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Inducing tissue specific tolerance in autoimmune disease with tolerogenic dendritic cells

机译:耐受性树突状细胞在自身免疫性疾病中诱导组织特异性耐受

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摘要

Current immunosuppressive therapy acts systemically, causing collateral damage and does not necessarily cope with the cause of rheumatoid arthritis. Tissue specific immune modulation may restore tolerance in patients with autoimmune diseases such as RA, but desires knowledge on relevant target autoantigens. We present the case of type 1 diabetes as prototype autoimmune disease with established autoantigens to set the stage for tissue-specific immune modulation using tolerogenic dendritic cells pulsed with autoantigen in RA. This approach induces autoantigen-specific regulatory T cells that exert their tissue-specific action through a combination of linked suppression and infectious tolerance, introducing a legacy of targeted, localised immune regulation in the proximity of the lesion. Several trials are in progress in RA employing various types of tolerogenic DCs. With knowledge on mode of action and confounding effects of concomitant immunosuppressive therapy, this strategy may provide novel immune intervention that may also prevent RA in high-risk subjects.
机译:当前的免疫抑制疗法具有全身作用,引起附带损害,并不一定能解决类风湿关节炎的病因。组织特异性免疫调节可恢复患有自身免疫性疾病(例如RA)的患者的耐受性,但需要了解相关靶标自身抗原。我们目前以已建立的自身抗原为原型自身免疫疾病的1型糖尿病病例,为在RA中使用自身抗原脉冲的耐受性树突状细胞为组织特异性免疫调节奠定基础。这种方法诱导了自身抗原特异性调节性T细胞,它们通过连锁抑制和感染耐受性的结合发挥其组织特异性作用,在病变附近引入了靶向的,局部免疫调节的遗留物。使用各种类型的致耐受性DC的RA正在进行多项试验。有了关于作用方式的知识以及伴随的免疫抑制疗法的混杂效应,该策略可以提供新颖的免疫干预措施,也可以预防高危受试者的RA。

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