Department of Chemistry and the International Institute for Nanotechnology, Northwestern University , Evanston, Illinois 60208, United States.
Interdisciplinary Biological Sciences Graduate Program, Northwestern University , Evanston, Illinois 60208, United States.
J Am Chem Soc. 2018 Jan 31;140(4):1227-1230. doi: 10.1021/jacs.7b12579. Epub 2018 Jan 22.
Spherical nucleic acids (SNAs) can be potent sequence-specific stimulators of antigen presenting cells (APCs). When loaded with peptide antigens, they can be used to activate the immune system to train T-cells to specifically kill cancer cells. Herein, the role of peptide chemical conjugation to the DNA, which is used to load SNAs with antigens via hybridization, is explored in the context of APC activation. Importantly, though the antigen chemistry does not impede TLR-9 regulated APC activation, it significantly augments the downstream T-cell response in terms of both activation and proliferation. A comparison of three linker types, (1) noncleavable, (2) cleavable but nontraceless, and (3) traceless, reveals up to an 8-fold improvement in T-cell proliferation when the traceless linker is used. This work underscores the critical importance of the choice of conjugation chemistry in vaccine development.
球形核酸(SNAs)可以作为抗原呈递细胞(APCs)的强有力的序列特异性刺激物。当负载肽抗原时,它们可以被用来激活免疫系统,训练 T 细胞特异性杀死癌细胞。本文探讨了在 APC 激活的背景下,将肽化学连接物与 DNA 结合的作用,该 DNA 用于通过杂交将 SNAs 加载抗原。重要的是,尽管抗原化学不会阻碍 TLR-9 调节的 APC 激活,但它在激活和增殖方面显著增强了下游 T 细胞反应。对三种连接体类型(1)不可裂解、(2)可裂解但无痕迹和(3)无痕迹的比较表明,当使用无痕迹连接体时,T 细胞增殖提高了 8 倍。这项工作强调了在疫苗开发中选择缀合化学的重要性。