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基于球形核酸的理性疫苗学。

Rational vaccinology with spherical nucleic acids.

机构信息

Interdisciplinary Biological Sciences Graduate Program, Northwestern University, Evanston, IL 60208.

Division of Hematology-Oncology, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611.

出版信息

Proc Natl Acad Sci U S A. 2019 May 21;116(21):10473-10481. doi: 10.1073/pnas.1902805116. Epub 2019 May 8.

Abstract

In the case of cancer immunotherapy, nanostructures are attractive because they can carry all of the necessary components of a vaccine, including both antigen and adjuvant. Herein, we explore how spherical nucleic acids (SNAs), an emerging class of nanotherapeutic materials, can be used to deliver peptide antigens and nucleic acid adjuvants to raise immune responses that kill cancer cells, reduce (or eliminate) tumor growth, and extend life in three established mouse tumor models. Three SNA structures that are compositionally nearly identical but structurally different markedly vary in their abilities to cross-prime antigen-specific CD8 T cells and raise subsequent antitumor immune responses. Importantly, the most effective structure is the one that exhibits synchronization of maximum antigen presentation and costimulatory marker expression. In the human papillomavirus-associated TC-1 model, vaccination with this structure improved overall survival, induced the complete elimination of tumors from 30% of the mice, and conferred curative protection from tumor rechallenges, consistent with immunological memory not otherwise achievable. The antitumor effect of SNA vaccination is dependent on the method of antigen incorporation within the SNA structure, underscoring the modularity of this class of nanostructures and the potential for the deliberate design of new vaccines, thereby defining a type of rational cancer vaccinology.

摘要

在癌症免疫疗法中,纳米结构很有吸引力,因为它们可以携带疫苗的所有必要成分,包括抗原和佐剂。在此,我们探讨了球形核酸 (SNA) 作为一类新兴的纳米治疗材料,如何能够递送肽抗原和核酸佐剂,以引发免疫反应,杀死癌细胞、减少(或消除)肿瘤生长并延长三种已建立的小鼠肿瘤模型的寿命。三种组成上几乎相同但结构不同的 SNA 结构在交叉引发抗原特异性 CD8 T 细胞和提高随后的抗肿瘤免疫反应的能力方面存在显著差异。重要的是,最有效的结构是表现出最大抗原呈递和共刺激标记物表达同步的结构。在人乳头瘤病毒相关的 TC-1 模型中,用这种结构进行疫苗接种可提高总生存率,使 30%的小鼠的肿瘤完全消除,并赋予对肿瘤再挑战的治愈性保护,这与否则无法实现的免疫记忆一致。SNA 疫苗接种的抗肿瘤作用取决于抗原在 SNA 结构内的掺入方式,突出了这种纳米结构的模块化以及新疫苗的精心设计的潜力,从而定义了一种理性癌症疫苗学。

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