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吲哚胺2,3双加氧酶与肿瘤免疫耐受

Indoleamine 2,3-dioxygenase and immune tolerance in tumor
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摘要 调节性T细胞(Treg)介导的克隆抑制,是引起肿瘤免疫耐受的主要因素之一。而吲哚胺2,3双加氧酶(IDO)通过对Treg细胞的作用下调各系统肿瘤微环境中的免疫反应,从而诱导宿主免疫耐受的形成。IDO抑制剂1-MT将有望成为治疗肿瘤的新靶点。 Clonal suppression induced by CD4 ^+ CD25 ^+ regulatory T cells is one of the principal factors to evoke the immune tolerance in tumor. Through the activation of CD^4+ CD25 ^+ regulatory T cells, the indoleamine 2,3-dioxygenase (IDO) reduces the immune response in tumor micro-environment of various systems, and induces the formation of host immune tolerance. IDO inhibitor 1 - MT is expected to become a new target for cancer treatment.
出处 《国际肿瘤学杂志》 CAS 2010年第4期276-278,共3页 Journal of International Oncology
关键词 肿瘤 免疫耐受 吲哚胺-吡咯2 3-双加氧酶 CD4^+CD25^+T细胞 Neoplasms Immune tolerance Indoleamine-pyrrole 2,3-dioxygenase CD4^+CD25^+ T cells
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  • 1Uyttenhove C,Pilotte L,Theate I,et al.Evidence for a tumoral immune resistance mechanism based on tryptophan degradation by indoleamine 2,3-dioxygenase.Nat Med,2003;9:1269-1274
  • 2Sakurai K,Enomoto K,Amano S,et al.Study of indoleamine 2,3-dioxygenase expression in patients of esophageal squamous cell carcinoma.Gan To Kagaku Ryoho,2004;31:1780-1782
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  • 4Munn DH,Mellor AL.IDO and tolerance to tumors.Trends Mol Med,2004;10:15-18

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