Molecular DNA dendron vaccines

被引:12
|
作者
Distler, Max E. [1 ,2 ]
Cavaliere, John P. [1 ,2 ]
Teplensky, Michelle H. [1 ,2 ]
Evangelopoulos, Michael [2 ,3 ]
Mirkin, Chad A. [1 ,2 ,3 ]
机构
[1] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
[2] Northwestern Univ, Int Inst Nanotechnol, Evanston, IL 60208 USA
[3] Northwestern Univ, Dept Biomed Engn, Evanston, IL 60208 USA
关键词
DNA dendrons; vaccines; DNA therapeutics; DRUG-DELIVERY; CANCER; BIOMATERIALS; ACTIVATION; NANOPARTICLES; THERAPEUTICS; EFFICIENT;
D O I
10.1073/pnas.2215091120
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A foundational principle of rational vaccinology is that vaccine structure plays a critical role in determining therapeutic efficacy, but in order to establish fundamental, effective, and translatable vaccine design parameters, a highly modular and well-defined platform is required. Herein, we report a DNA dendron vaccine, a molecular nanostructure that consists of an adjuvant DNA strand that splits into multiple DNA branches with a varied number of conjugated peptide antigens that is capable of dendritic cell uptake, immune activation, and potent cancer killing. We leveraged the well-defined architecture and chemical modularity of the DNA dendron to study structure-function relationships that dictate molecular vaccine efficacy, particularly regarding the delivery of immune-activating DNA sequences and antigenic peptides on a single chemical construct. We investigated how adjuvant and antigen placement and number impact dendron cellular uptake and immune activation, in vitro. These parameters also played a significant role in raising a potent and specific immune response against target cancer cells. By gaining this structural understanding of molecular vaccines, DNA dendrons successfully treated a mouse cervical human papillomavirus TC-1 cancer model, in vivo, where the vaccine structure defined its efficacy; the top-performing design effectively reduced tumor burden (<150 mm(3) through day 30) and maintained 100% survival through 44 d after tumor inoculation.
引用
收藏
页数:8
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