吲哚胺2,3-双加氧酶:骨肉瘤新的免疫治疗靶点。

Asim Farooq, Bilal Zulfiqar, Kashif Asghar
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引用次数: 0

摘要

肿瘤释放的分子在肿瘤微环境中诱导免疫抑制。一种免疫抑制酶,吲哚胺2,3-双加氧酶(IDO/IDO1),促进了包括骨肉瘤在内的几种恶性肿瘤的免疫逃逸。IDO的上调在肿瘤和肿瘤引流淋巴结中建立了耐受性环境。ido诱导的效应t细胞的下调和局部调节性t细胞的上调产生免疫抑制并促进转移。观察:骨肉瘤是最常见的骨肿瘤,其特征是肿瘤细胞形成未成熟的骨。近20%的骨肉瘤患者在诊断时出现肺转移。二十年来,骨肉瘤治疗方式的改进一直处于停滞阶段。因此,开发新的骨肉瘤免疫治疗靶点势在必行。IDO高表达与骨肉瘤患者的转移和预后不良有关。结论及意义:目前关于IDO在骨肉瘤中的作用的研究较少。本文综述了IDO不仅作为预后标志物,而且作为骨肉瘤免疫治疗靶点的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Indoleamine 2,3-Dioxygenase: A Novel Immunotherapeutic Target for Osteosarcoma.

Indoleamine 2,3-Dioxygenase: A Novel Immunotherapeutic Target for Osteosarcoma.

Indoleamine 2,3-Dioxygenase: A Novel Immunotherapeutic Target for Osteosarcoma.

Introduction: Tumour-emitted molecules induce immunosuppression in the tumour microenvironment. An immunosuppressive enzyme, indoleamine 2,3-dioxygenase (IDO/IDO1), facilitates immune escape in several malignant tumours, including osteosarcoma. Upregulation of IDO establishes a tolerogenic environment in the tumour and the tumour-draining lymph nodes. IDO-induced downregulation of effector T-cells and upregulation of local regulatory T-cells creates immunosuppression and promotes metastasis.

Observations: Osteosarcoma is the most common bone tumour characterised by immature bone formation by the tumour cells. Almost 20% of osteosarcoma patients present with pulmonary metastasis at the time of diagnosis. The improvement in therapeutic modalities for osteosarcoma has been in a stagnant phase for two decades. Therefore, the development of novel immunotherapeutic targets for osteosarcoma is emergent. High IDO expression is associated with metastasis and poor prognosis in osteosarcoma patients.

Conclusion and relevance: At present, only a few studies are available describing IDO's role in osteosarcoma. This review describes the prospects of IDO not only as a prognostic marker but also as an immunotherapeutic target for osteosarcoma.

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