The accelerated blood clearance (ABC) phenomenon: Clinical challenge and approaches to manage

被引:590
作者
Abu Lila, Amr S. [1 ,2 ]
Kiwada, Hiroshi [1 ]
Ishida, Tatsuhiro [1 ]
机构
[1] Univ Tokushima, Inst Hlth Biosci, Dept Pharmacokinet & Biopharmaceut, Subdiv Biopharmaceut Sci, Tokushima 7708505, Japan
[2] Zagazig Univ, Fac Pharm, Dept Pharmaceut & Ind Pharm, Zagazig, Egypt
关键词
Accelerated blood clearance (ABC) phenomenon; Anti; PEG IgM; Polyethylene glycol(PEG); Repeated administration; Splenic B cells; PEGYLATED LIPOSOMAL DOXORUBICIN; POLYETHYLENE-GLYCOL; REPEATED INJECTION; POLY(ETHYLENE GLYCOL); COVALENT ATTACHMENT; ANTITUMOR-ACTIVITY; IMMUNE-RESPONSE; MARGINAL ZONE; PEG; PHARMACOKINETICS;
D O I
10.1016/j.jconrel.2013.07.026
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Despite the clinical introduction of an increasing number of polyethylene glycol (PEG)-conjugated substances, PEG has been named as the cause of an unexpected immunogenic response known as the "accelerated blood clearance (ABC) phenomenon." This phenomenon has been extensively observed during the repeated administration of PEG-conjugated substances and PEGylated nanocarriers including PEGylated liposomes, PEGylated nanoparticles, PEGylated micelles, etc., resulting in the increased clearance and reduced efficacy of PEG-conjugated substances/PEGylated nanocarriers. In this review, therefore, we focused on the possible mechanisms underlying the induction of such a phenomenon and emphasized the factors affecting its magnitude. In addition, the clinical implications of the ABC phenomenon on the therapeutic efficacy of PEG-conjugated substances/PEGylated nanocarriers, along with the new approaches that can be applied to manage and/or abrogate the induction of the ABC phenomenon, are also discussed. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:38 / 47
页数:10
相关论文
共 91 条
[1]
Multiple administration of PEG-coated liposomal oxaliplatin enhances its therapeutic efficacy: A possible mechanism and the potential for clinical application [J].
Abu Lila, Amr S. ;
Eldin, Noha Essam ;
Ichihara, Masako ;
Ishida, Tatsuhiro ;
Kiwada, Hiroshi .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2012, 438 (1-2) :176-183
[2]
ABUCHOWSKI A, 1977, J BIOL CHEM, V252, P3582
[3]
ABUCHOWSKI A, 1977, J BIOL CHEM, V252, P3578
[4]
Controlling the physical behavior and biological performance of liposome formulations through use of surface grafted poly(ethylene glycol) [J].
Allen, C ;
Dos Santos, N ;
Gallagher, R ;
Chiu, GNC ;
Shu, Y ;
Li, WM ;
Johnstone, SA ;
Janoff, AS ;
Mayer, LD ;
Webb, MS ;
Bally, MB .
BIOSCIENCE REPORTS, 2002, 22 (02) :225-250
[5]
Drug delivery systems: Entering the mainstream [J].
Allen, TM ;
Cullis, PR .
SCIENCE, 2004, 303 (5665) :1818-1822
[6]
Stabilized plasmid-lipid particles containing PEG-diacylglycerols exhibit extended circulation lifetimes and tumor selective gene expression [J].
Ambegia, E ;
Ansell, S ;
Cullis, P ;
Heyes, J ;
Palmer, L ;
MacLachlan, I .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2005, 1669 (02) :155-163
[7]
Antibody against poly(ethylene glycol) adversely affects PEG-asparaginase therapy in acute lymphoblastic leukemia patients [J].
Armstrong, Jonathan K. ;
Hempel, Georg ;
Koling, Susanne ;
Chan, Linda S. ;
Fisher, Timothy ;
Meiselman, Herbert J. ;
Garratty, George .
CANCER, 2007, 110 (01) :103-111
[8]
Tc-99m-PEG-liposomes for the evaluation of colitis in Crohn's disease [J].
Brouwers, AH ;
De Jong, DJ ;
Dams, ETM ;
Oyen, WJG ;
Boerman, OC ;
Laverman, P ;
Naber, THJ ;
Storm, G ;
Corstens, FHM .
JOURNAL OF DRUG TARGETING, 2000, 8 (04) :225-233
[9]
Supramolecular Nanodevices: From Design Validation to Theranostic Nanomedicine [J].
Cabral, Horacio ;
Nishiyama, Nobuhiro ;
Kataoka, Kazunori .
ACCOUNTS OF CHEMICAL RESEARCH, 2011, 44 (10) :999-1008
[10]
Complement activation following first exposure to pegylated liposomal doxorubicin (Doxil): possible role in hypersensitivity reactions [J].
Chanan-Khan, A ;
Szebeni, J ;
Savay, S ;
Liebes, L ;
Rafique, NM ;
Alving, CR ;
Muggia, FM .
ANNALS OF ONCOLOGY, 2003, 14 (09) :1430-1437