TY - JOUR
T1 - Molecular DNA dendron vaccines
AU - Distler, Max E.
AU - Cavaliere, John P.
AU - Teplensky, Michelle H.
AU - Evangelopoulos, Michael
AU - Mirkin, Chad A.
N1 - Funding Information:
ACKNOWLEDGMENTS. This material is based upon work supported by the Polsky Urologic Cancer Institute of the Robert H. Lurie Comprehensive Cancer Center of Northwestern University at Northwestern Memorial Hospital, the Air Force Office of Scientific Research under award FA9550-17-1-0348, and the Lefkofsky Family Foundation. This research was also supported by the National Cancer Institute of the NIH under awards P50CA221747 and R01CA257926. M.H.T. acknowledges support from Northwestern University’s Cancer Nanotechnology Training Program supported by the National Cancer Institute of the NIH award T32CA186897 and support from Edward Bachrach. M.E. was partially supported by the Alexander S. Onassis Public Benefit Foundation. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.We thank Dr.Bin Zhang for supplying the TC-1 cervical cancer cells.This work made use of the IMSERC MS facility at Northwestern University, which has received support from the Soft and Hybrid Nanotechnology Experimental (SHyNE) Resource (NSF ECCS-2025633), the State of Illinois, and the International Institute for Nanotechnology (IIN). Imaging work was performed at the Northwestern University Center for Advanced Molecular Imaging generously supported by NCI CCSG P30 CA060553 awarded to the Robert H Lurie Comprehensive Cancer Center. Some figures were made using BioRender.
Publisher Copyright:
Copyright © 2023 the Author(s). Published by PNAS.
PY - 2023/1/31
Y1 - 2023/1/31
N2 - 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 mm3 through day 30) and maintained 100% survival through 44 d after tumor inoculation.
AB - 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 mm3 through day 30) and maintained 100% survival through 44 d after tumor inoculation.
KW - DNA dendrons
KW - DNA therapeutics
KW - vaccines
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U2 - 10.1073/pnas.2215091120
DO - 10.1073/pnas.2215091120
M3 - Article
C2 - 36696444
AN - SCOPUS:85146870113
SN - 0027-8424
VL - 120
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 5
M1 - e2215091120
ER -