Puccetti Paolo
Department of Experimental Medicine, University of Perugia, Perugia, Italy.
Eur J Immunol. 2007 Apr;37(4):876-9. doi: 10.1002/eji.200737184.
A series of recent studies, including an article in this issue of the European Journal of Immunology, have demonstrated that the immunoregulatory pathway of tryptophan catabolism, initiated by the enzyme indoleamine 2,3-dioxygenase (IDO), not only represents an effector mechanism of peripheral tolerance, but is also a critical participant in the promotion of an optimally protective immune response balanced between inflammation and tolerance. Although subjected to transcriptional regulation by type I/II IFN, IDO is itself required for the production of type I IFN in response to B7 signaling in CD19(+) DC. Such a bidirectional feedback loop could be part of an integrated response for preventing excessive inflammation and autoimmunity.
包括本期《欧洲免疫学杂志》上一篇文章在内的一系列近期研究表明,由吲哚胺2,3-双加氧酶(IDO)启动的色氨酸分解代谢免疫调节途径,不仅代表外周耐受的效应机制,也是促进炎症与耐受之间平衡的最佳保护性免疫反应的关键参与者。尽管IDO受I型/II型干扰素的转录调控,但IDO本身是CD19(+)树突状细胞(DC)中响应B7信号产生I型干扰素所必需的。这种双向反馈回路可能是预防过度炎症和自身免疫的综合反应的一部分。