Characterization of the in vitro and in vivo activity of monoclonal antibodies to human IL-18.

S Holmes, J A Abrahamson, N Al-Mahdi, S S Abdel-Meguid, Y S Ho
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引用次数: 16

Abstract

IL-18 is a cytokine with potent IFN-gamma inducing activities as well as an important mediator of Th1 polarized immune responses. In this study we demonstrated that IL-18 induces the concentration-dependent production of the proinflammatory mediators IFN-gamma, IL-6, and GM-CSF, but not the anti-inflammatory cytokine, IL-10 from peripheral blood lymphocytes in the presence of mitogen. Three neutralizing IL-18 monoclonal antibodies (MAbs) were investigated, one of which (2C10) inhibited IL-18 bioactivity with an IC50 of 0.1 nM and had a K(D) of 3.9 x 10(-11) M. A NOD/SCID mouse model engrafted with human peripheral blood lymphocytes was developed to test the in vivo efficacy of this MAb. The IFN-gamma production induced by LPS administration was inhibited approximately 90% by prior dosing of MAb 2C10. The therapeutic utility of a high-affinity IL-18 MAb may be of benefit in Th1-driven autoimmune diseases such as rheumatoid arthritis and Crohn's Disease, where elevated levels of IL-18 have been observed.

人IL-18单克隆抗体体外和体内活性的研究。
IL-18是一种具有强大的ifn - γ诱导活性的细胞因子,也是Th1极化免疫反应的重要介质。在这项研究中,我们证明了IL-18诱导促炎介质ifn - γ、IL-6和GM-CSF的浓度依赖性生产,但在有丝裂原存在的情况下,外周血淋巴细胞的抗炎细胞因子IL-10却没有。研究了3种中和IL-18的单克隆抗体(MAb),其中一种(2C10)抑制IL-18的生物活性,IC50为0.1 nM, K(D)为3.9 × 10(-11) M.建立了移植人外周血淋巴细胞的NOD/SCID小鼠模型,检测了该单克隆抗体的体内药效。通过事先给药MAb 2C10, LPS诱导的ifn - γ产生被抑制约90%。高亲和IL-18单抗的治疗效用可能有益于th1驱动的自身免疫性疾病,如类风湿关节炎和克罗恩病,在这些疾病中已观察到IL-18水平升高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Hybridoma
Hybridoma 医学-免疫学
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4-8 weeks
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