Optimizing Advances in Nanoparticle Delivery for Cancer Immunotherapy

被引:39
|
作者
Caster, Joseph M. [1 ]
Callaghan, Cameron [1 ]
Seyedin, Steven N. [1 ]
Henderson, Kelly [1 ]
Sun, Bp [2 ]
Wang, Andrew Z. [2 ]
机构
[1] Univ Iowa, Carver Coll Med, Dept Radiat Oncol, Iowa City, IA USA
[2] Univ N Carolina, Carolina Ctr Canc Nanotechnol Excellence, Carolina Inst Nanomed,Lab Nano & Translat Med, Lineberger Comprehens Canc Ctr,Dept Radiat Oncol, Chapel Hill, NC 27515 USA
基金
美国国家卫生研究院;
关键词
Nanomedicine; Nanoparticle; Immunotherapy; Cancer Immunotherapy; TUMOR-ASSOCIATED MACROPHAGES; CELL LUNG-CANCER; IMMUNE-CHECKPOINT BLOCKADE; IRON-OXIDE NANOPARTICLES; ANTIGEN-PRESENTING CELLS; THERAPEUTIC-EFFICACY; T-CELLS; HYBRID NANOPARTICLES; DENDRITIC CELLS; SIRNA DELIVERY;
D O I
10.1016/j.addr.2019.07.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cancer immunotherapy is one of the fastest growing and most promising fields in clinical oncology. T-cell checkpoint inhibitors are revolutionizing the management of advanced cancers including non-small cell lung cancer and melanoma. Unfortunately, many common cancers are not responsive to these drugs and resistance remains problematic. A growing number of novel cancer immunotherapies have been discovered but their clinical translation has been limited by shortcomings of conventional drug delivery. Immune signaling is tightly-regulated and often requires simultaneous or near-simultaneous activation of multiple signals in specific subpopulations of immune cells. Nucleic acid therapies, which require intact intracellular delivery, are among the most promising approaches to modulate the tumor microenvironment to a pro-immunogenic phenotype. Advanced nanomedicines can be precisely engineered to overcome many of these limitations and appear well-poised to enable the clinical translation of promising cancer immunotherapies. (C) 2019 Published by Elsevier B.V.
引用
收藏
页码:3 / 15
页数:13
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