Ishida Tatsuhiro, Kiwada Hiroshi
Institute of Health Biosciences, The University of Tokushima, Tokushima City, Japan.
Yakugaku Zasshi. 2008 Feb;128(2):233-43. doi: 10.1248/yakushi.128.233.
PEGylated liposomes (approximately 100 nm in diameter) lose their long-circulating characteristic upon repeated injection at certain intervals in the same animal (referred to as the "accelerated blood clearance (ABC) phenomenon"), as described by our group and by researchers in the Netherlands. Recently, it was demonstrated by our group that anti-PEG IgM, induced by the first dose of PEGylated liposomes, is responsible for the ABC phenomenon. The IgM produced in this manner then selectively bound to the surface of subsequently injected PEGylated liposomes, leading to substantial complement activation. It is generally believed that nanocarriers coated with a polymer, such as PEG, have no immunogenicity. However, unexpected immune responses occurred even in response to polymer-coated liposomes. This immunogenicity to PEGylated liposomes presents a serious concern in the development and clinical use of liposomal formulations. In this review, we demonstrate our recent observations regarding with the ABC phenomenon against liposomes.
聚乙二醇化脂质体(直径约100纳米)在同一动物体内以一定间隔重复注射时会失去其长循环特性(称为“加速血液清除(ABC)现象”),这是我们团队以及荷兰的研究人员所描述的。最近,我们团队证明,第一剂聚乙二醇化脂质体诱导产生的抗聚乙二醇IgM是ABC现象的原因。以这种方式产生的IgM随后选择性地结合到随后注射的聚乙二醇化脂质体表面,导致大量补体激活。一般认为,用聚合物(如聚乙二醇)包被的纳米载体没有免疫原性。然而,即使是对聚合物包被的脂质体也会出现意外的免疫反应。聚乙二醇化脂质体的这种免疫原性在脂质体制剂的开发和临床应用中是一个严重问题。在这篇综述中,我们展示了我们最近关于脂质体ABC现象的观察结果。