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分子 DNA 树突疫苗。

Molecular DNA dendron vaccines.

机构信息

Department of Chemistry, Northwestern University, Evanston, IL 60208.

International Institute for Nanotechnology, Northwestern University, Evanston, IL 60208.

出版信息

Proc Natl Acad Sci U S A. 2023 Jan 31;120(5):e2215091120. doi: 10.1073/pnas.2215091120. Epub 2023 Jan 25.

DOI:10.1073/pnas.2215091120
PMID:36696444
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9945956/
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 through day 30) and maintained 100% survival through 44 d after tumor inoculation.

摘要

理性疫苗学的一个基本原则是疫苗结构在决定治疗效果方面起着关键作用,但为了建立基本、有效和可转化的疫苗设计参数,需要一个高度模块化和定义明确的平台。在此,我们报告了一种 DNA 树突疫苗,它是一种由佐剂 DNA 链组成的分子纳米结构,该佐剂 DNA 链分裂成多个具有不同数量连接肽抗原的 DNA 分支,能够被树突状细胞摄取、免疫激活和有效杀伤癌症。我们利用 DNA 树突的明确结构和化学模块化来研究决定分子疫苗功效的结构-功能关系,特别是关于在单个化学构建体上递呈免疫激活 DNA 序列和抗原肽的问题。我们研究了佐剂和抗原的位置和数量如何影响树突细胞的摄取和免疫激活。这些参数在提高针对靶癌细胞的有效和特异性免疫反应方面也起着重要作用。通过对分子疫苗的这种结构理解,DNA 树突在体内成功治疗了小鼠宫颈人乳头瘤病毒 TC-1 癌症模型,其中疫苗结构决定了其疗效;表现最佳的设计有效降低了肿瘤负担(第 30 天<150mm),并在接种肿瘤后 44 天保持 100%的存活率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a05/9945956/7b04d786ca9f/pnas.2215091120fig05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a05/9945956/cd8e3fb24f68/pnas.2215091120fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a05/9945956/e304018ba6ea/pnas.2215091120fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a05/9945956/ec1d8324df61/pnas.2215091120fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a05/9945956/1c9da7a67da7/pnas.2215091120fig04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a05/9945956/7b04d786ca9f/pnas.2215091120fig05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a05/9945956/cd8e3fb24f68/pnas.2215091120fig01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a05/9945956/e304018ba6ea/pnas.2215091120fig02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a05/9945956/ec1d8324df61/pnas.2215091120fig03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a05/9945956/1c9da7a67da7/pnas.2215091120fig04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3a05/9945956/7b04d786ca9f/pnas.2215091120fig05.jpg

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