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Harnessing the properties of dendritic cells in the pursuit of immunological tolerance

机译:利用树突状细胞的特性追求免疫耐受

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摘要

The acquisition of self-perpetuating, immunological tolerance specific for graft alloantigens has long been described as the “holy grail” of clinical transplantation. By removing the need for life-long immunosuppression following engraftment, the adverse consequences of immunosuppressive regimens, including chronic infections and malignancy, may be avoided. Furthermore, autoimmune diseases and allergy are, by definition, driven by aberrant immunological responses to ordinarily innocuous antigens. The re-establishment of permanent tolerance towards instigating antigens may, therefore, provide a cure to these common diseases. Whilst various cell types exhibiting a tolerogenic phenotype have been proposed for such a task, tolerogenic dendritic cells (tol-DCs) are exquisitely adapted for antigen presentation and interact with many facets of the immune system: as such, they are attractive candidates for use in strategies for immune intervention. We review here our current understanding of tol-DC mediated induction and maintenance of immunological tolerance. Additionally, we discuss recent in vitro findings from animal models and clinical trials of tol-DC immunotherapy in the setting of transplantation, autoimmunity and allergy which highlight their promising therapeutic potential, and speculate how tol-DC therapy may be developed in the future.
机译:长期以来,获得针对移植同种异体抗原的自身永续的免疫耐受性一直被认为是临床移植的“圣杯”。通过消除移植后终身免疫抑制的需要,可以避免免疫抑制方案的不利后果,包括慢性感染和恶性肿瘤。此外,根据定义,自身免疫性疾病和变态反应是由对通常无害抗原的异常免疫反应所驱动。因此,对诱导抗原的永久耐受性的重建可以为这些常见疾病提供治愈方法。尽管已经提出了多种表现出致耐受性表型的细胞类型用于此任务,但是致耐受性树突状细胞(tol-DC)非常适合于抗原呈递并与免疫系统的许多方面相互作用:同样,它们是有吸引力的候选物,可用于免疫干预策略。我们在这里回顾我们目前对tol-DC介导的诱导和维持免疫耐受的理解。此外,我们讨论了动物模型的最新体外研究结果以及tol-DC免疫疗法在移植,自身免疫和变态反应方面的临床研究,这些研究突显了它们有希望的治疗潜力,并推测了将来如何开发tol-DC疗法。

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