Affiliation:
1. Department of Chemistry, Northwestern University, Evanston, IL 60208
2. International Institute for Nanotechnology, Northwestern University, Evanston, IL 60208
3. Department of Biomedical Engineering, Northwestern University, Evanston, IL 60208
Abstract
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.
Funder
DOD | USAF | AMC | Air Force Office of Scientific Research
HHS | NIH | National Cancer Institute
HHS | National Institutes of Health
National Science Foundation
Publisher
Proceedings of the National Academy of Sciences
Cited by
9 articles.
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