Engineering cancer vaccines using stimuli-responsive biomaterials

被引:0
作者
Zhao, Yu [1 ]
Guo, Yugang [1 ]
Tang, Li [1 ,2 ]
机构
[1] Ecole Polytech Fed Lausanne, Inst Bioengn, CH-1015 Lausanne, Switzerland
[2] Ecole Polytech Fed Lausanne, Inst Mat Sci & Engn, CH-1015 Lausanne, Switzerland
基金
瑞士国家科学基金会;
关键词
cancer vaccine; stimuli-responsive; biomaterial; nanoparticle; immune response; lymph node targeting; cross-presentation; MHC CLASS-I; PROTEIN-BASED VACCINES; T-CELL RESPONSES; DENDRITIC CELLS; DRUG-DELIVERY; ANTIGEN PRESENTATION; B-CELLS; NANOPARTICLE VACCINES; ANTITUMOR IMMUNITY; PH;
D O I
10.1007/s12274-018-2162-1
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Cancer vaccines aimed at expanding the pool or increasing the activity of tumor-specific T cells against malignancies is an important immunotherapy modality that has been extensively pursued in the past decades. However, the clinical efficacy of cancer vaccines remains modest in comparison to other immunotherapies, such as checkpoint blockade and adoptive T cell therapy. This unsatisfactory performance is likely due to the suboptimal selection of tumor antigens for vaccine and inefficient delivery platform. Recently, vaccines designed to target cancer neoantigens have shown marked promise in both preclinical and early clinical studies. However, enormous challenges need to be overcome to develop a highly efficient and safe delivery strategy for targeting cancer vaccines to professional antigen-presenting cells and eliciting optimized immune response against cancers. To meet these challenges, biomaterials, particularly biomaterials that are designed to respond to certain environmental stimuli, termed as stimuli-responsive biomaterials, are being actively developed to precisely manipulate the trafficking and release of cancer vaccines in vivo for enhanced therapeutic efficacy and safety. In this mini review, we provide a brief overview of the recent advances in applying stimuli-responsive biomaterials in enhancing non-cellular cancer vaccines while focusing on the chemistry and material design with varied responsiveness. We also discuss the present challenges and opportunities in the field and provide a perspective for future directions.
引用
收藏
页码:5355 / 5371
页数:17
相关论文
共 97 条
[1]   A nano-liposome vaccine carrying E75, a HER-2/neu-derived peptide, exhibits significant antitumour activity in mice [J].
Arab, Atefeh ;
Behravan, Javad ;
Razazan, Atefeh ;
Gholizadeh, Zahra ;
Nikpoor, Amin Reza ;
Barati, Nastaran ;
Mosaffa, Fatemeh ;
Badiee, Ali ;
Jaafari, Mahmoud Reza .
JOURNAL OF DRUG TARGETING, 2018, 26 (04) :365-372
[2]   Acid-degradable polyurethane particles for protein-based vaccines:: Biological evaluation and in vitro analysis of particle degradation products [J].
Bachelder, Eric M. ;
Beaudette, Tristan T. ;
Broaders, Kyle E. ;
Paramonov, Sergey E. ;
Dashe, Jesse ;
Frechet, Jean M. J. .
MOLECULAR PHARMACEUTICS, 2008, 5 (05) :876-884
[3]   Conductive polymers: Towards a smart biomaterial for tissue engineering [J].
Balint, Richard ;
Cassidy, Nigel J. ;
Cartmell, Sarah H. .
ACTA BIOMATERIALIA, 2014, 10 (06) :2341-2353
[4]   Chemisorbed poly(propylene sulphide)-based copolymers resist biomolecular interactions [J].
Bearinger, JP ;
Terrettaz, S ;
Michel, R ;
Tirelli, N ;
Vogel, H ;
Textor, M ;
Hubbell, JA .
NATURE MATERIALS, 2003, 2 (04) :259-264
[5]   Toll-dependent selection of microbial antigens for presentation by dendritic cells [J].
Blander, JM ;
Medzhitov, R .
NATURE, 2006, 440 (7085) :808-812
[6]   A VERSATILE VECTOR FOR GENE AND OLIGONUCLEOTIDE TRANSFER INTO CELLS IN CULTURE AND IN-VIVO - POLYETHYLENIMINE [J].
BOUSSIF, O ;
LEZOUALCH, F ;
ZANTA, MA ;
MERGNY, MD ;
SCHERMAN, D ;
DEMENEIX, B ;
BEHR, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) :7297-7301
[7]   Immunization with mimotopes prevents growth of carcinoembryonic antigen -: Positive tumors in BALB/c mice [J].
Braemswig, Kira H. ;
Knittelfelder, Regina ;
Gruber, Silke ;
Untersmayr, Eva ;
Riemer, Angelika B. ;
Szalai, Krisztina ;
Horvat, Reinhard ;
Kammerer, Robert ;
Zimmermann, Wolfgang ;
Zielinski, Christoph C. ;
Scheiner, Otto ;
Jensen-Jarolim, Erika .
CLINICAL CANCER RESEARCH, 2007, 13 (21) :6501-6508
[8]  
Broos Katrijn, 2016, Mol Ther Nucleic Acids, V5, pe326, DOI 10.1038/mtna.2016.38
[9]   Photothermally Controlled MHC Class I Restricted CD8+ T-Cell Responses Elicited by Hyaluronic Acid Decorated Gold Nanoparticles as a Vaccine for Cancer Immunotherapy [J].
Cao, Fengqiang ;
Yan, Mengmeng ;
Liu, Yijia ;
Liu, Lanxia ;
Ma, Guilei .
ADVANCED HEALTHCARE MATERIALS, 2018, 7 (10)
[10]   PROVENGE (Sipuleucel-T) in Prostate Cancer: The First FDA-Approved Therapeutic Cancer Vaccine [J].
Cheever, Martin A. ;
Higano, Celestia S. .
CLINICAL CANCER RESEARCH, 2011, 17 (11) :3520-3526