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用于癌症疫苗的转化型纳米颗粒工程

Translational nanoparticle engineering for cancer vaccines.

作者信息

Grippin Adam J, Sayour Elias J, Mitchell Duane A

机构信息

Preston A. Wells, Jr. Center for Brain Tumor Therapy, University of Florida Brain Tumor Immunotherapy Program, McKnight Brain Institute, Department of Neurosurgery, University of Florida, Gainesville, FL, USA.

J. Crayton Pruitt Family Department of Biomedical Engineering, Biomedical Sciences Building, University of Florida, Gainesville, FL, USA.

出版信息

Oncoimmunology. 2017 Feb 22;6(10):e1290036. doi: 10.1080/2162402X.2017.1290036. eCollection 2017.


DOI:10.1080/2162402X.2017.1290036
PMID:29123947
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5665077/
Abstract

Conventional cancer treatments remain insufficient to treat many therapy-resistant tumors. Cancer vaccines attempt to overcome this resistance by activating the patient's immune system to eliminate tumor cells without the toxicity of systemic chemotherapy and radiation. Nanoparticles (NPs) are promising as customizable, immunostimulatory carriers to protect and deliver antigen. Although many NP vaccines have been investigated in preclinical settings, a few have advanced into clinical application, and still fewer have demonstrated clinical benefit. This review incorporates observations from NP vaccines that have been evaluated in early phase clinical trials to make recommendations for the next generation of NP-based cancer vaccines.

摘要

传统的癌症治疗方法在治疗许多耐药性肿瘤方面仍然不足。癌症疫苗试图通过激活患者的免疫系统来消除肿瘤细胞,从而克服这种耐药性,同时避免全身化疗和放疗的毒性。纳米颗粒(NPs)作为可定制的免疫刺激载体,有望用于保护和递送抗原。尽管许多纳米颗粒疫苗已在临床前环境中进行了研究,但只有少数进入了临床应用,而且证明有临床益处的更少。本综述纳入了在早期临床试验中评估的纳米颗粒疫苗的观察结果,为下一代基于纳米颗粒的癌症疫苗提出建议。

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本文引用的文献

[1]
Systemic RNA delivery to dendritic cells exploits antiviral defence for cancer immunotherapy.

Nature. 2016-6-1

[2]
Efficacy of the MAGE-A3 cancer immunotherapeutic as adjuvant therapy in patients with resected MAGE-A3-positive non-small-cell lung cancer (MAGRIT): a randomised, double-blind, placebo-controlled, phase 3 trial.

Lancet Oncol. 2016-4-27

[3]
A non-randomized dose-escalation Phase I trial of a protein-based immunotherapeutic for the treatment of breast cancer patients with HER2-overexpressing tumors.

Breast Cancer Res Treat. 2016-4

[4]
Cancer statistics, 2016.

CA Cancer J Clin. 2016-1-7

[5]
Nanoparticle surface charge impacts distribution, uptake and lymph node trafficking by pulmonary antigen-presenting cells.

Nanomedicine. 2016-4

[6]
A randomized pilot trial testing the safety and immunologic effects of a MAGE-A3 protein plus AS15 immunostimulant administered into muscle or into dermal/subcutaneous sites.

Cancer Immunol Immunother. 2016-1

[7]
Identification of QS-21 as an Inflammasome-activating Molecular Component of Saponin Adjuvants.

J Biol Chem. 2016-1-15

[8]
Optimization of Lipid Nanoparticle Formulations for mRNA Delivery in Vivo with Fractional Factorial and Definitive Screening Designs.

Nano Lett. 2015-10-20

[9]
Survivin-targeted immunotherapy drives robust polyfunctional T cell generation and differentiation in advanced ovarian cancer patients.

Oncoimmunology. 2015-5-7

[10]
Safety and Immunogenicity of MAGE-A3 Cancer Immunotherapeutic with or without Adjuvant Chemotherapy in Patients with Resected Stage IB to III MAGE-A3-Positive Non-Small-Cell Lung Cancer.

J Thorac Oncol. 2015-10

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