Aberrant T-cell activation underlies many autoimmune disorders, yet most attempts to induce T-cell tolerance have failed. Building on previous strategies for tolerance induction that exploited natural mechanisms for clearing apoptotic debris, we show that antigen-decorated microparticles (500-nm diameter) induce long-term T-cell tolerance in mice with relapsing experimental autoimmune encephalomyelitis. Specifically, intravenous infusion of either polystyrene or biodegradable poly(lactide-co-glycolide) microparticles bearing encephalitogenic peptides prevents the onset and modifies the course of the disease. These beneficial effects require microparticle uptake by marginal zone macrophages expressing the scavenger receptor MARCO and are mediated in part by the activity of regulatory T cells, abortive T-cell activation and T-cell anergy. Together these data highlight the potential for using microparticles to target natural apoptotic clearance pathways to inactivate pathogenic T cells and halt the disease process in autoimmunity.

译文

异常的T细胞活化是许多自身免疫性疾病的基础,但大多数诱导T细胞耐受的尝试都失败了。在先前利用天然机制清除凋亡碎片的耐受性诱导策略的基础上,我们发现抗原修饰的微粒 (直径500 nm) 在患有复发性实验性自身免疫性脑脊髓炎的小鼠中诱导长期T细胞耐受性。具体来说,静脉内输注聚苯乙烯或可生物降解的带有脑源性肽的聚 (丙交酯-共-乙交酯) 微粒可防止发作并改变疾病的进程。这些有益作用需要表达清道夫受体MARCO的边缘区巨噬细胞摄取微粒,并且部分由调节性T细胞的活性,流产性T细胞活化和T细胞无反应性介导。这些数据共同强调了使用微粒靶向自然凋亡清除途径以使致病性T细胞失活并阻止自身免疫中的疾病过程的潜力。

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