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吲哚胺2,3-双加氧酶、肿瘤诱导的耐受性及反调节

Indoleamine 2,3-dioxygenase, tumor-induced tolerance and counter-regulation.

作者信息

Munn David H

机构信息

Immunotherapy Center and Department of Pediatrics, Medical College of Georgia, Augusta, Georgia 30912, USA.

出版信息

Curr Opin Immunol. 2006 Apr;18(2):220-5. doi: 10.1016/j.coi.2006.01.002. Epub 2006 Feb 7.

Abstract

Tumors create an abnormal state of tolerance toward themselves and their antigens. One mechanism that might contribute to this tolerance is the immunoregulatory enzyme indoleamine 2,3-dioxygenase (IDO). IDO-expressing antigen-presenting cells are found in tumor-draining lymph nodes, where they can create a tolerogenic microenvironment. IDO can also be expressed within the tumor itself, by tumor cells or host stromal cells, where it can inhibit the effector phase the immune response. Finally, emerging evidence suggests that IDO might also constitute a significant counter-regulatory mechanism, induced by clinically relevant pro-inflammatory signals, such as IFN-gamma, IFN-alpha, CpG oligodeoxynucleotides, and 4-1BB ligation. Strategies to inhibit the IDO pathway may thus assist in breaking tolerance to tumors, and might enhance the efficacy of other immunotherapy strategies by removing unwanted counter-regulation.

摘要

肿瘤会对自身及其抗原产生一种异常的耐受状态。吲哚胺2,3-双加氧酶(IDO)这种免疫调节酶可能是导致这种耐受的一种机制。在肿瘤引流淋巴结中可发现表达IDO的抗原呈递细胞,它们能营造一个促耐受性微环境。IDO也可在肿瘤自身内部由肿瘤细胞或宿主基质细胞表达,在那里它能抑制免疫反应的效应阶段。最后,新出现的证据表明,IDO可能还是一种由临床相关促炎信号(如γ干扰素、α干扰素、CpG寡脱氧核苷酸和4-1BB连接)诱导产生的重要负调节机制。因此,抑制IDO途径的策略可能有助于打破对肿瘤的耐受性,并且可能通过消除不必要的负调节来增强其他免疫治疗策略的疗效。

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