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Nat Commun ; 6: 8244, 2015 Sep 15.
Artigo em Inglês | MEDLINE | ID: mdl-26372309

RESUMO

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.


Assuntos
Barreira Hematoencefálica/metabolismo , Antígeno CTLA-4/imunologia , Proteínas de Transporte/metabolismo , Peptídeos Penetradores de Células/metabolismo , Encefalomielite Autoimune Experimental/imunologia , Linfócitos T/imunologia , Animais , Modelos Animais de Doenças , Células HeLa , Humanos , Técnicas In Vitro , Células Jurkat , Camundongos , Camundongos Endogâmicos C57BL , Fragmentos de Peptídeos/metabolismo , Células Th17/imunologia , Ubiquitina-Proteína Ligases/metabolismo
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