Cell-penetrating peptides: Application in vaccine delivery

被引:84
作者
Brooks, Nicole A. [1 ,2 ]
Pouniotis, Dodie S. [2 ]
Tang, Choon-Kit [1 ]
Apostolopoulos, Vasso [3 ]
Pietersz, Geoffrey A. [1 ]
机构
[1] Burnet Inst, Bioorgan & Med Chem Lab, Melbourne, Vic 3004, Australia
[2] RMIT Univ, Sch Med Sci, Melbourne, Vic, Australia
[3] Burnet Inst, Immunol & Vaccine Lab, Melbourne, Vic 3004, Australia
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2010年 / 1805卷 / 01期
关键词
Cell penetrating peptide; Cancer vaccine; Penetratin; Antigen presentation; Vaccine delivery; PROTEIN TRANSDUCTION DOMAINS; TAT-FUSION PROTEINS; VIRUS TYPE-1 VP22; CLASS-I PATHWAY; DENDRITIC CELLS; DNA VACCINE; ANTENNAPEDIA HOMEODOMAIN; MAMMALIAN-CELLS; T-CELLS; INTERCELLULAR TRAFFICKING;
D O I
10.1016/j.bbcan.2009.09.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recent years have seen a surge in interest in cell-penetrating peptides (CPP) as an efficient means for delivering therapeutic targets into cellular compartments. The cell membrane is impermeable to hydrophilic substances yet linking to CPP can facilitate delivery into cells. Thus the unique translocatory property of CPP ensures they remain an attractive carrier, with the capacity to deliver cargoes in an efficient manner having applications in drug delivery, gene transfer and DNA vaccination. Fundamental for an effective vaccine is the delivery of antigen epitopes to antigen-presenting cells, ensuing processing and presentation and induction of an immune response. Vaccination with proteins or synthetic peptides incorporating CTL epitopes have proven limited due to the failure for exogenous antigens to be presented efficiently to T cells. Linking of antigens to CPP overcomes such obstacles by facilitating cellular uptake, processing and presentation of exogenous antigen for the induction of potent immune responses. This review will encompass the various strategies for the delivery of whole proteins, T cell epitopes and preclinical studies utilizing CPP for cancer vaccines. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:25 / 34
页数:10
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