Aragnol D, Leserman L D
Proc Natl Acad Sci U S A. 1986 Apr;83(8):2699-703. doi: 10.1073/pnas.83.8.2699.
In a study designed to evaluate the potential for in vivo manipulation of the circulation and tissue distribution of injected liposomes, mice were passively injected with antidinitrophenyl (anti-DNP) monoclonal antibodies of the IgG2a or IgG2b subclasses or were immunized with the nitrophenyl hapten bound to a protein carrier. They were then injected i.v. with 125I- and carboxyfluorescein-labeled, DNP-bearing liposomes. Circulation time of the DNP-bearing liposomes was markedly reduced in actively and passively immune mice, with increased deposition of liposomes in the liver. The increased clearance of liposomes could be abrogated by injection of a monoclonal antibody directed against the murine IgG Fc receptor (2.4G2). The results suggest that clearance of ligand-bearing reagent in the face of an immune response may be modified by specific immunologic manipulation in vivo.
在一项旨在评估体内操纵注射脂质体的循环和组织分布潜力的研究中,给小鼠被动注射IgG2a或IgG2b亚类的抗二硝基苯基(抗DNP)单克隆抗体,或用与蛋白质载体结合的硝基苯基半抗原进行免疫。然后给它们静脉注射125I和羧基荧光素标记的、携带DNP的脂质体。在主动免疫和被动免疫的小鼠中,携带DNP的脂质体的循环时间显著缩短,脂质体在肝脏中的沉积增加。注射针对小鼠IgG Fc受体的单克隆抗体(2.4G2)可消除脂质体清除率的增加。结果表明,面对免疫反应时,携带配体试剂的清除率可能通过体内特定的免疫操作来改变。