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Neurooncol Adv. 2021 Aug 25;3(1):vdab118. doi: 10.1093/noajnl/vdab118. eCollection 2021 Jan-Dec.
2
Epigenetic scarring of exhausted T cells hinders memory differentiation upon eliminating chronic antigenic stimulation.耗竭的 T 细胞的表观遗传瘢痕阻碍了在消除慢性抗原刺激时记忆分化。
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A Phase I Study of APX005M and Cabiralizumab with or without Nivolumab in Patients with Melanoma, Kidney Cancer, or Non-Small Cell Lung Cancer Resistant to Anti-PD-1/PD-L1.APX005M 联合或不联合 Nivolumab 与 Cabiralizumab 治疗抗 PD-1/PD-L1 耐药的黑色素瘤、肾癌或非小细胞肺癌患者的 I 期研究
Clin Cancer Res. 2021 Sep 1;27(17):4757-4767. doi: 10.1158/1078-0432.CCR-21-0903. Epub 2021 Jun 17.
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Synergistic immunotherapy of glioblastoma by dual targeting of IL-6 and CD40.通过双重靶向白细胞介素 6 和 CD40 对胶质母细胞瘤进行协同免疫治疗。
Nat Commun. 2021 Jun 8;12(1):3424. doi: 10.1038/s41467-021-23832-3.
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Viral Gene Therapy for Glioblastoma Multiforme: A Promising Hope for the Current Dilemma.胶质母细胞瘤的病毒基因治疗:当前困境下的一线希望
Front Oncol. 2021 May 13;11:678226. doi: 10.3389/fonc.2021.678226. eCollection 2021.
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Targeting Treg cells with GITR activation alleviates resistance to immunotherapy in murine glioblastomas.靶向调节性 T 细胞(Treg)细胞表面的糖皮质激素诱导 TNF 受体(GITR)激活可缓解小鼠胶质母细胞瘤对免疫治疗的抵抗。
Nat Commun. 2021 May 11;12(1):2582. doi: 10.1038/s41467-021-22885-8.
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A vaccine targeting mutant IDH1 in newly diagnosed glioma.针对新诊断的神经胶质瘤中突变 IDH1 的疫苗。
Nature. 2021 Apr;592(7854):463-468. doi: 10.1038/s41586-021-03363-z. Epub 2021 Mar 24.
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J Thorac Oncol. 2021 Apr;16(4):665-676. doi: 10.1016/j.jtho.2020.12.019. Epub 2021 Jan 21.
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Adenosinergic Pathway: A Hope in the Immunotherapy of Glioblastoma.腺苷能通路:胶质母细胞瘤免疫治疗的希望
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胶质母细胞瘤中的免疫治疗耐药性

Immunotherapy Resistance in Glioblastoma.

作者信息

Wang Elaina J, Chen Jia-Shu, Jain Saket, Morshed Ramin A, Haddad Alexander F, Gill Sabraj, Beniwal Angad S, Aghi Manish K

机构信息

Department of Neurological Surgery, The Warren Alpert School of Medicine, Brown University, Providence, RI, United States.

Department of Neurological Surgery, University of California, San Francisco, San Francisco, CA, United States.

出版信息

Front Genet. 2021 Dec 17;12:750675. doi: 10.3389/fgene.2021.750675. eCollection 2021.

DOI:10.3389/fgene.2021.750675
PMID:34976006
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8718605/
Abstract

Glioblastoma is the most common malignant primary brain tumor in adults. Despite treatment consisting of surgical resection followed by radiotherapy and adjuvant chemotherapy, survival remains poor at a rate of 26.5% at 2 years. Recent successes in using immunotherapies to treat a number of solid and hematologic cancers have led to a growing interest in harnessing the immune system to target glioblastoma. Several studies have examined the efficacy of various immunotherapies, including checkpoint inhibitors, vaccines, adoptive transfer of lymphocytes, and oncolytic virotherapy in both pre-clinical and clinical settings. However, these therapies have yielded mixed results at best when applied to glioblastoma. While the initial failures of immunotherapy were thought to reflect the immunoprivileged environment of the brain, more recent studies have revealed immune escape mechanisms created by the tumor itself and adaptive resistance acquired in response to therapy. Several of these resistance mechanisms hijack key signaling pathways within the immune system to create a protumoral microenvironment. In this review, we discuss immunotherapies that have been trialed in glioblastoma, mechanisms of tumor resistance, and strategies to sensitize these tumors to immunotherapies. Insights gained from the studies summarized here may help pave the way for novel therapies to overcome barriers that have thus far limited the success of immunotherapy in glioblastoma.

摘要

胶质母细胞瘤是成人中最常见的原发性恶性脑肿瘤。尽管治疗方法包括手术切除,随后进行放疗和辅助化疗,但2年生存率仍很低,仅为26.5%。最近,利用免疫疗法治疗多种实体癌和血液癌取得了成功,这使得人们越来越有兴趣利用免疫系统来靶向胶质母细胞瘤。多项研究在临床前和临床环境中检验了各种免疫疗法的疗效,包括检查点抑制剂、疫苗、淋巴细胞过继转移和溶瘤病毒疗法。然而,这些疗法应用于胶质母细胞瘤时,充其量也只是取得了喜忧参半的结果。虽然免疫疗法最初的失败被认为反映了大脑的免疫豁免环境,但最近的研究揭示了肿瘤自身产生的免疫逃逸机制以及对治疗产生的适应性耐药性。其中一些耐药机制利用免疫系统内的关键信号通路来创建促肿瘤微环境。在这篇综述中,我们讨论了已在胶质母细胞瘤中进行试验的免疫疗法、肿瘤耐药机制以及使这些肿瘤对免疫疗法敏感的策略。从这里总结的研究中获得的见解可能有助于为新疗法铺平道路,以克服迄今为止限制免疫疗法在胶质母细胞瘤中取得成功的障碍。