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A DNA Microarray-based Analysis of the Host Response to a Nonviral Gene Carrier: A Strategy for Improving the Immune Response

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Please use this identifier to cite or link to this item:http://hdl.handle.net/2115/48250

Title: A DNA Microarray-based Analysis of the Host Response to a Nonviral Gene Carrier: A Strategy for Improving the Immune Response
Authors: Hatakeyama, Hiroto Browse this author
Ito, Erika Browse this author
Yamamoto, Momoko Browse this author
Akita, Hidetaka Browse this author
Hayashi, Yasuhiro Browse this author
Kajimoto, Kazuaki Browse this author
Kaji, Noritada Browse this author
Baba, Yoshinobu Browse this author
Harashima, Hideyoshi Browse this author
Issue Date: Aug-2011
Publisher: Nature Publishing
Journal Title: Molecular Therapy
Volume: 19
Issue: 8
Start Page: 1487
End Page: 1498
Publisher DOI: 10.1038/mt.2011.24
Abstract: The purpose of this study was to investigate the host response to systemically administered lipid nanoparticles (NPs) encapsulating pDNA in the spleen using a DNA microarray. As a model for NPs, we used a Multifunctional envelope-type nano device (MEND). Microarray analysis revealed that 1581 of the differentially expressed genes could be identified by PEG-unmodified NP using a 3-fold change relative to the control. As the result of PEGylation, the NP treatment resulted in the reduction in the expression of most of the genes. However, the expression of type I interferon (IFN) was specifically increased by PEGylation. Based on the microarray and a pathway analysis, we hypothesize that PEGylation inhibited the endosomal escape of NP, and extended the interaction of TLR9 with CpG-DNA accompanied by the production of type I IFN. This hypothesis was tested by introducing a pH-sensitive fusogenic peptide, GALA, which enhances the endosomal escape of PEGylated NP. As expected, type I IFN was reduced and IL-6 remained at the baseline. These findings indicate that a carrier design based on microarray analysis and the manipulation of intracellular trafficking constitutes a rational strategy for reducing the host immune response to NPs.
Type: article (author version)
URI: http://hdl.handle.net/2115/48250
Appears in Collections:薬学研究院 (Faculty of Pharmaceutical Sciences) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 畠山 浩人

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