[1]吴 勇 黄书岚.嵌合抗原受体T细胞治疗胶质母细胞瘤的研究进展[J].中国临床神经外科杂志,2021,26(01):43-45.[doi:10.13798/j.issn.1009-153X.2021.01.015]
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嵌合抗原受体T细胞治疗胶质母细胞瘤的研究进展()
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《中国临床神经外科杂志》[ISSN:1009-153X/CN:42-1603/TN]

卷:
26
期数:
2021年01期
页码:
43-45
栏目:
综述
出版日期:
2021-01-25

文章信息/Info

文章编号:
1009-153X(2021)01-0043-03
作者:
吴 勇 黄书岚
430060 武汉,武汉大学人民医院神经外科(吴 勇、黄书岚)
关键词:
胶质母细胞瘤嵌合抗原受体T细胞胶质瘤干细胞
分类号:
R 739.41; R 730.51
DOI:
10.13798/j.issn.1009-153X.2021.01.015
文献标志码:
A

参考文献/References:

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[7] Brown CE, Aguilar B, Starr R, et al. Optimization of IL13Rα2- targeted chimeric antigen receptor T cells for improved anti-tumor efficacy against glioblastoma [J]. Mol Ther,2018, 26(1): 31-44.
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[9] Keu KV, Witney TH, Yaghoubi S, et al. Reporter gene imag-ing of targeted T cell immunotherapy in recurrent glioma [J].Sci Transl Med, 2017, 9(373): 2196-2203.
[10] Villa GR, Mischel PS. Old player, new partner: EGFRVⅢ and cytokine receptor signaling in glioblastoma [J]. Nat Neurosci, 2016, 19(6): 765-767.
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[13] 郑 岩,谢甲贝,曹名波,等. EGFRvⅢ/CAR-T对EGFRvⅢ+ U87胶质瘤细胞和裸鼠移植瘤的特异性杀伤作用[J]. 中国肿瘤生物治疗杂志,2018,25(4):334-339.
[14] O’Rourke DM, Nasrallah MP, Desai A, et al. A single dose of peripherally infused EGFRVⅢ-directed CAR T cells mediates antigen loss and induces adaptive resistance in patients with recurrent glioblastoma [J]. Sci Transl Med, 2017, 9(399): 984-989.
[15] Felsberg J, Hentschel B, Kaulich K, et al. Epidermal growth factor receptor variantⅢ (EGFRVⅢ) positivity in egframp-lified glioblastomas: prognostic role and comparison between primary and recurrent tumors [J]. Clin Cancer Res, 2017, 23(22): 6846-6855.
[16] Rui Liu, Qu YP, Chen LH, et al. Genomic copy number gains of ErbB family members predict poor clinical out-comes in glioma patients [J]. Oncotarget, 2017, 8(54): 92275-92288.
[17] Morgan RA, Yang JC, Kitano M, et al. Case report of a seri-ous adverse event following the administration of T cells transduced with a chimeric antigen receptor recognizing ERBB2 [J]. Mol Ther, 2010, 18: 843-851.
[18] Ahmed N, Salsman VS, Kew Y, et al. HER2-specific T cellstarget primary glioblastoma stem cells and induce regressionof autologous experimental tumors [J]. Clin Cancer Res, 2010, 16(2): 474-485.
[19] Ahmed N, Brawley V, Hegde M, et al. HER2-specific chi-meric antigen receptor-modified virus-specific T cells for progressive glioblastoma: a phase 1 dose-escalation trial [J].JAMA Oncol, 2017, 3(8): 1094-1101.
[20] Hui M, Nickolas W, Hong G, et al. EphA2 promotes infil-trative invasion of glioma stem cells in vivo through cross-talk with akt and regulates stem properties [J]. Oncogene, 2015, 34(5): 558-567.
[21] Chow KK, Naik S, Kakarla S, et al. T cells redirected to EphA2 for the immunotherapy of glioblastoma[J]. Mol Ther,2013, 21(3): 629-637.
[22] Yi ZZ, Prinzing BL, Cao F, et al. Optimizing EphA2-CAR T Cells for the adoptive immunotherapy of glioma [J]. Mol Ther Methods Clin Dev, 2018, 9: 70-80.
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[25] 赵炜熠,初 明. 胶质瘤免疫抑制与治疗的研究进展[J]. 中国临床神经外科杂志,2018,23(3):212-214.
[26] Zheng Y, Gao N, Fu YL, et al. Generation of regulable EGFRVⅢ targeted chimeric antigen receptor T cells for adoptive cell therapy of glioblastoma [J]. Biochem Biophys Res Commun, 2018, 507(1-4): 59-66.

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备注/Memo

备注/Memo:
2019-01-03收稿
通讯作者:黄书岚,E-mail:donghufuyu@qq.com
更新日期/Last Update: 2021-01-25