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

机译:dNP2是一种血脑屏障渗透性肽能够传递ctCTLA-4蛋白从而改善实验性自身免疫性脑脊髓炎

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摘要

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.
机译:浸润中枢神经系统(CNS)的效应T细胞在多发性硬化症(MS)的发生和发展中起关键作用。然而,由于难以将药物输送到CNS中,目前用于MS的药物非常有限。在这里,我们确定了一种可渗透细胞的肽dNP2,该肽可将蛋白质有效地传递到小鼠和人类T细胞以及各种组织中。此外,它穿透了组织严密的血脑屏障,通过血管进入脑组织和驻留细胞。细胞毒性T淋巴细胞抗原4(dNP2-ctCTLA-4)的dNP2缀合的胞质域负调控活化的T细胞,在预防和治疗小鼠模型中均对实验性自身免疫性脑脊髓炎具有抑制作用,从而导致脱髓鞘和CNS-减少浸润T辅助细胞1和T辅助细胞17。因此,这项研究表明,dNP2是一种血脑屏障渗透肽,而dNP2-ctCTLA-4可能是治疗MS等中枢神经系统炎症性疾病的有效药物。

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