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DOI 10.1038/ncomms9244

Медицинская библиотека · Nature communications · 2015

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

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, Yun Kim Ji, Lee Jae-Ung, Hun Shin Jae, Kyun Kim Lark, Doh Junsang, Kim Hongtae, Lee Sang-Kyou, Bothwell Alfred L M, Suh Minah, Choi Je-Min

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

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.

Для цитирования: 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, Yun Kim Ji, Lee Jae-Ung, Hun Shin Jae, Kyun Kim Lark, Doh Junsang, Kim Hongtae, Lee Sang-Kyou, Bothwell Alfred L M, Suh Minah, Choi Je-Min. dNP2 is a blood-brain barrier-permeable peptide enabling ctCTLA-4 protein delivery to ameliorate experimental autoimmune encephalomyelitis.. Nature communications. 2015. DOI: 10.1038/ncomms9244.

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