Tuning CpG motif position in nanostructured DNA for efficient immune stimulation

Author:

Tan Mengmeng1,Makiguchi Natsuki2,Kusamori Kosuke2ORCID,Itakura Shoko2,Takahashi Yuki1,Takakura Yoshinobu1,Nishikawa Makiya2ORCID

Affiliation:

1. Department of Biopharmaceutics and Drug Metabolism Graduate School of Pharmaceutical Sciences Kyoto University Kyoto Japan

2. Laboratory of Biopharmaceutics Faculty of Pharmaceutical Sciences Tokyo University of Science Noda Chiba Japan

Abstract

AbstractIt was previously demonstrated that polypod‐like nanostructured DNA (polypodna) comprising three or more oligodeoxynucleotides (ODNs) were useful for the delivery of ODNs containing cytosine–phosphate–guanine (CpG) motifs, or CpG ODNs, to immune cells. Although the immunostimulatory activity of single‐stranded CpG ODNs is highly dependent on CpG motif sequence and position, little is known about how the position of the motif affects the immunostimulatory activity of CpG motif‐containing nanostructured DNAs. In the present study, four series of polypodna were designed, each comprising a CpG ODN with one potent CpG motif at varying positions and 2–5 CpG‐free ODNs, and investigated their immunostimulatory activity using Toll‐like receptor‐9 (TLR9)‐positive murine macrophage‐like RAW264.7 cells. Polypodnas with the CpG motif in the 5′‐overhang induced more tumor necrosis factor‐α release than those with the motif in the double‐stranded region, even though their cellular uptake were similar. Importantly, the rank order of the immunostimulatory activity of single‐stranded CpG ODNs changed after their incorporation into polypodna. These results indicate that the CpG ODN sequence as well as the motif location in nanostructured DNAs should be considered for designing the CpG motif‐containing nanostructured DNAs for immune stimulation.

Funder

Japan Society for the Promotion of Science

Publisher

Wiley

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