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dNP2 is a blood-brain barrier-permeable peptide enabling ctCTLA-4 protein delivery to ameliorate experimental autoimmune encephalomyelitis

Cited 79 time in Web of Science Cited 91 time in Scopus
Authors

Lim, Sangho; Kim, Won-Ju; Kim, Yeon-Ho; Lee, Sohee; Koo, Ja-Hyun; Lee, Jung-Ah; Yoon, Heeseok; Kim, Do-Hyun; Park, Hong-Jai; Kim, Hye-Mi; Lee, Hong-Gyun; Kim, Ji Yun; Lee, Jae-Ung; Shin, Jae Hun; Kim, Lark Kyun; Doh, Junsang; Kim, Hongtae; Lee, Sang-Kyou; Bothwell, Alfred L. M.; Suh, Minah; Choi, Je-Min

Issue Date
2015-09
Publisher
Nature Publishing Group
Citation
Nature Communications, Vol.6
Abstract
Central nervous system (CNS)-infiltrating effector T cells play critical roles in the development and progression of multiple sclerosis (MS). However, current drugs for MS are very limited due to the difficulty of delivering drugs into the CNS. Here we identify a cell-permeable peptide, dNP2, which efficiently delivers proteins into mouse and human T cells, as well as various tissues. Moreover, it enters the brain tissue and resident cells through blood vessels by penetrating the tightly organized blood-brain barrier. The dNP2-conjugated cytoplasmic domain of cytotoxic T-lymphocyte antigen 4 (dNP2-ctCTLA-4) negatively regulates activated T cells and shows inhibitory effects on experimental autoimmune encephalomyelitis in both preventive and therapeutic mouse models, resulting in the reduction of demyelination and CNS-infiltrating T helper 1 and T helper 17 cells. Thus, this study demonstrates that dNP2 is a blood-brain barrier-permeable peptide and dNP2-ctCTLA-4 could be an effective agent for treating CNS inflammatory diseases such as MS.
URI
https://hdl.handle.net/10371/203479
DOI
https://doi.org/10.1038/ncomms9244
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  • College of Engineering
  • Department of Materials Science & Engineering
Research Area Ex Vivo Models, Lymphocyte Biology, Smart Biomaterials

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