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用于癌症治疗的吲哚胺-2,3-双加氧酶抑制剂:我们能见树又见林吗?

Inhibitors of indoleamine-2,3-dioxygenase for cancer therapy: can we see the wood for the trees?

作者信息

Löb Stefan, Königsrainer Alfred, Rammensee Hans-Georg, Opelz Gerhard, Terness Peter

机构信息

Department of General, Visceral and Transplant Surgery, University Hospital of Tubingen, Hoppe-Seyler-Strasse 3, Tubingen, Germany.

出版信息

Nat Rev Cancer. 2009 Jun;9(6):445-52. doi: 10.1038/nrc2639.

Abstract

Indoleamine-2,3-dioxygenase (IDO) is an immunosuppressive enzyme capable of inhibiting a destructive maternal T cell response against allogeneic fetuses. Expression of IDO is evident in tumours and is thought to enable escape from immunologically mediated rejection. Consequently, clinical trials using an inhibitor of IDO, 1-methyltryptophan (1MT), have been initiated. However, a review of the current literature indicates that we are far from understanding the biological relevance of IDO expression during tumorigenesis. A better understanding of IDO biology is needed to comprehend the effect of IDO inhibitors and to provide a rationale for their therapeutic application in cancer.

摘要

吲哚胺-2,3-双加氧酶(IDO)是一种免疫抑制酶,能够抑制母体针对同种异体胎儿的破坏性T细胞反应。IDO在肿瘤中表达明显,被认为有助于逃避免疫介导的排斥反应。因此,已经启动了使用IDO抑制剂1-甲基色氨酸(1MT)的临床试验。然而,对当前文献的综述表明,我们远未理解IDO在肿瘤发生过程中表达的生物学相关性。需要更好地了解IDO生物学,以理解IDO抑制剂的作用,并为其在癌症治疗中的应用提供理论依据。

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