Munn David H, Mellor Andrew L
Immunotherapy Program, Department of Pediatrics, MCG Cancer Center, Medical College of Georgia, Augusta, GA 30912, USA.
J Clin Invest. 2007 May;117(5):1147-54. doi: 10.1172/JCI31178.
Tumors arise from normal cells of the body through genetic mutation. Although such genetic mutation often leads to the expression of abnormal antigens, the immune system fails to respond effectively to these antigens; that is, it is tolerant of these antigens. This acquired state of tolerance must be overcome for cancer immunotherapy to succeed. Indoleamine 2,3-dioxygenase (IDO) is one molecular mechanism that contributes to tumor-induced tolerance. IDO helps create a tolerogenic milieu in the tumor and the tumor-draining lymph nodes, both by direct suppression of T cells and enhancement of local Treg-mediated immunosuppression. It can also function as an antagonist to other activators of antitumor immunity. Therefore, strategies to block IDO might enhance the effectiveness of tumor immunotherapy.
肿瘤是通过基因突变从机体的正常细胞产生的。尽管这种基因突变常常导致异常抗原的表达,但免疫系统却无法对这些抗原做出有效反应;也就是说,免疫系统对这些抗原具有耐受性。癌症免疫疗法若要取得成功,就必须克服这种获得性耐受状态。吲哚胺2,3-双加氧酶(IDO)是导致肿瘤诱导耐受的一种分子机制。IDO通过直接抑制T细胞以及增强局部调节性T细胞介导的免疫抑制作用,有助于在肿瘤和肿瘤引流淋巴结中营造一种致耐受的微环境。它还可以作为抗肿瘤免疫其他激活剂的拮抗剂发挥作用。因此,阻断IDO的策略可能会提高肿瘤免疫疗法的有效性。