| Literature DB >> 25502904 |
Yeqin Wang1, Yoshinari Yamamoto2, Suguru Shigemori3, Takafumi Watanabe2, Kazushi Oshiro2, Xinyu Wang2, Pengfei Wang2, Takashi Sato4, Shinichi Yonekura5, Sachi Tanaka6, Haruki Kitazawa7, Takeshi Shimosato8.
Abstract
Here, we report a simple and low-cost oral oligodeoxynucleotide (ODN) delivery system targeted to the gut Peyer's patches (PPs). This system requires only Dulbecco's modified eagle's medium, calcium chloride, ODNs, and basic laboratory equipment. ODN nanocapsules (ODNcaps) were directly delivered to the PPs through oral administration and were taken up by macrophages in the PPs, where they induced an immune response. Long-term continuous oral dosing with inhibitory/suppressive ODNcaps (iODNcaps, "iSG3caps" in this study) was evaluated using an atopic dermatitis mouse model to visually monitor disease course. Administration of iSG3caps improved skin lesions and decreased epidermal thickness. Underlying this effect is the ability of iSG3 to bind to and prevent phosphorylation of signal transducer and activator of transcription 6, thereby blocking the interleukin-4 signaling cascade mediated by binding of allergens to type 2 helper T cells. The results of our iSG3cap oral delivery experiments suggest that iSG3 may be useful for treating allergic diseases.Entities:
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Year: 2014 PMID: 25502904 PMCID: PMC4445625 DOI: 10.1038/mt.2014.239
Source DB: PubMed Journal: Mol Ther ISSN: 1525-0016 Impact factor: 11.454