Ozmen L, Gribaudo G, Fountoulakis M, Gentz R, Landolfo S, Garotta G
F. Hoffmann-La Roche Ltd, Pharmaceutical Research-New Technologies, Basel, Switzerland.
J Immunol. 1993 Apr 1;150(7):2698-705.
With the purpose to use a soluble receptor as an IFN gamma antagonist in vivo, we assessed the immunogenicity, the half-life, the bioavailability, and the activity of the soluble receptor after injection into mice. No significant immunogenicity was detected after multiple chronic injections of mouse (Mo)IFN gamma-R or injections of MoIFN gamma-R in emulsion with CFA. Pharmacokinetic experiments using radiolabeled MoIFN gamma-R revealed that the half-life of the soluble MoIFN gamma-R is 3 h in the blood and 6 h in the lymphoid organs. When the MoIFN gamma-R protein was traced by the capacity of the animal sera to displace the binding of radiolabeled MoIFN gamma-R from affinity purified rabbit anti-MoIFN gamma-R antibodies, a blood half-life of 1 h was determined. Finally, the capacity of the injected receptor to bind and neutralize the IFN gamma-mediated antiviral activity was assessed in vivo. Treatment with IFN-gamma or IFN-alpha A/D protected the mice from the lethal infection with encephalomyocarditis virus. Mice treated with MoIFN-gamma-R neutralized the protective effect of IFN-gamma.
为了在体内将可溶性受体用作γ干扰素拮抗剂,我们评估了将可溶性受体注射到小鼠体内后的免疫原性、半衰期、生物利用度和活性。多次慢性注射小鼠(Mo)γ干扰素受体或在弗氏完全佐剂(CFA)乳液中注射Moγ干扰素受体后,未检测到明显的免疫原性。使用放射性标记的Moγ干扰素受体进行的药代动力学实验表明,可溶性Moγ干扰素受体在血液中的半衰期为3小时,在淋巴器官中的半衰期为6小时。当通过动物血清从亲和纯化的兔抗Moγ干扰素受体抗体中置换放射性标记的Moγ干扰素受体结合的能力来追踪Moγ干扰素受体蛋白时,确定其血液半衰期为1小时。最后,在体内评估了注射的受体结合和中和γ干扰素介导的抗病毒活性的能力。用γ干扰素或αA/D干扰素治疗可保护小鼠免受脑心肌炎病毒的致死性感染。用Moγ干扰素受体治疗的小鼠中和了γ干扰素的保护作用。