T cell-independent B cell response is responsible for ABC phenomenon induced by repeated injection of PEGylated liposomes

被引:113
作者
Koide, Hiroyuki [1 ,2 ]
Asai, Tomohiro [1 ,2 ]
Hatanaka, Kentaro [1 ,2 ]
Akai, Shuji [3 ]
Ishii, Takayuki [1 ,2 ]
Kenjo, Eriya [1 ,2 ]
Ishida, Tatsuhiro [4 ]
Kiwada, Hiroshi [4 ]
Tsukada, Hideo [5 ]
Oku, Naoto [1 ,2 ]
机构
[1] Univ Shizuoka, Dept Med Biochem, Grad Sch Pharmaceut Sci, Suruga Ku, Shizuoka 4228526, Japan
[2] Univ Shizuoka, Global COE Program, Grad Sch Pharmaceut Sci, Suruga Ku, Shizuoka 4228526, Japan
[3] Univ Shizuoka, Dept Synthet Organ Chem, Grad Sch Pharmaceut Sci, Suruga Ku, Shizuoka 4228526, Japan
[4] Univ Tokushima, Dept Pharmacokinet & Biopharmaceut, Inst Hlth Biosci, Tokushima 7708505, Japan
[5] Hamamatsu Photon KK, Cent Res Lab, Shizuoka, Japan
关键词
Polyethylene glycol; Liposome; Accelerated blood clearance; Thymus-independent type 2 antigen; Nanocarriers; ACCELERATED BLOOD CLEARANCE; STERICALLY STABILIZED LIPOSOMES; REDUCED CARDIOTOXICITY; MARGINAL-ZONE; DOXORUBICIN; ANTIGENS; IGM; PERMEABILITY; SURFACE; MEMORY;
D O I
10.1016/j.ijpharm.2010.03.022
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Repeated injection of polyethyleneglycol-modified (PEGylated) liposomes causes a rapid clearance of them from the bloodstream, this phenomenon is called accelerated blood clearance (ABC). In the present study, we focused on the immune system responsible for the ABC phenomenon. PEGylated liposomes were preadministered to BALB/c mice and [H-3]-labeled ones were then administered to them 3 days after the preadministration. Consistent with our previous results, the preadministration with PEGylated liposomes triggered the rapid clearance of [H-3]-labeled PEGylated liposomes from the bloodstream, but that with PEGylated liposomes encapsulating doxorubicin (Dox) did not. In addition, we found that the ABC phenomenon was observed when a mixture of free Dox and PEGylated liposomes was preadministered. These data indicate that immune cells responsible for the ABC phenomenon might be selectively damaged by the Dox encapsulated in PEGylated liposomes. The ABC phenomenon was also observed in BALB/c nu/nu mice, but not in BALB/c SCID mice. The amount of anti-PEG IgM antibody induced by the stimulation with the PEGylated liposomes was significantly increased in the BALB/c nu/nu mice, but not in the BALB/c SCID ones. These data indicate that a T cell-independent B cell response would play a significant role in the ABC phenomenon. Furthermore, the present study suggests that PEGylated liposomes might be recognized by B cells as a thymus-independent type 2 (TI-2) antigen. The present study provides important information for the future development of liposomal medicines. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:218 / 223
页数:6
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