6受体抗体,但尚无特异性靶向人IL-6以阻断IL-6信号通路用于RA治疗的单克隆抗体。在本研究中,我们开发了一种新型人源化抗IL-6单克隆抗体HZ-0408b,它对人IL-6具有强大的结合和中和活性。我们证明HZ-0408b具有高物种特异性和低交叉反应性。此外,HZ-0408b对IL-6信号通路的抑制作用比FDA批准的抗IL-6嵌合单克隆抗体Siltuximab更强。HZ-0408b与已经进入III期研究的抗IL-6人源化单克隆抗体Olokizumab相当。我们观察到,在食蟹猴中能够达到治疗性血清水平的剂量下,HZ-0408b耐受性良好。最重要的是,我们证明在猴胶原诱导的关节炎(CIA)模型中,HZ-0408b治疗能显著改善关节炎发作后的关节肿胀,并显著降低血浆C反应蛋白(CRP)水平。总体而言,我们使用非人灵长类动物的研究结果表明,人源化抗IL-6单克隆抗体HZ-0408b在RA治疗中具有出色的安全性和疗效。