Biomimetic Nanoparticle Vaccines for Cancer Therapy

被引:96
作者
Kroll, Ashley, V [1 ,2 ]
Jiang, Yao [1 ,2 ]
Zhou, Jiarong [1 ,2 ]
Holay, Maya [1 ,2 ]
Fang, Ronnie H. [1 ,2 ]
Zhang, Liangfang [1 ,2 ]
机构
[1] Univ Calif San Diego, Dept Nanoengn, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
anticancer vaccination; antigen presentation; biomimetic nanoparticle; immunotherapy; nanomedicine; ANTIGEN-PRESENTING CELLS; MEMBRANE-COATED NANOPARTICLES; IN-SITU VACCINATION; TARGETING DENDRITIC CELLS; POLYMERIC NANOPARTICLES; CHECKPOINT BLOCKADE; IMMUNE-RESPONSE; LYMPH-NODE; ANTITUMOR IMMUNITY; ANTIBODY-RESPONSES;
D O I
10.1002/adbi.201800219
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
It is currently understood that in order for a tumor to successfully grow, it must evolve means of evading immune surveillance. In the past several decades, researchers have leveraged increases in the knowledge of tumor immunology to develop therapies capable of augmenting endogenous immunity and eliciting strong antitumor responses. In particular, the goal of anticancer vaccination is to train the immune system to properly utilize its own resources in the fight against cancer. Although attractive in principle, there are currently only limited examples of anticancer vaccines that are successfully translated to the clinic. Recently, there has been a significant push toward the use of nanotechnology for designing vaccine candidates that exhibit enhanced potency and specificity. Here, the recent developments in the field of anticancer nanovaccines are discussed. By taking advantage of the flexibility offered by nanomedicine to purposefully program immune responses, this new generation of vaccines has the potential to address many of the hurdles facing traditional platforms. A specific emphasis is placed on the emergence of cell membrane-coated nanoparticles, a novel biomimetic platform that can be used to generate personalized nanovaccines that elicit strong, multiantigenic antitumor responses.
引用
收藏
页数:17
相关论文
共 186 条
[1]   Induction of necrotic cell death and activation of STING in the tumor microenvironment via cationic silica nanoparticles leading to enhanced antitumor immunity [J].
An, Myunggi ;
Yu, Chunsong ;
Xi, Jingchao ;
Reyes, Joyce ;
Mao, Guangzhao ;
Wei, Wei-Zen ;
Liu, Haipeng .
NANOSCALE, 2018, 10 (19) :9311-9319
[2]   Silica Nanoparticle as a Lymph Node Targeting Platform for Vaccine Delivery [J].
An, Myunggi ;
Li, Meng ;
Xi, Jingchao ;
Liu, Haipeng .
ACS APPLIED MATERIALS & INTERFACES, 2017, 9 (28) :23466-23475
[3]   Toxoid Vaccination against Bacterial Infection Using Cell Membrane-Coated Nanoparticles [J].
Angsantikul, Pavimol ;
Fang, Ronnie H. ;
Zhang, Liangfang .
BIOCONJUGATE CHEMISTRY, 2018, 29 (03) :604-612
[4]   Cell Membrane-Coated Nanoparticles As an Emerging Antibacterial Vaccine Platform [J].
Angsantikul, Pavimol ;
Thamphiwatana, Soracha ;
Gao, Weiwei ;
Zhang, Liangfang .
VACCINES, 2015, 3 (04) :814-828
[5]   Antibiotic-Resistant Bugs in the 21st Century -- A Clinical Super-Challenge. [J].
Arias, Cesar A. ;
Murray, Barbara E. .
NEW ENGLAND JOURNAL OF MEDICINE, 2009, 360 (05) :439-443
[6]  
Aryal S, 2013, NANOMEDICINE-UK, V8, P1271, DOI [10.2217/NNM.12.153, 10.2217/nnm.12.153]
[7]   Vaccine delivery: a matter of size, geometry, kinetics and molecular patterns [J].
Bachmann, Martin F. ;
Jennings, Gary T. .
NATURE REVIEWS IMMUNOLOGY, 2010, 10 (11) :787-796
[8]   Nanoparticle-Mediated Cytoplasmic Delivery of Proteins To Target Cellular Machinery [J].
Bale, Shyam Sundhar ;
Kwon, Seok Joon ;
Shah, Dhiral A. ;
Banerjee, Akhilesh ;
Dordick, Jonathan S. ;
Kane, Ravi S. .
ACS NANO, 2010, 4 (03) :1493-1500
[9]   Dendritic cells as therapeutic vaccines against cancer [J].
Banchereau, J ;
Palucka, AK .
NATURE REVIEWS IMMUNOLOGY, 2005, 5 (04) :296-306
[10]   The impact of nanoparticle ligand density on dendritic-cell targeted vaccines [J].
Bandyopadhyay, Arunima ;
Fine, Rebecca L. ;
Demento, Stacey ;
Bockenstedt, Linda K. ;
Fahmy, Tarek M. .
BIOMATERIALS, 2011, 32 (11) :3094-3105