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胶质母细胞瘤治疗中免疫疗法的进展。

Advances in immunotherapy for the treatment of glioblastoma.

作者信息

Tivnan Amanda, Heilinger Tatjana, Lavelle Ed C, Prehn Jochen H M

机构信息

Department of Physiology and Medical Physics and RCSI Centre for Systems Medicine, Royal College of Surgeons in Ireland, 123 St. Stephen's Green, Dublin 2, Ireland.

IMC Fachhochschule Krems, University of Applied Sciences, Piaristengasse 1, 3500, Krems, Austria.

出版信息

J Neurooncol. 2017 Jan;131(1):1-9. doi: 10.1007/s11060-016-2299-2. Epub 2016 Oct 14.

Abstract

Glioblastoma (GBM) is an aggressive brain tumour, associated with extremely poor prognosis and although there have been therapeutic advances, treatment options remain limited. This review focuses on the use of immunotherapy, harnessing the power of the host's immune system to reject cancer cells. Key challenges in glioma specific immunotherapy as with many other cancers are the limited immunogenicity of the cancer cells and the immunosuppressive environment of the tumour. Although specific antigens have been identified in several cancers; brain tumours, such as GBM, are considered poorly immunogenic. However, as detailed in this review, strategies aimed at circumventing these challenges are showing promise for GBM treatment; including identification of glioma specific antigens and endogenous immune cell activation in an attempt to overcome the immunosuppressive environment which is associated with GBM tumours. An up-to-date summary of current Phase I/II and ongoing Phase III GBM immunotherapy clinical trials is provided in addition to insights into promising preclinical approaches which are focused predominantly on increased induction of Type 1 helper T cell (T1) immune responses within patients.

摘要

胶质母细胞瘤(GBM)是一种侵袭性脑肿瘤,预后极差。尽管在治疗方面取得了进展,但治疗选择仍然有限。本综述重点关注免疫疗法的应用,即利用宿主免疫系统的力量来排斥癌细胞。与许多其他癌症一样,胶质瘤特异性免疫疗法的关键挑战在于癌细胞的免疫原性有限以及肿瘤的免疫抑制环境。尽管在几种癌症中已鉴定出特定抗原,但脑肿瘤,如GBM,被认为免疫原性较差。然而,正如本综述中所详述的,旨在规避这些挑战的策略对GBM治疗显示出前景;包括鉴定胶质瘤特异性抗原和激活内源性免疫细胞,以试图克服与GBM肿瘤相关的免疫抑制环境。除了对有前景的临床前方法的见解外,还提供了当前I/II期和正在进行的III期GBM免疫疗法临床试验的最新总结,这些方法主要集中在增强患者体内1型辅助性T细胞(T1)免疫反应的诱导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17ad/5258809/8dd8120057db/11060_2016_2299_Fig1_HTML.jpg

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